8-146017140-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017140
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017140
    reference: chr 8
allele count: 1
allele frequency: 8.286651861182008e-6
allele num: 120676
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.199+95G>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.280+18G>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.280+18G>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.280+18G>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.187+18G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.280+18G>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.322G>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.166+18G>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.365G>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.280+18G>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.280+18G>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.138+237G>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.26-260G>A
  variant of: http://identifiers.org/hgnc/10368
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12028
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28443
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

8-146017142-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017142
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017142
    reference: chr 8
allele count: 1
allele frequency: 8.284317786430287e-6
allele num: 120710
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.280+16G>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.280+16G>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.187+16G>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.26-262G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.280+16G>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.280+16G>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.320G>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.166+16G>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.280+16G>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.363G>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.280+16G>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.199+93G>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.138+235G>A
  variant of: http://identifiers.org/hgnc/10368
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2466
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28496
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12040
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

8-146017149-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017149
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017149
    reference: chr 8
allele count: 2
allele frequency: 1.655985559805918e-5
allele num: 120774
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.280+9C>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.187+9C>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.199+86C>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.280+9C>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.313C>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.26-269C>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.138+228C>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.166+9C>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.280+9C>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.280+9C>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.356C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.280+9C>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.280+9C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13101
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12050
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-146017159-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017159
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017159
    reference: chr 8
allele count: 1
allele frequency: 8.277186418792524e-6
allele num: 120814
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.199+76G>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.186G>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.279G>C
  hgvsp: ENSP00000433703.1:p.Lys93Asn
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.279G>C
  hgvsp: ENSP00000434535.1:p.Lys93Asn
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.279G>C
  hgvsp: ENSP00000433464.2:p.Lys93Asn
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.279G>C
  hgvsp: ENSP00000378378.2:p.Lys93Asn
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.279G>C
  hgvsp: ENSP00000262584.3:p.Lys93Asn
  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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.346G>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.303G>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.165G>C
  hgvsp: ENSP00000437062.1:p.Arg56Thr
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.279G>C
  hgvsp: ENSP00000435313.1:p.Lys93Asn
  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.26-279G>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.138+218G>C
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28625
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13118
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys93Asn
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

8-146017159-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017159
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017159
    reference: chr 8
allele count: 1
allele frequency: 8.277186418792524e-6
allele num: 120814
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.186G>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.303G>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.346G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.279G>A
  hgvsp: ENST00000532702.1:c.279G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.279G>A
  hgvsp: ENST00000394920.2:c.279G>A(p.%3D)
  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.199+76G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.279G>A
  hgvsp: ENST00000262584.3:c.279G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.165G>A
  hgvsp: ENSP00000437062.1:p.Arg56Lys
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.279G>A
  hgvsp: ENST00000533397.1:c.279G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.279G>A
  hgvsp: ENST00000528957.1:c.279G>A(p.%3D)
  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.138+218G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.279G>A
  hgvsp: ENST00000529920.1:c.279G>A(p.%3D)
  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.26-279G>A
  variant of: http://identifiers.org/hgnc/10368
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12052
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13118
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28625
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg56Lys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

8-146017163-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017163
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017163
    reference: chr 8
allele count: 1
allele frequency: 8.276775368316504e-6
allele num: 120820
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.275A>G
  hgvsp: ENSP00000378378.2:p.Lys92Arg
  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.275A>G
  hgvsp: ENSP00000262584.3:p.Lys92Arg
  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.182A>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.26-283A>G
  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.275A>G
  hgvsp: ENSP00000433464.2:p.Lys92Arg
  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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.342A>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.275A>G
  hgvsp: ENSP00000435313.1:p.Lys92Arg
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.275A>G
  hgvsp: ENSP00000434535.1:p.Lys92Arg
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.275A>G
  hgvsp: ENSP00000433703.1:p.Lys92Arg
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.161A>G
  hgvsp: ENSP00000437062.1:p.Arg55Gly
  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.138+214A>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.299A>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.199+72A>G
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13108
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys92Arg
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

8-146017171-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017171
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017171
    reference: chr 8
allele count: 3295
allele frequency: 2.727062056179961e-2
allele num: 120826
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.267T>C
  hgvsp: ENST00000533397.1:c.267T>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.291T>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.199+64T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.267T>C
  hgvsp: ENST00000529920.1:c.267T>C(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.267T>C
  hgvsp: ENST00000528957.1:c.267T>C(p.%3D)
  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.26-291T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.153T>C
  hgvsp: ENSP00000437062.1:p.Ile52Thr
  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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.334T>C
  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.267T>C
  hgvsp: ENST00000262584.3:c.267T>C(p.%3D)
  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.138+206T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.267T>C
  hgvsp: ENST00000532702.1:c.267T>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.267T>C
  hgvsp: ENST00000394920.2:c.267T>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.174T>C
  variant of: http://identifiers.org/hgnc/10368
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 12838
  bin: 2.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 3.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.25e1
  variant carriers: 139
genotype depth: GenotypeDepth
  all individuals: 11736
  bin: 3.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 28385
  bin: 2.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 81
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 9.75e1
  variant carriers: 2199
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.75e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 4.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 5.75e1
  variant carriers: 54
genotype quality: GenotypeQuality
hgvs: p.Ile52Thr
num of homozygotes: 103
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum

8-146017180-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017180
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017180
    reference: chr 8
allele count: 1300
allele frequency: 1.076426264800861e-2
allele num: 120770
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.258G>A
  hgvsp: ENST00000533397.1:c.258G>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.258G>A
  hgvsp: ENST00000394920.2:c.258G>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.258G>A
  hgvsp: ENST00000262584.3:c.258G>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: ENST00000526668
  gene symbol: RPL8
  hgvsc: ENST00000526668.1:n.165G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.258G>A
  hgvsp: ENST00000529920.1:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.144G>A
  hgvsp: ENSP00000437062.1:p.Ser49Asn
  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.138+197G>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.282G>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.258G>A
  hgvsp: ENST00000528957.1:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.258G>A
  hgvsp: ENST00000532702.1:c.258G>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.325G>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.199+55G>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.26-300G>A
  variant of: http://identifiers.org/hgnc/10368
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 29911
  bin: 2.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12305
  bin: 3.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 9.75e1
  variant carriers: 754
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 5.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 13264
  bin: 2.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 4.25e1
  variant carriers: 20
genotype quality: GenotypeQuality
hgvs: p.Ser49Asn
num of homozygotes: 80
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

8-146017181-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017181
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017181
    reference: chr 8
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.257A>G
  hgvsp: ENSP00000378378.2:p.Gln86Arg
  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.164A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.257A>G
  hgvsp: ENSP00000433703.1:p.Gln86Arg
  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.257A>G
  hgvsp: ENSP00000433464.2:p.Gln86Arg
  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.26-301A>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.257A>G
  hgvsp: ENSP00000435313.1:p.Gln86Arg
  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.257A>G
  hgvsp: ENSP00000262584.3:p.Gln86Arg
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.143A>G
  hgvsp: ENSP00000437062.1:p.Ser49Gly
  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.138+196A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.257A>G
  hgvsp: ENSP00000434535.1:p.Gln86Arg
  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.199+54A>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.281A>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.324A>G
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30449
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13439
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln86Arg
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum

8-146017185-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017185
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017185
    reference: chr 8
allele count: 2
allele frequency: 1.656342134031205e-5
allele num: 120748
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.253G>A
  hgvsp: ENSP00000262584.3:p.Gly85Ser
  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.253G>A
  hgvsp: ENSP00000378378.2:p.Gly85Ser
  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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.277G>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.253G>A
  hgvsp: ENSP00000435313.1:p.Gly85Ser
  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.160G>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.26-305G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.253G>A
  hgvsp: ENSP00000433703.1:p.Gly85Ser
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.139G>A
  hgvsp: ENST00000531975.1:c.139G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.253G>A
  hgvsp: ENSP00000434535.1:p.Gly85Ser
  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.199+50G>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.138+192G>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.253G>A
  hgvsp: ENSP00000433464.2:p.Gly85Ser
  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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.320G>A
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12536
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13428
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30451
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly85Ser
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

8-146017189-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017189
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017189
    reference: chr 8
allele count: 3
allele frequency: 2.485336514564072e-5
allele num: 120708
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.249C>T
  hgvsp: ENST00000394920.2:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.249C>T
  hgvsp: ENST00000529920.1:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.249C>T
  hgvsp: ENST00000532702.1:c.249C>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.249C>T
  hgvsp: ENST00000533397.1:c.249C>T(p.%3D)
  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.138+188C>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.249C>T
  hgvsp: ENST00000262584.3:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.135C>T
  hgvsp: ENSP00000437062.1:p.Thr46Ile
  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.249C>T
  hgvsp: ENST00000528957.1:c.249C>T(p.%3D)
  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.26-309C>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.273C>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.156C>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.199+46C>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.316C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13400
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30439
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr46Ile
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD

8-146017194-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017194
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017194
    reference: chr 8
allele count: 2
allele frequency: 1.657577616071872e-5
allele num: 120658
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.138+183A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.130A>G
  hgvsp: ENST00000531975.1:c.130A>G(p.%3D)
  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.244A>G
  hgvsp: ENSP00000262584.3:p.Ile82Val
  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.244A>G
  hgvsp: ENSP00000433464.2:p.Ile82Val
  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.26-314A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.244A>G
  hgvsp: ENSP00000434535.1:p.Ile82Val
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.244A>G
  hgvsp: ENSP00000433703.1:p.Ile82Val
  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.244A>G
  hgvsp: ENSP00000435313.1:p.Ile82Val
  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.244A>G
  hgvsp: ENSP00000378378.2:p.Ile82Val
  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.151A>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.199+41A>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.268A>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.311A>G
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30420
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12529
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile82Val
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

8-146017194-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017194
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017194
    reference: chr 8
allele count: 2
allele frequency: 1.657577616071872e-5
allele num: 120658
alternate allele: G
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.151A>C
  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.244A>C
  hgvsp: ENSP00000433464.2:p.Ile82Leu
  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.244A>C
  hgvsp: ENSP00000262584.3:p.Ile82Leu
  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.244A>C
  hgvsp: ENSP00000435313.1:p.Ile82Leu
  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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.311A>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.244A>C
  hgvsp: ENSP00000434535.1:p.Ile82Leu
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.244A>C
  hgvsp: ENSP00000433703.1:p.Ile82Leu
  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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.268A>C
  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.244A>C
  hgvsp: ENSP00000378378.2:p.Ile82Leu
  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.26-314A>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.130A>C
  hgvsp: ENST00000531975.1:c.130A>C(p.%3D)
  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.199+41A>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.138+183A>C
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12529
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13345
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile82Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-146017204-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017204
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017204
    reference: chr 8
allele count: 1
allele frequency: 8.294900295298451e-6
allele num: 120556
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.301C>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.258C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.234C>T
  hgvsp: ENST00000532702.1:c.234C>T(p.%3D)
  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.199+31C>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.234C>T
  hgvsp: ENST00000528957.1:c.234C>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.234C>T
  hgvsp: ENST00000262584.3:c.234C>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.141C>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.26-324C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.234C>T
  hgvsp: ENST00000529920.1:c.234C>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.234C>T
  hgvsp: ENST00000394920.2:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.120C>T
  hgvsp: ENSP00000437062.1:p.Pro41Leu
  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.138+173C>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.234C>T
  hgvsp: ENST00000533397.1:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12524
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13306
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2090
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro41Leu
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

8-146017215-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017215
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017215
    reference: chr 8
allele count: 2
allele frequency: 1.661074382910867e-5
allele num: 120404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.223C>T
  hgvsp: ENST00000528957.1:c.223C>T(p.%3D)
  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.199+20C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.109C>T
  hgvsp: ENST00000531975.1:c.109C>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.223C>T
  hgvsp: ENST00000394920.2:c.223C>T(p.%3D)
  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.26-335C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.223C>T
  hgvsp: ENST00000532702.1:c.223C>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.290C>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.130C>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.223C>T
  hgvsp: ENST00000533397.1:c.223C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.223C>T
  hgvsp: ENST00000529920.1:c.223C>T(p.%3D)
  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.138+162C>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.247C>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.223C>T
  hgvsp: ENST00000262584.3:c.223C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2086
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13190
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30318
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu75Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ

8-146017220-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017220
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017220
    reference: chr 8
allele count: 5
allele frequency: 4.155516031980851e-5
allele num: 120322
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.26-340C>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.218C>T
  hgvsp: ENSP00000262584.3:p.Thr73Met
  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.218C>T
  hgvsp: ENSP00000378378.2:p.Thr73Met
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.218C>T
  hgvsp: ENSP00000434535.1:p.Thr73Met
  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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.242C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.218C>T
  hgvsp: ENSP00000433703.1:p.Thr73Met
  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.218C>T
  hgvsp: ENSP00000433464.2:p.Thr73Met
  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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.285C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.104C>T
  hgvsp: ENSP00000437062.1:p.Arg36Trp
  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.218C>T
  hgvsp: ENSP00000435313.1:p.Thr73Met
  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.199+15C>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.125C>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.138+157C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13191
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30295
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr73Met
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

8-146017229-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017229
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017229
    reference: chr 8
allele count: 1
allele frequency: 8.319605983460623e-6
allele num: 120198
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.138+148A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.209A>G
  hgvsp: ENSP00000433703.1:p.Lys70Arg
  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.209A>G
  hgvsp: ENSP00000378378.2:p.Lys70Arg
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.95A>G
  hgvsp: ENSP00000437062.1:p.Arg33Gly
  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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.233A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.209A>G
  hgvsp: ENSP00000434535.1:p.Lys70Arg
  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.26-349A>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.209A>G
  hgvsp: ENSP00000435313.1:p.Lys70Arg
  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.209A>G
  hgvsp: ENSP00000433464.2:p.Lys70Arg
  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.209A>G
  hgvsp: ENSP00000262584.3:p.Lys70Arg
  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.199+6A>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.116A>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.276A>G
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30219
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys70Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

8-146017235-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017235
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017235
    reference: chr 8
allele count: 2
allele frequency: 1.665556295802798e-5
allele num: 120080
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.203G>A
  hgvsp: ENSP00000378378.2:p.Arg68Gln
  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.203G>A
  hgvsp: ENSP00000433464.2:p.Arg68Gln
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.89G>A
  hgvsp: ENSP00000437062.1:p.Gly31Ser
  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.26-355G>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.203G>A
  hgvsp: ENSP00000435313.1:p.Arg68Gln
  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.203G>A
  hgvsp: ENSP00000262584.3:p.Arg68Gln
  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.110G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.203G>A
  hgvsp: ENSP00000433703.1:p.Arg68Gln
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.199G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.203G>A
  hgvsp: ENSP00000434535.1:p.Arg68Gln
  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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.227G>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.270G>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.138+142G>A
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg68Gln
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

8-146017236-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017236
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017236
    reference: chr 8
allele count: 1
allele frequency: 8.328613785521537e-6
allele num: 120068
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.109C>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.226C>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.202C>T
  hgvsp: ENSP00000378378.2:p.Arg68Trp
  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.202C>T
  hgvsp: ENSP00000435313.1:p.Arg68Trp
  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.202C>T
  hgvsp: ENSP00000262584.3:p.Arg68Trp
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.202C>T
  hgvsp: ENSP00000433703.1:p.Arg68Trp
  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.26-356C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.202C>T
  hgvsp: ENSP00000434535.1:p.Arg68Trp
  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.202C>T
  hgvsp: ENSP00000433464.2:p.Arg68Trp
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.198C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.88C>T
  hgvsp: ENST00000531975.1:c.88C>T(p.%3D)
  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.138+141C>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.269C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30144
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2077
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg68Trp
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP

8-146017238-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017238
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017238
    reference: chr 8
allele count: 1
allele frequency: 8.332083520805212e-6
allele num: 120018
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.224A>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.267A>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.107A>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.26-358A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.200A>G
  hgvsp: ENSP00000433703.1:p.Tyr67Cys
  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.138+139A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.86A>G
  hgvsp: ENSP00000437062.1:p.Ile30Val
  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.200A>G
  hgvsp: ENSP00000435313.1:p.Tyr67Cys
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.200A>G
  hgvsp: ENSP00000434535.1:p.Tyr67Cys
  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.196A>G
  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.200A>G
  hgvsp: ENSP00000262584.3:p.Tyr67Cys
  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.200A>G
  hgvsp: ENSP00000433464.2:p.Tyr67Cys
  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.200A>G
  hgvsp: ENSP00000378378.2:p.Tyr67Cys
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30109
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12425
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr67Cys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

8-146017241-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017241
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017241
    reference: chr 8
allele count: 1
allele frequency: 8.335834083558401e-6
allele num: 119964
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.26-361C>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.264C>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.197C>T
  hgvsp: ENSP00000435313.1:p.Pro66Leu
  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.193C>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.197C>T
  hgvsp: ENSP00000378378.2:p.Pro66Leu
  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.138+136C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.83C>T
  hgvsp: ENSP00000437062.1:p.Arg29Cys
  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.197C>T
  hgvsp: ENSP00000262584.3:p.Pro66Leu
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.197C>T
  hgvsp: ENSP00000434535.1:p.Pro66Leu
  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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.221C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.197C>T
  hgvsp: ENSP00000433703.1:p.Pro66Leu
  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.104C>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.197C>T
  hgvsp: ENSP00000433464.2:p.Pro66Leu
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30090
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13058
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro66Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/8-146017243-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017243
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017243
    reference: chr 8
allele count: 1
allele frequency: 8.338753523123364e-6
allele num: 119922
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.195T>G
  hgvsp: ENSP00000434535.1:p.Asp65Glu
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.81T>G
  hgvsp: ENSP00000437062.1:p.Ile28Ser
  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.26-363T>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.262T>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.195T>G
  hgvsp: ENSP00000435313.1:p.Asp65Glu
  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.195T>G
  hgvsp: ENSP00000433464.2:p.Asp65Glu
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.195T>G
  hgvsp: ENSP00000433703.1:p.Asp65Glu
  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.102T>G
  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.195T>G
  hgvsp: ENSP00000262584.3:p.Asp65Glu
  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.195T>G
  hgvsp: ENSP00000378378.2:p.Asp65Glu
  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.138+134T>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.191T>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.219T>G
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 30063
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12392
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp65Glu
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD

8-146017254-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017254
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017254
    reference: chr 8
allele count: 1
allele frequency: 8.367220576668843e-6
allele num: 119514
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.208G>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.184G>A
  hgvsp: ENSP00000262584.3:p.Val62Ile
  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.26-374G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.70G>A
  hgvsp: ENSP00000437062.1:p.Trp24Ter
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.184G>A
  hgvsp: ENSP00000434535.1:p.Val62Ile
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.184G>A
  hgvsp: ENSP00000433703.1:p.Val62Ile
  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.184G>A
  hgvsp: ENSP00000378378.2:p.Val62Ile
  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.91G>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.184G>A
  hgvsp: ENSP00000433464.2:p.Val62Ile
  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.180G>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.184G>A
  hgvsp: ENSP00000435313.1:p.Val62Ile
  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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.251G>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.138+123G>A
  variant of: http://identifiers.org/hgnc/10368
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12954
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29848
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp24Ter
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff

8-146017257-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017257
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017257
    reference: chr 8
allele count: 1
allele frequency: 8.375069094320028e-6
allele num: 119402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.181G>A
  hgvsp: ENSP00000378378.2:p.Val61Met
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.181G>A
  hgvsp: ENSP00000434535.1:p.Val61Met
  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.177G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.67G>A
  hgvsp: ENST00000531975.1:c.67G>A(p.%3D)
  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.181G>A
  hgvsp: ENSP00000435313.1:p.Val61Met
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.205G>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.138+120G>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.248G>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.181G>A
  hgvsp: ENSP00000433464.2:p.Val61Met
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.181G>A
  hgvsp: ENSP00000433703.1:p.Val61Met
  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.181G>A
  hgvsp: ENSP00000262584.3:p.Val61Met
  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.26-377G>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.88G>A
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12954
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12193
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29813
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val61Met
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
reference allele: C
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

8-146017258-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017258
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017258
    reference: chr 8
allele count: 1
allele frequency: 8.376331836762046e-6
allele num: 119384
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.180G>C
  hgvsp: ENSP00000434535.1:p.Lys60Asn
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.180G>C
  hgvsp: ENSP00000433703.1:p.Lys60Asn
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.67-1G>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.138+119G>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.26-378G>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.87G>C
  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.180G>C
  hgvsp: ENSP00000433464.2:p.Lys60Asn
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.205-1G>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.247G>C
  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.180G>C
  hgvsp: ENSP00000262584.3:p.Lys60Asn
  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.176G>C
  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.180G>C
  hgvsp: ENSP00000378378.2:p.Lys60Asn
  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.180G>C
  hgvsp: ENSP00000435313.1:p.Lys60Asn
  variant of: http://identifiers.org/hgnc/10368
canonical: false
consequence: splice acceptor
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29813
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12955
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12174
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.67-1G>C
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff

8-146017259-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017259
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017259
    reference: chr 8
allele count: 2
allele frequency: 1.676164934629567e-5
allele num: 119320
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.179A>G
  hgvsp: ENSP00000434535.1:p.Lys60Arg
  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.179A>G
  hgvsp: ENSP00000262584.3:p.Lys60Arg
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.67-2A>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.246A>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.175A>G
  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.179A>G
  hgvsp: ENSP00000433464.2:p.Lys60Arg
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.205-2A>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.179A>G
  hgvsp: ENSP00000378378.2:p.Lys60Arg
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.179A>G
  hgvsp: ENSP00000433703.1:p.Lys60Arg
  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.179A>G
  hgvsp: ENSP00000435313.1:p.Lys60Arg
  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.86A>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.138+118A>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.26-379A>G
  variant of: http://identifiers.org/hgnc/10368
canonical: false
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12168
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12946
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29782
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.67-2A>G
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ

8-146017267-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017267
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017267
    reference: chr 8
allele count: 1
allele frequency: 8.398280032249395e-6
allele num: 119072
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.238C>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.138+110C>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.205-10C>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.78C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.171C>T
  hgvsp: ENST00000529920.1:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.171C>T
  hgvsp: ENST00000532702.1:c.171C>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.171C>T
  hgvsp: ENST00000262584.3:c.171C>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.171C>T
  hgvsp: ENST00000528957.1:c.171C>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.171C>T
  hgvsp: ENST00000394920.2:c.171C>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.171C>T
  hgvsp: ENST00000533397.1:c.171C>T(p.%3D)
  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.26-387C>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.167C>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.67-10C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12083
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12957
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29635
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro57Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

8-146017279-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017279
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017279
    reference: chr 8
allele count: 1
allele frequency: 8.424174009738345e-6
allele num: 118706
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.26-399C>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.159C>T
  hgvsp: ENST00000394920.2:c.159C>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.159C>T
  hgvsp: ENST00000262584.3:c.159C>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.66C>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.205-22C>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.155C>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.67-22C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.159C>T
  hgvsp: ENST00000529920.1:c.159C>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.159C>T
  hgvsp: ENST00000533397.1:c.159C>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.159C>T
  hgvsp: ENST00000528957.1:c.159C>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.226C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.159C>T
  hgvsp: ENST00000532702.1:c.159C>T(p.%3D)
  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.138+98C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11976
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29472
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12904
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly53Gly
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

8-146017283-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017283
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017283
    reference: chr 8
allele count: 1
allele frequency: 8.426729586247577e-6
allele num: 118670
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.155C>T
  hgvsp: ENSP00000433703.1:p.Pro52Leu
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.155C>T
  hgvsp: ENSP00000434535.1:p.Pro52Leu
  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.155C>T
  hgvsp: ENSP00000262584.3:p.Pro52Leu
  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.138+94C>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.26-403C>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.205-26C>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.155C>T
  hgvsp: ENSP00000435313.1:p.Pro52Leu
  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.151C>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.155C>T
  hgvsp: ENSP00000433464.2:p.Pro52Leu
  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.67-26C>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.222C>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.155C>T
  hgvsp: ENSP00000378378.2:p.Pro52Leu
  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.62C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11962
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12928
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro52Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD

8-146017285-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017285
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017285
    reference: chr 8
allele count: 2
allele frequency: 1.685999460480173e-5
allele num: 118624
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.153C>T
  hgvsp: ENST00000262584.3:c.153C>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.153C>T
  hgvsp: ENST00000533397.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.153C>T
  hgvsp: ENST00000532702.1:c.153C>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.153C>T
  hgvsp: ENST00000528957.1:c.153C>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.220C>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.26-405C>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.205-28C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.153C>T
  hgvsp: ENST00000529920.1:c.153C>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.149C>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.153C>T
  hgvsp: ENST00000394920.2:c.153C>T(p.%3D)
  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.138+92C>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.60C>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.67-28C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11957
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12950
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29404
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp51Asp
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

8-146017288-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017288
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017288
    reference: chr 8
allele count: 302
allele frequency: 2.547835183747849e-3
allele num: 118532
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.205-31C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.150C>T
  hgvsp: ENST00000529920.1:c.150C>T(p.%3D)
  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.67-31C>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.146C>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.217C>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.26-408C>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.150C>T
  hgvsp: ENST00000394920.2:c.150C>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.150C>T
  hgvsp: ENST00000533397.1:c.150C>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.150C>T
  hgvsp: ENST00000262584.3:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.150C>T
  hgvsp: ENST00000532702.1:c.150C>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.150C>T
  hgvsp: ENST00000528957.1:c.150C>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.57C>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.138+89C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 11940
  bin: 3.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12901
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 9.75e1
  variant carriers: 195
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 29351
  bin: 2.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 4.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.His50His
num of homozygotes: 6
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

8-146017291-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017291
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017291
    reference: chr 8
allele count: 78
allele frequency: 6.586502735931905e-4
allele num: 118424
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.67-34C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.147C>T
  hgvsp: ENST00000532702.1:c.147C>T(p.%3D)
  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.138+86C>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.143C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.147C>T
  hgvsp: ENST00000529920.1:c.147C>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.214C>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.147C>T
  hgvsp: ENST00000533397.1:c.147C>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.147C>T
  hgvsp: ENST00000394920.2:c.147C>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.147C>T
  hgvsp: ENST00000528957.1:c.147C>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.147C>T
  hgvsp: ENST00000262584.3:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.205-34C>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.26-411C>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.54C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12897
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11929
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Ile49Ile
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-146017297-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017297
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017297
    reference: chr 8
allele count: 2
allele frequency: 1.691732503256585e-5
allele num: 118222
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.137C>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.48C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.141C>T
  hgvsp: ENST00000394920.2:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.141C>T
  hgvsp: ENST00000528957.1:c.141C>T(p.%3D)
  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.138+80C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.141C>T
  hgvsp: ENST00000529920.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.141C>T
  hgvsp: ENST00000532702.1:c.141C>T(p.%3D)
  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.67-40C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.208C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.141C>T
  hgvsp: ENST00000262584.3:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.141C>T
  hgvsp: ENST00000533397.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.205-40C>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.26-417C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11910
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.141C>T
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

8-146017298-TCCTGTGGGCAGAGGCGGCGTGAGTGCGGCGTTCCGGCCGGGCGTCCCTTCCCCTCCCGCCCCGGCCAGCGTTCCGCA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017298
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017221
    reference: chr 8
allele count: 1
allele frequency: 8.463960456376747e-6
allele num: 118148
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  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
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000525232
  gene symbol: RPL8
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  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
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000531767
  gene symbol: RPL8
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: splice acceptor
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29293
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12802
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11904
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: TCCTGTGGGCAGAGGCGGCGTGAGTGCGGCGTTCCGGCCGGGCGTCCCTTCCCCTCCCGCCCCGGCCAGCGTTCCGCA
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

8-146017307-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017307
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017307
    reference: chr 8
allele count: 1
allele frequency: 8.510203734277399e-6
allele num: 117506
alternate allele: T
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.139-8G>A
  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.139-8G>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.139-8G>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.26-427G>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.139-8G>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.205-50G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.139-8G>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.38G>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.206-8G>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.135-8G>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.139-8G>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.67-50G>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.138+70G>A
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12497
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.139-8G>A
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

8-146017321-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017321
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017321
    reference: chr 8
allele count: 3
allele frequency: 2.573693421639614e-5
allele num: 116564
alternate allele: A
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.139-22C>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.138+56C>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.25+430C>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.139-22C>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.24C>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.139-22C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.139-22C>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.204+56C>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.139-22C>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.66+56C>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.206-22C>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.135-22C>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.139-22C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28766
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11664
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

8-146017321-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017321
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017321
    reference: chr 8
allele count: 1
allele frequency: 8.578978072132047e-6
allele num: 116564
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.206-22C>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.204+56C>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.139-22C>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.139-22C>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.138+56C>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.135-22C>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.139-22C>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.66+56C>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.139-22C>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.24C>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.139-22C>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.25+430C>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.139-22C>G
  variant of: http://identifiers.org/hgnc/10368
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28766
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11664
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12311
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

8-146017322-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017322
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017322
    reference: chr 8
allele count: 1
allele frequency: 8.589884551951622e-6
allele num: 116416
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.139-23A>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.204+55A>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.23A>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.206-23A>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.139-23A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.139-23A>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.25+429A>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.66+55A>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.135-23A>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.139-23A>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.139-23A>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.139-23A>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.138+55A>G
  variant of: http://identifiers.org/hgnc/10368
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11654
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

8-146017324-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017324
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017324
    reference: chr 8
allele count: 1
allele frequency: 8.608667206143144e-6
allele num: 116162
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.139-25G>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.21G>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.138+53G>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.139-25G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.139-25G>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.135-25G>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.139-25G>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.204+53G>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.66+53G>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.206-25G>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.139-25G>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.25+427G>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.139-25G>A
  variant of: http://identifiers.org/hgnc/10368
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11646
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12109
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

8-146017328-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017328
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017328
    reference: chr 8
allele count: 1
allele frequency: 8.616529951058109e-6
allele num: 116056
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.139-29C>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.17C>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.139-29C>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.206-29C>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.25+423C>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.138+49C>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.139-29C>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.135-29C>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.139-29C>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.204+49C>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.139-29C>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.139-29C>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.66+49C>G
  variant of: http://identifiers.org/hgnc/10368
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11578
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

8-146017330-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017330
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017330
    reference: chr 8
allele count: 14
allele frequency: 1.206605302168442e-4
allele num: 116028
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.139-31A>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.139-31A>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.15A>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.66+47A>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.25+421A>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.139-31A>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.204+47A>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.139-31A>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.206-31A>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.135-31A>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.139-31A>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.138+47A>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.139-31A>C
  variant of: http://identifiers.org/hgnc/10368
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11550
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28449
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

8-146017333-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017333
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017333
    reference: chr 8
allele count: 1
allele frequency: 8.629914736442405e-6
allele num: 115876
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.139-34C>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.204+44C>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.138+44C>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.12C>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.25+418C>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.66+44C>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.139-34C>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.135-34C>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.206-34C>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.139-34C>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.139-34C>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.139-34C>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.139-34C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11509
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12030
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS

8-146017337-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017337
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017337
    reference: chr 8
allele count: 1144
allele frequency: 9.873815401080595e-3
allele num: 115862
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.135-38C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.139-38C>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.8C>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.139-38C>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.139-38C>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.138+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.66+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.139-38C>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.139-38C>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.206-38C>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.204+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.139-38C>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.25+414C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 1.25e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 9.75e1
  variant carriers: 508
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 7.5e0
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 1.75e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 11395
  bin: 3.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 28208
  bin: 2.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 12051
  bin: 2.25e1
  variant carriers: 52
genotype quality: GenotypeQuality
num of homozygotes: 65
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/8-146017340-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017340
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017340
    reference: chr 8
allele count: 1
allele frequency: 8.648723448419014e-6
allele num: 115624
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.5G>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.204+37G>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.138+37G>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.138+37G>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.138+37G>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.138+37G>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.138+37G>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.66+37G>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.138+37G>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.205+37G>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.134+37G>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.138+37G>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.25+411G>T
  variant of: http://identifiers.org/hgnc/10368
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12096
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11551
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

8-146017344-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017344
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017344
    reference: chr 8
allele count: 1
allele frequency: 8.660558086363084e-6
allele num: 115466
alternate allele: T
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.138+33G>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.138+33G>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.138+33G>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.66+33G>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.25+407G>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.1G>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.138+33G>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.138+33G>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.204+33G>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.205+33G>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.138+33G>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.134+33G>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.138+33G>A
  variant of: http://identifiers.org/hgnc/10368
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1480
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11888
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28322
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11488
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

8-146017353-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017353
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017353
    reference: chr 8
allele count: 1
allele frequency: 8.691419830343484e-6
allele num: 115056
alternate allele: G
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.25+398G>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.205+24G>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.66+24G>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.138+24G>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.134+24G>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.204+24G>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.138+24G>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.138+24G>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.138+24G>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.138+24G>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.138+24G>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.138+24G>C
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11864
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11388
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2213
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28083
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/8-146017355-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017355
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017355
    reference: chr 8
allele count: 1
allele frequency: 8.689456213830139e-6
allele num: 115082
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.66+22G>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.138+22G>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.138+22G>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.138+22G>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.204+22G>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.134+22G>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.138+22G>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.138+22G>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.138+22G>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.138+22G>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.205+22G>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.25+396G>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11380
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28104
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11905
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-146017361-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017361
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017361
    reference: chr 8
allele count: 1
allele frequency: 8.702614265325304e-6
allele num: 114908
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.138+16C>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.205+16C>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.134+16C>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.66+16C>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.138+16C>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.25+390C>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.138+16C>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.138+16C>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.204+16C>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.138+16C>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.138+16C>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.138+16C>G
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27928
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11302
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12083
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

8-146017366-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017366
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017366
    reference: chr 8
allele count: 12
allele frequency: 1.044913881680918e-4
allele num: 114842
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.138+11C>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.134+11C>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.138+11C>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.205+11C>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.204+11C>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.138+11C>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.25+385C>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.138+11C>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.138+11C>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.138+11C>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.66+11C>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.138+11C>G
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12202
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27851
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD

8-146017368-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017368
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017368
    reference: chr 8
allele count: 1
allele frequency: 8.708677326087714e-6
allele num: 114828
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.66+9C>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.204+9C>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.138+9C>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.138+9C>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.138+9C>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.138+9C>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.205+9C>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.25+383C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.138+9C>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.134+9C>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.138+9C>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.138+9C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12248
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2420
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11248
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

8-146017368-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017368
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017368
    reference: chr 8
allele count: 2
allele frequency: 1.741735465217543e-5
allele num: 114828
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.138+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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.204+9C>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.138+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.138+9C>A
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.138+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.138+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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.205+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.138+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.138+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.25+383C>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.134+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.66+9C>A
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12248
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11248
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2420
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

8-146017373-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017373
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017373
    reference: chr 8
allele count: 1
allele frequency: 8.723872003349968e-6
allele num: 114628
alternate allele: A
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.134+4C>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.138+4C>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.25+378C>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.138+4C>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.204+4C>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.138+4C>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.205+4C>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.138+4C>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.66+4C>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.138+4C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.138+4C>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.138+4C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27749
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11229
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1758
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.138+4C>T
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD

8-146017378-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017378
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017378
    reference: chr 8
allele count: 1
allele frequency: 8.719764217575556e-6
allele num: 114682
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.137A>G
  hgvsp: ENSP00000436460.1:p.Lys46Arg
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.137A>G
  hgvsp: ENSP00000433464.2:p.Lys46Arg
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.137A>G
  hgvsp: ENSP00000378378.2:p.Lys46Arg
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.137A>G
  hgvsp: ENSP00000262584.3:p.Lys46Arg
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.203A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.137A>G
  hgvsp: ENSP00000435313.1:p.Lys46Arg
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.137A>G
  hgvsp: ENSP00000434535.1:p.Lys46Arg
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.204A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.65A>G
  hgvsp: ENSP00000437062.1:p.Arg23Gly
  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.25+373A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.137A>G
  hgvsp: ENSP00000433703.1:p.Lys46Arg
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.133A>G
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11211
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27754
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys46Arg
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

8-146017379-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017379
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017379
    reference: chr 8
allele count: 3
allele frequency: 2.615974886641088e-5
allele num: 114680
alternate allele: G
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.25+372A>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433464
  ensembl transcript: ENST00000528957
  gene symbol: RPL8
  hgvsc: ENST00000528957.1:c.136A>C
  hgvsp: ENSP00000433464.2:p.Lys46Gln
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.136A>C
  hgvsp: ENSP00000434535.1:p.Lys46Gln
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.136A>C
  hgvsp: ENSP00000262584.3:p.Lys46Gln
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.132A>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.136A>C
  hgvsp: ENSP00000436460.1:p.Lys46Gln
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.136A>C
  hgvsp: ENSP00000433703.1:p.Lys46Gln
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.203A>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.202A>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.136A>C
  hgvsp: ENSP00000378378.2:p.Lys46Gln
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.136A>C
  hgvsp: ENSP00000435313.1:p.Lys46Gln
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.64A>C
  hgvsp: ENST00000531975.1:c.64A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2560
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11207
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27754
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Lys46Gln
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

8-146017380-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017380
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017380
    reference: chr 8
allele count: 1
allele frequency: 8.721589422456349e-6
allele num: 114658
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000262584
  ensembl transcript: ENST00000262584
  gene symbol: RPL8
  hgvsc: ENST00000262584.3:c.135C>T
  hgvsp: ENST00000262584.3:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.135C>T
  hgvsp: ENST00000529920.1:c.135C>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.135C>T
  hgvsp: ENST00000533397.1:c.135C>T(p.%3D)
  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.25+371C>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.131C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.63C>T
  hgvsp: ENSP00000437062.1:p.Ser22Leu
  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.135C>T
  hgvsp: ENST00000527914.1:c.135C>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.202C>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.135C>T
  hgvsp: ENST00000528957.1:c.135C>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.201C>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.135C>T
  hgvsp: ENST00000394920.2:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.135C>T
  hgvsp: ENST00000532702.1:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27745
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2571
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11207
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser22Leu
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

8-146017380-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017380
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017380
    reference: chr 8
allele count: 1
allele frequency: 8.721589422456349e-6
allele num: 114658
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.135C>G
  hgvsp: ENST00000527914.1:c.135C>G(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.135C>G
  hgvsp: ENST00000262584.3:c.135C>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.202C>G
  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.135C>G
  hgvsp: ENST00000528957.1:c.135C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.135C>G
  hgvsp: ENST00000532702.1:c.135C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.63C>G
  hgvsp: ENSP00000437062.1:p.Ser22Ter
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.135C>G
  hgvsp: ENST00000529920.1:c.135C>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: ENST00000528296
  gene symbol: RPL8
  hgvsc: ENST00000528296.1:n.131C>G
  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.135C>G
  hgvsp: ENST00000533397.1:c.135C>G(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.135C>G
  hgvsp: ENST00000394920.2:c.135C>G(p.%3D)
  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.25+371C>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.201C>G
  variant of: http://identifiers.org/hgnc/10368
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27745
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11207
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2571
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser22Ter
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD

8-146017384-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017384
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017384
    reference: chr 8
allele count: 1
allele frequency: 8.733624454148471e-6
allele num: 114500
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.131T>C
  hgvsp: ENSP00000434535.1:p.Ile44Thr
  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.25+367T>C
  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.131T>C
  hgvsp: ENSP00000262584.3:p.Ile44Thr
  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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.198T>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.127T>C
  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.131T>C
  hgvsp: ENSP00000433464.2:p.Ile44Thr
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.131T>C
  hgvsp: ENSP00000433703.1:p.Ile44Thr
  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.131T>C
  hgvsp: ENSP00000435313.1:p.Ile44Thr
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.59T>C
  hgvsp: ENSP00000437062.1:p.Ser21Pro
  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.131T>C
  hgvsp: ENSP00000378378.2:p.Ile44Thr
  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.131T>C
  hgvsp: ENSP00000436460.1:p.Ile44Thr
  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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.197T>C
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11192
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2633
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27685
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1749
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12404
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile44Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD

8-146017386-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017386
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017386
    reference: chr 8
allele count: 6
allele frequency: 5.240357741755171e-5
allele num: 114496
alternate allele: A
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.125C>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.129C>T
  hgvsp: ENST00000533397.1:c.129C>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.129C>T
  hgvsp: ENST00000528957.1:c.129C>T(p.%3D)
  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.25+365C>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.195C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.57C>T
  hgvsp: ENSP00000437062.1:p.Ala20Val
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.129C>T
  hgvsp: ENST00000529920.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.129C>T
  hgvsp: ENST00000532702.1:c.129C>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.129C>T
  hgvsp: ENST00000262584.3:c.129C>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.129C>T
  hgvsp: ENST00000527914.1:c.129C>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.129C>T
  hgvsp: ENST00000394920.2:c.129C>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.196C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27695
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2633
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11188
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala20Val
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: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff

8-146017401-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017401
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017401
    reference: chr 8
allele count: 41
allele frequency: 3.596238860430847e-4
allele num: 114008
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.25+350C>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.110C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.114C>T
  hgvsp: ENST00000529920.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.114C>T
  hgvsp: ENST00000532702.1:c.114C>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.114C>T
  hgvsp: ENST00000528957.1:c.114C>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.114C>T
  hgvsp: ENST00000533397.1:c.114C>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.180C>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.114C>T
  hgvsp: ENST00000262584.3:c.114C>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.181C>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.114C>T
  hgvsp: ENST00000394920.2:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.42C>T
  hgvsp: ENSP00000437062.1:p.Thr15Met
  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.114C>T
  hgvsp: ENST00000527914.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12718
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2317
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1730
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 27458
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Thr15Met
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

8-146017403-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017403
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017403
    reference: chr 8
allele count: 1
allele frequency: 8.772237622372715e-6
allele num: 113996
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000436460
  ensembl transcript: ENST00000527914
  gene symbol: RPL8
  hgvsc: ENST00000527914.1:c.112C>G
  hgvsp: ENSP00000436460.1:p.His38Asp
  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.112C>G
  hgvsp: ENSP00000433464.2:p.His38Asp
  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.112C>G
  hgvsp: ENSP00000262584.3:p.His38Asp
  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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.178C>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.112C>G
  hgvsp: ENSP00000434535.1:p.His38Asp
  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.108C>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.112C>G
  hgvsp: ENSP00000378378.2:p.His38Asp
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.112C>G
  hgvsp: ENSP00000433703.1:p.His38Asp
  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.112C>G
  hgvsp: ENSP00000435313.1:p.His38Asp
  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.25+348C>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.40C>G
  hgvsp: ENST00000531975.1:c.40C>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.179C>G
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12756
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27463
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His38Asp
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

8-146017406-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017406
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017406
    reference: chr 8
allele count: 1
allele frequency: 8.778706369829343e-6
allele num: 113912
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.109C>T
  hgvsp: ENSP00000435313.1:p.Arg37Trp
  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.109C>T
  hgvsp: ENSP00000436460.1:p.Arg37Trp
  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.109C>T
  hgvsp: ENSP00000378378.2:p.Arg37Trp
  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.25+345C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.109C>T
  hgvsp: ENSP00000434535.1:p.Arg37Trp
  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.109C>T
  hgvsp: ENSP00000262584.3:p.Arg37Trp
  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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.175C>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.109C>T
  hgvsp: ENSP00000433464.2:p.Arg37Trp
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.109C>T
  hgvsp: ENSP00000433703.1:p.Arg37Trp
  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.105C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.37C>T
  hgvsp: ENST00000531975.1:c.37C>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.176C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12962
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1717
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27528
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11116
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg37Trp
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
reference allele: G
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD

8-146017410-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017410
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017410
    reference: chr 8
allele count: 4
allele frequency: 3.516359864268509e-5
allele num: 113754
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.105T>C
  hgvsp: ENST00000532702.1:c.105T>C(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.105T>C
  hgvsp: ENST00000527914.1:c.105T>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.101T>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.105T>C
  hgvsp: ENST00000528957.1:c.105T>C(p.%3D)
  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.25+341T>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.172T>C
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.105T>C
  hgvsp: ENST00000529920.1:c.105T>C(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.105T>C
  hgvsp: ENST00000533397.1:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.33T>C
  hgvsp: ENSP00000437062.1:p.Leu12Pro
  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.105T>C
  hgvsp: ENST00000394920.2:c.105T>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.105T>C
  hgvsp: ENST00000262584.3:c.105T>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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.171T>C
  variant of: http://identifiers.org/hgnc/10368
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2353
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27414
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11073
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12951
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2962
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu12Pro
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ

8-146017411-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017411
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017411
    reference: chr 8
allele count: 1
allele frequency: 8.793064031092274e-6
allele num: 113726
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.104C>T
  hgvsp: ENSP00000262584.3:p.Ala35Val
  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.104C>T
  hgvsp: ENSP00000435313.1:p.Ala35Val
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.104C>T
  hgvsp: ENSP00000434535.1:p.Ala35Val
  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.104C>T
  hgvsp: ENSP00000378378.2:p.Ala35Val
  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.104C>T
  hgvsp: ENSP00000436460.1:p.Ala35Val
  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.100C>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.104C>T
  hgvsp: ENSP00000433464.2:p.Ala35Val
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.32C>T
  hgvsp: ENST00000531975.1:c.32C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.104C>T
  hgvsp: ENSP00000433703.1:p.Ala35Val
  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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.170C>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.25+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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.171C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11071
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12969
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2964
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala35Val
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

8-146017411-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017411
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017411
    reference: chr 8
allele count: 4
allele frequency: 3.51722561243691e-5
allele num: 113726
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000435313
  ensembl transcript: ENST00000533397
  gene symbol: RPL8
  hgvsc: ENST00000533397.1:c.104C>G
  hgvsp: ENSP00000435313.1:p.Ala35Gly
  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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.171C>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.104C>G
  hgvsp: ENSP00000436460.1:p.Ala35Gly
  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.104C>G
  hgvsp: ENSP00000262584.3:p.Ala35Gly
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.104C>G
  hgvsp: ENSP00000433703.1:p.Ala35Gly
  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.100C>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.25+340C>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.104C>G
  hgvsp: ENSP00000434535.1:p.Ala35Gly
  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.104C>G
  hgvsp: ENSP00000433464.2:p.Ala35Gly
  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.104C>G
  hgvsp: ENSP00000378378.2:p.Ala35Gly
  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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.170C>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.32C>G
  hgvsp: ENSP00000437062.1:p.Leu12Val
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2964
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12969
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11071
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala35Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

8-146017417-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017417
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017417
    reference: chr 8
allele count: 1
allele frequency: 8.824723344923136e-6
allele num: 113318
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000378378
  ensembl transcript: ENST00000394920
  gene symbol: RPL8
  hgvsc: ENST00000394920.2:c.98A>G
  hgvsp: ENSP00000378378.2:p.Asp33Gly
  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.94A>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.165A>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.98A>G
  hgvsp: ENSP00000435313.1:p.Asp33Gly
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.26A>G
  hgvsp: ENSP00000437062.1:p.Ile10Val
  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.25+334A>G
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.98A>G
  hgvsp: ENSP00000433703.1:p.Asp33Gly
  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.98A>G
  hgvsp: ENSP00000262584.3:p.Asp33Gly
  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.98A>G
  hgvsp: ENSP00000433464.2:p.Asp33Gly
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.98A>G
  hgvsp: ENSP00000434535.1:p.Asp33Gly
  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.98A>G
  hgvsp: ENSP00000436460.1:p.Asp33Gly
  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: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.164A>G
  variant of: http://identifiers.org/hgnc/10368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3080
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10969
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27194
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp33Gly
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD

8-146017422-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017422
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017422
    reference: chr 8
allele count: 10
allele frequency: 8.909955984817435e-5
allele num: 112234
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161016
  ensembl transcript: ENST00000531767
  gene symbol: RPL8
  hgvsc: ENST00000531767.1:n.159C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000437062
  ensembl transcript: ENST00000531975
  gene symbol: RPL8
  hgvsc: ENST00000531975.1:c.21C>T
  hgvsp: ENSP00000437062.1:p.Pro8Leu
  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.93C>T
  hgvsp: ENST00000533397.1:c.93C>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.93C>T
  hgvsp: ENST00000527914.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000434535
  ensembl transcript: ENST00000532702
  gene symbol: RPL8
  hgvsc: ENST00000532702.1:c.93C>T
  hgvsp: ENST00000532702.1:c.93C>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: ENST00000525232
  gene symbol: RPL8
  hgvsc: ENST00000525232.1:n.160C>T
  variant of: http://identifiers.org/hgnc/10368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000161016
  ensembl protein: ENSP00000433703
  ensembl transcript: ENST00000529920
  gene symbol: RPL8
  hgvsc: ENST00000529920.1:c.93C>T
  hgvsp: ENST00000529920.1:c.93C>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.93C>T
  hgvsp: ENST00000262584.3:c.93C>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.93C>T
  hgvsp: ENST00000528957.1:c.93C>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.93C>T
  hgvsp: ENST00000394920.2:c.93C>T(p.%3D)
  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.25+329C>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.89C>T
  variant of: http://identifiers.org/hgnc/10368
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26645
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10551
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3317
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12708
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro8Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/8-146017424-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146017424
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146017424
allele count: 2
allele frequency: 1.78122940453501e-5
allele num: 112282
alternate allele: A
canonical: true
consequence: missense
filter: PASS
hgvs: p.Ala31Ser
num of homozygotes: 0
reference allele: C

GenotypeDepth
all individuals: 73
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 551
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 104
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1123
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 140
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3751
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9760
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38774
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2761
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2373
bin: 7.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.089392278650591e-5
allele num: 16422
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66264
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.024e0

VQSLOD
type: SiteQuality
SIO_000300: 4.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.893e0

FS
type: SiteQuality
SIO_000300: 2.028e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.01e0

QD
type: SiteQuality
SIO_000300: 1.273e1

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

DP
type: SiteQuality
SIO_000300: 1.74496e6

GenotypeDepth
all individuals: 180
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13002
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2377
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3750
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 21
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1122
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 434
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2764
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9784
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38906
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16434
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50879628232596e-5
allele num: 66278
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.291e1

MQRankSum
type: SiteQuality
SIO_000300: 8.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.06e-1

FS
type: SiteQuality
SIO_000300: 1.94e0

VQSLOD
type: SiteQuality
SIO_000300: 9.81e-1

DP
type: SiteQuality
SIO_000300: 1.746264e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.542e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.8e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 2466
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 74
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 48
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39129
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1120
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2386
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2763
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3756
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 382
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9796
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66306
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.319647413593134e-4
allele num: 8622
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.748706e6

VQSLOD
type: SiteQuality
SIO_000300: 7.38e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.55e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.72e0

QD
type: SiteQuality
SIO_000300: 1.26e1

FS
type: SiteQuality
SIO_000300: 4.286e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.35e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.14e-1

GenotypeDepth
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 8.75e1
variant carriers: 0

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

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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Other
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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FS
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QD
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MQ
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DP
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MQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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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
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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Other
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South Asian
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Latino
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FS
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VQSLOD
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MQ
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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ReadPosRankSum
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele num: 16488
num of homozygotes: 0

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

Latino
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East Asian
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Other
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African
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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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num of homozygotes: 0

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

MQ
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GenotypeDepth
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variant carriers: 45

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 9.257657034088942e-2
allele num: 11558
num of homozygotes: 56

African
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South Asian
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 1.239407738005488e-2
allele num: 66322
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Other
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East Asian
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BaseQRankSum
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InbreedingCoeff
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QD
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MQ
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DP
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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FS
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SIO_000300: 1.218e0

MQRankSum
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GenotypeDepth
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variant carriers: 22

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele num: 16494
num of homozygotes: 0

European (Finnish)
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allele count: 0
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Latino
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allele frequency: 4.760256188333045e-3
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African
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allele frequency: 1.181201550387597e-1
allele num: 10320
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East Asian
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Other
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European (Non-Finnish)
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ReadPosRankSum
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VQSLOD
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FS
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QD
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MQ
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MQRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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East Asian
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Latino
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European (Non-Finnish)
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South Asian
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European (Finnish)
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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DP
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FS
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MQ
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QD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Non-Finnish)
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East Asian
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MQRankSum
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FS
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ReadPosRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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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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European (Non-Finnish)
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South Asian
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Latino
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African
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MQRankSum
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InbreedingCoeff
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QD
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MQ
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FS
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DP
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VQSLOD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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VQSLOD
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InbreedingCoeff
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DP
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FS
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MQ
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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Other
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East Asian
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African
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South Asian
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QD
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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FS
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MQRankSum
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MQ
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DP
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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African
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Latino
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BaseQRankSum
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VQSLOD
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FS
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QD
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MQRankSum
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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ReadPosRankSum
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DP
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QD
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MQ
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African
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European (Non-Finnish)
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DP
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MQ
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FS
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Latino
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allele num: 11536
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Other
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European (Finnish)
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allele frequency: 0.0e0
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African
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South Asian
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East Asian
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FS
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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MQ
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Latino
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allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

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

East Asian
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South Asian
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European (Non-Finnish)
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allele num: 65766
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African
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Other
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FS
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VQSLOD
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MQ
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DP
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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num of homozygotes: 0

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

European (Non-Finnish)
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allele num: 65754
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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QD
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ClippingRankSum
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MQ
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ReadPosRankSum
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FS
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DP
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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African
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allele frequency: 0.0e0
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Other
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East Asian
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European (Non-Finnish)
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allele num: 65718
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Latino
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DP
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InbreedingCoeff
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MQRankSum
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FS
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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MQ
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VQSLOD
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

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

Other
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Latino
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 65240
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European (Finnish)
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South Asian
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ClippingRankSum
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MQRankSum
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FS
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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DP
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QD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 65068
num of homozygotes: 0

East Asian
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Other
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African
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Latino
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South Asian
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European (Finnish)
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MQRankSum
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DP
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ClippingRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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BaseQRankSum
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FS
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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European (Finnish)
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East Asian
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South Asian
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European (Non-Finnish)
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VQSLOD
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DP
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MQRankSum
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InbreedingCoeff
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MQ
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FS
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ClippingRankSum
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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Latino
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South Asian
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African
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East Asian
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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MQ
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FS
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BaseQRankSum
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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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
all individuals: 1841
bin: 2.25e1
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GenotypeQuality
all individuals: 1163
bin: 9.75e1
variant carriers: 2

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
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: 64764
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.018978396931153e-4
allele num: 9906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8508
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.305e1

MQRankSum
type: SiteQuality
SIO_000300: 2.25e0

DP
type: SiteQuality
SIO_000300: 1.64473e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -4.832e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.23e-1

MQ
type: SiteQuality
SIO_000300: 5.945e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.68e0

GenotypeDepth
all individuals: 67
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 132
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variant carriers: 3

GenotypeDepth
all individuals: 26
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GenotypeDepth
all individuals: 20
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variant carriers: 2

GenotypeDepth
all individuals: 15
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variant carriers: 1

GenotypeQuality
all individuals: 39770
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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: 293

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 946
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 9.25e1
variant carriers: 1

African
type: Population
allele count: 287
allele frequency: 2.901921132457027e-2
allele num: 9890
num of homozygotes: 6

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8506
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.545642832854184e-5
allele num: 64698
num of homozygotes: 0

Latino
type: Population
allele count: 13
allele frequency: 1.130828114126653e-3
allele num: 11496
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.123595505617978e-3
allele num: 890
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.99e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -1.195e0

InbreedingCoeff
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SIO_000300: 2.7e-2

VQSLOD
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SIO_000300: 6.38e0

QD
type: SiteQuality
SIO_000300: 1.368e1

DP
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SIO_000300: 1.672011e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.71e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

GenotypeDepth
all individuals: 480
bin: 4.25e1
variant carriers: 2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 45

GenotypeDepth
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GenotypeDepth
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variant carriers: 12

GenotypeQuality
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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: 1201
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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: 273
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 32
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GenotypeQuality
all individuals: 952
bin: 8.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.706251088281386e-5
allele num: 11486
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.186587478346944e-5
allele num: 64656
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16436
num of homozygotes: 0

African
type: Population
allele count: 73
allele frequency: 7.412672623883022e-3
allele num: 9848
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.794e0

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-2

QD
type: SiteQuality
SIO_000300: 1.274e1

VQSLOD
type: SiteQuality
SIO_000300: 5.62e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

DP
type: SiteQuality
SIO_000300: 1.657461e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.59e-1

GenotypeDepth
all individuals: 1940
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29312
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variant carriers: 0

GenotypeDepth
all individuals: 1210
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GenotypeDepth
all individuals: 41
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 31
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 370
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GenotypeQuality
all individuals: 18
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GenotypeQuality
all individuals: 69
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variant carriers: 0

GenotypeQuality
all individuals: 50
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variant carriers: 0

GenotypeQuality
all individuals: 2661
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GenotypeQuality
all individuals: 58
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variant carriers: 0

GenotypeQuality
all individuals: 288
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variant carriers: 0

GenotypeQuality
all individuals: 164
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GenotypeQuality
all individuals: 1129
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variant carriers: 2

GenotypeQuality
all individuals: 37
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GenotypeQuality
all individuals: 9839
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 59
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GenotypeQuality
all individuals: 2285
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16414
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9812
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.098661378284581e-5
allele num: 64544
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.57e-1

DP
type: SiteQuality
SIO_000300: 1.646416e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.12e-1

QD
type: SiteQuality
SIO_000300: 1.34e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.991e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

FS
type: SiteQuality
SIO_000300: 4.719e0

VQSLOD
type: SiteQuality
SIO_000300: 1.82e0

MQRankSum
type: SiteQuality
SIO_000300: 5.54e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 29
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 203
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variant carriers: 1

GenotypeDepth
all individuals: 31
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variant carriers: 0

GenotypeDepth
all individuals: 88
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variant carriers: 0

GenotypeDepth
all individuals: 1938
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variant carriers: 0

GenotypeDepth
all individuals: 41
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GenotypeDepth
all individuals: 201
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GenotypeQuality
all individuals: 288
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variant carriers: 0

GenotypeQuality
all individuals: 35
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GenotypeQuality
all individuals: 72
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variant carriers: 0

GenotypeQuality
all individuals: 157
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GenotypeQuality
all individuals: 320
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GenotypeQuality
all individuals: 273
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GenotypeQuality
all individuals: 62
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 74
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GenotypeQuality
all individuals: 381
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 39644
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16414
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.55053183241852e-5
allele num: 64494
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e0

QD
type: SiteQuality
SIO_000300: 2.9e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.829e0

MQ
type: SiteQuality
SIO_000300: 5.444e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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SIO_000300: -1.639e0

ReadPosRankSum
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SIO_000300: -2.127e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.46e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

DP
type: SiteQuality
SIO_000300: 1.645728e6

GenotypeDepth
all individuals: 43
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 123
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variant carriers: 0

GenotypeDepth
all individuals: 65
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variant carriers: 0

GenotypeDepth
all individuals: 41
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variant carriers: 0

GenotypeDepth
all individuals: 1926
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GenotypeDepth
all individuals: 475
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GenotypeQuality
all individuals: 367
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GenotypeQuality
all individuals: 197
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GenotypeQuality
all individuals: 104
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 70
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GenotypeQuality
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GenotypeQuality
all individuals: 287
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 35
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GenotypeQuality
all individuals: 35
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GenotypeQuality
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GenotypeQuality
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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: 2215
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GenotypeQuality
all individuals: 1124
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9686
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11438
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.558797855094152e-5
allele num: 64152
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.295e1

InbreedingCoeff
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MQ
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SIO_000300: 5.929e1

DP
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VQSLOD
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MQRankSum
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ClippingRankSum
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SIO_000300: -1.336e0

FS
type: SiteQuality
SIO_000300: 9.718999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.183e0

GenotypeDepth
all individuals: 195
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variant carriers: 1

GenotypeDepth
all individuals: 26
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variant carriers: 0

GenotypeDepth
all individuals: 12311
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 427
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GenotypeQuality
all individuals: 2271
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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: 283
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GenotypeQuality
all individuals: 270
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8382
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9514
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11408
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.852309212151148e-4
allele num: 16196
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.368e1

FS
type: SiteQuality
SIO_000300: 7.819e0

ClippingRankSum
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SIO_000300: -6.16e-1

MQRankSum
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MQ
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DP
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

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

Latino
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allele num: 11408
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South Asian
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Other
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ReadPosRankSum
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DP
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MQ
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InbreedingCoeff
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VQSLOD
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FS
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

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

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

South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 63350
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African
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Latino
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Other
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VQSLOD
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ReadPosRankSum
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QD
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MQRankSum
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InbreedingCoeff
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DP
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FS
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BaseQRankSum
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MQ
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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European (Non-Finnish)
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allele num: 63330
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Latino
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European (Finnish)
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East Asian
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South Asian
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InbreedingCoeff
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MQ
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ClippingRankSum
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DP
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MQRankSum
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ReadPosRankSum
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FS
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QD
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VQSLOD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 63236
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Latino
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African
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South Asian
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East Asian
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European (Finnish)
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Other
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BaseQRankSum
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ReadPosRankSum
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DP
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ClippingRankSum
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MQ
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InbreedingCoeff
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QD
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VQSLOD
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MQRankSum
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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allele frequency: 1.162790697674419e-1
allele num: 9460
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European (Finnish)
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Other
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allele count: 3
allele frequency: 3.488372093023256e-3
allele num: 860
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.744583267436344e-5
allele num: 63230
num of homozygotes: 0

Latino
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allele count: 38
allele frequency: 3.338604814619575e-3
allele num: 11382
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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QD
type: SiteQuality
SIO_000300: 1.57e1

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

East Asian
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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: 1.583430978243658e-5
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num of homozygotes: 0

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

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

East Asian
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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European (Finnish)
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allele frequency: 0.0e0
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African
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South Asian
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BaseQRankSum
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SIO_000300: -5.976e0

DP
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VQSLOD
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FS
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MQ
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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SIO_000300: -1.023e0

ClippingRankSum
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QD
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GenotypeDepth
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 850
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East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.588007368354189e-5
allele num: 62972
num of homozygotes: 0

Latino
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MQ
type: SiteQuality
SIO_000300: 5.954e1

ClippingRankSum
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SIO_000300: -2.93e-1

QD
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FS
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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MQRankSum
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DP
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SIO_000300: 1.551712e6

InbreedingCoeff
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SIO_000300: 0.0e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11360
num of homozygotes: 0

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15664
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.588511882068878e-5
allele num: 62952
num of homozygotes: 0

Latino
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num of homozygotes: 0

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

East Asian
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num of homozygotes: 0

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

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

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

African
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Other
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South Asian
type: Population
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allele num: 15612
num of homozygotes: 0

Latino
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62930
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: -1.711e0

VQSLOD
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ReadPosRankSum
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MQ
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DP
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SIO_000300: 1.547553e6

FS
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SIO_000300: 2.066e0

MQRankSum
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SIO_000300: 1.65e-1

QD
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ClippingRankSum
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SIO_000300: 3.69e-1

InbreedingCoeff
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SIO_000300: 3.4e-3

GenotypeDepth
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variant carriers: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8372
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9168
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11354
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.178134435086604e-5
allele num: 62930
num of homozygotes: 0

MQ
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SIO_000300: 5.892e1

MQRankSum
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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FS
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DP
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InbreedingCoeff
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SIO_000300: 3.4e-3

VQSLOD
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9168
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11342
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8370
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62856
num of homozygotes: 0

South Asian
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allele frequency: 6.442468754026543e-5
allele num: 15522
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6530
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.09e-1

ReadPosRankSum
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FS
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SIO_000300: 2.392e0

MQRankSum
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ClippingRankSum
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InbreedingCoeff
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MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -1.589e0

DP
type: SiteQuality
SIO_000300: 1.545697e6

QD
type: SiteQuality
SIO_000300: 1.103e1

GenotypeDepth
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.435006435006435e-5
allele num: 15540
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6522
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62876
num of homozygotes: 0

DP
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SIO_000300: 1.545742e6

InbreedingCoeff
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SIO_000300: -2.0e-4

FS
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SIO_000300: 0.0e0

BaseQRankSum
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MQRankSum
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SIO_000300: -5.55e-1

VQSLOD
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ClippingRankSum
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SIO_000300: 9.350000000000001e-1

ReadPosRankSum
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SIO_000300: -8.110000000000001e-1

QD
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SIO_000300: 8.5e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 3
allele frequency: 3.270111183780249e-4
allele num: 9174
num of homozygotes: 0

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

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

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

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

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

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

European (Non-Finnish)
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Other
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South Asian
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East Asian
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European (Finnish)
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African
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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FS
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ClippingRankSum
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MQ
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DP
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62814
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.091464745688714e-4
allele num: 9162
num of homozygotes: 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: 11332
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8376
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15492
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6490
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.86e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.84e0

FS
type: SiteQuality
SIO_000300: 6.329e0

DP
type: SiteQuality
SIO_000300: 1.543742e6

QD
type: SiteQuality
SIO_000300: 8.49e0

VQSLOD
type: SiteQuality
SIO_000300: -1.14e-2

GenotypeDepth
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bin: 5.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 6

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.553835865099838e-5
allele num: 62802
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15500
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6486
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8380
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9162
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.544546e6

FS
type: SiteQuality
SIO_000300: 5.5e-1

QD
type: SiteQuality
SIO_000300: 1.16e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.327e0

MQRankSum
type: SiteQuality
SIO_000300: 8.129999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.45e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

GenotypeDepth
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bin: 9.75e1
variant carriers: 8

GenotypeDepth
all individuals: 8
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variant carriers: 4

GenotypeDepth
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bin: 6.25e1
variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 41

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 235
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variant carriers: 0

GenotypeQuality
all individuals: 9096
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9104
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15412
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6422
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 41
allele frequency: 6.555175390912289e-4
allele num: 62546
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11306
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8386
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.74e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.142e0

DP
type: SiteQuality
SIO_000300: 1.539279e6

QD
type: SiteQuality
SIO_000300: 1.357e1

VQSLOD
type: SiteQuality
SIO_000300: 4.85e0

MQRankSum
type: SiteQuality
SIO_000300: 5.7e-2

MQ
type: SiteQuality
SIO_000300: 5.96e1

GenotypeDepth
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bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 6.25e1
variant carriers: 1

GenotypeDepth
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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: 711
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 874
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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: 2485
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9086
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.598721023181455e-5
allele num: 62550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15426
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8386
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6416
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11298
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.923e1

DP
type: SiteQuality
SIO_000300: 1.536764e6

VQSLOD
type: SiteQuality
SIO_000300: -2.61e0

QD
type: SiteQuality
SIO_000300: 3.048e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.8e-1

FS
type: SiteQuality
SIO_000300: 1.7048e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.068e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.77e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 0
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variant carriers: 0

GenotypeDepth
all individuals: 900
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variant carriers: 0

GenotypeQuality
all individuals: 726
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GenotypeQuality
all individuals: 118
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2115
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 65
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 127
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variant carriers: 0

GenotypeQuality
all individuals: 9080
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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
all individuals: 174
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 38069
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GenotypeQuality
all individuals: 344
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.599795226211045e-5
allele num: 62508
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15408
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9074
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8382
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11296
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.383e1

DP
type: SiteQuality
SIO_000300: 1.538346e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 4.83e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

BaseQRankSum
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SIO_000300: -1.746e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.42e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 9
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variant carriers: 0

GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 115
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variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6386
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.388915432393693e-4
allele num: 8372
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11284
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62434
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9044
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.297690111601349e-4
allele num: 15412
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

FS
type: SiteQuality
SIO_000300: 9.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e-1

DP
type: SiteQuality
SIO_000300: 1.53445e6

MQRankSum
type: SiteQuality
SIO_000300: -1.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.94e-1

QD
type: SiteQuality
SIO_000300: 9.619999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.7e-2

MQ
type: SiteQuality
SIO_000300: 5.937e1

GenotypeDepth
all individuals: 1
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11278
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9040
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.602050624799744e-5
allele num: 62420
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6386
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.34e-1

FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.304e1

DP
type: SiteQuality
SIO_000300: 1.534757e6

BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.25e-1

MQ
type: SiteQuality
SIO_000300: 5.869e1

GenotypeDepth
all individuals: 4
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variant carriers: 0

GenotypeDepth
all individuals: 0
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GenotypeDepth
all individuals: 28
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2477
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GenotypeQuality
all individuals: 305
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GenotypeQuality
all individuals: 553
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 864
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.204101249599487e-5
allele num: 62420
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11278
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8372
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6386
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.212389380530973e-4
allele num: 9040
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.195e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.25e-1

FS
type: SiteQuality
SIO_000300: 5.75e-1

QD
type: SiteQuality
SIO_000300: 1.304e1

MQ
type: SiteQuality
SIO_000300: 5.869e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.5e-2

DP
type: SiteQuality
SIO_000300: 1.534757e6

GenotypeDepth
all individuals: 12808
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 100
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1693
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9027
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 830
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2087
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2453
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4446
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 173
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 131
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37557
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 857
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6338
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8354
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.877840909090909e-5
allele num: 11264
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15388
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8984
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62172
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.406e0

VQSLOD
type: SiteQuality
SIO_000300: -1.523e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.48e0

FS
type: SiteQuality
SIO_000300: 7.592e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.56e-1

DP
type: SiteQuality
SIO_000300: 1.526087e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.37e-1

MQ
type: SiteQuality
SIO_000300: 5.909e1

QD
type: SiteQuality
SIO_000300: 1.325e1

GenotypeDepth
all individuals: 10
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 720
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1888
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 806
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 2233
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8440
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 854
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 913
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35751
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 754
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4540
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 755
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8328
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.616088947024199e-4
allele num: 15290
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.743739647276625e-5
allele num: 61578
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11214
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8772
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6246
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.362e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.48e-1

FS
type: SiteQuality
SIO_000300: 2.644e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

MQRankSum
type: SiteQuality
SIO_000300: 6.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.8e-1

DP
type: SiteQuality
SIO_000300: 1.504015e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.600000000000001e-1