16-731914-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731914
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731914
    reference: chr 16
allele count: 5
allele frequency: 4.17160306362529e-5
allele num: 119858
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.404+11G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.329+34G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1220G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*880C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.612+34G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*880C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.396+34G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1962C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.555+34G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*880C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*880C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1759C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.211+34G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1783C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.742G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.396+34G>A
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7823
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11015
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-731918-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731918
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731918
    reference: chr 16
allele count: 3
allele frequency: 2.502711270543088e-5
allele num: 119870
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.329+38G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*876C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.396+38G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1779C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.211+38G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1224G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.746G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*876C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*876C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.404+15G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*876C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1755C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.612+38G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.555+38G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1958C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.396+38G>A
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5287
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11028
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

16-731919-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731919
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731919
    reference: chr 16
allele count: 1
allele frequency: 8.34125752798492e-6
allele num: 119886
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*875A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*875A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.612+39T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.329+39T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*875A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*875A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.396+39T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1225T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1957A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1778A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.555+39T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.404+16T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.747T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1754A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.396+39T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.211+39T>C
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13904
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11022
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

http://identifiers.org/exac.variant/16-731922-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731922
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731922
    reference: chr 16
allele count: 1
allele frequency: 8.340840089413805e-6
allele num: 119892
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*872T>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.396+42A>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.396+42A>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.404+19A>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1954T>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1751T>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*872T>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1228A>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.211+42A>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.750A>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*872T>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*872T>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.612+42A>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.555+42A>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1775T>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.329+42A>C
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7826
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

16-731923-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731923
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731923
    reference: chr 16
allele count: 5
allele frequency: 4.170280910122106e-5
allele num: 119896
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1774G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1953G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.612+43C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.404+20C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.555+43C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.396+43C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1750G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*871G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.396+43C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.329+43C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*871G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*871G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*871G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.211+43C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.751C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1229C>T
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5294
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7828
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12967
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-731924-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731924
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731924
    reference: chr 16
allele count: 6
allele frequency: 5.003752814610959e-5
allele num: 119910
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1773C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.555+44G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1952C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.329+44G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*870C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.396+44G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.752G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*870C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.396+44G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.404+21G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1230G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*870C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1749C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*870C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.612+44G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.211+44G>A
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11072
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7828
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ

16-731928-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731928
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731928
    reference: chr 16
allele count: 18
allele frequency: 1.501200960768615e-4
allele num: 119904
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*866G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.756C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1745G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.612+48C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1234C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*866G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.211+48C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*866G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1948G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.555+48C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*866G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.404+25C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.396+48C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.329+48C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.396+48C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1769G>A
  variant of: http://identifiers.org/hgnc/14148
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11088
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13959
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum

16-731929-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731929
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731929
    reference: chr 16
allele count: 6
allele frequency: 5.002668089647812e-5
allele num: 119936
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*865C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*865C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1744C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.329+49G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*865C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.757G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*865C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.612+49G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1768C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1235G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1947C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.555+49G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.404+26G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.396+49G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.396+49G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.211+49G>A
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12938
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3412
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13984
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

16-731933-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731933
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731933
    reference: chr 16
allele count: 1061
allele frequency: 8.845499716543836e-3
allele num: 119948
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1740C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1764C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1943C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.761G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.612+53G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.211+53G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*861C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1239G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*861C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*861C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.555+53G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.404+30G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*861C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.396+53G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.329+53G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.396+53G>A
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 102
genotype depth: GenotypeDepth
  all individuals: 2124
  bin: 5.25e1
  variant carriers: 100
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3428
  bin: 4.75e1
  variant carriers: 83
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 6.75e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 6.25e1
  variant carriers: 119
genotype depth: GenotypeDepth
  all individuals: 12735
  bin: 2.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
num of homozygotes: 5
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

16-731936-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731936
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731936
    reference: chr 16
allele count: 1
allele frequency: 8.33694600993764e-6
allele num: 119948
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1940G>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*858G>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.396+56C>G
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.764C>G
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.396+56C>G
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1761G>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1242C>G
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.612+56C>G
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*858G>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*858G>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1737G>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*858G>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.329+56C>G
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.211+56C>G
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.404+33C>G
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.555+56C>G
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12726
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

http://identifiers.org/exac.variant/16-731937-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731937
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731937
    reference: chr 16
allele count: 1
allele frequency: 8.335695113615524e-6
allele num: 119966
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*857T>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1243A>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*857T>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.612+57A>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.555+57A>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1939T>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*857T>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1760T>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.396+57A>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.404+34A>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*857T>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.765A>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.396+57A>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.329+57A>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1736T>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.211+57A>C
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13922
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5343
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12733
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3452
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
reference allele: A
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-731942-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731942
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731942
    reference: chr 16
allele count: 1
allele frequency: 8.337363058811759e-6
allele num: 119942
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1934G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*852G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1731G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*852G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1755G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*852G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.329+62C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1248C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*852G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.555+62C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.770C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.404+39C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.396+62C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.612+62C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.211+62C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.396+62C>T
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3455
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7834
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ

16-731943-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731943
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731943
    reference: chr 16
allele count: 7
allele frequency: 5.836348780203105e-5
allele num: 119938
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.396+63G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*851C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.771G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.329+63G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*851C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.555+63G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1754C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1249G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.211+63G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.396+63G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*851C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*851C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1933C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1730C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.404+40G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.612+63G>A
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11001
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7837
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12693
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

16-731943-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731943
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731943
    reference: chr 16
allele count: 2
allele frequency: 1.667528222915173e-5
allele num: 119938
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1933C>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*851C>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.771G>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.211+63G>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.404+40G>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1754C>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1730C>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.329+63G>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*851C>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.612+63G>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*851C>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*851C>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1249G>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.396+63G>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.555+63G>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.396+63G>C
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5356
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11001
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13919
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

16-731944-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731944
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731944
    reference: chr 16
allele count: 1
allele frequency: 8.337085021593051e-6
allele num: 119946
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*850G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.396+64C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1753G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*850G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.555+64C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*850G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1250C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*850G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1729G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.612+64C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.329+64C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.396+64C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.211+64C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1932G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.404+41C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.772C>T
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12719
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13928
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10992
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD

16-731946-TTG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731946
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731944
    reference: chr 16
allele count: 1
allele frequency: 8.337641114575865e-6
allele num: 119938
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.404+47_404+48delGT
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*846_*847delCA
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.556-69_555+70delGT
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*846_*847delCA
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1256_1257delGT
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1725_1726delCA
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.613-69_612+70delGT
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.778_779delGT
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1749_1750delCA
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*846_*847delCA
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.211+70_211+71delGT
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1928_1929delCA
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*846_*847delCA
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.397-69_396+70delGT
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.397-69_396+70delGT
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.330-69_329+70delGT
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13927
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5360
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7833
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
reference allele: TTG
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-731953-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731953
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731953
    reference: chr 16
allele count: 196
allele frequency: 1.633932441895362e-3
allele num: 119956
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*841C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.330-67G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1923C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*841C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.211+73G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1744C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.404+50G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*841C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*841C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.556-67G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.397-67G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1720C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.397-67G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.781G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.613-67G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1259G>A
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 5.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 7823
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 13901
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5354
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 10960
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3457
  bin: 4.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
num of homozygotes: 3
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

16-731955-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731955
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731955
    reference: chr 16
allele count: 10
allele frequency: 8.335834083558401e-5
allele num: 119964
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*839C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*839C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*839C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*839C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1718C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.556-65G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.330-65G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1742C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.404+52G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1921C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.211+75G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.613-65G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.397-65G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1261G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.783G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.397-65G>A
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13907
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10969
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/16-731962-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731962
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731962
    reference: chr 16
allele count: 1
allele frequency: 8.340840089413805e-6
allele num: 119892
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1735G>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1914G>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.790C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.397-58C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.397-58C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*832G>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.613-58C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*832G>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1711G>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.211+82C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*832G>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*832G>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.405-58C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.556-58C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1268C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.330-58C>A
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7836
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12547
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10984
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

16-731962-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731962
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731962
    reference: chr 16
allele count: 1
allele frequency: 8.340840089413805e-6
allele num: 119892
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.397-58C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.556-58C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.397-58C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1735G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1711G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*832G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.405-58C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*832G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*832G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1268C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1914G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.211+82C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.330-58C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.790C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*832G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.613-58C>T
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10984
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13901
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7836
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

16-731963-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731963
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731963
    reference: chr 16
allele count: 1
allele frequency: 8.339588024351597e-6
allele num: 119910
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1734G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1710G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*831G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.397-57C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.330-57C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.211+83C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*831G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.791C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.556-57C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*831G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*831G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.397-57C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1913G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.613-57C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.405-57C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1269C>T
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7833
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13901
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3471
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

16-731967-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731967
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731967
    reference: chr 16
allele count: 1
allele frequency: 8.339727124128499e-6
allele num: 119908
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1730A>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.397-53T>G
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*827A>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.397-53T>G
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*827A>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.211+87T>G
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.795T>G
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*827A>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1706A>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*827A>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1909A>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.556-53T>G
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.405-53T>G
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.613-53T>G
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1273T>G
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.330-53T>G
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7836
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10962
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD

16-731971-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731971
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731971
    reference: chr 16
allele count: 1
allele frequency: 8.342649291709075e-6
allele num: 119866
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.405-49G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.799G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1905C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*823C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1726C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1702C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*823C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.397-49G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*823C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.613-49G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.556-49G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.212-88G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*823C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1277G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.397-49G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.330-49G>A
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3471
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7839
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12389
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13827
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-731974-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731974
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731974
    reference: chr 16
allele count: 1
allele frequency: 8.343623802689983e-6
allele num: 119852
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1699C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.405-46G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1280G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.212-85G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*820C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1902C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.613-46G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.397-46G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*820C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1723C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.330-46G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*820C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*820C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.397-46G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.556-46G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.802G>A
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7838
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13809
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

16-731975-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731975
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731975
    reference: chr 16
allele count: 1
allele frequency: 8.344180768332166e-6
allele num: 119844
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*819C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.803G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.613-45G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1901C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.405-45G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*819C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1698C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.330-45G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1281G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*819C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*819C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.556-45G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.212-84G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1722C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.397-45G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.397-45G>A
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10962
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7835
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5351
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

16-731979-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731979
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731978
    reference: chr 16
allele count: 2
allele frequency: 1.669978791269351e-5
allele num: 119762
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.397-40delT
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1717delA
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.330-40delT
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1286delT
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.397-40delT
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1896delA
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*814delA
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1693delA
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*814delA
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.212-79delT
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.556-40delT
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.613-40delT
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*814delA
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*814delA
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.808delT
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.405-40delT
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13757
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: GT
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP

16-731982-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731982
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731982
    reference: chr 16
allele count: 1
allele frequency: 8.353660574063554e-6
allele num: 119708
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.397-38G>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*812C>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*812C>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*812C>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1691C>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.810G>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.330-38G>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*812C>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1894C>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1288G>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.212-77G>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.556-38G>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.405-38G>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1715C>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.397-38G>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.613-38G>C
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10957
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12184
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7844
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum

16-731983-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731983
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731983
    reference: chr 16
allele count: 1
allele frequency: 8.354777261638205e-6
allele num: 119692
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*811C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1714C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.556-37G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.212-76G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*811C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.811G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*811C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*811C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.330-37G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.613-37G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1690C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.397-37G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.397-37G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1289G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.405-37G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1893C>T
  variant of: http://identifiers.org/hgnc/14148
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13691
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7845
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12161
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

16-731988-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731988
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731988
    reference: chr 16
allele count: 1
allele frequency: 8.373526259378349e-6
allele num: 119424
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1709G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1294C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.212-71C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*806G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1888G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.330-32C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1685G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*806G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*806G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*806G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.405-32C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.397-32C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.397-32C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.816C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.556-32C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.613-32C>T
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7841
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3475
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13633
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10965
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

16-731989-TCCC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731989
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731986
    reference: chr 16
allele count: 143
allele frequency: 1.197654941373534e-3
allele num: 119400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1705_1707delGGG
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*802_*804delGGG
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.330-28_330-26delCCC
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1681_1683delGGG
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*802_*804delGGG
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.397-28_397-26delCCC
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.405-28_405-26delCCC
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.556-28_556-26delCCC
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1884_1886delGGG
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*802_*804delGGG
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.820_822delCCC
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1298_1300delCCC
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*802_*804delGGG
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.397-28_397-26delCCC
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.613-28_613-26delCCC
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.212-67_212-65delCCC
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13618
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 7828
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10953
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11802
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3471
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 5.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
num of homozygotes: 3
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
reference allele: TCCC
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/16-731990-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731990
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731990
    reference: chr 16
allele count: 1
allele frequency: 8.399973120086016e-6
allele num: 119048
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.556-30C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.397-30C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1707G>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1886G>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*804G>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1296C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*804G>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1683G>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*804G>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.613-30C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.818C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.330-30C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.405-30C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*804G>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.212-69C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.397-30C>A
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5345
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10939
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

16-731991-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731991
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731991
    reference: chr 16
allele count: 4
allele frequency: 3.358691453809596e-5
allele num: 119094
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1885G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.819C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*803G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1682G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*803G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.397-29C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*803G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1706G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.556-29C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.397-29C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.330-29C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.613-29C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.212-68C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1297C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*803G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.405-29C>T
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

16-731994-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731994
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731994
    reference: chr 16
allele count: 4
allele frequency: 3.357845606259024e-5
allele num: 119124
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*800G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.822C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1300C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.212-65C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1679G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.556-26C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*800G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*800G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*800G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1703G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1882G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.330-26C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.397-26C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.613-26C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.397-26C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.405-26C>T
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10937
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13522
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/16-731998-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 731998
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731998
    reference: chr 16
allele count: 7
allele frequency: 5.884231939610968e-5
allele num: 118962
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.556-22C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*796G>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.405-22C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*796G>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.613-22C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.330-22C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*796G>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.826C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1304C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1878G>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*796G>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.212-61C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.397-22C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.397-22C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1675G>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1699G>T
  variant of: http://identifiers.org/hgnc/14148
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3467
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13442
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-732002-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 732002
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 732002
    reference: chr 16
allele count: 2
allele frequency: 1.682566924099406e-5
allele num: 118866
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.830G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.613-18G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*792C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.556-18G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.397-18G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1874C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1695C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.405-18G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*792C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*792C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*792C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1308G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1671C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.330-18G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.397-18G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.212-57G>A
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10907
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5347
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

16-732003-CACTCA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 732003
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731998
    reference: chr 16
allele count: 1
allele frequency: 8.421478137842754e-6
allele num: 118744
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*786_*790delTGAGT
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*786_*790delTGAGT
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1868_1872delTGAGT
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.556-12_556-8delAACTC
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1314_1318delAACTC
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*786_*790delTGAGT
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1665_1669delTGAGT
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*786_*790delTGAGT
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1689_1693delTGAGT
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.330-12_330-8delAACTC
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.613-12_613-8delAACTC
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.397-12_397-8delAACTC
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.836_840delAACTC
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.405-12_405-8delAACTC
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.397-12_397-8delAACTC
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.212-51_212-47delAACTC
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13335
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11248
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7821
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
reference allele: CACTCA
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

16-732004-ACTCAACTCTT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 732004
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 731994
    reference: chr 16
allele count: 1
allele frequency: 8.422896802668375e-6
allele num: 118724
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10904
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13319
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7817
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5344
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11210
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.613-14_613-5delTCAACTCTTC
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: ACTCAACTCTT
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD

16-732006-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 732006
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 732006
    reference: chr 16
allele count: 2
allele frequency: 1.686397517622854e-5
allele num: 118596
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*788A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.397-14T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*788A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.212-53T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*788A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*788A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1312T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1667A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.834T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.330-14T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.397-14T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1870A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.556-14T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.613-14T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.405-14T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1691A>G
  variant of: http://identifiers.org/hgnc/14148
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10904
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13239
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum

16-732007-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 732007
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 732007
    reference: chr 16
allele count: 1
allele frequency: 8.442665856170744e-6
allele num: 118446
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*787G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.613-13C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1869G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.835C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.212-52C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1313C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*787G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*787G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*787G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.556-13C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.397-13C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.397-13C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1666G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1690G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.405-13C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.330-13C>T
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10908
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13215
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10931
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

16-732029-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 732029
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 732029
    reference: chr 16
allele count: 1
allele frequency: 8.560617734175697e-6
allele num: 116814
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.565A>G
  hgvsp: ENSP00000456591.1:p.Met189Val
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.406A>G
  hgvsp: ENSP00000456875.1:p.Met136Val
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.212-30A>G
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*765T>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*765T>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1644T>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*765T>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*765T>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1847T>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.857A>G
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.339A>G
  hgvsp: ENSP00000457583.1:p.Met114Val
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.622A>G
  hgvsp: ENSP00000219548.4:p.Met208Val
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.414A>G
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.406A>G
  hgvsp: ENSP00000457228.1:p.Met136Val
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1335A>G
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1668T>C
  variant of: http://identifiers.org/hgnc/14148
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12791
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9814
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met208Val
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum

16-732033-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 732033
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 732033
    reference: chr 16
allele count: 3
allele frequency: 2.581933351693748e-5
allele num: 116192
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.410C>T
  hgvsp: ENSP00000456875.1:p.Ala137Val
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.626C>T
  hgvsp: ENSP00000219548.4:p.Ala209Val
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.212-26C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.569C>T
  hgvsp: ENSP00000456591.1:p.Ala190Val
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*761G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*761G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.861C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1843G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1664G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.410C>T
  hgvsp: ENSP00000457228.1:p.Ala137Val
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*761G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.343C>T
  hgvsp: ENSP00000457583.1:p.Ala115Val
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.418C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1339C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*761G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1640G>A
  variant of: http://identifiers.org/hgnc/14148
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5343
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10849
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12725
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala209Val
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

16-732034-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 732034
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 732034
    reference: chr 16
allele count: 2
allele frequency: 1.719513033908797e-5
allele num: 116312
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*760C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.212-25G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.627G>A
  hgvsp: ENST00000219548.4:c.627G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*760C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1340G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.411G>A
  hgvsp: ENST00000565677.1:c.411G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1663C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.570G>A
  hgvsp: ENST00000567173.1:c.570G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.411G>A
  hgvsp: ENST00000564370.1:c.411G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*760C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.862G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1842C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.344G>A
  hgvsp: ENST00000566408.1:c.344G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*760C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1639C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.419G>A
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10835
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12738
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7816
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9729
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Ala209Ala
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

16-732038-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 732038
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 732038
    reference: chr 16
allele count: 1
allele frequency: 8.613116053125699e-6
allele num: 116102
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1659T>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.415A>G
  hgvsp: ENSP00000457228.1:p.Met139Val
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.415A>G
  hgvsp: ENSP00000456875.1:p.Met139Val
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1635T>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1344A>G
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.348A>G
  hgvsp: ENSP00000457583.1:p.Met117Val
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.212-21A>G
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*756T>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.631A>G
  hgvsp: ENSP00000219548.4:p.Met211Val
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.423A>G
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*756T>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*756T>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1838T>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.574A>G
  hgvsp: ENSP00000456591.1:p.Met192Val
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*756T>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.866A>G
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5343
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9720
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met211Val
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

16-732042-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 732042
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 732042
    reference: chr 16
allele count: 1
allele frequency: 8.632745731107236e-6
allele num: 115838
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1348A>G
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.419A>G
  hgvsp: ENSP00000456875.1:p.Asp140Gly
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.352A>G
  hgvsp: ENSP00000457583.1:p.Asp118Gly
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.427A>G
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1631T>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*752T>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.419A>G
  hgvsp: ENSP00000457228.1:p.Asp140Gly
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*752T>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.578A>G
  hgvsp: ENSP00000456591.1:p.Asp193Gly
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.635A>G
  hgvsp: ENSP00000219548.4:p.Asp212Gly
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*752T>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1834T>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1655T>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.870A>G
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*752T>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.212-17A>G
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12659
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5343
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9693
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp212Gly
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

16-732043-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 732043
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 732043
    reference: chr 16
allele count: 3
allele frequency: 2.594437525944375e-5
allele num: 115632
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.353C>T
  hgvsp: ENST00000566408.1:c.353C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.212-16C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*751G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1630G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.871C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.420C>T
  hgvsp: ENST00000564370.1:c.420C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*751G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.636C>T
  hgvsp: ENST00000219548.4:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.579C>T
  hgvsp: ENST00000567173.1:c.579C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1833G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*751G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.420C>T
  hgvsp: ENST00000565677.1:c.420C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*751G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.428C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1654G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1349C>T
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7812
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10831
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp212Asp
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

16-732046-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 732046
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 732046
    reference: chr 16
allele count: 1
allele frequency: 8.653363562416712e-6
allele num: 115562
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.423G>A
  hgvsp: ENST00000565677.1:c.423G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.431G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.356G>A
  hgvsp: ENST00000566408.1:c.356G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*748C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.639G>A
  hgvsp: ENST00000219548.4:c.639G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*748C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1627C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1830C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.874G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*748C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.582G>A
  hgvsp: ENST00000567173.1:c.582G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.423G>A
  hgvsp: ENST00000564370.1:c.423G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1651C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*748C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1352G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.212-13G>A
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7812
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12637
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9641
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu213Glu
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

16-732049-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 732049
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 732049
    reference: chr 16
allele count: 519
allele frequency: 4.498959778085992e-3
allele num: 115360
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*745A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.426T>C
  hgvsp: ENST00000565677.1:c.426T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.585T>C
  hgvsp: ENST00000567173.1:c.585T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1827A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1355T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.359T>C
  hgvsp: ENST00000566408.1:c.359T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.212-10T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.642T>C
  hgvsp: ENST00000219548.4:c.642T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.426T>C
  hgvsp: ENST00000564370.1:c.426T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.434T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*745A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*745A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1624A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.877T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*745A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1648A>G
  variant of: http://identifiers.org/hgnc/14148
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 1.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2131
  bin: 1.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 12555
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7767
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5307
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10760
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9512
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu214Leu
num of homozygotes: 14
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum

16-732064-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 732064
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 732064
    reference: chr 16
allele count: 2
allele frequency: 1.744683078318823e-5
allele num: 114634
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1812A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.600T>C
  hgvsp: ENST00000567173.1:c.600T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1633A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1370T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.441T>C
  hgvsp: ENST00000565677.1:c.441T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*730A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1609A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.657T>C
  hgvsp: ENST00000219548.4:c.657T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*730A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.374T>C
  hgvsp: ENST00000566408.1:c.374T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.217T>C
  hgvsp: ENST00000564316.1:c.217T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.449T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.441T>C
  hgvsp: ENST00000564370.1:c.441T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.892T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*730A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*730A>G
  variant of: http://identifiers.org/hgnc/14148
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12532
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10783
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9414
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp219Asp
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP

16-732064-TGAG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 732064
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 732061
    reference: chr 16
allele count: 1
allele frequency: 8.723415391594117e-6
allele num: 114634
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*727_*729delCTC
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1371_1373delGAG
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*727_*729delCTC
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1809_1811delCTC
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*727_*729delCTC
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.658_660delGAG
  hgvsp: ENSP00000219548.4:p.Glu220del
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1630_1632delCTC
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*727_*729delCTC
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.601_603delGAG
  hgvsp: ENSP00000456591.1:p.Glu201del
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.442_444delGAG
  hgvsp: ENSP00000456875.1:p.Glu148del
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.375_377delGAG
  hgvsp: ENSP00000457583.1:p.Glu126del
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.442_444delGAG
  hgvsp: ENSP00000457228.1:p.Glu148del
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.450_452delGAG
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1606_1608delCTC
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.218_220delGAG
  hgvsp: ENSP00000457090.1:p.Glu74del
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9414
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12532
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7795
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5350
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu220del
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: TGAG
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

16-732065-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 732065
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 732065
    reference: chr 16
allele count: 1
allele frequency: 8.726764988218868e-6
allele num: 114590
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.658G>A
  hgvsp: ENSP00000219548.4:p.Glu220Lys
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*729C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1608C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1371G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.218G>A
  hgvsp: ENSP00000457090.1:p.Glu74Lys
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*729C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.450G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*729C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.601G>A
  hgvsp: ENSP00000456591.1:p.Glu201Lys
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.893G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.442G>A
  hgvsp: ENSP00000456875.1:p.Glu148Lys
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.442G>A
  hgvsp: ENSP00000457228.1:p.Glu148Lys
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*729C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1811C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1632C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.375G>A
  hgvsp: ENSP00000457583.1:p.Glu126Lys
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7795
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2619
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9408
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu220Lys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-732066-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 732066
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 732066
    reference: chr 16
allele count: 1
allele frequency: 8.732709235713287e-6
allele num: 114512
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000563505
  gene symbol: STUB1
  hgvsc: ENST00000563505.1:n.894A>G
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.602A>G
  hgvsp: ENSP00000456591.1:p.Glu201Gly
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.443A>G
  hgvsp: ENSP00000456875.1:p.Glu148Gly
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1631T>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.219A>G
  hgvsp: ENSP00000457090.1:p.Glu74Gly
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*728T>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1372A>G
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.376A>G
  hgvsp: ENSP00000457583.1:p.Glu126Gly
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*728T>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*728T>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.443A>G
  hgvsp: ENSP00000457228.1:p.Glu148Gly
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1810T>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.659A>G
  hgvsp: ENSP00000219548.4:p.Glu220Gly
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.451A>G
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*728T>C
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1607T>C
  variant of: http://identifiers.org/hgnc/14148
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2628
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10786
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7795
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu220Gly
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-732067-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 732067
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 732067
    reference: chr 16
allele count: 16
allele frequency: 1.397501965237139e-4
allele num: 114490
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*727C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.377G>A
  hgvsp: ENST00000566408.1:c.377G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.660G>A
  hgvsp: ENST00000219548.4:c.660G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1809C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*727C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.220G>A
  hgvsp: ENST00000564316.1:c.220G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.444G>A
  hgvsp: ENST00000565677.1:c.444G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*727C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.444G>A
  hgvsp: ENST00000564370.1:c.444G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.452G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1606C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.603G>A
  hgvsp: ENST00000567173.1:c.603G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1373G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1630C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*727C>T
  variant of: http://identifiers.org/hgnc/14148
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2642
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12525
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1904
  bin: 1.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Glu220Glu
num of homozygotes: 1
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-732067-GAA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 732067
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 732065
    reference: chr 16
allele count: 1
allele frequency: 8.734387282732117e-6
allele num: 114490
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.445_446delAA
  hgvsp: ENSP00000456875.1:p.Lys149GlufsTer17
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*725_*726delTT
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1374_1375delAA
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.661_662delAA
  hgvsp: ENSP00000219548.4:p.Lys221GlufsTer17
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1628_1629delTT
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1604_1605delTT
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*725_*726delTT
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.378_379delAA
  hgvsp: ENSP00000457583.1:p.Lys127GlufsTer17
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.604_605delAA
  hgvsp: ENSP00000456591.1:p.Lys202GlufsTer?
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.445_446delAA
  hgvsp: ENSP00000457228.1:p.Lys149GlufsTer17
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.221_222delAA
  hgvsp: ENSP00000457090.1:p.Lys75GlufsTer17
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1807_1808delTT
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*725_*726delTT
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*725_*726delTT
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.453_454delAA
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7796
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12525
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1904
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys221GlufsTer17
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: GAA
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

16-732072-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 732072
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 732072
    reference: chr 16
allele count: 2
allele frequency: 1.747946163258172e-5
allele num: 114420
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.382G>A
  hgvsp: ENSP00000457583.1:p.Arg128Lys
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*722C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1625C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.665G>A
  hgvsp: ENSP00000219548.4:p.Arg222Lys
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.449G>A
  hgvsp: ENSP00000456875.1:p.Arg150Lys
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1804C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*722C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.225G>A
  hgvsp: ENSP00000457090.1:p.Arg76Lys
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*722C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.457G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.608G>A
  hgvsp: ENSP00000456591.1:p.Arg203Lys
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*722C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.449G>A
  hgvsp: ENSP00000457228.1:p.Arg150Lys
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1601C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1378G>A
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2677
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7795
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg222Lys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD

16-732073-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 732073
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 732073
    reference: chr 16
allele count: 1
allele frequency: 8.745692746322435e-6
allele num: 114342
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.450G>A
  hgvsp: ENST00000564370.1:c.450G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.609G>A
  hgvsp: ENST00000567173.1:c.609G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.383G>A
  hgvsp: ENST00000566408.1:c.383G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.458G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.450G>A
  hgvsp: ENST00000565677.1:c.450G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1803C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.226G>A
  hgvsp: ENST00000564316.1:c.226G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.666G>A
  hgvsp: ENST00000219548.4:c.666G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*721C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*721C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1600C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*721C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1379G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*721C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1624C>T
  variant of: http://identifiers.org/hgnc/14148
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12525
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10786
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2694
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7795
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg222Arg
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

16-732076-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 732076
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 732076
    reference: chr 16
allele count: 1
allele frequency: 8.746763697431951e-6
allele num: 114328
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1382G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*718C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.386G>A
  hgvsp: ENST00000566408.1:c.386G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*718C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.461G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.612G>A
  hgvsp: ENST00000567173.1:c.612G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*718C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.453G>A
  hgvsp: ENST00000565677.1:c.453G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*718C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1621C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.453G>A
  hgvsp: ENST00000564370.1:c.453G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.229G>A
  hgvsp: ENST00000564316.1:c.229G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.669G>A
  hgvsp: ENST00000219548.4:c.669G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1800C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568313
  gene symbol: JMJD8
  hgvsc: ENST00000568313.1:n.953C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1597C>T
  variant of: http://identifiers.org/hgnc/14148
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7795
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.669G>A
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
population: Latino
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum

16-732080-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 732080
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 732080
    reference: chr 16
allele count: 2
allele frequency: 1.751068151572459e-5
allele num: 114216
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.386+4A>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.612+4A>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.453+4A>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*714T>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*714T>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.461+4A>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.669+4A>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*714T>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1796T>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.453+4A>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*714T>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.229+4A>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568313
  gene symbol: JMJD8
  hgvsc: ENST00000568313.1:n.949T>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1617T>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1593T>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1382+4A>T
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7795
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9323
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.669+4A>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

16-732081-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 732081
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 732081
    reference: chr 16
allele count: 1
allele frequency: 8.755340757862296e-6
allele num: 114216
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*713C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.461+5G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.453+5G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1616C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.612+5G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1592C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.669+5G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*713C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1795C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.453+5G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.386+5G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*713C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1382+5G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.229+5G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568313
  gene symbol: JMJD8
  hgvsc: ENST00000568313.1:n.948C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*713C>T
  variant of: http://identifiers.org/hgnc/14148
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7795
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9315
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12514
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.669+5G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

16-732082-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 732082
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 732082
    reference: chr 16
allele count: 1
allele frequency: 8.760096010652276e-6
allele num: 114154
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1382+6T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*712A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.461+6T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.669+6T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1615A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*712A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.453+6T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*712A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.612+6T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.229+6T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.386+6T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568313
  gene symbol: JMJD8
  hgvsc: ENST00000568313.1:n.947A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.453+6T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1794A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*712A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1591A>G
  variant of: http://identifiers.org/hgnc/14148
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.669+6T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

16-732089-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 732089
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 732089
    reference: chr 16
allele count: 55
allele frequency: 4.827356188670634e-4
allele num: 113934
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.386+13C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*705G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.453+13C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.612+13C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*705G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1382+13C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1584G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*705G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.669+13C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*705G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1608G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1787G>A
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.461+13C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.453+13C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.229+13C>T
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568313
  gene symbol: JMJD8
  hgvsc: ENST00000568313.1:n.940G>A
  variant of: http://identifiers.org/hgnc/14148
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2839
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7796
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10786
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9279
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

16-732090-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 732090
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 732090
    reference: chr 16
allele count: 197
allele frequency: 1.727161143257934e-3
allele num: 114060
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*704C>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1382+14G>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1583C>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*704C>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.669+14G>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568313
  gene symbol: JMJD8
  hgvsc: ENST00000568313.1:n.939C>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.612+14G>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1786C>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*704C>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.386+14G>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1607C>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.453+14G>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*704C>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.229+14G>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.453+14G>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.461+14G>C
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10751
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12468
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 6.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
num of homozygotes: 3
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ

16-732090-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 732090
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 732090
    reference: chr 16
allele count: 14
allele frequency: 1.227424162721375e-4
allele num: 114060
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.386+14G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*704C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.453+14G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1583C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*704C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1382+14G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.461+14G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.229+14G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*704C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.612+14G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.669+14G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568313
  gene symbol: JMJD8
  hgvsc: ENST00000568313.1:n.939C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1786C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.453+14G>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*704C>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1607C>T
  variant of: http://identifiers.org/hgnc/14148
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5348
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

16-732092-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 732092
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 732092
    reference: chr 16
allele count: 1
allele frequency: 8.759635599159075e-6
allele num: 114160
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1605A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1382+16T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*702A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*702A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.229+16T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1784A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*702A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.453+16T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1581A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.386+16T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.669+16T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*702A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.453+16T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568313
  gene symbol: JMJD8
  hgvsc: ENST00000568313.1:n.937A>G
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.612+16T>C
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.461+16T>C
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10765
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1785
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7793
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9250
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ

http://identifiers.org/exac.variant/16-732099-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 732099
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 732099
    reference: chr 16
allele count: 1
allele frequency: 8.76024949190553e-6
allele num: 114152
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000569248
  gene symbol: STUB1
  hgvsc: ENST00000569248.1:n.1382+23C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000293882
  ensembl transcript: ENST00000293882
  gene symbol: JMJD8
  hgvsc: ENST00000293882.4:c.*695G>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457583
  ensembl transcript: ENST00000566408
  gene symbol: STUB1
  hgvsc: ENST00000566408.1:c.386+23C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000219548
  ensembl transcript: ENST00000219548
  gene symbol: STUB1
  hgvsc: ENST00000219548.4:c.669+23C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000567120
  gene symbol: JMJD8
  hgvsc: ENST00000567120.1:n.1777G>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000394147
  ensembl transcript: ENST00000454700
  gene symbol: JMJD8
  hgvsc: ENST00000454700.1:c.*695G>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl transcript: ENST00000566181
  gene symbol: STUB1
  hgvsc: ENST00000566181.2:n.461+23C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000565302
  gene symbol: JMJD8
  hgvsc: ENST00000565302.1:n.1574G>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568313
  gene symbol: JMJD8
  hgvsc: ENST00000568313.1:n.930G>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000477481
  ensembl transcript: ENST00000609261
  gene symbol: JMJD8
  hgvsc: ENST00000609261.1:c.*695G>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456591
  ensembl transcript: ENST00000567173
  gene symbol: STUB1
  hgvsc: ENST00000567173.1:c.612+23C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000161999
  ensembl transcript: ENST00000568689
  gene symbol: JMJD8
  hgvsc: ENST00000568689.1:n.1598G>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000456875
  ensembl transcript: ENST00000564370
  gene symbol: STUB1
  hgvsc: ENST00000564370.1:c.453+23C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457228
  ensembl transcript: ENST00000565677
  gene symbol: STUB1
  hgvsc: ENST00000565677.1:c.453+23C>A
  variant of: http://identifiers.org/hgnc/11427
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000161999
  ensembl protein: ENSP00000399475
  ensembl transcript: ENST00000412368
  gene symbol: JMJD8
  hgvsc: ENST00000412368.2:c.*695G>T
  variant of: http://identifiers.org/hgnc/14148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103266
  ensembl protein: ENSP00000457090
  ensembl transcript: ENST00000564316
  gene symbol: STUB1
  hgvsc: ENST00000564316.1:c.229+23C>A
  variant of: http://identifiers.org/hgnc/11427
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: C

GenotypeDepth
all individuals: 286
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 460
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 382
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 321
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2059
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13026
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13857
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 126
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 135
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23101
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 533
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2823
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10598
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 67
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8099
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3954
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4774
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3550
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1987
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10214
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.099420555047271e-5
allele num: 65580
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.090875867949811e-5
allele num: 16418
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 4.01e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

QD
type: SiteQuality
SIO_000300: 1.517e1

FS
type: SiteQuality
SIO_000300: 1.34e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.991586e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.557e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.6e-2

GenotypeDepth
all individuals: 3396
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 261
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 456
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7824
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 77
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13894
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 221
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2059
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 126
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1988
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 533
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4774
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23286
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 100
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10598
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3956
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2823
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3557
bin: 7.25e1
variant carriers: 0

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

Other
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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 frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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allele count: 2
allele frequency: 3.031221582297666e-4
allele num: 6598
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.524762137106611e-5
allele num: 65584
num of homozygotes: 0

ClippingRankSum
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MQ
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MQRankSum
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DP
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SIO_000300: 1.992695e6

InbreedingCoeff
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VQSLOD
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FS
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SIO_000300: 1.815e0

ReadPosRankSum
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SIO_000300: 5.09e-1

QD
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BaseQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

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

Other
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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: 1.524622655892666e-5
allele num: 65590
num of homozygotes: 0

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

Other
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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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

MQ
type: SiteQuality
SIO_000300: 5.981e1

QD
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ClippingRankSum
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SIO_000300: -1.521e0

VQSLOD
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InbreedingCoeff
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FS
type: SiteQuality
SIO_000300: 1.714e0

BaseQRankSum
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SIO_000300: 5.81e0

MQRankSum
type: SiteQuality
SIO_000300: 1.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.35e-1

DP
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SIO_000300: 1.993567e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 16414
num of homozygotes: 0

European (Non-Finnish)
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allele num: 65610
num of homozygotes: 0

Other
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African
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Latino
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allele frequency: 8.676036786395974e-5
allele num: 11526
num of homozygotes: 0

European (Finnish)
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DP
type: SiteQuality
SIO_000300: 1.994066e6

FS
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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QD
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VQSLOD
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MQ
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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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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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South Asian
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 65614
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East Asian
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African
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allele frequency: 0.0e0
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Latino
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Other
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European (Finnish)
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MQRankSum
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FS
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DP
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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QD
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ClippingRankSum
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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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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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East Asian
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European (Finnish)
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African
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Other
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South Asian
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Latino
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European (Non-Finnish)
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allele num: 65606
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FS
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DP
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BaseQRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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QD
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10248
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.09570252971655e-5
allele num: 65620
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
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: 2
allele frequency: 1.218917601170161e-4
allele num: 16408
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.48e0

FS
type: SiteQuality
SIO_000300: 3.441e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.86e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.19e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.996579e6

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

QD
type: SiteQuality
SIO_000300: 1.277e1

GenotypeDepth
all individuals: 224
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 13778
bin: 2.75e1
variant carriers: 15

GenotypeDepth
all individuals: 183
bin: 1.75e1
variant carriers: 6

GenotypeDepth
all individuals: 5287
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variant carriers: 70

GenotypeDepth
all individuals: 59
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variant carriers: 28

GenotypeDepth
all individuals: 203
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variant carriers: 71

GenotypeDepth
all individuals: 290
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variant carriers: 70

GenotypeDepth
all individuals: 10926
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variant carriers: 36

GenotypeDepth
all individuals: 1270
bin: 5.75e1
variant carriers: 104

GenotypeDepth
all individuals: 7759
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variant carriers: 59

GenotypeQuality
all individuals: 76
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 1948
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 56
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11328
bin: 9.75e1
variant carriers: 1054

African
type: Population
allele count: 27
allele frequency: 2.634660421545667e-3
allele num: 10248
num of homozygotes: 0

Latino
type: Population
allele count: 94
allele frequency: 8.152645273200346e-3
allele num: 11530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 816
allele frequency: 1.243182302934276e-2
allele num: 65638
num of homozygotes: 5

Other
type: Population
allele count: 7
allele frequency: 7.847533632286996e-3
allele num: 892
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157943492357573e-4
allele num: 8636
num of homozygotes: 0

South Asian
type: Population
allele count: 105
allele frequency: 6.404782237403928e-3
allele num: 16394
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 11
allele frequency: 1.664145234493192e-3
allele num: 6610
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.82e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.72e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.306e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

QD
type: SiteQuality
SIO_000300: 1.423e1

DP
type: SiteQuality
SIO_000300: 2.028635e6

GenotypeDepth
all individuals: 5342
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 172
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variant carriers: 0

GenotypeDepth
all individuals: 7818
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 13907
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 165
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GenotypeDepth
all individuals: 147
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GenotypeDepth
all individuals: 1262
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variant carriers: 0

GenotypeQuality
all individuals: 88
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variant carriers: 0

GenotypeQuality
all individuals: 44
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variant carriers: 0

GenotypeQuality
all individuals: 2817
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variant carriers: 0

GenotypeQuality
all individuals: 202
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variant carriers: 0

GenotypeQuality
all individuals: 10779
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 54
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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: 3928
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1992
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10254
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65640
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.102770657878677e-5
allele num: 16386
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.4279e1

DP
type: SiteQuality
SIO_000300: 2.013913e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.72e0

QD
type: SiteQuality
SIO_000300: 1.46e1

MQRankSum
type: SiteQuality
SIO_000300: -4.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.274e0

GenotypeDepth
all individuals: 70
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 433
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variant carriers: 0

GenotypeDepth
all individuals: 262
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variant carriers: 0

GenotypeDepth
all individuals: 214
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GenotypeDepth
all individuals: 2108
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variant carriers: 1

GenotypeDepth
all individuals: 42
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GenotypeDepth
all individuals: 165
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variant carriers: 0

GenotypeDepth
all individuals: 98
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variant carriers: 0

GenotypeDepth
all individuals: 10978
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variant carriers: 0

GenotypeDepth
all individuals: 147
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variant carriers: 0

GenotypeQuality
all individuals: 196
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variant carriers: 0

GenotypeQuality
all individuals: 42
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GenotypeQuality
all individuals: 23455
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variant carriers: 0

GenotypeQuality
all individuals: 520
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variant carriers: 0

GenotypeQuality
all individuals: 44
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variant carriers: 0

GenotypeQuality
all individuals: 8163
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variant carriers: 0

GenotypeQuality
all individuals: 48
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variant carriers: 0

GenotypeQuality
all individuals: 68
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variant carriers: 0

GenotypeQuality
all individuals: 23
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GenotypeQuality
all individuals: 85
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GenotypeQuality
all individuals: 87
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variant carriers: 0

GenotypeQuality
all individuals: 28
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GenotypeQuality
all individuals: 10780
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1990
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variant carriers: 0

GenotypeQuality
all individuals: 48
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variant carriers: 0

GenotypeQuality
all individuals: 39
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2819
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variant carriers: 0

GenotypeQuality
all individuals: 4785
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variant carriers: 0

GenotypeQuality
all individuals: 3527
bin: 7.25e1
variant carriers: 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: 1
allele frequency: 1.523043650431021e-5
allele num: 65658
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16386
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10256
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.014007e6

QD
type: SiteQuality
SIO_000300: 1.351e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.42e-1

MQ
type: SiteQuality
SIO_000300: 5.894e1

FS
type: SiteQuality
SIO_000300: 1.373e0

MQRankSum
type: SiteQuality
SIO_000300: 1.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.47e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

GenotypeDepth
all individuals: 1261
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 433
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 207
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variant carriers: 0

GenotypeDepth
all individuals: 13908
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
all individuals: 262
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GenotypeDepth
all individuals: 11001
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
all individuals: 80
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GenotypeQuality
all individuals: 23420
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1995
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 551
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.522950869604947e-5
allele num: 65662
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10260
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.426e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e-1

FS
type: SiteQuality
SIO_000300: 4.994e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.36e-1

QD
type: SiteQuality
SIO_000300: 1.395e1

DP
type: SiteQuality
SIO_000300: 2.014967e6

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

MQ
type: SiteQuality
SIO_000300: 5.989e1

GenotypeDepth
all individuals: 2109
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1263
bin: 5.75e1
variant carriers: 2

GenotypeDepth
all individuals: 163
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 202
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 262
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GenotypeDepth
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bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3455
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13919
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 433
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10790
bin: 9.75e1
variant carriers: 7

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65668
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10266
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.285539365740174e-4
allele num: 16334
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: 8638
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.99e0

FS
type: SiteQuality
SIO_000300: 1.163e0

MQRankSum
type: SiteQuality
SIO_000300: 3.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.33e-1

DP
type: SiteQuality
SIO_000300: 2.015338e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.7e-1

MQ
type: SiteQuality
SIO_000300: 5.982e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.07e-1

QD
type: SiteQuality
SIO_000300: 1.307e1

GenotypeDepth
all individuals: 735
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 99
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 12693
bin: 2.25e1
variant carriers: 0

GenotypeDepth
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bin: 4.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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bin: 3.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23399
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8159
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1996
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3530
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 65
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10790
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2821
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 1.75e1
variant carriers: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10266
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.045623439117987e-5
allele num: 65668
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

VQSLOD
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BaseQRankSum
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SIO_000300: 4.7e-1

DP
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SIO_000300: 2.015338e6

MQRankSum
type: SiteQuality
SIO_000300: 3.83e-1

InbreedingCoeff
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SIO_000300: 1.4e-3

ClippingRankSum
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SIO_000300: -1.07e-1

FS
type: SiteQuality
SIO_000300: 1.163e0

MQ
type: SiteQuality
SIO_000300: 5.982e1

ReadPosRankSum
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SIO_000300: 2.33e-1

QD
type: SiteQuality
SIO_000300: 1.307e1

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10264
num of homozygotes: 0

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

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16336
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.522718966987453e-5
allele num: 65672
num of homozygotes: 0

ClippingRankSum
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SIO_000300: -1.1e0

BaseQRankSum
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SIO_000300: -4.1e-1

MQ
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SIO_000300: 5.956e1

MQRankSum
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SIO_000300: -5.97e-1

ReadPosRankSum
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FS
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InbreedingCoeff
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SIO_000300: -7.0e-4

DP
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SIO_000300: 2.015235e6

VQSLOD
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SIO_000300: 2.39e-1

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.125199068969742e-5
allele num: 16326
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65664
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 2.015474e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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SIO_000300: 8.599999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.09e0

MQ
type: SiteQuality
SIO_000300: 5.896e1

InbreedingCoeff
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SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.528e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.07e-1

BaseQRankSum
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SIO_000300: 2.05e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.24e-1

GenotypeDepth
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variant carriers: 50

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

African
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allele count: 184
allele frequency: 1.78988326848249e-2
allele num: 10280
num of homozygotes: 3

European (Non-Finnish)
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allele count: 1
allele frequency: 1.522209029743965e-5
allele num: 65694
num of homozygotes: 0

South Asian
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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

Latino
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allele count: 11
allele frequency: 9.537020981446159e-4
allele num: 11534
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

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: 1.43e-2

ClippingRankSum
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SIO_000300: -1.96e-1

BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.976e1

VQSLOD
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SIO_000300: 5.44e0

QD
type: SiteQuality
SIO_000300: 1.458e1

MQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.98e-1

DP
type: SiteQuality
SIO_000300: 2.024718e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 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: 10284
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.521884702014975e-5
allele num: 65708
num of homozygotes: 0

European (Finnish)
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allele count: 9
allele frequency: 1.360749924402782e-3
allele num: 6614
num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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allele frequency: 0.0e0
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African
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allele count: 0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.52151421094273e-5
allele num: 65724
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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Other
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MQRankSum
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MQ
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FS
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BaseQRankSum
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ReadPosRankSum
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DP
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ClippingRankSum
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InbreedingCoeff
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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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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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Latino
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European (Non-Finnish)
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East Asian
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European (Finnish)
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Other
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InbreedingCoeff
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FS
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MQRankSum
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DP
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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MQ
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ClippingRankSum
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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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African
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East Asian
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European (Non-Finnish)
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South Asian
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BaseQRankSum
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QD
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DP
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MQRankSum
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FS
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ClippingRankSum
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MQ
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VQSLOD
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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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East Asian
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Latino
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African
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European (Non-Finnish)
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European (Finnish)
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South Asian
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BaseQRankSum
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MQ
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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DP
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ClippingRankSum
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QD
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FS
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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East Asian
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European (Finnish)
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Other
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South Asian
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ClippingRankSum
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MQ
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QD
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FS
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VQSLOD
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DP
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeQuality
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African
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East Asian
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Latino
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QD
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FS
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VQSLOD
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MQRankSum
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DP
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MQ
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DP
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FS
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VQSLOD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65818
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.252661906551422e-4
allele num: 15966
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 3.3e-3

ClippingRankSum
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SIO_000300: -6.46e-1

VQSLOD
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BaseQRankSum
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SIO_000300: -1.505e0

MQ
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SIO_000300: 6.086e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

QD
type: SiteQuality
SIO_000300: 1.777e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.99e-1

DP
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SIO_000300: 2.017346e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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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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bin: 7.25e1
variant carriers: 0

South Asian
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allele count: 1
allele frequency: 6.291682395872656e-5
allele num: 15894
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65824
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 8.42e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.18e-1

BaseQRankSum
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SIO_000300: -1.625e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.021e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -5.911999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.016388e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.669999999999999e-1

GenotypeDepth
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bin: 8.25e1
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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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519387383007172e-5
allele num: 65816
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15888
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.521e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.239e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.87e0

VQSLOD
type: SiteQuality
SIO_000300: 7.97e-1

ReadPosRankSum
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SIO_000300: 1.43e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 6.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

QD
type: SiteQuality
SIO_000300: 1.434e1

DP
type: SiteQuality
SIO_000300: 2.016133e6

GenotypeDepth
all individuals: 102
bin: 8.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.664009703690868e-5
allele num: 11542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65758
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15678
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.63e-1

MQ
type: SiteQuality
SIO_000300: 5.984e1

QD
type: SiteQuality
SIO_000300: 1.523e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 6.61e-1

BaseQRankSum
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SIO_000300: -2.545e0

FS
type: SiteQuality
SIO_000300: 1.699e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.47e-1

DP
type: SiteQuality
SIO_000300: 2.012147e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.57e-1

GenotypeDepth
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variant carriers: 3

GenotypeDepth
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variant carriers: 5

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 10

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

South Asian
type: Population
allele count: 113
allele frequency: 7.214915081087983e-3
allele num: 15662
num of homozygotes: 3

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.041917624870719e-5
allele num: 65748
num of homozygotes: 0

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

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

East Asian
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allele count: 27
allele frequency: 3.126447429365447e-3
allele num: 8636
num of homozygotes: 0

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

African
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allele count: 1
allele frequency: 9.704968944099378e-5
allele num: 10304
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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MQRankSum
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FS
type: SiteQuality
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ReadPosRankSum
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MQ
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VQSLOD
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BaseQRankSum
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SIO_000300: 8.49e-1

ClippingRankSum
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SIO_000300: -1.06e-1

QD
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SIO_000300: 1.789e1

DP
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GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65724
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15392
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.706853038245001e-5
allele num: 10302
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Other
type: Population
allele count: 0
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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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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South Asian
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African
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 65732
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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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num of homozygotes: 0

DP
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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FS
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VQSLOD
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MQ
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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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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

South Asian
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allele frequency: 2.591680704937152e-4
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European (Finnish)
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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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Other
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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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BaseQRankSum
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FS
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MQRankSum
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DP
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ClippingRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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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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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 frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 8.105604446503011e-4
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Other
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African
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South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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num of homozygotes: 0

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

Other
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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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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.048594597890372e-5
allele num: 65604
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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.03e0

InbreedingCoeff
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SIO_000300: -3.0e-4

DP
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SIO_000300: 2.00423e6

ClippingRankSum
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VQSLOD
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BaseQRankSum
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QD
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SIO_000300: 1.402e1

FS
type: SiteQuality
SIO_000300: 1.061e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-2

GenotypeDepth
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variant carriers: 0

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

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

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

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

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

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

Other
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.525553012967201e-5
allele num: 65550
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQ
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QD
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BaseQRankSum
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FS
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SIO_000300: 3.266e0

MQRankSum
type: SiteQuality
SIO_000300: 7.76e-1

VQSLOD
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SIO_000300: 1.97e0

DP
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SIO_000300: 2.002846e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

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

Latino
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allele num: 11522
num of homozygotes: 0

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

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

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

BaseQRankSum
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SIO_000300: 2.27e0

FS
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SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 7.29e-1

MQ
type: SiteQuality
SIO_000300: 5.943e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.37e-1

InbreedingCoeff
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SIO_000300: -8.0e-4

QD
type: SiteQuality
SIO_000300: 1.169e1

DP
type: SiteQuality
SIO_000300: 1.980027e6

MQRankSum
type: SiteQuality
SIO_000300: 5.8e-2

GenotypeDepth
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
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South Asian
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allele count: 2
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allele num: 13322
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 1
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allele num: 8626
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64968
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.977542e6

QD
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MQ
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FS
type: SiteQuality
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -1.1e-3

VQSLOD
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GenotypeDepth
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 65016
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Latino
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African
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European (Finnish)
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num of homozygotes: 0

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

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

South Asian
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Other
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Latino
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European (Finnish)
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African
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European (Non-Finnish)
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allele num: 64954
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East Asian
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MQ
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InbreedingCoeff
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FS
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ReadPosRankSum
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QD
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MQRankSum
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VQSLOD
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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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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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Latino
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num of homozygotes: 0

Other
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num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.541259517277519e-5
allele num: 64882
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.972838e6

ReadPosRankSum
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SIO_000300: 4.47e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

VQSLOD
type: SiteQuality
SIO_000300: 7.38e-1

MQRankSum
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SIO_000300: 9.389999999999999e-1

FS
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SIO_000300: 5.764e0

QD
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.4e-1

BaseQRankSum
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SIO_000300: 5.97e0

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

Latino
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allele frequency: 8.686587908269631e-5
allele num: 11512
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.084801184563655e-5
allele num: 64834
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MQRankSum
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SIO_000300: 2.72e-1

InbreedingCoeff
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SIO_000300: -1.2e-3

MQ
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SIO_000300: 5.985e1

FS
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ClippingRankSum
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QD
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VQSLOD
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BaseQRankSum
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SIO_000300: 1.47e0

ReadPosRankSum
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SIO_000300: 3.62e-1

DP
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SIO_000300: 1.972641e6

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
allele num: 10276
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.542828931128116e-5
allele num: 64816
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -5.944e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.75e-1

FS
type: SiteQuality
SIO_000300: 1.342e0

InbreedingCoeff
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SIO_000300: -1.0e-3

DP
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SIO_000300: 1.971026e6

MQRankSum
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SIO_000300: -1.304e0

VQSLOD
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SIO_000300: -7.47e-2

QD
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SIO_000300: 1.434e1

MQ
type: SiteQuality
SIO_000300: 5.943e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

GenotypeDepth
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variant carriers: 3

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele num: 848
num of homozygotes: 0

South Asian
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allele frequency: 8.337266005977662e-3
allele num: 12714
num of homozygotes: 4

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

African
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allele count: 371
allele frequency: 3.610354223433242e-2
allele num: 10276
num of homozygotes: 10

Latino
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allele frequency: 7.822005909960021e-4
allele num: 11506
num of homozygotes: 0

East Asian
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allele count: 27
allele frequency: 3.132977488976561e-3
allele num: 8618
num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 7.717955050629786e-5
allele num: 64784
num of homozygotes: 0

VQSLOD
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DP
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ReadPosRankSum
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MQ
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FS
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ClippingRankSum
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BaseQRankSum
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QD
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InbreedingCoeff
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SIO_000300: 4.04e-2

MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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European (Finnish)
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Other
type: Population
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.095783542814686e-5
allele num: 64604
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South Asian
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MQRankSum
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MQ
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BaseQRankSum
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ReadPosRankSum
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FS
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

African
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allele frequency: 0.0e0
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Other
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European (Non-Finnish)
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allele num: 64604
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South Asian
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European (Finnish)
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Latino
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InbreedingCoeff
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FS
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MQ
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BaseQRankSum
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VQSLOD
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DP
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ClippingRankSum
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MQRankSum
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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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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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European (Non-Finnish)
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Latino
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African
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European (Finnish)
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East Asian
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VQSLOD
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QD
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FS
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MQ
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InbreedingCoeff
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MQRankSum
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DP
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Non-Finnish)
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Latino
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European (Finnish)
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Other
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MQRankSum
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FS
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BaseQRankSum
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InbreedingCoeff
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QD
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VQSLOD
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DP
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MQ
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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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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African
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Latino
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European (Finnish)
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Other
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South Asian
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European (Non-Finnish)
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MQ
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BaseQRankSum
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QD
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VQSLOD
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MQRankSum
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FS
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DP
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InbreedingCoeff
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ClippingRankSum
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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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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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Other
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European (Non-Finnish)
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Latino
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African
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East Asian
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South Asian
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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MQ
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DP
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FS
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BaseQRankSum
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InbreedingCoeff
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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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East Asian
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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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VQSLOD
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InbreedingCoeff
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FS
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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MQ
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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European (Finnish)
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East Asian
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African
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European (Non-Finnish)
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MQ
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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FS
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QD
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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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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
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num of homozygotes: 0

South Asian
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allele frequency: 8.344459279038718e-5
allele num: 11984
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

MQ
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
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SIO_000300: -1.3e-3

FS
type: SiteQuality
SIO_000300: 6.226e0

VQSLOD
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SIO_000300: -1.747e0

QD
type: SiteQuality
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MQRankSum
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SIO_000300: 1.93e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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

Other
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num of homozygotes: 0

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

South Asian
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allele frequency: 1.681802892700975e-4
allele num: 11892
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 (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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ReadPosRankSum
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DP
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FS
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ClippingRankSum
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SIO_000300: 3.23e-1

BaseQRankSum
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SIO_000300: -1.485e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 64520
num of homozygotes: 0

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

Latino
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allele num: 11498
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10248
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 6.69e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

ReadPosRankSum
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InbreedingCoeff
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SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
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MQRankSum
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QD
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DP
type: SiteQuality
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BaseQRankSum
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SIO_000300: -2.361e0

ClippingRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 1
allele frequency: 1.550628004341758e-5
allele num: 64490
num of homozygotes: 0

South Asian
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num of homozygotes: 0

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

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

East Asian
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allele count: 0
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BaseQRankSum
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SIO_000300: -5.56e-1

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 55

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

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

Latino
type: Population
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allele frequency: 8.695652173913044e-5
allele num: 11500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.551975665021572e-5
allele num: 64434
num of homozygotes: 0

African
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allele count: 53
allele frequency: 5.176792342254347e-3
allele num: 10238
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Other
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East Asian
type: Population
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FS
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 1
allele frequency: 1.204819277108434e-3
allele num: 830
num of homozygotes: 0

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

Latino
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allele num: 11498
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East Asian
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South Asian
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African
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allele count: 186
allele frequency: 1.816761086149639e-2
allele num: 10238
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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FS
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DP
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: 1.14e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.95e-1

QD
type: SiteQuality
SIO_000300: 1.456e1

MQ
type: SiteQuality
SIO_000300: 5.971e1

GenotypeDepth
all individuals: 133
bin: 8.25e1
variant carriers: 2

GenotypeDepth
all individuals: 204
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2842
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3480
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9243
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12468
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7779
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10751
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 316
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 764
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1969
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4728
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7819
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3900
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2915
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3439
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2799
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19293
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10916
bin: 9.75e1
variant carriers: 14

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11788
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.101640767966254e-5
allele num: 64482
num of homozygotes: 0

African
type: Population
allele count: 12
allele frequency: 1.172103926548154e-3
allele num: 10238
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.9e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.95e-1

DP
type: SiteQuality
SIO_000300: 1.985083e6

MQ
type: SiteQuality
SIO_000300: 5.971e1

FS
type: SiteQuality
SIO_000300: 5.47e-1

QD
type: SiteQuality
SIO_000300: 1.456e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.14e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.81e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.11e0

VQSLOD
type: SiteQuality
SIO_000300: 3.82e0

GenotypeDepth
all individuals: 375
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 488
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2867
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 12482
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1344
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 62
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5358
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2179
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3500
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 806
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 754
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10751
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4746
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1973
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 567
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3915
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7856
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3022
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19393
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2812
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3453
bin: 7.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.767532721234616e-5
allele num: 10238
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11868
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64496
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.88e0

VQSLOD
type: SiteQuality
SIO_000300: -1.415e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

DP
type: SiteQuality
SIO_000300: 1.971465e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e0

FS
type: SiteQuality
SIO_000300: 5.264e0

QD
type: SiteQuality
SIO_000300: 1.378e1

MQRankSum
type: SiteQuality
SIO_000300: 1.96e0

MQ
type: SiteQuality
SIO_000300: 5.968e1