5-137506687-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506687
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506687
    reference: chr 5
allele count: 6
allele frequency: 4.949923276189219e-5
allele num: 121214
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.340+40T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.359+40T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.359+40T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*135+40T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*142+40T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000407129
  ensembl transcript: ENST00000453824
  gene symbol: BRD8
  hgvsc: ENST00000453824.1:c.23+40T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.374+40T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.344+40T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.374+40T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*262+40T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*244+40T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.359+40T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.344+40T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.236+40T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.359+40T>C
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3359
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5800
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6328
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4237
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

5-137506688-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506688
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506688
    reference: chr 5
allele count: 2
allele frequency: 1.649919978881024e-5
allele num: 121218
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.359+39A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.359+39A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*135+39A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*142+39A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.344+39A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.374+39A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.359+39A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*262+39A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.236+39A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.374+39A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.340+39A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000407129
  ensembl transcript: ENST00000453824
  gene symbol: BRD8
  hgvsc: ENST00000453824.1:c.23+39A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.359+39A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*244+39A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.344+39A>G
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4230
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4698
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
reference allele: T
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

5-137506690-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506690
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506690
    reference: chr 5
allele count: 5
allele frequency: 4.124799947202561e-5
allele num: 121218
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*142+37A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*262+37A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.236+37A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.359+37A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.344+37A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.344+37A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.359+37A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.374+37A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000407129
  ensembl transcript: ENST00000453824
  gene symbol: BRD8
  hgvsc: ENST00000453824.1:c.23+37A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*244+37A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*135+37A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.340+37A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.374+37A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.359+37A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.359+37A>C
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3359
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4099
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5942
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4230
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

5-137506692-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506692
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506692
    reference: chr 5
allele count: 1
allele frequency: 8.250416646040625e-6
allele num: 121206
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.340+35A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.344+35A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.374+35A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*135+35A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*262+35A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*142+35A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.236+35A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.359+35A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000407129
  ensembl transcript: ENST00000453824
  gene symbol: BRD8
  hgvsc: ENST00000453824.1:c.23+35A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.359+35A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.359+35A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.359+35A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.344+35A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*244+35A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.374+35A>G
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6329
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5953
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4219
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

5-137506693-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506693
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506694
    reference: chr 5
allele count: 1
allele frequency: 8.250552787036732e-6
allele num: 121204
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.359+33_359+34insT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*135+33_*135+34insT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000407129
  ensembl transcript: ENST00000453824
  gene symbol: BRD8
  hgvsc: ENST00000453824.1:c.23+33_23+34insT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.359+33_359+34insT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.236+33_236+34insT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.344+33_344+34insT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.374+33_374+34insT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.374+33_374+34insT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.344+33_344+34insT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*142+33_*142+34insT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.340+33_340+34insT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*244+33_*244+34insT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.359+33_359+34insT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.359+33_359+34insT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*262+33_*262+34insT
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: intron
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5954
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6333
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3853
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4209
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5801
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

5-137506694-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506694
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506694
    reference: chr 5
allele count: 1
allele frequency: 8.250144377526608e-6
allele num: 121210
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.344+33A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.344+33A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.374+33A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.236+33A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.374+33A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.359+33A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.359+33A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.340+33A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*135+33A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*244+33A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.359+33A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*142+33A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*262+33A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.359+33A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000407129
  ensembl transcript: ENST00000453824
  gene symbol: BRD8
  hgvsc: ENST00000453824.1:c.23+33A>G
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5957
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2230
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5801
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

5-137506699-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506699
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506699
    reference: chr 5
allele count: 3
allele frequency: 2.47520667975776e-5
allele num: 121202
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.344+28T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000407129
  ensembl transcript: ENST00000453824
  gene symbol: BRD8
  hgvsc: ENST00000453824.1:c.23+28T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.374+28T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.359+28T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*244+28T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*262+28T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.374+28T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.340+28T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.344+28T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.236+28T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.359+28T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*142+28T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.359+28T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.359+28T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*135+28T>C
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2230
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3853
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5800
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6334
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

5-137506700-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506700
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506700
    reference: chr 5
allele count: 1
allele frequency: 8.250688932525866e-6
allele num: 121202
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.359+27A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.359+27A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.344+27A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.374+27A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*244+27A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.340+27A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.359+27A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.374+27A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*142+27A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.236+27A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.359+27A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.344+27A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*135+27A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*262+27A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000407129
  ensembl transcript: ENST00000453824
  gene symbol: BRD8
  hgvsc: ENST00000453824.1:c.23+27A>C
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5148
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6454
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4221
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4089
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6335
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

5-137506719-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506719
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506720
    reference: chr 5
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: AT
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.359+7dupA
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.359+7dupA
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000407129
  ensembl transcript: ENST00000453824
  gene symbol: BRD8
  hgvsc: ENST00000453824.1:c.23+7dupA
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*262+7dupA
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.344+7dupA
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.236+7dupA
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*244+7dupA
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.359+7dupA
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*142+7dupA
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*135+7dupA
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.340+7dupA
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.359+7dupA
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.344+7dupA
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.374+7dupA
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.374+7dupA
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6336
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3358
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6458
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.359+7dupA
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

5-137506729-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506729
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506729
    reference: chr 5
allele count: 4
allele frequency: 3.298860243785772e-5
allele num: 121254
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.357T>C
  hgvsp: ENST00000402931.1:c.357T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.357T>C
  hgvsp: ENST00000254900.5:c.357T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.357T>C
  hgvsp: ENST00000230901.5:c.357T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.372T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.338T>C
  hgvsp: ENST00000441656.1:c.338T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.234T>C
  hgvsp: ENST00000455658.2:c.234T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*140T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*133T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.372T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.342T>C
  hgvsp: ENST00000418329.1:c.342T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.357T>C
  hgvsp: ENST00000411594.2:c.357T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.342T>C
  hgvsp: ENST00000454473.1:c.342T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*242T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*260T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000407129
  ensembl transcript: ENST00000453824
  gene symbol: BRD8
  hgvsc: ENST00000453824.1:c.21T>C
  hgvsp: ENST00000453824.1:c.21T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.357T>C
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/5-137506731-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506731
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506731
    reference: chr 5
allele count: 1
allele frequency: 8.247014580721778e-6
allele num: 121256
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.355T>G
  hgvsp: ENSP00000394330.2:p.Tyr119Asp
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.355T>G
  hgvsp: ENSP00000230901.5:p.Tyr119Asp
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.355T>G
  hgvsp: ENSP00000384845.1:p.Tyr119Asp
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*138T>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.232T>G
  hgvsp: ENSP00000408396.2:p.Tyr78Asp
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.336T>G
  hgvsp: ENSP00000398084.1:p.Tyr113Asp
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.370T>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.370T>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*258T>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.340T>G
  hgvsp: ENSP00000398067.1:p.Tyr114Asp
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000407129
  ensembl transcript: ENST00000453824
  gene symbol: BRD8
  hgvsc: ENST00000453824.1:c.19T>G
  hgvsp: ENSP00000407129.1:p.Tyr7Asp
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.355T>G
  hgvsp: ENSP00000254900.5:p.Tyr119Asp
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.340T>G
  hgvsp: ENSP00000398873.1:p.Tyr114Asp
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*240T>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*131T>G
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5800
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr119Asp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP

5-137506745-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506745
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506745
    reference: chr 5
allele count: 1
allele frequency: 8.242935804015958e-6
allele num: 121316
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*244A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.341A>C
  hgvsp: ENSP00000230901.5:p.Glu114Ala
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.322A>C
  hgvsp: ENSP00000398084.1:p.Glu108Ala
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.218A>C
  hgvsp: ENSP00000408396.2:p.Glu73Ala
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.326A>C
  hgvsp: ENSP00000398873.1:p.Glu109Ala
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*226A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000407129
  ensembl transcript: ENST00000453824
  gene symbol: BRD8
  hgvsc: ENST00000453824.1:c.5A>C
  hgvsp: ENSP00000407129.1:p.Glu2Ala
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.356A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.326A>C
  hgvsp: ENSP00000398067.1:p.Glu109Ala
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.356A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.341A>C
  hgvsp: ENSP00000394330.2:p.Glu114Ala
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*124A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.341A>C
  hgvsp: ENSP00000384845.1:p.Glu114Ala
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*117A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.341A>C
  hgvsp: ENSP00000254900.5:p.Glu114Ala
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4703
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5800
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4363
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Glu114Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

5-137506754-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506754
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506754
    reference: chr 5
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.317T>C
  hgvsp: ENSP00000398067.1:p.Val106Ala
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.332T>C
  hgvsp: ENSP00000254900.5:p.Val111Ala
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.347T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.332T>C
  hgvsp: ENSP00000230901.5:p.Val111Ala
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.317T>C
  hgvsp: ENSP00000398873.1:p.Val106Ala
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*115T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.347T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.332T>C
  hgvsp: ENSP00000384845.1:p.Val111Ala
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.332T>C
  hgvsp: ENSP00000394330.2:p.Val111Ala
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.209T>C
  hgvsp: ENSP00000408396.2:p.Val70Ala
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.313T>C
  hgvsp: ENSP00000398084.1:p.Val105Ala
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*217T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*235T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*108T>C
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6062
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4703
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5800
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val111Ala
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

5-137506760-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506760
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506760
    reference: chr 5
allele count: 2
allele frequency: 1.648098094798602e-5
allele num: 121352
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.341A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.326A>C
  hgvsp: ENSP00000254900.5:p.Lys109Thr
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.326A>C
  hgvsp: ENSP00000384845.1:p.Lys109Thr
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.307A>C
  hgvsp: ENSP00000398084.1:p.Lys103Thr
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*109A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.326A>C
  hgvsp: ENSP00000230901.5:p.Lys109Thr
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*211A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.311A>C
  hgvsp: ENSP00000398067.1:p.Lys104Thr
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.311A>C
  hgvsp: ENSP00000398873.1:p.Lys104Thr
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*229A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.326A>C
  hgvsp: ENSP00000394330.2:p.Lys109Thr
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.203A>C
  hgvsp: ENSP00000408396.2:p.Lys68Thr
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*102A>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.341A>C
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4381
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6465
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4081
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6065
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys109Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

5-137506762-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506762
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506762
    reference: chr 5
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*227A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*100A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.201A>G
  hgvsp: ENST00000455658.2:c.201A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.309A>G
  hgvsp: ENST00000418329.1:c.309A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.324A>G
  hgvsp: ENST00000230901.5:c.324A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.339A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.324A>G
  hgvsp: ENST00000411594.2:c.324A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.324A>G
  hgvsp: ENST00000402931.1:c.324A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.305A>G
  hgvsp: ENST00000441656.1:c.305A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.339A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*209A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.309A>G
  hgvsp: ENST00000454473.1:c.309A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*107A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.324A>G
  hgvsp: ENST00000254900.5:c.324A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6465
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6342
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4379
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu108Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ

5-137506764-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506764
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506764
    reference: chr 5
allele count: 2
allele frequency: 1.647962294622699e-5
allele num: 121362
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.322C>T
  hgvsp: ENST00000402931.1:c.322C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.337C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.199C>T
  hgvsp: ENST00000455658.2:c.199C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.307C>T
  hgvsp: ENST00000454473.1:c.307C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.322C>T
  hgvsp: ENST00000254900.5:c.322C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.303C>T
  hgvsp: ENST00000441656.1:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.337C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*225C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.322C>T
  hgvsp: ENST00000411594.2:c.322C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*207C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*105C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.307C>T
  hgvsp: ENST00000418329.1:c.307C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*98C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.322C>T
  hgvsp: ENST00000230901.5:c.322C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6067
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4379
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6342
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5800
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu108Leu
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/5-137506771-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506771
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506771
    reference: chr 5
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.300T>G
  hgvsp: ENST00000454473.1:c.300T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*200T>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.315T>G
  hgvsp: ENST00000411594.2:c.315T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.330T>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.300T>G
  hgvsp: ENST00000418329.1:c.300T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*218T>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*98T>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.192T>G
  hgvsp: ENST00000455658.2:c.192T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.315T>G
  hgvsp: ENST00000402931.1:c.315T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.315T>G
  hgvsp: ENST00000254900.5:c.315T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.296T>G
  hgvsp: ENST00000441656.1:c.296T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*91T>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.315T>G
  hgvsp: ENST00000230901.5:c.315T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.330T>G
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4705
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5800
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6341
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val105Val
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

5-137506780-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506780
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506780
    reference: chr 5
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.183T>C
  hgvsp: ENST00000455658.2:c.183T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.306T>C
  hgvsp: ENST00000230901.5:c.306T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.306T>C
  hgvsp: ENST00000411594.2:c.306T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.287T>C
  hgvsp: ENST00000441656.1:c.287T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.291T>C
  hgvsp: ENST00000418329.1:c.291T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*89T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.321T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.306T>C
  hgvsp: ENST00000254900.5:c.306T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.321T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.291T>C
  hgvsp: ENST00000454473.1:c.291T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*191T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.306T>C
  hgvsp: ENST00000402931.1:c.306T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*82T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*209T>C
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4705
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6069
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala102Ala
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

5-137506785-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506785
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506784
    reference: chr 5
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*76delG
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*83delG
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.177delG
  hgvsp: ENSP00000408396.2:p.Thr60LeufsTer8
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.315delG
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.315delG
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.300delG
  hgvsp: ENSP00000384845.1:p.Thr101LeufsTer8
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.285delG
  hgvsp: ENSP00000398067.1:p.Thr96LeufsTer8
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.285delG
  hgvsp: ENSP00000398873.1:p.Thr96LeufsTer8
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.300delG
  hgvsp: ENSP00000254900.5:p.Thr101LeufsTer8
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*203delG
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.300delG
  hgvsp: ENSP00000230901.5:p.Thr101LeufsTer8
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.281delG
  hgvsp: ENSP00000398084.1:p.Thr95LeufsTer8
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.300delG
  hgvsp: ENSP00000394330.2:p.Thr101LeufsTer8
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*185delG
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6070
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6467
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4704
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4077
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6339
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr101LeufsTer8
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: TC
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

5-137506786-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506786
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506786
    reference: chr 5
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.177G>C
  hgvsp: ENSP00000408396.2:p.Leu59Phe
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*83G>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.300G>C
  hgvsp: ENSP00000230901.5:p.Leu100Phe
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.300G>C
  hgvsp: ENSP00000254900.5:p.Leu100Phe
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.315G>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.285G>C
  hgvsp: ENSP00000398873.1:p.Leu95Phe
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.285G>C
  hgvsp: ENSP00000398067.1:p.Leu95Phe
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.300G>C
  hgvsp: ENSP00000384845.1:p.Leu100Phe
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.281G>C
  hgvsp: ENSP00000398084.1:p.Leu94Phe
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.315G>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*185G>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.300G>C
  hgvsp: ENSP00000394330.2:p.Leu100Phe
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*203G>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*76G>C
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6070
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu100Phe
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD

5-137506787-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506787
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506787
    reference: chr 5
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.299T>C
  hgvsp: ENSP00000384845.1:p.Leu100Ser
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.314T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.280T>C
  hgvsp: ENSP00000398084.1:p.Leu94Ser
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*75T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*82T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*184T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.176T>C
  hgvsp: ENSP00000408396.2:p.Leu59Ser
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.299T>C
  hgvsp: ENSP00000394330.2:p.Leu100Ser
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.299T>C
  hgvsp: ENSP00000230901.5:p.Leu100Ser
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.284T>C
  hgvsp: ENSP00000398067.1:p.Leu95Ser
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.299T>C
  hgvsp: ENSP00000254900.5:p.Leu100Ser
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.314T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.284T>C
  hgvsp: ENSP00000398873.1:p.Leu95Ser
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*202T>C
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4704
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6467
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu100Ser
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

5-137506812-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506812
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506812
    reference: chr 5
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.274G>C
  hgvsp: ENSP00000384845.1:p.Val92Leu
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.255G>C
  hgvsp: ENSP00000398084.1:p.Val86Leu
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*57G>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*50G>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*159G>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.259G>C
  hgvsp: ENSP00000398067.1:p.Val87Leu
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.289G>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.274G>C
  hgvsp: ENSP00000230901.5:p.Val92Leu
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.289G>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.274G>C
  hgvsp: ENSP00000254900.5:p.Val92Leu
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.151G>C
  hgvsp: ENSP00000408396.2:p.Val51Leu
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.274G>C
  hgvsp: ENSP00000394330.2:p.Val92Leu
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.259G>C
  hgvsp: ENSP00000398873.1:p.Val87Leu
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*177G>C
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4704
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3853
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5150
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5800
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3359
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val92Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum

5-137506819-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506819
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506819
    reference: chr 5
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*43G>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.282G>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.248G>A
  hgvsp: ENST00000441656.1:c.248G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.252G>A
  hgvsp: ENST00000454473.1:c.252G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.267G>A
  hgvsp: ENST00000254900.5:c.267G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*170G>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.267G>A
  hgvsp: ENST00000230901.5:c.267G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.267G>A
  hgvsp: ENST00000402931.1:c.267G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.144G>A
  hgvsp: ENST00000455658.2:c.144G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*50G>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.267G>A
  hgvsp: ENST00000411594.2:c.267G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*152G>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.252G>A
  hgvsp: ENST00000418329.1:c.252G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.282G>A
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6465
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6342
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5800
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6073
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val89Val
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

5-137506820-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506820
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506820
    reference: chr 5
allele count: 4
allele frequency: 3.295381522795802e-5
allele num: 121382
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.266T>C
  hgvsp: ENSP00000384845.1:p.Val89Ala
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*151T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.251T>C
  hgvsp: ENSP00000398067.1:p.Val84Ala
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.247T>C
  hgvsp: ENSP00000398084.1:p.Val83Ala
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.143T>C
  hgvsp: ENSP00000408396.2:p.Val48Ala
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.251T>C
  hgvsp: ENSP00000398873.1:p.Val84Ala
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.266T>C
  hgvsp: ENSP00000254900.5:p.Val89Ala
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*49T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*42T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.281T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*169T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.266T>C
  hgvsp: ENSP00000230901.5:p.Val89Ala
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.266T>C
  hgvsp: ENSP00000394330.2:p.Val89Ala
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.281T>C
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4073
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4704
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5800
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val89Ala
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/5-137506837-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506837
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506837
    reference: chr 5
allele count: 13
allele frequency: 1.071316730670974e-4
allele num: 121346
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*152T>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.249T>G
  hgvsp: ENST00000411594.2:c.249T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*25T>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.126T>G
  hgvsp: ENST00000455658.2:c.126T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*32T>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.230T>G
  hgvsp: ENST00000441656.1:c.230T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.249T>G
  hgvsp: ENST00000230901.5:c.249T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.234T>G
  hgvsp: ENST00000418329.1:c.234T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.249T>G
  hgvsp: ENST00000254900.5:c.249T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.249T>G
  hgvsp: ENST00000402931.1:c.249T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*134T>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.264T>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.264T>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.234T>G
  hgvsp: ENST00000454473.1:c.234T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4070
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3361
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5803
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3852
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6469
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4368
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4705
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly83Gly
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP

5-137506852-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506852
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506852
    reference: chr 5
allele count: 1
allele frequency: 8.250416646040625e-6
allele num: 121206
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*20-3C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.237-3C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.252-3C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.222-3C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*13-3C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.237-3C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*122-3C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.222-3C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.114-3C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.237-3C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.218-3C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.237-3C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*140-3C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.252-3C>T
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4705
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5906
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3358
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.237-3C>T
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum

5-137506854-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506854
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506854
    reference: chr 5
allele count: 6
allele frequency: 4.950576742190465e-5
allele num: 121198
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.237-5C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.252-5C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.237-5C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*140-5C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*20-5C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.218-5C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.252-5C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.114-5C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.222-5C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*13-5C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*122-5C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.237-5C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.222-5C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.237-5C>T
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2837
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4276
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3851
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5788
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3358
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.237-5C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

5-137506855-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506855
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506855
    reference: chr 5
allele count: 3
allele frequency: 2.475982965237199e-5
allele num: 121164
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.114-6C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.218-6C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.252-6C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.252-6C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.222-6C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*13-6C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.222-6C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.237-6C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.237-6C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*122-6C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.237-6C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*140-6C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*20-6C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.237-6C>T
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5887
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3358
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5771
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6168
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4349
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.237-6C>T
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff

5-137506861-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506861
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506861
    reference: chr 5
allele count: 1
allele frequency: 8.25722920416825e-6
allele num: 121106
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.218-12A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.114-12A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.237-12A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*122-12A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.237-12A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*140-12A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*20-12A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.252-12A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.222-12A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*13-12A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.237-12A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.237-12A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.222-12A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.252-12A>G
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3849
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4443
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5721
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5995
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4696
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum

5-137506862-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506862
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506863
    reference: chr 5
allele count: 961
allele frequency: 9.821556323201766e-3
allele num: 97846
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*122-14dupT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.237-14dupT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.114-14dupT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*13-14dupT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.222-14dupT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.237-14dupT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.252-14dupT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.237-14dupT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*20-14dupT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.222-14dupT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*140-14dupT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.252-14dupT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.218-14dupT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.237-14dupT
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1650
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 7.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 2.25e1
  variant carriers: 214
genotype depth: GenotypeDepth
  all individuals: 7096
  bin: 4.25e1
  variant carriers: 193
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5608
  bin: 5.25e1
  variant carriers: 83
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 6640
  bin: 3.75e1
  variant carriers: 219
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 1.75e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 4849
  bin: 2.75e1
  variant carriers: 311
genotype depth: GenotypeDepth
  all individuals: 6334
  bin: 4.75e1
  variant carriers: 109
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

5-137506862-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506862
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506861
    reference: chr 5
allele count: 1201
allele frequency: 1.227439036853832e-2
allele num: 97846
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.222-14delT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.252-14delT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.252-14delT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.114-14delT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.237-14delT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*140-14delT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.237-14delT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.222-14delT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.237-14delT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.237-14delT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*122-14delT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*13-14delT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*20-14delT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.218-14delT
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 2.25e1
  variant carriers: 141
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4849
  bin: 2.75e1
  variant carriers: 281
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 8.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 1650
  bin: 7.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 6.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7096
  bin: 4.25e1
  variant carriers: 143
genotype depth: GenotypeDepth
  all individuals: 4775
  bin: 5.75e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 6334
  bin: 4.75e1
  variant carriers: 118
genotype depth: GenotypeDepth
  all individuals: 6640
  bin: 3.75e1
  variant carriers: 201
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 1.75e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 6346
  bin: 3.25e1
  variant carriers: 254
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: GA
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

5-137506862-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506862
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506862
    reference: chr 5
allele count: 1
allele frequency: 1.022014185556896e-5
allele num: 97846
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*122-13C>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.237-13C>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.237-13C>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*13-13C>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.237-13C>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.222-13C>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*20-13C>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.252-13C>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.222-13C>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.218-13C>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.252-13C>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.114-13C>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*140-13C>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.237-13C>A
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3509
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1650
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7096
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5608
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4849
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

5-137506869-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506869
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506869
    reference: chr 5
allele count: 1
allele frequency: 8.268836409340477e-6
allele num: 120936
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*140-20T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*13-20T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.237-20T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.237-20T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.252-20T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.114-20T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*122-20T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.222-20T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.252-20T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.237-20T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.218-20T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.222-20T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*20-20T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.237-20T>C
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9308
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7627
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6031
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4551
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9456
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3012
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8230
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD

5-137506874-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506874
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506874
    reference: chr 5
allele count: 3
allele frequency: 2.484760137821362e-5
allele num: 120736
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.114-25A>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.222-25A>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.237-25A>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.252-25A>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*13-25A>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.222-25A>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.252-25A>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.237-25A>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*122-25A>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.218-25A>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.237-25A>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*140-25A>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*20-25A>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.237-25A>T
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9058
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3012
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
reference allele: T
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

5-137506877-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506877
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506877
    reference: chr 5
allele count: 1
allele frequency: 8.276227364518158e-6
allele num: 120828
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.222-28T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*13-28T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.252-28T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.114-28T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.237-28T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*122-28T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.218-28T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.252-28T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*140-28T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*20-28T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.237-28T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.237-28T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.222-28T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.237-28T>A
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9009
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6010
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4543
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2747
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8878
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3008
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8084
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

5-137506880-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506880
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506880
    reference: chr 5
allele count: 2
allele frequency: 1.655190677966102e-5
allele num: 120832
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.252-31A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*20-31A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.218-31A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.237-31A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*122-31A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*13-31A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.222-31A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.237-31A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*140-31A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.114-31A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.252-31A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.237-31A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.237-31A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.222-31A>G
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2747
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4544
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8058
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8877
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6004
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7547
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum

5-137506884-AATAAC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506884
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506879
    reference: chr 5
allele count: 2
allele frequency: 1.655930715858849e-5
allele num: 120778
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*13-40_*13-36delGTTAT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.237-40_237-36delGTTAT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.237-40_237-36delGTTAT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.218-40_218-36delGTTAT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.252-40_252-36delGTTAT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*20-40_*20-36delGTTAT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.237-40_237-36delGTTAT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.114-40_114-36delGTTAT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.252-40_252-36delGTTAT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.222-40_222-36delGTTAT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.237-40_237-36delGTTAT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*140-40_*140-36delGTTAT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*122-40_*122-36delGTTAT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.222-40_222-36delGTTAT
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3007
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2716
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8580
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: AATAAC
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

5-137506890-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506890
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506890
    reference: chr 5
allele count: 3356
allele frequency: 2.781184738290185e-2
allele num: 120668
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*122-41T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*140-41T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.252-41T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.218-41T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.237-41T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.114-41T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.237-41T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*20-41T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.222-41T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.252-41T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*13-41T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.237-41T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.237-41T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.222-41T>C
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8118
  bin: 3.25e1
  variant carriers: 331
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 1.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 8.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 7.75e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 7437
  bin: 2.75e1
  variant carriers: 273
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 9.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 3519
  bin: 2.25e1
  variant carriers: 158
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 8.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 3015
  bin: 5.75e1
  variant carriers: 256
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 1.75e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6006
  bin: 4.75e1
  variant carriers: 342
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 7.25e1
  variant carriers: 82
genotype quality: GenotypeQuality
num of homozygotes: 60
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

5-137506894-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506894
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506894
    reference: chr 5
allele count: 4
allele frequency: 3.320494089520521e-5
allele num: 120464
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*122-45G>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.237-45G>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.252-45G>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.222-45G>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.237-45G>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.237-45G>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.222-45G>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.114-45G>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*140-45G>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.237-45G>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*20-45G>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.252-45G>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*13-45G>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.218-45G>A
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7144
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4463
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4161
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8020
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8002
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7491
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/5-137506901-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137506901
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137506901
    reference: chr 5
allele count: 68
allele frequency: 5.649248151532774e-4
allele num: 120370
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.237-52G>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.222-52G>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*122-52G>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.222-52G>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.252-52G>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*140-52G>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*13-52G>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.114-52G>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.252-52G>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.237-52G>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.218-52G>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.237-52G>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*20-52G>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.237-52G>T
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4464
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6865
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6007
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7993
  bin: 3.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

5-137507001-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137507001
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137507001
    reference: chr 5
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.217+49T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*12+33T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*121+49T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.236+49T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.221+49T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.236+49T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*19+49T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*139+49T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.113+49T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.236+49T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.251+49T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.251+49T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.221+49T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.236+49T>A
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6006
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2940
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4294
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

5-137507020-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137507020
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137507020
    reference: chr 5
allele count: 15
allele frequency: 1.235727349117691e-4
allele num: 121386
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*19+30A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.236+30A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.236+30A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.221+30A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.236+30A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.217+30A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*121+30A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*12+14A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.251+30A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.221+30A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.113+30A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.236+30A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*139+30A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.251+30A>G
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6239
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7114
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7766
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1730
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7539
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

5-137507027-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137507027
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137507027
    reference: chr 5
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.236+23C>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.113+23C>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.221+23C>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.236+23C>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.236+23C>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.221+23C>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.251+23C>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*121+23C>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*19+23C>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.251+23C>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*12+7C>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*139+23C>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.217+23C>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.236+23C>G
  variant of: http://identifiers.org/hgnc/19874
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6010
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4110
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7765
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2940
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.*12+7C>G
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

5-137507031-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137507031
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137507031
    reference: chr 5
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.236+19A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*121+19A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.236+19A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.221+19A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*139+19A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.251+19A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.236+19A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.251+19A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.113+19A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*12+3A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.221+19A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.236+19A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.217+19A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*19+19A>G
  variant of: http://identifiers.org/hgnc/19874
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4541
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4110
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7117
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7765
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2940
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.*12+3A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP

5-137507042-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137507042
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137507042
    reference: chr 5
allele count: 5
allele frequency: 4.118819711023609e-5
allele num: 121394
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*121+8C>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.221+8C>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*19+8C>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.251+8C>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.217+8C>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.236+8C>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.236+8C>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.251+8C>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.*4C>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*139+8C>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.113+8C>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.236+8C>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.221+8C>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.236+8C>G
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4109
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1716
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4540
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7536
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2942
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: c.236+8C>G
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD

5-137507060-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137507060
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137507060
    reference: chr 5
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.226G>A
  hgvsp: ENSP00000384845.1:p.Glu76Lys
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*111G>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.226G>A
  hgvsp: ENSP00000254900.5:p.Glu76Lys
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.226G>A
  hgvsp: ENSP00000230901.5:p.Glu76Lys
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.241G>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.241G>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.211G>A
  hgvsp: ENSP00000398067.1:p.Glu71Lys
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000407414
  ensembl transcript: ENST00000430331
  gene symbol: BRD8
  hgvsc: ENST00000430331.1:c.358G>A
  hgvsp: ENSP00000407414.1:p.Glu120Lys
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.207G>A
  hgvsp: ENSP00000398084.1:p.Glu70Lys
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.211G>A
  hgvsp: ENSP00000398873.1:p.Glu71Lys
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*9G>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.226G>A
  hgvsp: ENSP00000398676.1:p.Glu76Lys
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.103G>A
  hgvsp: ENSP00000408396.2:p.Glu35Lys
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.226G>A
  hgvsp: ENSP00000394330.2:p.Glu76Lys
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*129G>A
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4109
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6011
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4543
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu76Lys
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

5-137507061-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137507061
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137507061
    reference: chr 5
allele count: 2
allele frequency: 1.647690761397901e-5
allele num: 121382
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.210T>C
  hgvsp: ENST00000418329.1:c.210T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.225T>C
  hgvsp: ENST00000230901.5:c.225T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*8T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000407414
  ensembl transcript: ENST00000430331
  gene symbol: BRD8
  hgvsc: ENST00000430331.1:c.357T>C
  hgvsp: ENST00000430331.1:c.357T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.225T>C
  hgvsp: ENST00000411594.2:c.225T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.206T>C
  hgvsp: ENST00000441656.1:c.206T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*128T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.102T>C
  hgvsp: ENST00000455658.2:c.102T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.225T>C
  hgvsp: ENST00000254900.5:c.225T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.225T>C
  hgvsp: ENST00000402931.1:c.225T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.225T>C
  hgvsp: ENST00000432618.1:c.225T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*110T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.210T>C
  hgvsp: ENST00000454473.1:c.210T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.240T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.240T>C
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2928
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6013
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4301
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr75Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

5-137507061-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137507061
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137507061
    reference: chr 5
allele count: 2
allele frequency: 1.647690761397901e-5
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.225T>A
  hgvsp: ENST00000254900.5:c.225T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.225T>A
  hgvsp: ENST00000402931.1:c.225T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.225T>A
  hgvsp: ENST00000230901.5:c.225T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.225T>A
  hgvsp: ENST00000432618.1:c.225T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*110T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.225T>A
  hgvsp: ENST00000411594.2:c.225T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.240T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.206T>A
  hgvsp: ENST00000441656.1:c.206T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.102T>A
  hgvsp: ENST00000455658.2:c.102T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.*8T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*128T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.240T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.210T>A
  hgvsp: ENST00000454473.1:c.210T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.210T>A
  hgvsp: ENST00000418329.1:c.210T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000407414
  ensembl transcript: ENST00000430331
  gene symbol: BRD8
  hgvsc: ENST00000430331.1:c.357T>A
  hgvsp: ENST00000430331.1:c.357T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7763
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6013
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr75Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

5-137507075-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137507075
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137507075
    reference: chr 5
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.211C>T
  hgvsp: ENSP00000384845.1:p.Leu71Phe
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.226C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.196C>T
  hgvsp: ENSP00000398873.1:p.Leu66Phe
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.211C>T
  hgvsp: ENSP00000230901.5:p.Leu71Phe
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000407414
  ensembl transcript: ENST00000430331
  gene symbol: BRD8
  hgvsc: ENST00000430331.1:c.343C>T
  hgvsp: ENSP00000407414.1:p.Leu115Phe
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.211C>T
  hgvsp: ENSP00000254900.5:p.Leu71Phe
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.196C>T
  hgvsp: ENSP00000398067.1:p.Leu66Phe
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.192C>T
  hgvsp: ENSP00000398084.1:p.Leu65Phe
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.88C>T
  hgvsp: ENSP00000408396.2:p.Leu30Phe
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*114C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*96C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.226C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.211C>T
  hgvsp: ENSP00000394330.2:p.Leu71Phe
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.211C>T
  hgvsp: ENSP00000398676.1:p.Leu71Phe
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.141C>T
  hgvsp: ENST00000512140.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4111
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu71Phe
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

5-137507088-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137507088
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137507088
    reference: chr 5
allele count: 1
allele frequency: 8.24347940778844e-6
allele num: 121308
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.198C>T
  hgvsp: ENST00000411594.2:c.198C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.183C>T
  hgvsp: ENST00000418329.1:c.183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.213C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*101C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.213C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.198C>T
  hgvsp: ENST00000432618.1:c.198C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.128C>T
  hgvsp: ENSP00000427475.1:p.Pro43Leu
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.75C>T
  hgvsp: ENST00000455658.2:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*83C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.183C>T
  hgvsp: ENST00000454473.1:c.183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.198C>T
  hgvsp: ENST00000254900.5:c.198C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.198C>T
  hgvsp: ENST00000402931.1:c.198C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.198C>T
  hgvsp: ENST00000230901.5:c.198C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.179C>T
  hgvsp: ENST00000441656.1:c.179C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000407414
  ensembl transcript: ENST00000430331
  gene symbol: BRD8
  hgvsc: ENST00000430331.1:c.330C>T
  hgvsp: ENST00000430331.1:c.330C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19874
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6014
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4291
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro43Leu
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

5-137507089-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137507089
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137507089
    reference: chr 5
allele count: 1
allele frequency: 8.24715060946443e-6
allele num: 121254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.74C>T
  hgvsp: ENSP00000408396.2:p.Ser25Phe
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.197C>T
  hgvsp: ENSP00000254900.5:p.Ser66Phe
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*82C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000407414
  ensembl transcript: ENST00000430331
  gene symbol: BRD8
  hgvsc: ENST00000430331.1:c.329C>T
  hgvsp: ENSP00000407414.1:p.Ser110Phe
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.178C>T
  hgvsp: ENSP00000398084.1:p.Ser60Phe
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.197C>T
  hgvsp: ENSP00000394330.2:p.Ser66Phe
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.197C>T
  hgvsp: ENSP00000384845.1:p.Ser66Phe
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.182C>T
  hgvsp: ENSP00000398873.1:p.Ser61Phe
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*100C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.127C>T
  hgvsp: ENSP00000427475.1:p.Pro43Ser
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.212C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.197C>T
  hgvsp: ENSP00000230901.5:p.Ser66Phe
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.212C>T
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.182C>T
  hgvsp: ENSP00000398067.1:p.Ser61Phe
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.197C>T
  hgvsp: ENSP00000398676.1:p.Ser66Phe
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6003
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7766
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4541
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser66Phe
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD

5-137507102-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137507102
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137507101
    reference: chr 5
allele count: 1
allele frequency: 9.51782688976453e-6
allele num: 105066
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.187-4delA
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.202-4delA
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.187-4delA
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.64-4delA
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.172-4delA
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.117-4delA
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000407414
  ensembl transcript: ENST00000430331
  gene symbol: BRD8
  hgvsc: ENST00000430331.1:c.319-4delA
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*90-4delA
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.168-4delA
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.187-4delA
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.202-4delA
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.172-4delA
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.187-4delA
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*72-4delA
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.187-4delA
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3423
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6348
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3851
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.187-4delA
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: AT
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

5-137507104-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137507104
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137507105
    reference: chr 5
allele count: 783
allele frequency: 7.605042832999864e-3
allele num: 102958
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.172-6dupT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.187-6dupT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*90-6dupT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.202-6dupT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.202-6dupT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.168-6dupT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.64-6dupT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.187-6dupT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.187-6dupT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.187-6dupT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.172-6dupT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*72-6dupT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.117-6dupT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.187-6dupT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000407414
  ensembl transcript: ENST00000430331
  gene symbol: BRD8
  hgvsc: ENST00000430331.1:c.319-6dupT
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8111
  bin: 3.75e1
  variant carriers: 101
genotype depth: GenotypeDepth
  all individuals: 2364
  bin: 1.25e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 5046
  bin: 1.75e1
  variant carriers: 191
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10644
  bin: 3.25e1
  variant carriers: 198
genotype depth: GenotypeDepth
  all individuals: 10749
  bin: 2.75e1
  variant carriers: 263
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 5.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

5-137507104-T-TAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137507104
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137507106
    reference: chr 5
allele count: 34
allele frequency: 3.302317449833913e-4
allele num: 102958
alternate allele: TAA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.172-7_172-6dupTT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.187-7_187-6dupTT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.172-7_172-6dupTT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.117-7_117-6dupTT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.202-7_202-6dupTT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000407414
  ensembl transcript: ENST00000430331
  gene symbol: BRD8
  hgvsc: ENST00000430331.1:c.319-7_319-6dupTT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.64-7_64-6dupTT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.168-7_168-6dupTT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*90-7_*90-6dupTT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.187-7_187-6dupTT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.187-7_187-6dupTT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.187-7_187-6dupTT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.187-7_187-6dupTT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.202-7_202-6dupTT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*72-7_*72-6dupTT
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2364
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5189
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3010
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8507
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1749
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5046
  bin: 1.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

5-137507104-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137507104
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137507103
    reference: chr 5
allele count: 47873
allele frequency: 4.649760096349968e-1
allele num: 102958
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.172-6delT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.64-6delT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*90-6delT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.187-6delT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.202-6delT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.187-6delT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.202-6delT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.168-6delT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.117-6delT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000407414
  ensembl transcript: ENST00000430331
  gene symbol: BRD8
  hgvsc: ENST00000430331.1:c.319-6delT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*72-6delT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.172-6delT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.187-6delT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.187-6delT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.187-6delT
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10749
  bin: 2.75e1
  variant carriers: 9819
genotype depth: GenotypeDepth
  all individuals: 5046
  bin: 1.75e1
  variant carriers: 4513
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.25e1
  variant carriers: 387
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 5.75e1
  variant carriers: 946
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 6.75e1
  variant carriers: 473
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 168
genotype depth: GenotypeDepth
  all individuals: 10644
  bin: 3.25e1
  variant carriers: 9804
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 7.5e0
  variant carriers: 681
genotype depth: GenotypeDepth
  all individuals: 2364
  bin: 1.25e1
  variant carriers: 1995
genotype depth: GenotypeDepth
  all individuals: 8111
  bin: 3.75e1
  variant carriers: 7503
genotype quality: GenotypeQuality
num of homozygotes: 316
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: TA
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD

5-137507104-TAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137507104
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137507102
    reference: chr 5
allele count: 25145
allele frequency: 2.442258008119816e-1
allele num: 102958
alternate allele: T
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 6.25e1
  variant carriers: 342
genotype depth: GenotypeDepth
  all individuals: 8507
  bin: 2.25e1
  variant carriers: 3758
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.75e1
  variant carriers: 152
genotype depth: GenotypeDepth
  all individuals: 3010
  bin: 4.75e1
  variant carriers: 1681
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 5.75e1
  variant carriers: 532
genotype depth: GenotypeDepth
  all individuals: 10749
  bin: 2.75e1
  variant carriers: 4918
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 7.5e0
  variant carriers: 210
genotype depth: GenotypeDepth
  all individuals: 2364
  bin: 1.25e1
  variant carriers: 856
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 6.75e1
  variant carriers: 231
genotype depth: GenotypeDepth
  all individuals: 10644
  bin: 3.25e1
  variant carriers: 5226
genotype depth: GenotypeDepth
  all individuals: 5189
  bin: 4.25e1
  variant carriers: 2848
genotype depth: GenotypeDepth
  all individuals: 5046
  bin: 1.75e1
  variant carriers: 2029
genotype depth: GenotypeDepth
  all individuals: 1749
  bin: 5.25e1
  variant carriers: 952
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.25e1
  variant carriers: 191
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.75e1
  variant carriers: 99
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.25e1
  variant carriers: 120
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 9.75e1
  variant carriers: 352
genotype depth: GenotypeDepth
  all individuals: 8111
  bin: 3.75e1
  variant carriers: 4192
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 90
genotype quality: GenotypeQuality
  all individuals: 1506
  bin: 7.25e1
  variant carriers: 670
genotype quality: GenotypeQuality
  all individuals: 2071
  bin: 2.25e1
  variant carriers: 896
genotype quality: GenotypeQuality
  all individuals: 1986
  bin: 3.25e1
  variant carriers: 913
genotype quality: GenotypeQuality
  all individuals: 1707
  bin: 4.75e1
  variant carriers: 732
genotype quality: GenotypeQuality
  all individuals: 26225
  bin: 9.75e1
  variant carriers: 13501
genotype quality: GenotypeQuality
  all individuals: 1831
  bin: 6.25e1
  variant carriers: 821
genotype quality: GenotypeQuality
  all individuals: 1987
  bin: 4.25e1
  variant carriers: 894
genotype quality: GenotypeQuality
  all individuals: 2146
  bin: 1.75e1
  variant carriers: 974
genotype quality: GenotypeQuality
  all individuals: 2351
  bin: 2.5e0
  variant carriers: 804
genotype quality: GenotypeQuality
  all individuals: 1684
  bin: 5.75e1
  variant carriers: 769
genotype quality: GenotypeQuality
  all individuals: 2095
  bin: 7.5e0
  variant carriers: 926
genotype quality: GenotypeQuality
  all individuals: 1924
  bin: 2.75e1
  variant carriers: 917
genotype quality: GenotypeQuality
  all individuals: 2075
  bin: 1.25e1
  variant carriers: 900
genotype quality: GenotypeQuality
  all individuals: 1918
  bin: 3.75e1
  variant carriers: 911
genotype quality: GenotypeQuality
  all individuals: 1456
  bin: 8.75e1
  variant carriers: 688
genotype quality: GenotypeQuality
  all individuals: 1283
  bin: 9.25e1
  variant carriers: 557
genotype quality: GenotypeQuality
  all individuals: 1536
  bin: 7.75e1
  variant carriers: 716
genotype quality: GenotypeQuality
  all individuals: 1589
  bin: 8.25e1
  variant carriers: 733
genotype quality: GenotypeQuality
  all individuals: 1709
  bin: 5.25e1
  variant carriers: 772
genotype quality: GenotypeQuality
  all individuals: 1579
  bin: 6.75e1
  variant carriers: 706
num of homozygotes: 109
population: European (Non-Finnish)
  type: Population
  allele count: 15042
  allele frequency: 2.630824122009235e-1
  allele num: 57176
  num of homozygotes: 67
population: Latino
  type: Population
  allele count: 2487
  allele frequency: 2.597117794486216e-1
  allele num: 9576
  num of homozygotes: 10
population: Other
  type: Population
  allele count: 204
  allele frequency: 2.635658914728682e-1
  allele num: 774
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 1292
  allele frequency: 2.141199867417965e-1
  allele num: 6034
  num of homozygotes: 12
population: East Asian
population: African
population: South Asian
reference allele: TAA
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

5-137507104-TAAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137507104
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137507101
    reference: chr 5
allele count: 699
allele frequency: 6.78917616892325e-3
allele num: 102958
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.187-8_187-6delTTT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.172-8_172-6delTTT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*72-8_*72-6delTTT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.187-8_187-6delTTT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.172-8_172-6delTTT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.117-8_117-6delTTT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.64-8_64-6delTTT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000407414
  ensembl transcript: ENST00000430331
  gene symbol: BRD8
  hgvsc: ENST00000430331.1:c.319-8_319-6delTTT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.168-8_168-6delTTT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.187-8_187-6delTTT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.202-8_202-6delTTT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.202-8_202-6delTTT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.187-8_187-6delTTT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.187-8_187-6delTTT
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*90-8_*90-6delTTT
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 7.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2364
  bin: 1.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 5.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8507
  bin: 2.25e1
  variant carriers: 154
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 6.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
hgvs: c.187-8_187-6delTTT
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: TAAA
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

5-137507104-TAAAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137507104
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137507100
    reference: chr 5
allele count: 6
allele frequency: 5.82761902911867e-5
allele num: 102958
alternate allele: T
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8507
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5046
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5189
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1749
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2364
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10644
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10749
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3010
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8111
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2146
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1707
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1579
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1831
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1684
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1987
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2071
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1918
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1986
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2095
  bin: 7.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1536
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2351
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1506
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1589
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2075
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1456
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1924
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26225
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1283
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1709
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9576
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 774
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7144
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6034
  num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: TAAAA
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/5-137507105-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137507105
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137507105
    reference: chr 5
allele count: 1
allele frequency: 1.449275362318841e-3
allele num: 690
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000407414
  ensembl transcript: ENST00000430331
  gene symbol: BRD8
  hgvsc: ENST00000430331.1:c.319-6T>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.64-6T>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.117-6T>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.202-6T>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.187-6T>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.172-6T>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.202-6T>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.172-6T>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.168-6T>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.187-6T>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*72-6T>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.187-6T>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.187-6T>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.187-6T>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*90-6T>G
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 2.75e1
  variant carriers: 332
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 2.25e1
  variant carriers: 240
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 3.25e1
  variant carriers: 388
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.75e1
  variant carriers: 117
genotype quality: GenotypeQuality
hgvs: c.187-6T>G
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

5-137507106-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137507106
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137507106
    reference: chr 5
allele count: 1
allele frequency: 1.655629139072848e-3
allele num: 604
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.172-7T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.187-7T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.168-7T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.202-7T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.187-7T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*72-7T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.117-7T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.187-7T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.64-7T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.187-7T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.172-7T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000407414
  ensembl transcript: ENST00000430331
  gene symbol: BRD8
  hgvsc: ENST00000430331.1:c.319-7T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.187-7T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.202-7T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*90-7T>A
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: splice region
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.187-7T>A
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

5-137507120-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137507120
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137507120
    reference: chr 5
allele count: 5
allele frequency: 4.274307989536494e-5
allele num: 116978
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.172-21T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.187-21T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.187-21T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.64-21T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.187-21T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.202-21T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.202-21T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.168-21T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*90-21T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000407414
  ensembl transcript: ENST00000430331
  gene symbol: BRD8
  hgvsc: ENST00000430331.1:c.319-21T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.187-21T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.172-21T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.187-21T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.117-21T>A
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*72-21T>A
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8930
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5914
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2946
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD

5-137507128-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137507128
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137507128
    reference: chr 5
allele count: 1
allele frequency: 8.368621018628551e-6
allele num: 119494
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.187-29A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.168-29A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.172-29A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.187-29A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*90-29A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.172-29A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.187-29A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.187-29A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.64-29A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.202-29A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.202-29A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.187-29A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*72-29A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.117-29A>G
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000407414
  ensembl transcript: ENST00000430331
  gene symbol: BRD8
  hgvsc: ENST00000430331.1:c.319-29A>G
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16283
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14525
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ

5-137507704-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137507704
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137507704
    reference: chr 5
allele count: 2
allele frequency: 1.648016612007449e-5
allele num: 121358
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.171+50T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.186+50T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*71+50T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.186+50T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.186+50T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.186+50T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.117-605T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000407414
  ensembl transcript: ENST00000430331
  gene symbol: BRD8
  hgvsc: ENST00000430331.1:c.318+50T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.186+50T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.201+50T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.171+50T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.167+50T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.201+50T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*89+50T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.64-605T>C
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9099
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8870
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1730
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8068
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD

5-137507705-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137507705
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137507705
    reference: chr 5
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.186+49G>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.186+49G>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000407414
  ensembl transcript: ENST00000430331
  gene symbol: BRD8
  hgvsc: ENST00000430331.1:c.318+49G>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.64-606G>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.201+49G>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.201+49G>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.167+49G>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.117-606G>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.186+49G>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.171+49G>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.186+49G>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*89+49G>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.186+49G>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.171+49G>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*71+49G>C
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4231
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1730
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

5-137507711-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 137507711
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 137507711
    reference: chr 5
allele count: 2
allele frequency: 1.647935137272997e-5
allele num: 121364
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398084
  ensembl transcript: ENST00000441656
  gene symbol: BRD8
  hgvsc: ENST00000441656.1:c.167+43T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000407414
  ensembl transcript: ENST00000430331
  gene symbol: BRD8
  hgvsc: ENST00000430331.1:c.318+43T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000254900
  ensembl transcript: ENST00000254900
  gene symbol: BRD8
  hgvsc: ENST00000254900.5:c.186+43T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000414625
  ensembl transcript: ENST00000428808
  gene symbol: BRD8
  hgvsc: ENST00000428808.1:c.*71+43T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000394330
  ensembl transcript: ENST00000411594
  gene symbol: BRD8
  hgvsc: ENST00000411594.2:c.186+43T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000427475
  ensembl transcript: ENST00000512140
  gene symbol: BRD8
  hgvsc: ENST00000512140.1:c.117-612T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000425764
  gene symbol: BRD8
  hgvsc: ENST00000425764.1:n.201+43T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000396487
  ensembl transcript: ENST00000450756
  gene symbol: BRD8
  hgvsc: ENST00000450756.1:c.*89+43T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398067
  ensembl transcript: ENST00000454473
  gene symbol: BRD8
  hgvsc: ENST00000454473.1:c.171+43T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000384845
  ensembl transcript: ENST00000402931
  gene symbol: BRD8
  hgvsc: ENST00000402931.1:c.186+43T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000408396
  ensembl transcript: ENST00000455658
  gene symbol: BRD8
  hgvsc: ENST00000455658.2:c.64-612T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl transcript: ENST00000515254
  gene symbol: BRD8
  hgvsc: ENST00000515254.1:n.201+43T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000230901
  ensembl transcript: ENST00000230901
  gene symbol: BRD8
  hgvsc: ENST00000230901.5:c.186+43T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398873
  ensembl transcript: ENST00000418329
  gene symbol: BRD8
  hgvsc: ENST00000418329.1:c.171+43T>C
  variant of: http://identifiers.org/hgnc/19874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112983
  ensembl protein: ENSP00000398676
  ensembl transcript: ENST00000432618
  gene symbol: BRD8
  hgvsc: ENST00000432618.1:c.186+43T>C
  variant of: http://identifiers.org/hgnc/19874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9097
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1730
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7899
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6240
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8874
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

GenotypeDepth
all individuals: 994
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1337
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1795
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2832
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 280
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4103
bin: 9.75e1
variant carriers: 3

GenotypeDepth
all individuals: 2229
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5940
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5148
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6799
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 82
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4652
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3825
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3256
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2328
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 32686
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 55
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3566
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2867
bin: 7.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 6
allele frequency: 5.852516582130316e-4
allele num: 10252
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

MQ
type: SiteQuality
SIO_000300: 5.978e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

QD
type: SiteQuality
SIO_000300: 1.598e1

MQRankSum
type: SiteQuality
SIO_000300: -2.99e-1

FS
type: SiteQuality
SIO_000300: 1.258e0

VQSLOD
type: SiteQuality
SIO_000300: 1.53e0

DP
type: SiteQuality
SIO_000300: 3.40203e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.84e0

GenotypeDepth
all individuals: 6328
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5800
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3359
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2229
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1795
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5942
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5148
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4101
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 3854
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2869
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 70
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3825
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 80
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6799
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2330
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3567
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32682
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4652
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3256
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.59e0

DP
type: SiteQuality
SIO_000300: 3.401641e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

MQ
type: SiteQuality
SIO_000300: 5.899e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.24e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e0

MQRankSum
type: SiteQuality
SIO_000300: -1.73e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.31e-1

QD
type: SiteQuality
SIO_000300: 1.509e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.362e0

GenotypeDepth
all individuals: 6328
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2832
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1035
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4699
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5801
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5148
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3854
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 271
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2872
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4647
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2328
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6803
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3822
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3259
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3573
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32682
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

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num of homozygotes: 0

South Asian
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allele frequency: 3.029935765361775e-4
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European (Non-Finnish)
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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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African
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allele frequency: 0.0e0
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Other
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FS
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ClippingRankSum
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DP
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MQRankSum
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MQ
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VQSLOD
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QD
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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European (Non-Finnish)
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East Asian
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Other
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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QD
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BaseQRankSum
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MQ
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VQSLOD
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ClippingRankSum
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MQRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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European (Non-Finnish)
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num of homozygotes: 0

African
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allele num: 10248
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Other
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South Asian
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allele frequency: 0.0e0
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Latino
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ClippingRankSum
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QD
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MQ
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VQSLOD
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DP
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FS
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele num: 11578
num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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Other
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European (Non-Finnish)
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allele num: 66712
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East Asian
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European (Finnish)
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QD
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ReadPosRankSum
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DP
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VQSLOD
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FS
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InbreedingCoeff
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MQRankSum
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MQ
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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African
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Latino
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Other
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South Asian
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MQ
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BaseQRankSum
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ClippingRankSum
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FS
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ReadPosRankSum
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VQSLOD
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QD
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MQRankSum
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InbreedingCoeff
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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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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African
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Latino
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East Asian
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South Asian
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DP
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MQ
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QD
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ReadPosRankSum
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FS
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InbreedingCoeff
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VQSLOD
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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Latino
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European (Non-Finnish)
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East Asian
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allele frequency: 0.0e0
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African
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BaseQRankSum
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MQRankSum
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QD
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FS
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InbreedingCoeff
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DP
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VQSLOD
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ReadPosRankSum
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MQ
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ClippingRankSum
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SIO_000300: 2.01e-1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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Latino
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East Asian
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European (Non-Finnish)
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African
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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DP
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FS
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ClippingRankSum
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VQSLOD
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MQ
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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 (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

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

East Asian
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allele frequency: 1.15606936416185e-4
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num of homozygotes: 0

Latino
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num of homozygotes: 0

South Asian
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Other
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ClippingRankSum
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SIO_000300: -6.81e-1

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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num of homozygotes: 0

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

Other
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66726
num of homozygotes: 0

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

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

European (Non-Finnish)
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num of homozygotes: 0

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

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

MQ
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SIO_000300: 5.972e1

MQRankSum
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SIO_000300: 9.73e-1

DP
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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QD
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VQSLOD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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Other
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South Asian
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VQSLOD
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BaseQRankSum
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FS
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ClippingRankSum
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MQ
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QD
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DP
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InbreedingCoeff
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

East 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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num of homozygotes: 0

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

European (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
allele num: 10396
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.43e-1

InbreedingCoeff
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SIO_000300: -2.0e-4

MQ
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SIO_000300: 5.979e1

DP
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SIO_000300: 3.404878e6

MQRankSum
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FS
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QD
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ClippingRankSum
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VQSLOD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 4
allele frequency: 5.994485073732166e-5
allele num: 66728
num of homozygotes: 0

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

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

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

InbreedingCoeff
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SIO_000300: -3.0e-4

VQSLOD
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FS
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SIO_000300: 2.16e0

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

Latino
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allele frequency: 0.0e0
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East Asian
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Other
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South Asian
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 1.948616482297569e-4
allele num: 66714
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VQSLOD
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QD
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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FS
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MQ
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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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num of homozygotes: 0

South Asian
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European (Non-Finnish)
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African
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East Asian
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European (Finnish)
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Other
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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DP
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MQRankSum
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FS
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QD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
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African
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South Asian
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European (Finnish)
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Latino
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East Asian
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Other
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DP
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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VQSLOD
type: SiteQuality
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MQ
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SIO_000300: 5.973e1

FS
type: SiteQuality
SIO_000300: 4.166e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.54e-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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bin: 3.75e1
variant carriers: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

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

South Asian
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allele frequency: 1.818843215714805e-4
allele num: 16494
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 8.85e-1

VQSLOD
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ReadPosRankSum
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QD
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MQ
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SIO_000300: 5.939e1

FS
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MQRankSum
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BaseQRankSum
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DP
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SIO_000300: 3.389924e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

GenotypeDepth
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variant carriers: 0

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

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5008254539997e-5
allele num: 66630
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.519e0

QD
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InbreedingCoeff
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SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

DP
type: SiteQuality
SIO_000300: 3.385513e6

BaseQRankSum
type: SiteQuality
SIO_000300: 8.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -4.1e-2

FS
type: SiteQuality
SIO_000300: 7.146e0

MQ
type: SiteQuality
SIO_000300: 5.857e1

ClippingRankSum
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SIO_000300: 2.0e0

GenotypeDepth
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variant carriers: 6

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2471
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East Asian
type: Population
allele count: 48
allele frequency: 6.715165081141578e-3
allele num: 7148
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 10
allele frequency: 1.610305958132045e-3
allele num: 6210
num of homozygotes: 0

African
type: Population
allele count: 61
allele frequency: 7.042253521126761e-3
allele num: 8662
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 373
allele frequency: 6.761656152563266e-3
allele num: 55164
num of homozygotes: 0

Other
type: Population
allele count: 6
allele frequency: 8.356545961002786e-3
allele num: 718
num of homozygotes: 0

Latino
type: Population
allele count: 64
allele frequency: 6.980802792321117e-3
allele num: 9168
num of homozygotes: 0

South Asian
type: Population
allele count: 399
allele frequency: 3.702672605790646e-2
allele num: 10776
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.18e0

MQRankSum
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SIO_000300: 2.35e-1

FS
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SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

InbreedingCoeff
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SIO_000300: 6.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.79e-1

BaseQRankSum
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SIO_000300: -3.86e-1

DP
type: SiteQuality
SIO_000300: 3.222631e6

QD
type: SiteQuality
SIO_000300: 7.2e-1

GenotypeDepth
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variant carriers: 35

GenotypeDepth
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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: 251
allele frequency: 2.329250185597624e-2
allele num: 10776
num of homozygotes: 0

East Asian
type: Population
allele count: 74
allele frequency: 1.035254616675993e-2
allele num: 7148
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 718
allele frequency: 1.301573489957219e-2
allele num: 55164
num of homozygotes: 0

Other
type: Population
allele count: 8
allele frequency: 1.114206128133705e-2
allele num: 718
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Latino
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allele count: 63
allele frequency: 6.8717277486911e-3
allele num: 9168
num of homozygotes: 0

European (Finnish)
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allele count: 4
allele frequency: 6.441223832528181e-4
allele num: 6210
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African
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allele count: 83
allele frequency: 9.582082659893789e-3
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VQSLOD
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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FS
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QD
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MQ
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SIO_000300: 5.964e1

DP
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InbreedingCoeff
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SIO_000300: 6.5e-2

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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East Asian
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allele count: 0
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Latino
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num of homozygotes: 0

Other
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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: 1.812776448408382e-5
allele num: 55164
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VQSLOD
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DP
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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MQ
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BaseQRankSum
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FS
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

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

Other
type: Population
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East Asian
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allele count: 0
allele frequency: 0.0e0
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African
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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: 1.502945773716484e-5
allele num: 66536
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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FS
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MQRankSum
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MQ
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InbreedingCoeff
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DP
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QD
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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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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22063
bin: 9.75e1
variant carriers: 3

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66438
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.496503496503497e-4
allele num: 8580
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10236
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16410
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.757149e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: -6.474e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.91e-1

QD
type: SiteQuality
SIO_000300: 6.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.07e-1

GenotypeDepth
all individuals: 433
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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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GenotypeQuality
all individuals: 6059
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 562
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variant carriers: 0

GenotypeQuality
all individuals: 3702
bin: 7.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10230
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503895088278642e-5
allele num: 66494
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.971e1

VQSLOD
type: SiteQuality
SIO_000300: 1.68e-1

DP
type: SiteQuality
SIO_000300: 2.746261e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.07e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.06e0

QD
type: SiteQuality
SIO_000300: 1.527e1

FS
type: SiteQuality
SIO_000300: 3.8e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.379e0

GenotypeDepth
all individuals: 382
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 2816
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66504
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.215657670799903e-4
allele num: 16452
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.591e1

DP
type: SiteQuality
SIO_000300: 2.742084e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.39e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

FS
type: SiteQuality
SIO_000300: 9.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.71e0

GenotypeDepth
all individuals: 4541
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 433
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variant carriers: 0

GenotypeDepth
all individuals: 623
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variant carriers: 0

GenotypeDepth
all individuals: 8013
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
all individuals: 3525
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GenotypeQuality
all individuals: 53
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GenotypeQuality
all individuals: 470
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 4102
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 782
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 3673
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variant carriers: 0

GenotypeQuality
all individuals: 4576
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66486
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.08198515995621e-5
allele num: 16442
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.168497312456181e-4
allele num: 8558
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.82e0

MQ
type: SiteQuality
SIO_000300: 5.463e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.96e0

FS
type: SiteQuality
SIO_000300: 2.181e0

MQRankSum
type: SiteQuality
SIO_000300: -2.054e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.6e-1

DP
type: SiteQuality
SIO_000300: 2.733735e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.54e-1

GenotypeDepth
all individuals: 2755
bin: 9.75e1
variant carriers: 199

GenotypeDepth
all individuals: 7510
bin: 4.25e1
variant carriers: 395

GenotypeDepth
all individuals: 1866
bin: 6.25e1
variant carriers: 176

GenotypeDepth
all individuals: 1283
bin: 6.75e1
variant carriers: 129

GenotypeDepth
all individuals: 7966
bin: 3.75e1
variant carriers: 377

GenotypeDepth
all individuals: 4528
bin: 5.25e1
variant carriers: 309

GenotypeQuality
all individuals: 1012
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
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GenotypeQuality
all individuals: 391
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 62
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variant carriers: 0

GenotypeQuality
all individuals: 8016
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variant carriers: 3

GenotypeQuality
all individuals: 52
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variant carriers: 0

GenotypeQuality
all individuals: 619
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variant carriers: 0

GenotypeQuality
all individuals: 744
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 17
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GenotypeQuality
all individuals: 770
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variant carriers: 1

GenotypeQuality
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bin: 3.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 4

GenotypeQuality
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bin: 7.25e1
variant carriers: 2

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 3278

GenotypeQuality
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variant carriers: 4

GenotypeQuality
all individuals: 3332
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 5346
bin: 6.75e1
variant carriers: 3

European (Finnish)
type: Population
allele count: 385
allele frequency: 5.829800121138703e-2
allele num: 6604
num of homozygotes: 9

Latino
type: Population
allele count: 105
allele frequency: 9.083044982698962e-3
allele num: 11560
num of homozygotes: 0

South Asian
type: Population
allele count: 312
allele frequency: 1.900121802679659e-2
allele num: 16420
num of homozygotes: 3

Other
type: Population
allele count: 22
allele frequency: 2.433628318584071e-2
allele num: 904
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

African
type: Population
allele count: 51
allele frequency: 5.003924646781789e-3
allele num: 10192
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 2481
allele frequency: 3.733971464692071e-2
allele num: 66444
num of homozygotes: 46

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.05e-2

MQ
type: SiteQuality
SIO_000300: 5.956e1

VQSLOD
type: SiteQuality
SIO_000300: 5.1e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.53e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.18e-1

QD
type: SiteQuality
SIO_000300: 1.557e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.82e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e-1

DP
type: SiteQuality
SIO_000300: 2.721193e6

GenotypeDepth
all individuals: 380
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 825
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 526
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2549
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6011
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 440
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variant carriers: 0

GenotypeQuality
all individuals: 2739
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GenotypeQuality
all individuals: 94
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GenotypeQuality
all individuals: 22329
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variant carriers: 4

GenotypeQuality
all individuals: 718
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variant carriers: 0

GenotypeQuality
all individuals: 993
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GenotypeQuality
all individuals: 85
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GenotypeQuality
all individuals: 42
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GenotypeQuality
all individuals: 5409
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GenotypeQuality
all individuals: 3508
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GenotypeQuality
all individuals: 7687
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GenotypeQuality
all individuals: 470
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variant carriers: 0

GenotypeQuality
all individuals: 788
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GenotypeQuality
all individuals: 1041
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GenotypeQuality
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GenotypeQuality
all individuals: 89
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GenotypeQuality
all individuals: 514
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GenotypeQuality
all individuals: 723
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GenotypeQuality
all individuals: 1354
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4062
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4524
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16364
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.520523175215478e-5
allele num: 66364
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.832841691248771e-5
allele num: 10170
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.6e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.11e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

MQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.604e0

DP
type: SiteQuality
SIO_000300: 2.700152e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.17e-1

QD
type: SiteQuality
SIO_000300: 1.139e1

GenotypeDepth
all individuals: 7478
bin: 4.25e1
variant carriers: 6

GenotypeDepth
all individuals: 7826
bin: 3.25e1
variant carriers: 7

GenotypeDepth
all individuals: 2932
bin: 5.75e1
variant carriers: 2

GenotypeDepth
all individuals: 380
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variant carriers: 0

GenotypeDepth
all individuals: 4727
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variant carriers: 1

GenotypeDepth
all individuals: 825
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variant carriers: 0

GenotypeQuality
all individuals: 37
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GenotypeQuality
all individuals: 22377
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variant carriers: 66

GenotypeQuality
all individuals: 637
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variant carriers: 0

GenotypeQuality
all individuals: 4073
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variant carriers: 0

GenotypeQuality
all individuals: 788
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GenotypeQuality
all individuals: 1415
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variant carriers: 0

GenotypeQuality
all individuals: 492
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variant carriers: 0

GenotypeQuality
all individuals: 98
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GenotypeQuality
all individuals: 3504
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variant carriers: 0

GenotypeQuality
all individuals: 80
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GenotypeQuality
all individuals: 726
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GenotypeQuality
all individuals: 155
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GenotypeQuality
all individuals: 7031
bin: 6.25e1
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GenotypeQuality
all individuals: 1500
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GenotypeQuality
all individuals: 4555
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GenotypeQuality
all individuals: 629
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GenotypeQuality
all individuals: 5283
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GenotypeQuality
all individuals: 3543
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1031
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2751
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.854158454867954e-5
allele num: 10148
num of homozygotes: 0

Latino
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allele count: 2
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East Asian
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DP
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FS
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VQSLOD
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MQ
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InbreedingCoeff
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ReadPosRankSum
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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 (Finnish)
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DP
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VQSLOD
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InbreedingCoeff
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MQ
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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East Asian
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African
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VQSLOD
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MQ
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FS
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InbreedingCoeff
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MQRankSum
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DP
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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African
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European (Non-Finnish)
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European (Finnish)
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MQRankSum
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VQSLOD
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InbreedingCoeff
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FS
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DP
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QD
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MQ
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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South Asian
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European (Finnish)
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African
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Latino
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East Asian
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FS
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MQ
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VQSLOD
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QD
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DP
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African
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European (Non-Finnish)
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VQSLOD
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SIO_000300: -1.641e0

ClippingRankSum
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SIO_000300: -3.48e-1

QD
type: SiteQuality
SIO_000300: 2.11e1

DP
type: SiteQuality
SIO_000300: 3.758287e6

FS
type: SiteQuality
SIO_000300: 2.576e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

BaseQRankSum
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SIO_000300: -2.606e0

MQ
type: SiteQuality
SIO_000300: 5.873e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.62e-1

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
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
allele num: 10392
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

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

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

InbreedingCoeff
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SIO_000300: 0.0e0

VQSLOD
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SIO_000300: -4.253e-1

MQ
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SIO_000300: 5.894e1

MQRankSum
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SIO_000300: -1.93e-1

FS
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SIO_000300: 4.135e0

ClippingRankSum
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SIO_000300: -3.36e-1

BaseQRankSum
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SIO_000300: -9.88e-1

DP
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SIO_000300: 3.75821e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.22e-1

QD
type: SiteQuality
SIO_000300: 1.027e1

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.997242536866083e-5
allele num: 66728
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
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
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.93e-1

MQ
type: SiteQuality
SIO_000300: 5.894e1

BaseQRankSum
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SIO_000300: -9.88e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.253e-1

QD
type: SiteQuality
SIO_000300: 1.027e1

FS
type: SiteQuality
SIO_000300: 4.135e0

InbreedingCoeff
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SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.22e-1

DP
type: SiteQuality
SIO_000300: 3.75821e6

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10388
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

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

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

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

East Asian
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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

InbreedingCoeff
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SIO_000300: -1.0e-4

BaseQRankSum
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QD
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ReadPosRankSum
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FS
type: SiteQuality
SIO_000300: 8.4e-1

DP
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SIO_000300: 3.756534e6

MQRankSum
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ClippingRankSum
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VQSLOD
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SIO_000300: -2.346e-1

MQ
type: SiteQuality
SIO_000300: 5.841e1

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

South Asian
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allele count: 1
allele frequency: 6.06060606060606e-5
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Other
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num of homozygotes: 0

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

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

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

South Asian
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Other
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Latino
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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European (Non-Finnish)
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allele num: 66670
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MQRankSum
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ReadPosRankSum
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MQ
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BaseQRankSum
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InbreedingCoeff
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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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GenotypeDepth
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GenotypeDepth
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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 count: 0
allele frequency: 0.0e0
allele num: 7428
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 57570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14606
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10210
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.220703125e-4
allele num: 8192
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.086e0

DP
type: SiteQuality
SIO_000300: 3.362124e6

MQ
type: SiteQuality
SIO_000300: 5.863e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.01e-1

QD
type: SiteQuality
SIO_000300: 1.53e0

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.9e-1

GenotypeDepth
all individuals: 905
bin: 7.5e0
variant carriers: 18

GenotypeDepth
all individuals: 3010
bin: 4.75e1
variant carriers: 20

GenotypeDepth
all individuals: 1749
bin: 5.25e1
variant carriers: 13

GenotypeDepth
all individuals: 661
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 677
bin: 6.25e1
variant carriers: 6

GenotypeDepth
all individuals: 5189
bin: 4.25e1
variant carriers: 55

GenotypeDepth
all individuals: 8507
bin: 2.25e1
variant carriers: 273

GenotypeDepth
all individuals: 269
bin: 8.25e1
variant carriers: 2

GenotypeDepth
all individuals: 346
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variant carriers: 2

GenotypeQuality
all individuals: 1709
bin: 5.25e1
variant carriers: 38

GenotypeQuality
all individuals: 2075
bin: 1.25e1
variant carriers: 100

GenotypeQuality
all individuals: 26225
bin: 9.75e1
variant carriers: 95

GenotypeQuality
all individuals: 1579
bin: 6.75e1
variant carriers: 46

GenotypeQuality
all individuals: 1506
bin: 7.25e1
variant carriers: 22

GenotypeQuality
all individuals: 1987
bin: 4.25e1
variant carriers: 67

GenotypeQuality
all individuals: 1456
bin: 8.75e1
variant carriers: 11

GenotypeQuality
all individuals: 1924
bin: 2.75e1
variant carriers: 72

GenotypeQuality
all individuals: 2146
bin: 1.75e1
variant carriers: 72

GenotypeQuality
all individuals: 2351
bin: 2.5e0
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GenotypeQuality
all individuals: 1684
bin: 5.75e1
variant carriers: 38

GenotypeQuality
all individuals: 2071
bin: 2.25e1
variant carriers: 124

GenotypeQuality
all individuals: 1589
bin: 8.25e1
variant carriers: 25

GenotypeQuality
all individuals: 2095
bin: 7.5e0
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GenotypeQuality
all individuals: 1831
bin: 6.25e1
variant carriers: 36

GenotypeQuality
all individuals: 1918
bin: 3.75e1
variant carriers: 52

GenotypeQuality
all individuals: 1283
bin: 9.25e1
variant carriers: 17

GenotypeQuality
all individuals: 1707
bin: 4.75e1
variant carriers: 76

GenotypeQuality
all individuals: 1986
bin: 3.25e1
variant carriers: 57

GenotypeQuality
all individuals: 1536
bin: 7.75e1
variant carriers: 22

European (Finnish)
type: Population
allele count: 75
allele frequency: 1.242956579383494e-2
allele num: 6034
num of homozygotes: 0

Latino
type: Population
allele count: 47
allele frequency: 4.908103592314118e-3
allele num: 9576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 475
allele frequency: 8.307681544704071e-3
allele num: 57176
num of homozygotes: 0

African
type: Population
allele count: 54
allele frequency: 6.446991404011461e-3
allele num: 8376
num of homozygotes: 0

Other
type: Population
allele count: 5
allele frequency: 6.459948320413436e-3
allele num: 774
num of homozygotes: 0

East Asian
type: Population
allele count: 49
allele frequency: 6.858902575587906e-3
allele num: 7144
num of homozygotes: 0

South Asian
type: Population
allele count: 78
allele frequency: 5.620406398616515e-3
allele num: 13878
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.3e-2

QD
type: SiteQuality
SIO_000300: 9.99e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.91e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.003e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.93e-2

DP
type: SiteQuality
SIO_000300: 2.013197e6

GenotypeDepth
all individuals: 512
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 92
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 10749
bin: 2.75e1
variant carriers: 11

GenotypeDepth
all individuals: 10644
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variant carriers: 3

GenotypeDepth
all individuals: 677
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 177
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 417
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variant carriers: 1

GenotypeDepth
all individuals: 214
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8111
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2095
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 1986
bin: 3.25e1
variant carriers: 3

GenotypeQuality
all individuals: 2146
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1456
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1283
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1709
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2075
bin: 1.25e1
variant carriers: 5

GenotypeQuality
all individuals: 1918
bin: 3.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1579
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2071
bin: 2.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1831
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2351
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 1684
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1589
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1924
bin: 2.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1707
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1987
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variant carriers: 6

GenotypeQuality
all individuals: 1536
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 26225
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1506
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 5
allele frequency: 5.969436485195798e-4
allele num: 8376
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.657275439177991e-4
allele num: 6034
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.441129845799107e-4
allele num: 13878
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 24
allele frequency: 4.197565412061005e-4
allele num: 57176
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9576
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.799552071668533e-4
allele num: 7144
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.3e-2

DP
type: SiteQuality
SIO_000300: 2.013197e6

MQ
type: SiteQuality
SIO_000300: 5.946e1

VQSLOD
type: SiteQuality
SIO_000300: 6.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.93e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.003e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.91e-1

QD
type: SiteQuality
SIO_000300: 9.99e0

GenotypeDepth
all individuals: 661
bin: 9.75e1
variant carriers: 624

GenotypeDepth
all individuals: 269
bin: 8.25e1
variant carriers: 251

GenotypeDepth
all individuals: 1749
bin: 5.25e1
variant carriers: 1602

GenotypeDepth
all individuals: 8507
bin: 2.25e1
variant carriers: 7744

GenotypeDepth
all individuals: 3010
bin: 4.75e1
variant carriers: 2771

GenotypeDepth
all individuals: 214
bin: 8.75e1
variant carriers: 200

GenotypeDepth
all individuals: 677
bin: 6.25e1
variant carriers: 620

GenotypeDepth
all individuals: 346
bin: 7.75e1
variant carriers: 321

GenotypeDepth
all individuals: 5189
bin: 4.25e1
variant carriers: 4771

GenotypeQuality
all individuals: 1831
bin: 6.25e1
variant carriers: 1695

GenotypeQuality
all individuals: 1707
bin: 4.75e1
variant carriers: 1564

GenotypeQuality
all individuals: 1456
bin: 8.75e1
variant carriers: 1356

GenotypeQuality
all individuals: 2351
bin: 2.5e0
variant carriers: 1767

GenotypeQuality
all individuals: 1506
bin: 7.25e1
variant carriers: 1394

GenotypeQuality
all individuals: 1987
bin: 4.25e1
variant carriers: 1823

GenotypeQuality
all individuals: 1709
bin: 5.25e1
variant carriers: 1562

GenotypeQuality
all individuals: 1579
bin: 6.75e1
variant carriers: 1459

GenotypeQuality
all individuals: 2071
bin: 2.25e1
variant carriers: 1893

GenotypeQuality
all individuals: 1684
bin: 5.75e1
variant carriers: 1554

GenotypeQuality
all individuals: 2075
bin: 1.25e1
variant carriers: 1828

GenotypeQuality
all individuals: 2095
bin: 7.5e0
variant carriers: 1789

GenotypeQuality
all individuals: 1924
bin: 2.75e1
variant carriers: 1713

GenotypeQuality
all individuals: 2146
bin: 1.75e1
variant carriers: 1897

GenotypeQuality
all individuals: 1536
bin: 7.75e1
variant carriers: 1410

GenotypeQuality
all individuals: 1589
bin: 8.25e1
variant carriers: 1482

GenotypeQuality
all individuals: 1918
bin: 3.75e1
variant carriers: 1740

GenotypeQuality
all individuals: 1283
bin: 9.25e1
variant carriers: 1199

GenotypeQuality
all individuals: 26225
bin: 9.75e1
variant carriers: 24326

GenotypeQuality
all individuals: 1986
bin: 3.25e1
variant carriers: 1801

African
type: Population
allele count: 4018
allele frequency: 4.797039159503343e-1
allele num: 8376
num of homozygotes: 46

South Asian
type: Population
allele count: 6695
allele frequency: 4.824182158812509e-1
allele num: 13878
num of homozygotes: 32

European (Non-Finnish)
type: Population
allele count: 25961
allele frequency: 4.540541485938156e-1
allele num: 57176
num of homozygotes: 159

European (Finnish)
type: Population
allele count: 2649
allele frequency: 4.390122638382499e-1
allele num: 6034
num of homozygotes: 7

Other
type: Population
allele count: 361
allele frequency: 4.664082687338501e-1
allele num: 774
num of homozygotes: 5

Latino
type: Population
allele count: 4611
allele frequency: 4.815162907268171e-1
allele num: 9576
num of homozygotes: 28

East Asian
type: Population
allele count: 3578
allele frequency: 5.008398656215005e-1
allele num: 7144
num of homozygotes: 39

BaseQRankSum
type: SiteQuality
SIO_000300: -3.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.003e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.93e-2

MQ
type: SiteQuality
SIO_000300: 5.946e1

DP
type: SiteQuality
SIO_000300: 2.013197e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.91e-1

QD
type: SiteQuality
SIO_000300: 9.99e0

East Asian
type: Population
allele count: 790
allele frequency: 1.105823068309071e-1
allele num: 7144
num of homozygotes: 0

African
type: Population
allele count: 1933
allele frequency: 2.307784145176695e-1
allele num: 8376
num of homozygotes: 14

South Asian
type: Population
allele count: 3397
allele frequency: 2.447759043089782e-1
allele num: 13878
num of homozygotes: 6

MQRankSum
type: SiteQuality
SIO_000300: 3.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.91e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.93e-2

QD
type: SiteQuality
SIO_000300: 9.99e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.003e0

MQ
type: SiteQuality
SIO_000300: 5.946e1

DP
type: SiteQuality
SIO_000300: 2.013197e6

GenotypeDepth
all individuals: 3010
bin: 4.75e1
variant carriers: 53

GenotypeDepth
all individuals: 5189
bin: 4.25e1
variant carriers: 104

GenotypeDepth
all individuals: 512
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 10749
bin: 2.75e1
variant carriers: 148

GenotypeDepth
all individuals: 8111
bin: 3.75e1
variant carriers: 116

GenotypeDepth
all individuals: 5046
bin: 1.75e1
variant carriers: 113

GenotypeDepth
all individuals: 214
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variant carriers: 1

GenotypeDepth
all individuals: 10644
bin: 3.25e1
variant carriers: 156

GenotypeDepth
all individuals: 346
bin: 7.75e1
variant carriers: 2

GenotypeDepth
all individuals: 1749
bin: 5.25e1
variant carriers: 36

GenotypeDepth
all individuals: 269
bin: 8.25e1
variant carriers: 3

GenotypeDepth
all individuals: 661
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 2146
bin: 1.75e1
variant carriers: 61

GenotypeQuality
all individuals: 1684
bin: 5.75e1
variant carriers: 25

GenotypeQuality
all individuals: 1579
bin: 6.75e1
variant carriers: 26

GenotypeQuality
all individuals: 1986
bin: 3.25e1
variant carriers: 48

GenotypeQuality
all individuals: 2095
bin: 7.5e0
variant carriers: 69

GenotypeQuality
all individuals: 1831
bin: 6.25e1
variant carriers: 30

GenotypeQuality
all individuals: 1918
bin: 3.75e1
variant carriers: 45

GenotypeQuality
all individuals: 1589
bin: 8.25e1
variant carriers: 16

GenotypeQuality
all individuals: 1456
bin: 8.75e1
variant carriers: 24

GenotypeQuality
all individuals: 1506
bin: 7.25e1
variant carriers: 33

GenotypeQuality
all individuals: 2351
bin: 2.5e0
variant carriers: 90

GenotypeQuality
all individuals: 2071
bin: 2.25e1
variant carriers: 50

GenotypeQuality
all individuals: 1924
bin: 2.75e1
variant carriers: 51

GenotypeQuality
all individuals: 1707
bin: 4.75e1
variant carriers: 36

GenotypeQuality
all individuals: 2075
bin: 1.25e1
variant carriers: 58

GenotypeQuality
all individuals: 1536
bin: 7.75e1
variant carriers: 30

GenotypeQuality
all individuals: 1987
bin: 4.25e1
variant carriers: 44

GenotypeQuality
all individuals: 1283
bin: 9.25e1
variant carriers: 17

GenotypeQuality
all individuals: 1709
bin: 5.25e1
variant carriers: 48

GenotypeQuality
all individuals: 26225
bin: 9.75e1
variant carriers: 186

European (Finnish)
type: Population
allele count: 11
allele frequency: 1.823002983095791e-3
allele num: 6034
num of homozygotes: 0

Latino
type: Population
allele count: 61
allele frequency: 6.370091896407686e-3
allele num: 9576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 491
allele frequency: 8.587519238841473e-3
allele num: 57176
num of homozygotes: 0

Other
type: Population
allele count: 6
allele frequency: 7.751937984496124e-3
allele num: 774
num of homozygotes: 0

East Asian
type: Population
allele count: 9
allele frequency: 1.25979843225084e-3
allele num: 7144
num of homozygotes: 0

African
type: Population
allele count: 38
allele frequency: 4.536771728748806e-3
allele num: 8376
num of homozygotes: 0

South Asian
type: Population
allele count: 83
allele frequency: 5.980688860066292e-3
allele num: 13878
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.003e0

QD
type: SiteQuality
SIO_000300: 9.99e0

MQRankSum
type: SiteQuality
SIO_000300: 3.23e-1

DP
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SIO_000300: 2.013197e6

MQ
type: SiteQuality
SIO_000300: 5.946e1

VQSLOD
type: SiteQuality
SIO_000300: 6.0e0

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.93e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.3e-2

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 1.049391353015251e-4
allele num: 57176
num of homozygotes: 0

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

South Asian
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allele num: 13878
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.23e-1

VQSLOD
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.3e-2

DP
type: SiteQuality
SIO_000300: 2.013197e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.91e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

QD
type: SiteQuality
SIO_000300: 9.99e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.93e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.003e0

GenotypeDepth
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 152
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GenotypeDepth
all individuals: 61
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GenotypeDepth
all individuals: 110
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variant carriers: 4

GenotypeDepth
all individuals: 22
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GenotypeDepth
all individuals: 99
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GenotypeDepth
all individuals: 393
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variant carriers: 295

GenotypeDepth
all individuals: 15
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GenotypeDepth
all individuals: 17
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variant carriers: 14

GenotypeDepth
all individuals: 25
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GenotypeDepth
all individuals: 27
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GenotypeDepth
all individuals: 240
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variant carriers: 189

GenotypeQuality
all individuals: 40
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GenotypeQuality
all individuals: 99
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variant carriers: 0

GenotypeQuality
all individuals: 97
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GenotypeQuality
all individuals: 2467
bin: 2.5e0
variant carriers: 1979

GenotypeQuality
all individuals: 115
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GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
all individuals: 48
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variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 16
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GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 69
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GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 61
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GenotypeQuality
all individuals: 1
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.923076923076923e-2
allele num: 52
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 418
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 76
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 9.8878e4

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.41e-1

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