6-136590700-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590700
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590700
    reference: chr 6
allele count: 1
allele frequency: 8.256820133430213e-6
allele num: 121112
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.260T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.398T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2088T>A
  hgvsp: ENSP00000436142.1:p.Asp696Glu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2088T>A
  hgvsp: ENSP00000229446.5:p.Asp696Glu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1575T>A
  hgvsp: ENSP00000436501.1:p.Asp525Glu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2091T>A
  hgvsp: ENSP00000431734.1:p.Asp697Glu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2094T>A
  hgvsp: ENSP00000436216.1:p.Asp698Glu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*392T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2088T>A
  hgvsp: ENSP00000434826.1:p.Asp696Glu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2094T>A
  hgvsp: ENSP00000435441.1:p.Asp698Glu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2094T>A
  hgvsp: ENSP00000433505.1:p.Asp698Glu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.221T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2088T>A
  hgvsp: ENSP00000376159.2:p.Asp696Glu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2094T>A
  hgvsp: ENSP00000435210.1:p.Asp698Glu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.179T>A
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5341
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5633
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4245
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5430
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp698Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

6-136590703-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590703
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590703
    reference: chr 6
allele count: 1
allele frequency: 8.25722920416825e-6
allele num: 121106
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*389T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2088T>C
  hgvsp: ENST00000529826.1:c.2088T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2085T>C
  hgvsp: ENST00000392348.2:c.2085T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2091T>C
  hgvsp: ENST00000527613.1:c.2091T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.395T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2085T>C
  hgvsp: ENST00000353331.4:c.2085T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2085T>C
  hgvsp: ENST00000530429.1:c.2085T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1572T>C
  hgvsp: ENST00000530767.1:c.1572T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2085T>C
  hgvsp: ENST00000527759.1:c.2085T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2091T>C
  hgvsp: ENST00000531224.1:c.2091T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2091T>C
  hgvsp: ENST00000527536.1:c.2091T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2091T>C
  hgvsp: ENST00000532384.1:c.2091T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.218T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.176T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.257T>C
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4529
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4932
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile697Ile
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

6-136590710-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590710
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590710
    reference: chr 6
allele count: 13
allele frequency: 1.073705771581486e-4
allele num: 121076
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2084A>G
  hgvsp: ENSP00000436216.1:p.His695Arg
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.388A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2084A>G
  hgvsp: ENSP00000435210.1:p.His695Arg
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2078A>G
  hgvsp: ENSP00000436142.1:p.His693Arg
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2078A>G
  hgvsp: ENSP00000376159.2:p.His693Arg
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*382A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.211A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1565A>G
  hgvsp: ENSP00000436501.1:p.His522Arg
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2084A>G
  hgvsp: ENSP00000433505.1:p.His695Arg
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.250A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2078A>G
  hgvsp: ENSP00000229446.5:p.His693Arg
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2078A>G
  hgvsp: ENSP00000434826.1:p.His693Arg
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2084A>G
  hgvsp: ENSP00000435441.1:p.His695Arg
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.169A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2081A>G
  hgvsp: ENSP00000431734.1:p.His694Arg
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5430
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3561
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2348
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4244
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His695Arg
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

6-136590711-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590711
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590711
    reference: chr 6
allele count: 2
allele frequency: 1.651827747402501e-5
allele num: 121078
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2080C>T
  hgvsp: ENSP00000431734.1:p.His694Tyr
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2083C>T
  hgvsp: ENSP00000436216.1:p.His695Tyr
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2077C>T
  hgvsp: ENSP00000434826.1:p.His693Tyr
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2077C>T
  hgvsp: ENSP00000436142.1:p.His693Tyr
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.210C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.249C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2083C>T
  hgvsp: ENSP00000435441.1:p.His695Tyr
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.387C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.168C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2077C>T
  hgvsp: ENSP00000229446.5:p.His693Tyr
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2083C>T
  hgvsp: ENSP00000435210.1:p.His695Tyr
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2077C>T
  hgvsp: ENSP00000376159.2:p.His693Tyr
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*381C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1564C>T
  hgvsp: ENSP00000436501.1:p.His522Tyr
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2083C>T
  hgvsp: ENSP00000433505.1:p.His695Tyr
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12175
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3560
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5342
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His695Tyr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

6-136590712-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590712
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590712
    reference: chr 6
allele count: 60266
allele frequency: 4.991882579020608e-1
allele num: 120728
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2082G>A
  hgvsp: ENST00000527613.1:c.2082G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.167G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2076G>A
  hgvsp: ENST00000392348.2:c.2076G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2079G>A
  hgvsp: ENST00000529826.1:c.2079G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2076G>A
  hgvsp: ENST00000527759.1:c.2076G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2076G>A
  hgvsp: ENST00000353331.4:c.2076G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.248G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*380G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.209G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1563G>A
  hgvsp: ENST00000530767.1:c.1563G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2082G>A
  hgvsp: ENST00000531224.1:c.2082G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2082G>A
  hgvsp: ENST00000527536.1:c.2082G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2076G>A
  hgvsp: ENST00000530429.1:c.2076G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2082G>A
  hgvsp: ENST00000532384.1:c.2082G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.386G>A
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: synonymous
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 3.75e1
  variant carriers: 1449
genotype depth: GenotypeDepth
  all individuals: 5653
  bin: 6.25e1
  variant carriers: 5639
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 201
genotype depth: GenotypeDepth
  all individuals: 4345
  bin: 7.75e1
  variant carriers: 4339
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 8.75e1
  variant carriers: 3025
genotype depth: GenotypeDepth
  all individuals: 5404
  bin: 5.75e1
  variant carriers: 5400
genotype depth: GenotypeDepth
  all individuals: 3473
  bin: 4.75e1
  variant carriers: 3461
genotype depth: GenotypeDepth
  all individuals: 12063
  bin: 9.75e1
  variant carriers: 12046
genotype quality: GenotypeQuality
hgvs: p.Arg694Arg
num of homozygotes: 1
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD

6-136590714-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590714
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590714
    reference: chr 6
allele count: 19
allele frequency: 1.573160230509373e-4
allele num: 120776
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2074C>T
  hgvsp: ENSP00000229446.5:p.Arg692Trp
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2074C>T
  hgvsp: ENSP00000376159.2:p.Arg692Trp
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2080C>T
  hgvsp: ENSP00000436216.1:p.Arg694Trp
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2074C>T
  hgvsp: ENSP00000434826.1:p.Arg692Trp
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2080C>T
  hgvsp: ENSP00000435210.1:p.Arg694Trp
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1561C>T
  hgvsp: ENSP00000436501.1:p.Arg521Trp
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2077C>T
  hgvsp: ENSP00000431734.1:p.Arg693Trp
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2080C>T
  hgvsp: ENSP00000433505.1:p.Arg694Trp
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.246C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2074C>T
  hgvsp: ENSP00000436142.1:p.Arg692Trp
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*378C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.384C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.165C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.207C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2080C>T
  hgvsp: ENSP00000435441.1:p.Arg694Trp
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2778
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12363
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5512
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg694Trp
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD

6-136590714-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590714
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590714
    reference: chr 6
allele count: 2
allele frequency: 1.655958137378287e-5
allele num: 120776
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2080C>A
  hgvsp: ENST00000527536.1:c.2080C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2074C>A
  hgvsp: ENST00000353331.4:c.2074C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.165C>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2080C>A
  hgvsp: ENST00000527613.1:c.2080C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2074C>A
  hgvsp: ENST00000392348.2:c.2074C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1561C>A
  hgvsp: ENST00000530767.1:c.1561C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2077C>A
  hgvsp: ENST00000529826.1:c.2077C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2074C>A
  hgvsp: ENST00000527759.1:c.2074C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2080C>A
  hgvsp: ENST00000532384.1:c.2080C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.384C>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2080C>A
  hgvsp: ENST00000531224.1:c.2080C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.246C>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.207C>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*378C>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2074C>A
  hgvsp: ENST00000530429.1:c.2074C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 12363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2778
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3722
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg694Arg
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-136590717-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590717
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590717
    reference: chr 6
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2077C>A
  hgvsp: ENSP00000433505.1:p.Leu693Ile
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2077C>A
  hgvsp: ENSP00000436216.1:p.Leu693Ile
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2071C>A
  hgvsp: ENSP00000436142.1:p.Leu691Ile
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2071C>A
  hgvsp: ENSP00000229446.5:p.Leu691Ile
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1558C>A
  hgvsp: ENSP00000436501.1:p.Leu520Ile
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.162C>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2074C>A
  hgvsp: ENSP00000431734.1:p.Leu692Ile
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2077C>A
  hgvsp: ENSP00000435210.1:p.Leu693Ile
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2071C>A
  hgvsp: ENSP00000434826.1:p.Leu691Ile
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*375C>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.381C>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2071C>A
  hgvsp: ENSP00000376159.2:p.Leu691Ile
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.243C>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2077C>A
  hgvsp: ENSP00000435441.1:p.Leu693Ile
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.204C>A
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12349
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6595
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu693Ile
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD

6-136590718-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590718
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590718
    reference: chr 6
allele count: 5
allele frequency: 4.14167853947848e-5
allele num: 120724
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2076C>T
  hgvsp: ENST00000532384.1:c.2076C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2073C>T
  hgvsp: ENST00000529826.1:c.2073C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2076C>T
  hgvsp: ENST00000527536.1:c.2076C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2076C>T
  hgvsp: ENST00000531224.1:c.2076C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2076C>T
  hgvsp: ENST00000527613.1:c.2076C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2070C>T
  hgvsp: ENST00000530429.1:c.2070C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2070C>T
  hgvsp: ENST00000353331.4:c.2070C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2070C>T
  hgvsp: ENST00000527759.1:c.2070C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.242C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1557C>T
  hgvsp: ENST00000530767.1:c.1557C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*374C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2070C>T
  hgvsp: ENST00000392348.2:c.2070C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.380C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.161C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.203C>T
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6532
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11108
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8073
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp692Asp
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

6-136590718-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590718
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590718
    reference: chr 6
allele count: 1
allele frequency: 8.283357078956959e-6
allele num: 120724
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.203C>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2070C>A
  hgvsp: ENSP00000229446.5:p.Asp690Glu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.161C>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2076C>A
  hgvsp: ENSP00000433505.1:p.Asp692Glu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2073C>A
  hgvsp: ENSP00000431734.1:p.Asp691Glu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2070C>A
  hgvsp: ENSP00000376159.2:p.Asp690Glu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.380C>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2076C>A
  hgvsp: ENSP00000435441.1:p.Asp692Glu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2076C>A
  hgvsp: ENSP00000435210.1:p.Asp692Glu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2076C>A
  hgvsp: ENSP00000436216.1:p.Asp692Glu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.242C>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2070C>A
  hgvsp: ENSP00000434826.1:p.Asp690Glu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1557C>A
  hgvsp: ENSP00000436501.1:p.Asp519Glu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2070C>A
  hgvsp: ENSP00000436142.1:p.Asp690Glu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*374C>A
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6532
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8073
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11108
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp692Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

6-136590722-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590722
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590722
    reference: chr 6
allele count: 3
allele frequency: 2.485130635033715e-5
allele num: 120718
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2072C>T
  hgvsp: ENSP00000435441.1:p.Ala691Val
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2072C>T
  hgvsp: ENSP00000435210.1:p.Ala691Val
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2072C>T
  hgvsp: ENSP00000433505.1:p.Ala691Val
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.157C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2072C>T
  hgvsp: ENSP00000436216.1:p.Ala691Val
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2066C>T
  hgvsp: ENSP00000229446.5:p.Ala689Val
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1553C>T
  hgvsp: ENSP00000436501.1:p.Ala518Val
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2069C>T
  hgvsp: ENSP00000431734.1:p.Ala690Val
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2066C>T
  hgvsp: ENSP00000434826.1:p.Ala689Val
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2066C>T
  hgvsp: ENSP00000436142.1:p.Ala689Val
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.238C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.199C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*370C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.376C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2066C>T
  hgvsp: ENSP00000376159.2:p.Ala689Val
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11104
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12284
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala691Val
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD

6-136590723-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590723
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590723
    reference: chr 6
allele count: 1
allele frequency: 8.285690612312537e-6
allele num: 120690
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1552G>C
  hgvsp: ENSP00000436501.1:p.Ala518Pro
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2065G>C
  hgvsp: ENSP00000434826.1:p.Ala689Pro
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2065G>C
  hgvsp: ENSP00000436142.1:p.Ala689Pro
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.198G>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.156G>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2068G>C
  hgvsp: ENSP00000431734.1:p.Ala690Pro
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2071G>C
  hgvsp: ENSP00000436216.1:p.Ala691Pro
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2065G>C
  hgvsp: ENSP00000229446.5:p.Ala689Pro
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2071G>C
  hgvsp: ENSP00000435441.1:p.Ala691Pro
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2065G>C
  hgvsp: ENSP00000376159.2:p.Ala689Pro
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2071G>C
  hgvsp: ENSP00000435210.1:p.Ala691Pro
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2071G>C
  hgvsp: ENSP00000433505.1:p.Ala691Pro
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*369G>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.375G>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.237G>C
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8072
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11095
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3718
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala691Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

6-136590725-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590725
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590725
    reference: chr 6
allele count: 6
allele frequency: 4.972650422675286e-5
allele num: 120660
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*367C>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2063C>G
  hgvsp: ENSP00000434826.1:p.Ser688Cys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2063C>G
  hgvsp: ENSP00000229446.5:p.Ser688Cys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2063C>G
  hgvsp: ENSP00000376159.2:p.Ser688Cys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2066C>G
  hgvsp: ENSP00000431734.1:p.Ser689Cys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2069C>G
  hgvsp: ENSP00000435441.1:p.Ser690Cys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2069C>G
  hgvsp: ENSP00000436216.1:p.Ser690Cys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2063C>G
  hgvsp: ENSP00000436142.1:p.Ser688Cys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1550C>G
  hgvsp: ENSP00000436501.1:p.Ser517Cys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2069C>G
  hgvsp: ENSP00000435210.1:p.Ser690Cys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.373C>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2069C>G
  hgvsp: ENSP00000433505.1:p.Ser690Cys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.235C>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.154C>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.196C>G
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8068
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2774
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5509
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser690Cys
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

6-136590729-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590729
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590729
    reference: chr 6
allele count: 2
allele frequency: 1.659007581664648e-5
allele num: 120554
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2065G>A
  hgvsp: ENSP00000436216.1:p.Asp689Asn
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.150G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*363G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1546G>A
  hgvsp: ENSP00000436501.1:p.Asp516Asn
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2059G>A
  hgvsp: ENSP00000229446.5:p.Asp687Asn
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.231G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2065G>A
  hgvsp: ENSP00000433505.1:p.Asp689Asn
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2062G>A
  hgvsp: ENSP00000431734.1:p.Asp688Asn
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2059G>A
  hgvsp: ENSP00000376159.2:p.Asp687Asn
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.369G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2065G>A
  hgvsp: ENSP00000435441.1:p.Asp689Asn
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2059G>A
  hgvsp: ENSP00000436142.1:p.Asp687Asn
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2059G>A
  hgvsp: ENSP00000434826.1:p.Asp687Asn
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2065G>A
  hgvsp: ENSP00000435210.1:p.Asp689Asn
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.192G>A
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6221
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12142
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2564
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11077
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp689Asn
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

6-136590732-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590732
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590732
    reference: chr 6
allele count: 1
allele frequency: 8.298204268596276e-6
allele num: 120508
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.228T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2062T>A
  hgvsp: ENSP00000436216.1:p.Cys688Ser
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.366T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2062T>A
  hgvsp: ENSP00000433505.1:p.Cys688Ser
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2062T>A
  hgvsp: ENSP00000435210.1:p.Cys688Ser
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2059T>A
  hgvsp: ENSP00000431734.1:p.Cys687Ser
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2056T>A
  hgvsp: ENSP00000376159.2:p.Cys686Ser
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1543T>A
  hgvsp: ENSP00000436501.1:p.Cys515Ser
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*360T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2056T>A
  hgvsp: ENSP00000434826.1:p.Cys686Ser
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2056T>A
  hgvsp: ENSP00000229446.5:p.Cys686Ser
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2062T>A
  hgvsp: ENSP00000435441.1:p.Cys688Ser
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.189T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.147T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2056T>A
  hgvsp: ENSP00000436142.1:p.Cys686Ser
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11058
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3713
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6047
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8057
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2770
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys688Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

6-136590739-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590739
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590739
    reference: chr 6
allele count: 1
allele frequency: 8.316976612661764e-6
allele num: 120236
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*353A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.182A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2055A>G
  hgvsp: ENST00000532384.1:c.2055A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2049A>G
  hgvsp: ENST00000353331.4:c.2049A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2055A>G
  hgvsp: ENST00000527613.1:c.2055A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.221A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2052A>G
  hgvsp: ENST00000529826.1:c.2052A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1536A>G
  hgvsp: ENST00000530767.1:c.1536A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2055A>G
  hgvsp: ENST00000527536.1:c.2055A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2055A>G
  hgvsp: ENST00000531224.1:c.2055A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2049A>G
  hgvsp: ENST00000527759.1:c.2049A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2049A>G
  hgvsp: ENST00000392348.2:c.2049A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.140A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2049A>G
  hgvsp: ENST00000530429.1:c.2049A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.359A>G
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2769
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11592
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3713
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2563
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Lys685Lys
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

6-136590739-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590739
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590739
    reference: chr 6
allele count: 55
allele frequency: 4.574337136963971e-4
allele num: 120236
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2049A>C
  hgvsp: ENSP00000229446.5:p.Lys683Asn
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.221A>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.359A>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2052A>C
  hgvsp: ENSP00000431734.1:p.Lys684Asn
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2055A>C
  hgvsp: ENSP00000435210.1:p.Lys685Asn
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.182A>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2049A>C
  hgvsp: ENSP00000436142.1:p.Lys683Asn
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1536A>C
  hgvsp: ENSP00000436501.1:p.Lys512Asn
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2055A>C
  hgvsp: ENSP00000435441.1:p.Lys685Asn
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2055A>C
  hgvsp: ENSP00000436216.1:p.Lys685Asn
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2049A>C
  hgvsp: ENSP00000434826.1:p.Lys683Asn
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*353A>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.140A>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2049A>C
  hgvsp: ENSP00000376159.2:p.Lys683Asn
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2055A>C
  hgvsp: ENSP00000433505.1:p.Lys685Asn
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11592
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys685Asn
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

6-136590746-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590746
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590746
    reference: chr 6
allele count: 3
allele frequency: 2.518891687657431e-5
allele num: 119100
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.133A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2042A>G
  hgvsp: ENSP00000436142.1:p.Asp681Gly
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2045A>G
  hgvsp: ENSP00000431734.1:p.Asp682Gly
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2048A>G
  hgvsp: ENSP00000435210.1:p.Asp683Gly
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2048A>G
  hgvsp: ENSP00000433505.1:p.Asp683Gly
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2042A>G
  hgvsp: ENSP00000229446.5:p.Asp681Gly
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2042A>G
  hgvsp: ENSP00000434826.1:p.Asp681Gly
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2042A>G
  hgvsp: ENSP00000376159.2:p.Asp681Gly
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1529A>G
  hgvsp: ENSP00000436501.1:p.Asp510Gly
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2048A>G
  hgvsp: ENSP00000436216.1:p.Asp683Gly
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*346A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2048A>G
  hgvsp: ENSP00000435441.1:p.Asp683Gly
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.214A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.352A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.175A>G
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4306
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9042
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2559
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6557
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1901
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp683Gly
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

6-136590750-C-CCTTTTGATTTTCTTCTTTAAAAACTCTCTCTTCCCCTG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590750
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590788
    reference: chr 6
allele count: 107
allele frequency: 9.00688563780535e-4
allele num: 118798
alternate allele: CCTTTTGATTTTCTTCTTTAAAAACTCTCTCTTCCCCTG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsp: ENSP00000434826.1:p.Gly680GlnfsTer18
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsp: ENSP00000431734.1:p.Gly681GlnfsTer18
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsp: ENSP00000229446.5:p.Gly680GlnfsTer18
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsp: ENSP00000435441.1:p.Gly682GlnfsTer18
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsp: ENSP00000436142.1:p.Gly680GlnfsTer18
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsp: ENSP00000436216.1:p.Gly682GlnfsTer18
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsp: ENSP00000376159.2:p.Gly680GlnfsTer18
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsp: ENSP00000433505.1:p.Gly682GlnfsTer18
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsp: ENSP00000436501.1:p.Gly509GlnfsTer18
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsp: ENSP00000435210.1:p.Gly682GlnfsTer18
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8519
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 6881
  bin: 4.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 3588
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9215
  bin: 3.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 4.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
hgvs: p.Gly682GlnfsTer18
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum

6-136590751-C-CTTTTGATTTTCTTCTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590751
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590767
    reference: chr 6
allele count: 697
allele frequency: 5.894590846047157e-3
allele num: 118244
alternate allele: CTTTTGATTTTCTTCTT
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: splice acceptor
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 1.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 6758
  bin: 4.25e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 9218
  bin: 3.25e1
  variant carriers: 153
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 5.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 4.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 5.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 1.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 8443
  bin: 3.75e1
  variant carriers: 132
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 7.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: c.2044-2_2044-1insAAGAAGAAAATCAAAA
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-136590751-C-CTTTTGATTTTCTTCTTTAAAAACTCTCTCTTCCCCTGCTAAACGGG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590751
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590797
    reference: chr 6
allele count: 984
allele frequency: 8.321775312066574e-3
allele num: 118244
alternate allele: CTTTTGATTTTCTTCTTTAAAAACTCTCTCTTCCCCTGCTAAACGGG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: splice acceptor
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 9.75e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 8.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 9218
  bin: 3.25e1
  variant carriers: 154
genotype depth: GenotypeDepth
  all individuals: 7516
  bin: 2.75e1
  variant carriers: 100
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 5.25e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 6.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 1.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 4537
  bin: 2.25e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 4.75e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 6.25e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 8443
  bin: 3.75e1
  variant carriers: 143
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

6-136590751-C-CTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590751
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590753
    reference: chr 6
allele count: 1
allele frequency: 8.457088731774973e-6
allele num: 118244
alternate allele: CTT
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2038-2_2038-1insAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.171-2_171-1insAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2041-2_2041-1insAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1525-2_1525-1insAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*342-2_*342-1insAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2044-2_2044-1insAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2038-2_2038-1insAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2044-2_2044-1insAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2044-2_2044-1insAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2038-2_2038-1insAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2044-2_2044-1insAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.210-2_210-1insAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.127_128insAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2038-2_2038-1insAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.346_347insAA
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: splice acceptor
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 7516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6758
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2044-2_2044-1insAA
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

6-136590751-C-CTTTTGATTTTCTTCTTTAAAAACTCTCTCTTCCCCTGCTAAACGGGTATCCTTCCTCAGGG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590751
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590812
    reference: chr 6
allele count: 63
allele frequency: 5.327965901018233e-4
allele num: 118244
alternate allele: CTTTTGATTTTCTTCTTTAAAAACTCTCTCTTCCCCTGCTAAACGGGTATCCTTCCTCAGGG
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: splice acceptor
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 8443
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9218
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7516
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 9.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4537
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-136590752-T-TTTTG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590752
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590756
    reference: chr 6
allele count: 4983
allele frequency: 4.254029504166097e-2
allele num: 117136
alternate allele: TTTTG
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*342-3_*342-2insCAAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2044-3_2044-2insCAAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.171-3_171-2insCAAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2044-3_2044-2insCAAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.345_346insCAAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2041-3_2041-2insCAAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2038-3_2038-2insCAAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2044-3_2044-2insCAAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.210-3_210-2insCAAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2038-3_2038-2insCAAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1525-3_1525-2insCAAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2044-3_2044-2insCAAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.126_127insCAAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2038-3_2038-2insCAAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2038-3_2038-2insCAAA
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 7.25e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 9.75e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 8363
  bin: 3.75e1
  variant carriers: 780
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 1.75e1
  variant carriers: 288
genotype depth: GenotypeDepth
  all individuals: 9290
  bin: 3.25e1
  variant carriers: 960
genotype depth: GenotypeDepth
  all individuals: 2657
  bin: 5.75e1
  variant carriers: 203
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 8.75e1
  variant carriers: 30
genotype quality: GenotypeQuality
hgvs: c.2044-3_2044-2insCAAA
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum

6-136590752-T-TTTTGATTTTCTTCTTTAAAAACTCTCTCTTCCCCTGCTAAACGGGTATCCTTCCTC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590752
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590808
    reference: chr 6
allele count: 66
allele frequency: 5.634476164458408e-4
allele num: 117136
alternate allele: TTTTGATTTTCTTCTTTAAAAACTCTCTCTTCCCCTGCTAAACGGGTATCCTTCCTC
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 3545
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2657
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4575
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6747
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7558
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5055
  bin: 4.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

6-136590752-T-TTTTGATTTTCTTCTTTAAAAACTCTCTCTTCCCCTGCTAAACGGGTATCCTTCCTCAGGGTACTTGGTGAGATGTCA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590752
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590829
    reference: chr 6
allele count: 65
allele frequency: 5.549105313481764e-4
allele num: 117136
alternate allele: TTTTGATTTTCTTCTTTAAAAACTCTCTCTTCCCCTGCTAAACGGGTATCCTTCCTCAGGGTACTTGGTGAGATGTCA
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 6747
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8363
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 9.75e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

6-136590753-A-AGATTTTCTTCTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590753
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590765
    reference: chr 6
allele count: 1
allele frequency: 7.390983000739098e-5
allele num: 13530
alternate allele: AGATTTTCTTCTT
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2373
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8203
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4863
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7995
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6462
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2044-4_2044-3insAAGAAGAAAATC
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD

6-136590753-A-ATTTTCTTCTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590753
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590763
    reference: chr 6
allele count: 2973
allele frequency: 2.197339246119734e-1
allele num: 13530
alternate allele: ATTTTCTTCTT
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 2373
  bin: 1.75e1
  variant carriers: 172
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 6.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 1.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 9484
  bin: 3.25e1
  variant carriers: 580
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 9.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 5.75e1
  variant carriers: 122
genotype depth: GenotypeDepth
  all individuals: 7995
  bin: 2.75e1
  variant carriers: 456
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 8203
  bin: 3.75e1
  variant carriers: 475
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 7.75e1
  variant carriers: 32
genotype quality: GenotypeQuality
hgvs: c.2044-4_2044-3insAAGAAGAAAA
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

6-136590753-A-ATTTTCTTCTTTAAAAACTCTCTCTTCCCCTGC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590753
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590785
    reference: chr 6
allele count: 150
allele frequency: 1.108647450110865e-2
allele num: 13530
alternate allele: ATTTTCTTCTTTAAAAACTCTCTCTTCCCCTGC
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 4827
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 6462
  bin: 4.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7995
  bin: 2.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 9484
  bin: 3.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

6-136590753-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590753
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590753
    reference: chr 6
allele count: 190
allele frequency: 1.404286770140429e-2
allele num: 13530
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*342-3T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.345T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2038-3T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2041-3T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.171-3T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2038-3T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.210-3T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2044-3T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1525-3T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2044-3T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2038-3T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.126T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2044-3T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2044-3T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2038-3T>A
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 1.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8203
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2373
  bin: 1.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7995
  bin: 2.75e1
  variant carriers: 57
genotype quality: GenotypeQuality
hgvs: c.2044-3T>A
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ

6-136590754-T-TTTTCTTCTTTA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590754
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590765
    reference: chr 6
allele count: 1572
allele frequency: 1.335962198728626e-2
allele num: 117668
alternate allele: TTTTCTTCTTTA
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 6.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 1.75e1
  variant carriers: 93
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8147
  bin: 3.75e1
  variant carriers: 246
genotype depth: GenotypeDepth
  all individuals: 5622
  bin: 2.25e1
  variant carriers: 171
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 6.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 1.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 9636
  bin: 3.25e1
  variant carriers: 320
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
hgvs: c.2044-5_2044-4insTAAAGAAGAAA
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD

6-136590754-T-TTTTCTTCTTTAAAAACTCCG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590754
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590774
    reference: chr 6
allele count: 1
allele frequency: 8.498487269266071e-6
allele num: 117668
alternate allele: TTTTCTTCTTTAAAAACTCCG
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8689
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8147
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5990
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2044-5_2044-4insCGGAGTTTTTAAAGAAGAAA
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

6-136590755-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590755
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590755
    reference: chr 6
allele count: 189
allele frequency: 1.592786111579302e-2
allele num: 11866
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.210-5T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2044-5T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.343T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2041-5T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.124T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2044-5T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.171-5T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2038-5T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2038-5T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2044-5T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*342-5T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2038-5T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2038-5T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2044-5T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1525-5T>A
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: splice region
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3876
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9621
  bin: 3.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7494
  bin: 3.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: c.2044-5T>A
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: A
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

6-136590756-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590756
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590756
    reference: chr 6
allele count: 188
allele frequency: 1.403823178016726e-2
allele num: 13392
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.342T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1525-6T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2038-6T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.210-6T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*342-6T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.171-6T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2044-6T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2038-6T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2038-6T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.123T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2044-6T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2038-6T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2041-6T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2044-6T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2044-6T>C
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: splice region
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7383
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6658
  bin: 2.25e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 1.75e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2044-6T>C
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

6-136590758-A-AACTCTCTCTTCCCCT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590758
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590773
    reference: chr 6
allele count: 1
allele frequency: 5.853430110044486e-5
allele num: 17084
alternate allele: AACTCTCTCTTCCCCT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 10363
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8740
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5566
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10033
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6703
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

6-136590758-A-AACTCTCTCTTCCCCTGCTAAAC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590758
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590780
    reference: chr 6
allele count: 727
allele frequency: 4.255443690002341e-2
allele num: 17084
alternate allele: AACTCTCTCTTCCCCTGCTAAAC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 5566
  bin: 3.75e1
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 6.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 8.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6703
  bin: 1.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 8740
  bin: 3.25e1
  variant carriers: 116
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 1.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 3879
  bin: 4.25e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 4.75e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 6.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 7.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 5.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

6-136590759-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590759
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590759
    reference: chr 6
allele count: 797
allele frequency: 4.641276496622409e-2
allele num: 17172
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2038-9C>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2041-9C>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2044-9C>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2038-9C>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2044-9C>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.339C>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.171-9C>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2038-9C>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2038-9C>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2044-9C>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.210-9C>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1525-9C>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.120C>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*342-9C>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2044-9C>G
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10101
  bin: 2.25e1
  variant carriers: 133
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2595
  bin: 4.75e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 5.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 1.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 8670
  bin: 3.25e1
  variant carriers: 132
genotype depth: GenotypeDepth
  all individuals: 5519
  bin: 3.75e1
  variant carriers: 110
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD

6-136590759-G-GCTAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590759
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590763
    reference: chr 6
allele count: 1
allele frequency: 5.823433496389471e-5
allele num: 17172
alternate allele: GCTAA
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2038-10_2038-9insTTAG
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.210-10_210-9insTTAG
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.171-10_171-9insTTAG
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2044-10_2044-9insTTAG
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.338_339insTTAG
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2041-10_2041-9insTTAG
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2038-10_2038-9insTTAG
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.119_120insTTAG
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2038-10_2038-9insTTAG
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2038-10_2038-9insTTAG
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2044-10_2044-9insTTAG
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2044-10_2044-9insTTAG
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2044-10_2044-9insTTAG
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*342-10_*342-9insTTAG
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1525-10_1525-9insTTAG
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6789
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10101
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8670
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

6-136590760-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590760
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590760
    reference: chr 6
allele count: 797
allele frequency: 4.496727600993004e-2
allele num: 17724
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.338T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2044-10T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2038-10T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2038-10T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2044-10T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2044-10T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.210-10T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.119T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.171-10T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2038-10T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2044-10T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1525-10T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*342-10T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2038-10T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2041-10T>A
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 5.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 4.75e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 8593
  bin: 3.25e1
  variant carriers: 127
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10117
  bin: 2.25e1
  variant carriers: 143
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 5.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 6864
  bin: 1.75e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 3568
  bin: 1.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 4.25e1
  variant carriers: 82
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

6-136590763-GAT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590763
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590761
    reference: chr 6
allele count: 1
allele frequency: 5.626828719333783e-5
allele num: 17772
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2038-15_2038-14delAT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2041-15_2041-14delAT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2044-15_2044-14delAT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2044-15_2044-14delAT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2038-15_2038-14delAT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2044-15_2044-14delAT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.210-15_210-14delAT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*342-15_*342-14delAT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2044-15_2044-14delAT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.171-15_171-14delAT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.333_334delAT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.114_115delAT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1525-15_1525-14delAT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2038-15_2038-14delAT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2038-15_2038-14delAT
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 7159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5384
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10070
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3623
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8442
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: GAT
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ

6-136590767-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590767
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590767
    reference: chr 6
allele count: 1
allele frequency: 8.743245842586601e-6
allele num: 114374
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2044-17A>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2044-17A>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.331A>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2038-17A>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*342-17A>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.112A>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2044-17A>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2044-17A>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.210-17A>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2038-17A>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2041-17A>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2038-17A>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2038-17A>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1525-17A>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.171-17A>T
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9779
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5073
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8065
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

6-136590768-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590768
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590768
    reference: chr 6
allele count: 6
allele frequency: 2.453385672227674e-4
allele num: 24456
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2044-18T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2044-18T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.111T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2038-18T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*342-18T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.171-18T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1525-18T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2044-18T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2038-18T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2041-18T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2044-18T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.330T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2038-18T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2038-18T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.210-18T>C
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 10180
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4833
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

6-136590771-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590771
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590771
    reference: chr 6
allele count: 1
allele frequency: 8.897588753447816e-6
allele num: 112390
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.108T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2044-21T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2044-21T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2044-21T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1525-21T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.171-21T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.210-21T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2041-21T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*342-21T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2038-21T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.327T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2038-21T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2038-21T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2038-21T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2044-21T>C
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6978
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6900
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10856
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9935
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4105
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9716
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

6-136590774-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590774
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590774
    reference: chr 6
allele count: 1
allele frequency: 9.076222113307556e-6
allele num: 110178
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2044-24G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*342-24G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2044-24G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.105G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.210-24G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2044-24G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.171-24G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.324G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1525-24G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2038-24G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2041-24G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2038-24G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2038-24G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2044-24G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2038-24G>A
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11298
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8818
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3481
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8463
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2741
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

6-136590776-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590776
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590776
    reference: chr 6
allele count: 1
allele frequency: 4.188306248952924e-5
allele num: 23876
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2044-26C>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2044-26C>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2044-26C>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.103C>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1525-26C>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2038-26C>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2044-26C>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2038-26C>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*342-26C>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2038-26C>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.322C>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.171-26C>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2041-26C>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2038-26C>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.210-26C>A
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3370
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12925
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2745
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

6-136590783-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590783
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590783
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 30574
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.96C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2038-33C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.210-33C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2038-33C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1525-33C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2044-33C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.315C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*342-33C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2038-33C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2038-33C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2044-33C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.171-33C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2044-33C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2044-33C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2041-33C>T
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16979
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff

6-136590792-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590792
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590792
    reference: chr 6
allele count: 79
allele frequency: 2.722072910206051e-3
allele num: 29022
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2044-42A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2044-42A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2038-42A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.87A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2044-42A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2038-42A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.210-42A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.306A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2044-42A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1525-42A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*342-42A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2041-42A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.171-42A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2038-42A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2038-42A>G
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12483
  bin: 1.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12934
  bin: 7.5e0
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 4497
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

6-136590798-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590798
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590798
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 29476
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2038-48T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.81T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2044-48T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2044-48T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1525-48T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2041-48T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2038-48T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2038-48T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.210-48T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.300T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2044-48T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2038-48T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2044-48T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*342-48T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.171-48T>A
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19080
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4695
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

6-136590801-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136590801
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136590801
    reference: chr 6
allele count: 1
allele frequency: 3.260940455227288e-5
allele num: 30666
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1525-51A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2044-51A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*342-51A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000529917
  gene symbol: BCLAF1
  hgvsc: ENST00000529917.1:n.297A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.210-51A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2038-51A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2041-51A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2044-51A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2038-51A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2038-51A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534321
  gene symbol: BCLAF1
  hgvsc: ENST00000534321.1:n.78A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2044-51A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2044-51A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2038-51A>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.171-51A>G
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5480
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21723
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7354
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17168
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2940
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  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: T
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

6-136593082-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136593082
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136593082
    reference: chr 6
allele count: 2
allele frequency: 1.845324869443266e-5
allele num: 108382
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2037+51G>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2037+51G>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1524+51G>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2043+51G>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2040+51G>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2043+51G>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.170+51G>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*341+51G>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2043+51G>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2043+51G>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000476194
  gene symbol: BCLAF1
  hgvsc: ENST00000476194.1:n.605G>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.148+51G>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2037+51G>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2037+51G>C
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4852
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5717
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12312
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9246
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

6-136593082-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136593082
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136593082
    reference: chr 6
allele count: 1
allele frequency: 9.226624347216328e-6
allele num: 108382
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2043+51G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2040+51G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2043+51G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2037+51G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2037+51G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2037+51G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*341+51G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.170+51G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2043+51G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.148+51G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2043+51G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000476194
  gene symbol: BCLAF1
  hgvsc: ENST00000476194.1:n.605G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2037+51G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1524+51G>A
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5717
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13461
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9246
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4852
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum

6-136593100-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136593100
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136593099
    reference: chr 6
allele count: 1
allele frequency: 9.06306077688557e-6
allele num: 110338
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*341+32delT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2043+32delT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2037+32delT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2037+32delT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2043+32delT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1524+32delT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000476194
  gene symbol: BCLAF1
  hgvsc: ENST00000476194.1:n.586delT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2037+32delT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2043+32delT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.170+32delT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2037+32delT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.148+32delT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2040+32delT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2043+32delT
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9799
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19039
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3985
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4712
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2155
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6958
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4764
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: TA
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP

6-136593104-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136593104
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136593104
    reference: chr 6
allele count: 1
allele frequency: 9.009333669681791e-6
allele num: 110996
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2037+29T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*341+29T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2037+29T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2037+29T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2043+29T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2043+29T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000476194
  gene symbol: BCLAF1
  hgvsc: ENST00000476194.1:n.583T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2043+29T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1524+29T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.148+29T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2043+29T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2040+29T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2037+29T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.170+29T>C
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21417
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2182
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8145
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1741
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP

6-136593105-CG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136593105
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136593104
    reference: chr 6
allele count: 1
allele frequency: 8.99830831803621e-6
allele num: 111132
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*341+27delC
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2043+27delC
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2040+27delC
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2043+27delC
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2043+27delC
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000476194
  gene symbol: BCLAF1
  hgvsc: ENST00000476194.1:n.581delC
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1524+27delC
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.148+27delC
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2037+27delC
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2037+27delC
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2043+27delC
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2037+27delC
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.170+27delC
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2037+27delC
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3181
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7618
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21910
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7847
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: CG
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

6-136593106-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136593106
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136593106
    reference: chr 6
allele count: 2
allele frequency: 1.878181169355596e-5
allele num: 106486
alternate allele: A
canonical: false
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3761
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5490
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9531
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3728
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19309
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6683
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3360
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8875
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 846
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1730
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 995
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17962
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2912
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 713
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4985
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1478
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1551
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4029
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1467
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1128
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2539
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 836
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1537
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1986
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1037
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7622
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 57188
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9428
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6022
  num of homozygotes: 0
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

6-136593106-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136593106
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136593107
    reference: chr 6
allele count: 1
allele frequency: 9.390905846777981e-6
allele num: 106486
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2037+26dupT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.170+26dupT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2037+26dupT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2043+26dupT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000476194
  gene symbol: BCLAF1
  hgvsc: ENST00000476194.1:n.580dupT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2043+26dupT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2037+26dupT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.148+26dupT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2043+26dupT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2037+26dupT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2040+26dupT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2043+26dupT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1524+26dupT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*341+26dupT
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 5490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6683
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3761
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3728
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19309
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9531
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS

6-136593106-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136593106
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136593105
    reference: chr 6
allele count: 37
allele frequency: 3.474635163307853e-4
allele num: 106486
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.170+26delT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2040+26delT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2037+26delT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2043+26delT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*341+26delT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2037+26delT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2043+26delT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.148+26delT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2037+26delT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2043+26delT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000476194
  gene symbol: BCLAF1
  hgvsc: ENST00000476194.1:n.580delT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2037+26delT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2043+26delT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1524+26delT
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3761
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19309
  bin: 2.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9531
  bin: 2.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3728
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 5490
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: GA
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/6-136593110-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136593110
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136593110
    reference: chr 6
allele count: 29
allele frequency: 2.548599149295181e-4
allele num: 113788
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2040+23T>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2043+23T>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2043+23T>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2037+23T>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2043+23T>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2037+23T>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.170+23T>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.148+23T>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2037+23T>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000476194
  gene symbol: BCLAF1
  hgvsc: ENST00000476194.1:n.577T>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*341+23T>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1524+23T>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2043+23T>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2037+23T>G
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9746
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4682
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21604
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2591
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6337
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

6-136593133-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136593133
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136593133
    reference: chr 6
allele count: 1
allele frequency: 8.341675008341675e-6
allele num: 119880
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.148G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*341G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2043G>A
  hgvsp: ENST00000527536.1:c.2043G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2043G>A
  hgvsp: ENST00000527613.1:c.2043G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2043G>A
  hgvsp: ENST00000531224.1:c.2043G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2037G>A
  hgvsp: ENST00000392348.2:c.2037G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2037G>A
  hgvsp: ENST00000527759.1:c.2037G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2037G>A
  hgvsp: ENST00000353331.4:c.2037G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2043G>A
  hgvsp: ENST00000532384.1:c.2043G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.170G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2040G>A
  hgvsp: ENST00000529826.1:c.2040G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000476194
  gene symbol: BCLAF1
  hgvsc: ENST00000476194.1:n.554G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2037G>A
  hgvsp: ENST00000530429.1:c.2037G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1524G>A
  hgvsp: ENST00000530767.1:c.1524G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9301
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10238
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5963
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3723
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2043G>A
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum

6-136593147-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136593147
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136593147
    reference: chr 6
allele count: 2
allele frequency: 1.657440249279014e-5
allele num: 120668
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2029G>A
  hgvsp: ENSP00000435210.1:p.Glu677Lys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.156G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2026G>A
  hgvsp: ENSP00000431734.1:p.Glu676Lys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2023G>A
  hgvsp: ENSP00000434826.1:p.Glu675Lys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2023G>A
  hgvsp: ENSP00000229446.5:p.Glu675Lys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2029G>A
  hgvsp: ENSP00000435441.1:p.Glu677Lys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*327G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.134G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2023G>A
  hgvsp: ENSP00000436142.1:p.Glu675Lys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000476194
  gene symbol: BCLAF1
  hgvsc: ENST00000476194.1:n.540G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2029G>A
  hgvsp: ENSP00000436216.1:p.Glu677Lys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2029G>A
  hgvsp: ENSP00000433505.1:p.Glu677Lys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1510G>A
  hgvsp: ENSP00000436501.1:p.Glu504Lys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2023G>A
  hgvsp: ENSP00000376159.2:p.Glu675Lys
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3726
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9467
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16213
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu677Lys
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

6-136593149-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136593149
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136593149
    reference: chr 6
allele count: 1
allele frequency: 8.285004142502071e-6
allele num: 120700
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2024A>T
  hgvsp: ENSP00000431734.1:p.Lys675Ile
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2027A>T
  hgvsp: ENSP00000435210.1:p.Lys676Ile
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1508A>T
  hgvsp: ENSP00000436501.1:p.Lys503Ile
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2021A>T
  hgvsp: ENSP00000436142.1:p.Lys674Ile
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.154A>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2027A>T
  hgvsp: ENSP00000433505.1:p.Lys676Ile
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2021A>T
  hgvsp: ENSP00000434826.1:p.Lys674Ile
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*325A>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2021A>T
  hgvsp: ENSP00000229446.5:p.Lys674Ile
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2027A>T
  hgvsp: ENSP00000435441.1:p.Lys676Ile
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000476194
  gene symbol: BCLAF1
  hgvsc: ENST00000476194.1:n.538A>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2021A>T
  hgvsp: ENSP00000376159.2:p.Lys674Ile
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.132A>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2027A>T
  hgvsp: ENSP00000436216.1:p.Lys676Ile
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10357
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6013
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3726
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9473
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys676Ile
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum

6-136593155-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136593155
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136593155
    reference: chr 6
allele count: 2
allele frequency: 1.656095258599275e-5
allele num: 120766
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*319T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.148T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.126T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2015T>C
  hgvsp: ENSP00000376159.2:p.Val672Ala
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2018T>C
  hgvsp: ENSP00000431734.1:p.Val673Ala
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2021T>C
  hgvsp: ENSP00000433505.1:p.Val674Ala
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2015T>C
  hgvsp: ENSP00000229446.5:p.Val672Ala
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2015T>C
  hgvsp: ENSP00000436142.1:p.Val672Ala
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2021T>C
  hgvsp: ENSP00000436216.1:p.Val674Ala
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2021T>C
  hgvsp: ENSP00000435210.1:p.Val674Ala
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2015T>C
  hgvsp: ENSP00000434826.1:p.Val672Ala
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1502T>C
  hgvsp: ENSP00000436501.1:p.Val501Ala
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000476194
  gene symbol: BCLAF1
  hgvsc: ENST00000476194.1:n.532T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2021T>C
  hgvsp: ENSP00000435441.1:p.Val674Ala
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3726
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16258
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val674Ala
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

6-136593155-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136593155
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136593155
    reference: chr 6
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2021T>A
  hgvsp: ENSP00000435210.1:p.Val674Asp
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000476194
  gene symbol: BCLAF1
  hgvsc: ENST00000476194.1:n.532T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2021T>A
  hgvsp: ENSP00000435441.1:p.Val674Asp
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2015T>A
  hgvsp: ENSP00000436142.1:p.Val672Asp
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.126T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2018T>A
  hgvsp: ENSP00000431734.1:p.Val673Asp
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2021T>A
  hgvsp: ENSP00000433505.1:p.Val674Asp
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.148T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2015T>A
  hgvsp: ENSP00000434826.1:p.Val672Asp
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2021T>A
  hgvsp: ENSP00000436216.1:p.Val674Asp
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2015T>A
  hgvsp: ENSP00000376159.2:p.Val672Asp
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1502T>A
  hgvsp: ENSP00000436501.1:p.Val501Asp
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*319T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2015T>A
  hgvsp: ENSP00000229446.5:p.Val672Asp
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6017
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3726
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9476
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val674Asp
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP

6-136593156-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136593156
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136593156
    reference: chr 6
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.125G>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2014G>C
  hgvsp: ENSP00000436142.1:p.Val672Leu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2014G>C
  hgvsp: ENSP00000376159.2:p.Val672Leu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2020G>C
  hgvsp: ENSP00000435210.1:p.Val674Leu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2020G>C
  hgvsp: ENSP00000436216.1:p.Val674Leu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2017G>C
  hgvsp: ENSP00000431734.1:p.Val673Leu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2014G>C
  hgvsp: ENSP00000434826.1:p.Val672Leu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2014G>C
  hgvsp: ENSP00000229446.5:p.Val672Leu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*318G>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2020G>C
  hgvsp: ENSP00000433505.1:p.Val674Leu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2020G>C
  hgvsp: ENSP00000435441.1:p.Val674Leu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000476194
  gene symbol: BCLAF1
  hgvsc: ENST00000476194.1:n.531G>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1501G>C
  hgvsp: ENSP00000436501.1:p.Val501Leu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.147G>C
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5352
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1949
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val674Leu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

6-136593162-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136593162
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136593162
    reference: chr 6
allele count: 4
allele frequency: 3.31087456751701e-5
allele num: 120814
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000534792
  gene symbol: BCLAF1
  hgvsc: ENST00000534792.1:n.141G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.2014G>A
  hgvsp: ENSP00000433505.1:p.Glu672Lys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.2014G>A
  hgvsp: ENSP00000435210.1:p.Glu672Lys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.2014G>A
  hgvsp: ENSP00000436216.1:p.Glu672Lys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.2011G>A
  hgvsp: ENSP00000431734.1:p.Glu671Lys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.2008G>A
  hgvsp: ENSP00000376159.2:p.Glu670Lys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.2008G>A
  hgvsp: ENSP00000436142.1:p.Glu670Lys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.*312G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.2008G>A
  hgvsp: ENSP00000434826.1:p.Glu670Lys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.1495G>A
  hgvsp: ENSP00000436501.1:p.Glu499Lys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.2008G>A
  hgvsp: ENSP00000229446.5:p.Glu670Lys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000476194
  gene symbol: BCLAF1
  hgvsc: ENST00000476194.1:n.525G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.2014G>A
  hgvsp: ENSP00000435441.1:p.Glu672Lys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000532076
  gene symbol: BCLAF1
  hgvsc: ENST00000532076.1:n.119G>A
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9477
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3725
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu672Lys
num of homozygotes: 0
reference allele: C

GenotypeDepth
all individuals: 847
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3490
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2350
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2969
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12174
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 262
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3559
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 551
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4529
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4932
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 90
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57337
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 409
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 39
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 181
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 727
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500330072615976e-5
allele num: 66652
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.26e0

DP
type: SiteQuality
SIO_000300: 4.735882e6

MQRankSum
type: SiteQuality
SIO_000300: -2.03e0

FS
type: SiteQuality
SIO_000300: 2.823e0

MQ
type: SiteQuality
SIO_000300: 5.582e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.11e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.18e-1

QD
type: SiteQuality
SIO_000300: 1.36e0

GenotypeDepth
all individuals: 3491
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1457
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5430
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5633
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2404
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12175
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 534
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2969
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2349
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5342
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 400
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variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11424
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500330072615976e-5
allele num: 66652
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.503e1

FS
type: SiteQuality
SIO_000300: 4.276e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

ReadPosRankSum
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SIO_000300: 1.51e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.2e0

MQRankSum
type: SiteQuality
SIO_000300: 3.52e0

QD
type: SiteQuality
SIO_000300: 1.029e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.48e0

DP
type: SiteQuality
SIO_000300: 4.735677e6

GenotypeDepth
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bin: 7.25e1
variant carriers: 2

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11422
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.50073536032656e-4
allele num: 66634
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.546832373446499e-4
allele num: 6598
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 4.735331e6

VQSLOD
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SIO_000300: -3.38e0

MQRankSum
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SIO_000300: -2.884e0

ClippingRankSum
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SIO_000300: -4.99e-1

FS
type: SiteQuality
SIO_000300: 1.0307e1

BaseQRankSum
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SIO_000300: 4.47e-1

ReadPosRankSum
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SIO_000300: 1.3e0

QD
type: SiteQuality
SIO_000300: 1.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.46e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 1

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

Latino
type: Population
allele count: 2
allele frequency: 1.751006828926633e-4
allele num: 11422
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66638
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 4.735302e6

QD
type: SiteQuality
SIO_000300: 1.48e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.6e-2

MQ
type: SiteQuality
SIO_000300: 5.296e1

FS
type: SiteQuality
SIO_000300: 6.214e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -3.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.46e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.013e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.351e0

GenotypeDepth
all individuals: 327
bin: 2.25e1
variant carriers: 315

GenotypeDepth
all individuals: 4970
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variant carriers: 4962

GenotypeDepth
all individuals: 3549
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variant carriers: 3547

GenotypeDepth
all individuals: 149
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variant carriers: 109

GenotypeDepth
all individuals: 460
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variant carriers: 444

GenotypeDepth
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variant carriers: 32

GenotypeDepth
all individuals: 796
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variant carriers: 782

GenotypeDepth
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variant carriers: 2232

GenotypeDepth
all individuals: 5412
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variant carriers: 5406

GenotypeDepth
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variant carriers: 2499

GenotypeDepth
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variant carriers: 4468

GenotypeQuality
all individuals: 166
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variant carriers: 17

GenotypeQuality
all individuals: 50
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variant carriers: 44

GenotypeQuality
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GenotypeQuality
all individuals: 58
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GenotypeQuality
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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: 34

GenotypeQuality
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variant carriers: 32

GenotypeQuality
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variant carriers: 25

GenotypeQuality
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variant carriers: 18

GenotypeQuality
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variant carriers: 59696

GenotypeQuality
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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: 61
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variant carriers: 57

GenotypeQuality
all individuals: 53
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variant carriers: 51

European (Non-Finnish)
type: Population
allele count: 33193
allele frequency: 4.99338087071637e-1
allele num: 66474
num of homozygotes: 0

African
type: Population
allele count: 5159
allele frequency: 4.9961262831687e-1
allele num: 10326
num of homozygotes: 0

Latino
type: Population
allele count: 5664
allele frequency: 4.985915492957746e-1
allele num: 11360
num of homozygotes: 0

Other
type: Population
allele count: 452
allele frequency: 4.988962472406181e-1
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 4256
allele frequency: 4.962686567164179e-1
allele num: 8576
num of homozygotes: 0

South Asian
type: Population
allele count: 8245
allele frequency: 5.0e-1
allele num: 16490
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3297
allele frequency: 4.998483929654336e-1
allele num: 6596
num of homozygotes: 1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.869e-1

MQ
type: SiteQuality
SIO_000300: 5.413e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.04e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.43e0

VQSLOD
type: SiteQuality
SIO_000300: 9.238e1

ClippingRankSum
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SIO_000300: -1.232e0

DP
type: SiteQuality
SIO_000300: 4.740239e6

FS
type: SiteQuality
SIO_000300: 7.264e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.981e0

QD
type: SiteQuality
SIO_000300: 8.710000000000001e0

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: 1

East Asian
type: Population
allele count: 6
allele frequency: 6.946052326927529e-4
allele num: 8638
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.636667252592723e-4
allele num: 11378
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.949317738791423e-4
allele num: 10260
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.818843215714805e-4
allele num: 16494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.517440461871541e-5
allele num: 66512
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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BaseQRankSum
type: SiteQuality
SIO_000300: -6.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.389999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.495e1

MQRankSum
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SIO_000300: -2.872e0

DP
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SIO_000300: 2.75697e6

FS
type: SiteQuality
SIO_000300: 3.819e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.34e-1

QD
type: SiteQuality
SIO_000300: 1.88e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8
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variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11378
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.006976184748617e-5
allele num: 66512
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.872e0

FS
type: SiteQuality
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QD
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MQ
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VQSLOD
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DP
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: 9.389999999999999e-1

InbreedingCoeff
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SIO_000300: 2.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.34e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 1.503533303262667e-5
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European (Finnish)
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allele frequency: 0.0e0
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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FS
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VQSLOD
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DP
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SIO_000300: 2.753946e6

BaseQRankSum
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SIO_000300: -2.282e0

MQ
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QD
type: SiteQuality
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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

African
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South Asian
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Latino
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East Asian
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European (Non-Finnish)
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Other
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InbreedingCoeff
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MQ
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FS
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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VQSLOD
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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South Asian
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Other
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European (Finnish)
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MQRankSum
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ReadPosRankSum
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FS
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BaseQRankSum
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InbreedingCoeff
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DP
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MQ
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VQSLOD
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ClippingRankSum
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QD
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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

East Asian
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European (Finnish)
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South Asian
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Latino
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African
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Other
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ClippingRankSum
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MQ
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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DP
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MQRankSum
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FS
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Other
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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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MQRankSum
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FS
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BaseQRankSum
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VQSLOD
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DP
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MQ
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InbreedingCoeff
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ClippingRankSum
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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African
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East Asian
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Other
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European (Finnish)
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European (Non-Finnish)
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Latino
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South Asian
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FS
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QD
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MQRankSum
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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DP
type: SiteQuality
SIO_000300: 2.746842e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.455e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.7e-2

GenotypeDepth
all individuals: 2772
bin: 5.75e1
variant carriers: 1

GenotypeDepth
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bin: 8.25e1
variant carriers: 0

GenotypeDepth
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bin: 4.75e1
variant carriers: 1

GenotypeDepth
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bin: 7.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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bin: 1.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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bin: 6.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4816
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10162
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.010869237948996e-5
allele num: 66426
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.849e0

MQ
type: SiteQuality
SIO_000300: 5.537e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 8.877000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.662e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.159999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.04e-1

QD
type: SiteQuality
SIO_000300: 1.72e0

DP
type: SiteQuality
SIO_000300: 2.7413e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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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
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 25
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.070171178827243e-5
allele num: 16474
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66422
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10138
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11358
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.647e1

VQSLOD
type: SiteQuality
SIO_000300: -1.918e0

FS
type: SiteQuality
SIO_000300: 3.373e0

DP
type: SiteQuality
SIO_000300: 2.73679e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.72e0

QD
type: SiteQuality
SIO_000300: 7.75e0

MQRankSum
type: SiteQuality
SIO_000300: 2.67e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

GenotypeDepth
all individuals: 1651
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 755
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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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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 1908
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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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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 26
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2979
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16470
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11340
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: 1
allele frequency: 1.507977199384745e-5
allele num: 66314
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10012
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.948e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.67e1

MQRankSum
type: SiteQuality
SIO_000300: -1.693e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.3e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.514e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.484e0

VQSLOD
type: SiteQuality
SIO_000300: -3.501e0

QD
type: SiteQuality
SIO_000300: 1.7e0

DP
type: SiteQuality
SIO_000300: 2.719577e6

GenotypeDepth
all individuals: 1651
bin: 1.75e1
variant carriers: 4

GenotypeDepth
all individuals: 5303
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 923
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variant carriers: 2

GenotypeDepth
all individuals: 3713
bin: 5.25e1
variant carriers: 5

GenotypeDepth
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variant carriers: 5

GenotypeDepth
all individuals: 11022
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variant carriers: 9

GenotypeDepth
all individuals: 8042
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variant carriers: 6

GenotypeDepth
all individuals: 371
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variant carriers: 0

GenotypeDepth
all individuals: 1908
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variant carriers: 4

GenotypeDepth
all individuals: 2769
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variant carriers: 7

GenotypeDepth
all individuals: 2563
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variant carriers: 2

GenotypeQuality
all individuals: 15792
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 2979
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variant carriers: 1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 26
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variant carriers: 1

GenotypeQuality
all individuals: 647
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variant carriers: 4

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 1386
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variant carriers: 3

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 95
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variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3069
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 17274
bin: 9.75e1
variant carriers: 27

African
type: Population
allele count: 51
allele frequency: 5.093887335197763e-3
allele num: 10012
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507977199384745e-5
allele num: 66314
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.763668430335097e-4
allele num: 11340
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.071645415907711e-5
allele num: 16470
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.719577e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.3e0

VQSLOD
type: SiteQuality
SIO_000300: -3.501e0

FS
type: SiteQuality
SIO_000300: 9.948e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.484e0

MQRankSum
type: SiteQuality
SIO_000300: -1.693e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

QD
type: SiteQuality
SIO_000300: 1.7e0

MQ
type: SiteQuality
SIO_000300: 5.67e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.514e0

GenotypeDepth
all individuals: 194
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3626
bin: 5.25e1
variant carriers: 2

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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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
all individuals: 3645
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2904
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1677
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11290
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.569826955885937e-5
allele num: 65648
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9712
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.773e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.15e-1

DP
type: SiteQuality
SIO_000300: 2.634245e6

MQRankSum
type: SiteQuality
SIO_000300: -4.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.96e0

VQSLOD
type: SiteQuality
SIO_000300: -8.895999999999999e-1

QD
type: SiteQuality
SIO_000300: 8.539999999999999e0

GenotypeDepth
all individuals: 7329
bin: 2.75e1
variant carriers: 13

GenotypeDepth
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variant carriers: 5

GenotypeDepth
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variant carriers: 3

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
all individuals: 542
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GenotypeDepth
all individuals: 945
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variant carriers: 2

GenotypeDepth
all individuals: 4465
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variant carriers: 9

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
all individuals: 7165
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GenotypeQuality
all individuals: 438
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variant carriers: 0

GenotypeQuality
all individuals: 35
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GenotypeQuality
all individuals: 912
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 328
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variant carriers: 1

GenotypeQuality
all individuals: 1524
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 3542
bin: 5.25e1
variant carriers: 4

GenotypeQuality
all individuals: 2407
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variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 3

GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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bin: 3.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 1674
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variant carriers: 2

GenotypeQuality
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bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 3387
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variant carriers: 1

GenotypeQuality
all individuals: 17245
bin: 9.75e1
variant carriers: 81

GenotypeQuality
all individuals: 1675
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4918
bin: 6.75e1
variant carriers: 3

Latino
type: Population
allele count: 3
allele frequency: 2.660989888238425e-4
allele num: 11274
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 54
allele frequency: 8.244526550429021e-4
allele num: 65498
num of homozygotes: 0

South Asian
type: Population
allele count: 24
allele frequency: 1.470227885322225e-3
allele num: 16324
num of homozygotes: 0

East Asian
type: Population
allele count: 11
allele frequency: 1.282051282051282e-3
allele num: 8580
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 1.03327133705311e-3
allele num: 9678
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.110601894286587e-4
allele num: 6546
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.11358574610245e-3
allele num: 898
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.709e0

VQSLOD
type: SiteQuality
SIO_000300: -5.348000000000001e-1

DP
type: SiteQuality
SIO_000300: 2.618264e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.84e-1

QD
type: SiteQuality
SIO_000300: 2.3e-1

MQ
type: SiteQuality
SIO_000300: 5.577e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 6.52e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.448e0

GenotypeDepth
all individuals: 743
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2542
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 409
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 7516
bin: 2.75e1
variant carriers: 133

GenotypeDepth
all individuals: 4537
bin: 2.25e1
variant carriers: 88

GenotypeQuality
all individuals: 1531
bin: 4.25e1
variant carriers: 20

GenotypeQuality
all individuals: 462
bin: 7.5e0
variant carriers: 11

GenotypeQuality
all individuals: 2860
bin: 9.25e1
variant carriers: 31

GenotypeQuality
all individuals: 1921
bin: 5.75e1
variant carriers: 25

GenotypeQuality
all individuals: 5637
bin: 6.25e1
variant carriers: 31

GenotypeQuality
all individuals: 3835
bin: 5.25e1
variant carriers: 17

GenotypeQuality
all individuals: 240
bin: 1.25e1
variant carriers: 15

GenotypeQuality
all individuals: 86
bin: 2.5e0
variant carriers: 12

GenotypeQuality
all individuals: 3564
bin: 8.25e1
variant carriers: 14

GenotypeQuality
all individuals: 1677
bin: 3.25e1
variant carriers: 23

GenotypeQuality
all individuals: 2311
bin: 3.75e1
variant carriers: 31

GenotypeQuality
all individuals: 1651
bin: 8.75e1
variant carriers: 20

GenotypeQuality
all individuals: 465
bin: 1.75e1
variant carriers: 16

GenotypeQuality
all individuals: 716
bin: 2.75e1
variant carriers: 15

GenotypeQuality
all individuals: 4675
bin: 6.75e1
variant carriers: 21

GenotypeQuality
all individuals: 3914
bin: 7.75e1
variant carriers: 21

GenotypeQuality
all individuals: 3342
bin: 4.75e1
variant carriers: 24

GenotypeQuality
all individuals: 2356
bin: 7.25e1
variant carriers: 27

GenotypeQuality
all individuals: 1479
bin: 2.25e1
variant carriers: 25

GenotypeQuality
all individuals: 17857
bin: 9.75e1
variant carriers: 353

East Asian
type: Population
allele count: 51
allele frequency: 5.970498712245376e-3
allele num: 8542
num of homozygotes: 0

African
type: Population
allele count: 38
allele frequency: 3.945182724252492e-3
allele num: 9632
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 31
allele frequency: 4.745866503368034e-3
allele num: 6532
num of homozygotes: 0

Latino
type: Population
allele count: 59
allele frequency: 5.257529852076279e-3
allele num: 11222
num of homozygotes: 0

Other
type: Population
allele count: 7
allele frequency: 7.865168539325843e-3
allele num: 890
num of homozygotes: 0

South Asian
type: Population
allele count: 98
allele frequency: 6.022615535889872e-3
allele num: 16272
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 413
allele frequency: 6.338828007489947e-3
allele num: 65154
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.11e-2

FS
type: SiteQuality
SIO_000300: 3.73e0

VQSLOD
type: SiteQuality
SIO_000300: -5.042e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.568e0

DP
type: SiteQuality
SIO_000300: 2.608243e6

QD
type: SiteQuality
SIO_000300: 3.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.42e-1

MQ
type: SiteQuality
SIO_000300: 5.57e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.52e-1

GenotypeDepth
all individuals: 6758
bin: 4.25e1
variant carriers: 91

GenotypeDepth
all individuals: 409
bin: 8.75e1
variant carriers: 18

GenotypeDepth
all individuals: 2700
bin: 5.75e1
variant carriers: 47

GenotypeDepth
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variant carriers: 13

GenotypeDepth
all individuals: 929
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variant carriers: 24

GenotypeQuality
all individuals: 1651
bin: 8.75e1
variant carriers: 11

GenotypeQuality
all individuals: 1921
bin: 5.75e1
variant carriers: 6

GenotypeQuality
all individuals: 4675
bin: 6.75e1
variant carriers: 11

GenotypeQuality
all individuals: 240
bin: 1.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1479
bin: 2.25e1
variant carriers: 9

GenotypeQuality
all individuals: 3342
bin: 4.75e1
variant carriers: 12

GenotypeQuality
all individuals: 3835
bin: 5.25e1
variant carriers: 8

GenotypeQuality
all individuals: 86
bin: 2.5e0
variant carriers: 6

GenotypeQuality
all individuals: 465
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1531
bin: 4.25e1
variant carriers: 8

GenotypeQuality
all individuals: 2311
bin: 3.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2860
bin: 9.25e1
variant carriers: 10

GenotypeQuality
all individuals: 462
bin: 7.5e0
variant carriers: 4

GenotypeQuality
all individuals: 3564
bin: 8.25e1
variant carriers: 20

GenotypeQuality
all individuals: 5637
bin: 6.25e1
variant carriers: 10

GenotypeQuality
all individuals: 716
bin: 2.75e1
variant carriers: 15

GenotypeQuality
all individuals: 1677
bin: 3.25e1
variant carriers: 9

GenotypeQuality
all individuals: 3914
bin: 7.75e1
variant carriers: 14

GenotypeQuality
all individuals: 2356
bin: 7.25e1
variant carriers: 7

GenotypeQuality
all individuals: 17857
bin: 9.75e1
variant carriers: 832

Latino
type: Population
allele count: 50
allele frequency: 4.455533772945999e-3
allele num: 11222
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 69
allele frequency: 1.056338028169014e-2
allele num: 6532
num of homozygotes: 0

East Asian
type: Population
allele count: 51
allele frequency: 5.970498712245376e-3
allele num: 8542
num of homozygotes: 0

Other
type: Population
allele count: 12
allele frequency: 1.348314606741573e-2
allele num: 890
num of homozygotes: 0

African
type: Population
allele count: 88
allele frequency: 9.136212624584718e-3
allele num: 9632
num of homozygotes: 0

South Asian
type: Population
allele count: 280
allele frequency: 1.720747295968535e-2
allele num: 16272
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 434
allele frequency: 6.661141296006385e-3
allele num: 65154
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.57e1

FS
type: SiteQuality
SIO_000300: 3.73e0

DP
type: SiteQuality
SIO_000300: 2.608243e6

MQRankSum
type: SiteQuality
SIO_000300: -3.568e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.11e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.52e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.042e-1

QD
type: SiteQuality
SIO_000300: 3.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.19e-1

GenotypeDepth
all individuals: 2700
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4537
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9218
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 929
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8443
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variant carriers: 1

GenotypeDepth
all individuals: 2163
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 547
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variant carriers: 0

GenotypeDepth
all individuals: 362
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variant carriers: 0

GenotypeDepth
all individuals: 409
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variant carriers: 0

GenotypeQuality
all individuals: 5637
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variant carriers: 0

GenotypeQuality
all individuals: 716
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variant carriers: 0

GenotypeQuality
all individuals: 1677
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3914
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4675
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 462
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variant carriers: 0

GenotypeQuality
all individuals: 2356
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1479
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17857
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1531
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3835
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variant carriers: 0

GenotypeQuality
all individuals: 240
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variant carriers: 0

GenotypeQuality
all individuals: 3342
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3564
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 1651
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2860
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1921
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2311
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.170686022008897e-4
allele num: 8542
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9632
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16272
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11222
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65154
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.73e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.11e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.568e0

MQ
type: SiteQuality
SIO_000300: 5.57e1

QD
type: SiteQuality
SIO_000300: 3.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.42e-1

DP
type: SiteQuality
SIO_000300: 2.608243e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.19e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.042e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.52e-1

GenotypeDepth
all individuals: 743
bin: 7.75e1
variant carriers: 2

GenotypeDepth
all individuals: 929
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3580
bin: 5.25e1
variant carriers: 2

GenotypeDepth
all individuals: 5064
bin: 4.75e1
variant carriers: 5

GenotypeDepth
all individuals: 6758
bin: 4.25e1
variant carriers: 5

GenotypeQuality
all individuals: 1479
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5637
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2356
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4675
bin: 6.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1531
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3342
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 462
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variant carriers: 0

GenotypeQuality
all individuals: 3564
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variant carriers: 0

GenotypeQuality
all individuals: 240
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variant carriers: 1

GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 1677
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 716
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1921
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1651
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2860
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3914
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variant carriers: 0

GenotypeQuality
all individuals: 2311
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variant carriers: 0

GenotypeQuality
all individuals: 17857
bin: 9.75e1
variant carriers: 54

GenotypeQuality
all individuals: 3835
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 45
allele frequency: 6.906713325352242e-4
allele num: 65154
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 5.853430110044487e-4
allele num: 8542
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.7822135091784e-4
allele num: 11222
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 1.038205980066445e-3
allele num: 9632
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.145526057030482e-5
allele num: 16272
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.568e0

DP
type: SiteQuality
SIO_000300: 2.608243e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.52e-1

QD
type: SiteQuality
SIO_000300: 3.0e-1

MQ
type: SiteQuality
SIO_000300: 5.57e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.42e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.042e-1

FS
type: SiteQuality
SIO_000300: 3.73e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.11e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.19e-1

GenotypeDepth
all individuals: 1295
bin: 6.75e1
variant carriers: 77

GenotypeDepth
all individuals: 564
bin: 7.5e0
variant carriers: 17

GenotypeDepth
all individuals: 4575
bin: 2.25e1
variant carriers: 585

GenotypeDepth
all individuals: 1107
bin: 1.25e1
variant carriers: 68

GenotypeDepth
all individuals: 7558
bin: 2.75e1
variant carriers: 799

GenotypeDepth
all individuals: 5055
bin: 4.75e1
variant carriers: 440

GenotypeDepth
all individuals: 730
bin: 7.75e1
variant carriers: 46

GenotypeDepth
all individuals: 532
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variant carriers: 25

GenotypeDepth
all individuals: 6747
bin: 4.25e1
variant carriers: 576

GenotypeDepth
all individuals: 3545
bin: 5.25e1
variant carriers: 282

GenotypeDepth
all individuals: 1868
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variant carriers: 131

GenotypeDepth
all individuals: 346
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variant carriers: 12

GenotypeQuality
all individuals: 2255
bin: 3.75e1
variant carriers: 125

GenotypeQuality
all individuals: 1555
bin: 4.25e1
variant carriers: 151

GenotypeQuality
all individuals: 3718
bin: 7.75e1
variant carriers: 137

GenotypeQuality
all individuals: 4437
bin: 6.75e1
variant carriers: 147

GenotypeQuality
all individuals: 5552
bin: 6.25e1
variant carriers: 140

GenotypeQuality
all individuals: 387
bin: 1.25e1
variant carriers: 118

GenotypeQuality
all individuals: 625
bin: 7.5e0
variant carriers: 126

GenotypeQuality
all individuals: 187
bin: 2.5e0
variant carriers: 69

GenotypeQuality
all individuals: 1625
bin: 8.75e1
variant carriers: 130

GenotypeQuality
all individuals: 1725
bin: 5.75e1
variant carriers: 137

GenotypeQuality
all individuals: 820
bin: 2.75e1
variant carriers: 135

GenotypeQuality
all individuals: 3627
bin: 5.25e1
variant carriers: 168

GenotypeQuality
all individuals: 1648
bin: 3.25e1
variant carriers: 115

GenotypeQuality
all individuals: 3180
bin: 4.75e1
variant carriers: 139

GenotypeQuality
all individuals: 2280
bin: 7.25e1
variant carriers: 149

GenotypeQuality
all individuals: 2722
bin: 9.25e1
variant carriers: 141

GenotypeQuality
all individuals: 1609
bin: 2.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2918

GenotypeQuality
all individuals: 593
bin: 1.75e1
variant carriers: 132

GenotypeQuality
all individuals: 3382
bin: 8.25e1
variant carriers: 142

European (Finnish)
type: Population
allele count: 293
allele frequency: 4.552517091361094e-2
allele num: 6436
num of homozygotes: 0

African
type: Population
allele count: 399
allele frequency: 4.175387191293428e-2
allele num: 9556
num of homozygotes: 0

South Asian
type: Population
allele count: 790
allele frequency: 4.885590599876314e-2
allele num: 16170
num of homozygotes: 0

Latino
type: Population
allele count: 406
allele frequency: 3.670222382932562e-2
allele num: 11062
num of homozygotes: 0

Other
type: Population
allele count: 33
allele frequency: 3.699551569506727e-2
allele num: 892
num of homozygotes: 0

East Asian
type: Population
allele count: 387
allele frequency: 4.583135954523922e-2
allele num: 8444
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2675
allele frequency: 4.142405847373637e-2
allele num: 64576
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.63e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.562e0

QD
type: SiteQuality
SIO_000300: 1.61e0

VQSLOD
type: SiteQuality
SIO_000300: -9.464e-1

FS
type: SiteQuality
SIO_000300: 1.015e0

MQRankSum
type: SiteQuality
SIO_000300: -3.189e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.29e0

DP
type: SiteQuality
SIO_000300: 2.601515e6

MQ
type: SiteQuality
SIO_000300: 5.617e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.99e-1

GenotypeDepth
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bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 211
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GenotypeDepth
all individuals: 9290
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GenotypeDepth
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GenotypeDepth
all individuals: 346
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GenotypeDepth
all individuals: 1295
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GenotypeDepth
all individuals: 2550
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variant carriers: 17

GenotypeDepth
all individuals: 2228
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GenotypeQuality
all individuals: 387
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GenotypeQuality
all individuals: 625
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GenotypeQuality
all individuals: 593
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variant carriers: 0

GenotypeQuality
all individuals: 820
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variant carriers: 0

GenotypeQuality
all individuals: 3180
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GenotypeQuality
all individuals: 2255
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variant carriers: 0

GenotypeQuality
all individuals: 187
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GenotypeQuality
all individuals: 1648
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GenotypeQuality
all individuals: 2280
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GenotypeQuality
all individuals: 1725
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variant carriers: 0

GenotypeQuality
all individuals: 3627
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variant carriers: 0

GenotypeQuality
all individuals: 1609
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 3718
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1555
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5552
bin: 6.25e1
variant carriers: 3

GenotypeQuality
all individuals: 4437
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3382
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variant carriers: 0

GenotypeQuality
all individuals: 2722
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1625
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 18651
bin: 9.75e1
variant carriers: 53

South Asian
type: Population
allele count: 3
allele frequency: 1.855287569573284e-4
allele num: 16170
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 7.325240686479698e-4
allele num: 9556
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.553760099440646e-4
allele num: 6436
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 42
allele frequency: 6.50396432111001e-4
allele num: 64576
num of homozygotes: 0

East Asian
type: Population
allele count: 7
allele frequency: 8.289909995262909e-4
allele num: 8444
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.51997830410414e-4
allele num: 11062
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.121076233183856e-3
allele num: 892
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.015e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.63e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.562e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.99e-1

DP
type: SiteQuality
SIO_000300: 2.601515e6

MQRankSum
type: SiteQuality
SIO_000300: -3.189e0

MQ
type: SiteQuality
SIO_000300: 5.617e1

VQSLOD
type: SiteQuality
SIO_000300: -9.464e-1

QD
type: SiteQuality
SIO_000300: 1.61e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 65

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2280
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variant carriers: 0

GenotypeQuality
all individuals: 4437
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 7
allele frequency: 6.327969625745796e-4
allele num: 11062
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 43
allele frequency: 6.658820614469772e-4
allele num: 64576
num of homozygotes: 0

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

African
type: Population
allele count: 10
allele frequency: 1.046462955211385e-3
allele num: 9556
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.473716759431045e-4
allele num: 16170
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.18427285646613e-4
allele num: 8444
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6436
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.015e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.63e-2

MQ
type: SiteQuality
SIO_000300: 5.617e1

QD
type: SiteQuality
SIO_000300: 1.61e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.562e0

MQRankSum
type: SiteQuality
SIO_000300: -3.189e0

VQSLOD
type: SiteQuality
SIO_000300: -9.464e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.99e-1

DP
type: SiteQuality
SIO_000300: 2.601515e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 94
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GenotypeQuality
all individuals: 260
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variant carriers: 0

GenotypeQuality
all individuals: 2016
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 1
allele frequency: 8.576329331046312e-4
allele num: 1166
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 96
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1394
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1816
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1040
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7256
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.14e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.647e0

FS
type: SiteQuality
SIO_000300: 1.014e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.748e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.5e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.68e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.080000000000001e-1

DP
type: SiteQuality
SIO_000300: 2.543318e6

MQ
type: SiteQuality
SIO_000300: 5.629e1

QD
type: SiteQuality
SIO_000300: 7.9e-1

GenotypeDepth
all individuals: 394
bin: 8.75e1
variant carriers: 21

GenotypeDepth
all individuals: 3360
bin: 5.25e1
variant carriers: 181

GenotypeDepth
all individuals: 1680
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variant carriers: 83

GenotypeDepth
all individuals: 874
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variant carriers: 45

GenotypeDepth
all individuals: 4863
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variant carriers: 303

GenotypeDepth
all individuals: 4827
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variant carriers: 249

GenotypeDepth
all individuals: 328
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variant carriers: 8

GenotypeDepth
all individuals: 6462
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variant carriers: 349

GenotypeQuality
all individuals: 485
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variant carriers: 82

GenotypeQuality
all individuals: 293
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variant carriers: 83

GenotypeQuality
all individuals: 2016
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variant carriers: 1786

GenotypeQuality
all individuals: 598
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variant carriers: 70

GenotypeQuality
all individuals: 683
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variant carriers: 67

GenotypeQuality
all individuals: 260
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variant carriers: 82

GenotypeQuality
all individuals: 329
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variant carriers: 80

GenotypeQuality
all individuals: 1068
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variant carriers: 52

GenotypeQuality
all individuals: 403
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variant carriers: 64

GenotypeQuality
all individuals: 342
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variant carriers: 70

GenotypeQuality
all individuals: 94
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variant carriers: 75

GenotypeQuality
all individuals: 51033
bin: 2.5e0
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GenotypeQuality
all individuals: 882
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variant carriers: 61

GenotypeQuality
all individuals: 103
bin: 9.25e1
variant carriers: 80

GenotypeQuality
all individuals: 219
bin: 6.75e1
variant carriers: 94

GenotypeQuality
all individuals: 317
bin: 4.75e1
variant carriers: 85

GenotypeQuality
all individuals: 655
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variant carriers: 84

GenotypeQuality
all individuals: 111
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variant carriers: 87

GenotypeQuality
all individuals: 116
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variant carriers: 77

GenotypeQuality
all individuals: 162
bin: 7.25e1
variant carriers: 99

South Asian
type: Population
allele count: 515
allele frequency: 2.835903083700441e-1
allele num: 1816
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1531
allele frequency: 2.109977949283352e-1
allele num: 7256
num of homozygotes: 0

East Asian
type: Population
allele count: 229
allele frequency: 1.963979416809606e-1
allele num: 1166
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 185
allele frequency: 2.427821522309711e-1
allele num: 762
num of homozygotes: 0

African
type: Population
allele count: 235
allele frequency: 2.259615384615385e-1
allele num: 1040
num of homozygotes: 0

Latino
type: Population
allele count: 254
allele frequency: 1.822094691535151e-1
allele num: 1394
num of homozygotes: 0

Other
type: Population
allele count: 24
allele frequency: 2.5e-1
allele num: 96
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.647e0

DP
type: SiteQuality
SIO_000300: 2.543318e6

QD
type: SiteQuality
SIO_000300: 7.9e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.14e0

FS
type: SiteQuality
SIO_000300: 1.014e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.5e0

MQ
type: SiteQuality
SIO_000300: 5.629e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.748e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.080000000000001e-1

GenotypeDepth
all individuals: 4863
bin: 2.25e1
variant carriers: 12

GenotypeDepth
all individuals: 8203
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variant carriers: 23

GenotypeDepth
all individuals: 1233
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variant carriers: 2

GenotypeDepth
all individuals: 874
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variant carriers: 5

GenotypeDepth
all individuals: 3360
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variant carriers: 7

GenotypeDepth
all individuals: 328
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GenotypeDepth
all individuals: 2373
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variant carriers: 5

GenotypeDepth
all individuals: 394
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variant carriers: 2

GenotypeQuality
all individuals: 103
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GenotypeQuality
all individuals: 598
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GenotypeQuality
all individuals: 260
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GenotypeQuality
all individuals: 485
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GenotypeQuality
all individuals: 94
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GenotypeQuality
all individuals: 683
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GenotypeQuality
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GenotypeQuality
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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: 329
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GenotypeQuality
all individuals: 293
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GenotypeQuality
all individuals: 317
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GenotypeQuality
all individuals: 1068
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2016
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variant carriers: 118

GenotypeQuality
all individuals: 116
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variant carriers: 2

East Asian
type: Population
allele count: 10
allele frequency: 8.576329331046312e-3
allele num: 1166
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 2.624671916010499e-3
allele num: 762
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 2.869440459110474e-3
allele num: 1394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 87
allele frequency: 1.199007717750827e-2
allele num: 7256
num of homozygotes: 0

South Asian
type: Population
allele count: 32
allele frequency: 1.762114537444934e-2
allele num: 1816
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.041666666666667e-2
allele num: 96
num of homozygotes: 0

African
type: Population
allele count: 14
allele frequency: 1.346153846153846e-2
allele num: 1040
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.14e0

DP
type: SiteQuality
SIO_000300: 2.543318e6

QD
type: SiteQuality
SIO_000300: 7.9e-1

FS
type: SiteQuality
SIO_000300: 1.014e0

VQSLOD
type: SiteQuality
SIO_000300: 8.080000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.647e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.748e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.5e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.68e-1

MQ
type: SiteQuality
SIO_000300: 5.629e1

GenotypeDepth
all individuals: 394
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variant carriers: 0

GenotypeDepth
all individuals: 493
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variant carriers: 0

GenotypeDepth
all individuals: 4863
bin: 2.25e1
variant carriers: 61

GenotypeDepth
all individuals: 9484
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variant carriers: 30

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 213
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GenotypeDepth
all individuals: 2518
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variant carriers: 0

GenotypeDepth
all individuals: 4827
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variant carriers: 5

GenotypeDepth
all individuals: 1233
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
all individuals: 2414
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GenotypeQuality
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variant carriers: 15

GenotypeQuality
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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: 54

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11

GenotypeQuality
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GenotypeQuality
all individuals: 94
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variant carriers: 3

GenotypeQuality
all individuals: 103
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GenotypeQuality
all individuals: 219
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GenotypeQuality
all individuals: 260
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variant carriers: 13

African
type: Population
allele count: 7
allele frequency: 6.730769230769231e-3
allele num: 1040
num of homozygotes: 0

East Asian
type: Population
allele count: 9
allele frequency: 7.718696397941681e-3
allele num: 1166
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.041666666666667e-2
allele num: 96
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 120
allele frequency: 1.65380374862183e-2
allele num: 7256
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 7
allele frequency: 9.186351706036745e-3
allele num: 762
num of homozygotes: 0

Latino
type: Population
allele count: 19
allele frequency: 1.362984218077475e-2
allele num: 1394
num of homozygotes: 0

South Asian
type: Population
allele count: 27
allele frequency: 1.486784140969163e-2
allele num: 1816
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.647e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.5e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.68e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.14e0

DP
type: SiteQuality
SIO_000300: 2.543318e6

FS
type: SiteQuality
SIO_000300: 1.014e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.748e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.080000000000001e-1

QD
type: SiteQuality
SIO_000300: 7.9e-1

MQ
type: SiteQuality
SIO_000300: 5.629e1

GenotypeDepth
all individuals: 4517
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variant carriers: 157

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
all individuals: 588
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GenotypeDepth
all individuals: 5990
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variant carriers: 182

GenotypeDepth
all individuals: 2139
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GenotypeDepth
all individuals: 8689
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GenotypeDepth
all individuals: 456
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GenotypeQuality
all individuals: 553
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GenotypeQuality
all individuals: 1577
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GenotypeQuality
all individuals: 5748
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GenotypeQuality
all individuals: 3575
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GenotypeQuality
all individuals: 2661
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GenotypeQuality
all individuals: 2470
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GenotypeQuality
all individuals: 4090
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GenotypeQuality
all individuals: 1697
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GenotypeQuality
all individuals: 2015
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GenotypeQuality
all individuals: 3428
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GenotypeQuality
all individuals: 3980
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variant carriers: 48

GenotypeQuality
all individuals: 76
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GenotypeQuality
all individuals: 2214
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GenotypeQuality
all individuals: 540
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GenotypeQuality
all individuals: 2199
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GenotypeQuality
all individuals: 237
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GenotypeQuality
all individuals: 777
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variant carriers: 36

GenotypeQuality
all individuals: 16397
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variant carriers: 914

GenotypeQuality
all individuals: 4750
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GenotypeQuality
all individuals: 1587
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variant carriers: 40

African
type: Population
allele count: 130
allele frequency: 1.358979719841104e-2
allele num: 9566
num of homozygotes: 0

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

East Asian
type: Population
allele count: 128
allele frequency: 1.506236761590963e-2
allele num: 8498
num of homozygotes: 0

South Asian
type: Population
allele count: 206
allele frequency: 1.270506969285802e-2
allele num: 16214
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 94
allele frequency: 1.446598953524161e-2
allele num: 6498
num of homozygotes: 0

Latino
type: Population
allele count: 127
allele frequency: 1.136160314904276e-2
allele num: 11178
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 880
allele frequency: 1.357563790071272e-2
allele num: 64822
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.24e0

DP
type: SiteQuality
SIO_000300: 2.454445e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.09e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.176e0

FS
type: SiteQuality
SIO_000300: 4.191e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.473e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.71e-1

MQ
type: SiteQuality
SIO_000300: 5.654e1

MQRankSum
type: SiteQuality
SIO_000300: -3.132e0

QD
type: SiteQuality
SIO_000300: 6.8e-1

GenotypeDepth
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bin: 7.5e0
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2661
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GenotypeQuality
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bin: 3.75e1
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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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 16397
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variant carriers: 1

GenotypeQuality
all individuals: 2214
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8498
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11178
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9566
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16214
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.542686125080991e-5
allele num: 64822
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6498
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.132e0

VQSLOD
type: SiteQuality
SIO_000300: -1.176e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.71e-1

MQ
type: SiteQuality
SIO_000300: 5.654e1

QD
type: SiteQuality
SIO_000300: 6.8e-1

FS
type: SiteQuality
SIO_000300: 4.191e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.473e0

DP
type: SiteQuality
SIO_000300: 2.454445e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.24e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.09e-2

GenotypeDepth
all individuals: 5520
bin: 4.25e1
variant carriers: 4

GenotypeDepth
all individuals: 313
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variant carriers: 0

GenotypeDepth
all individuals: 806
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variant carriers: 5

GenotypeDepth
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variant carriers: 44

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 42

GenotypeDepth
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variant carriers: 28

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 70

GenotypeDepth
all individuals: 514
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GenotypeDepth
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GenotypeQuality
all individuals: 136
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variant carriers: 13

GenotypeQuality
all individuals: 251
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variant carriers: 10

GenotypeQuality
all individuals: 539
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GenotypeQuality
all individuals: 1066
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variant carriers: 10

GenotypeQuality
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variant carriers: 11

GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 8

GenotypeQuality
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bin: 4.75e1
variant carriers: 15

GenotypeQuality
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variant carriers: 9

GenotypeQuality
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bin: 8.25e1
variant carriers: 6

GenotypeQuality
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GenotypeQuality
all individuals: 19
bin: 9.25e1
variant carriers: 7

GenotypeQuality
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bin: 2.75e1
variant carriers: 10

GenotypeQuality
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variant carriers: 11

GenotypeQuality
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variant carriers: 7

GenotypeQuality
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bin: 9.75e1
variant carriers: 54

GenotypeQuality
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variant carriers: 6

GenotypeQuality
all individuals: 423
bin: 3.75e1
variant carriers: 7

GenotypeQuality
all individuals: 225
bin: 5.25e1
variant carriers: 10

East Asian
type: Population
allele count: 9
allele frequency: 8.181818181818182e-3
allele num: 1100
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 120
allele frequency: 1.838235294117647e-2
allele num: 6528
num of homozygotes: 0

South Asian
type: Population
allele count: 27
allele frequency: 2.246256239600666e-2
allele num: 1202
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 6
allele frequency: 9.009009009009009e-3
allele num: 666
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 7.641921397379912e-3
allele num: 916
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.25e-2
allele num: 80
num of homozygotes: 0

Latino
type: Population
allele count: 19
allele frequency: 1.382823871906841e-2
allele num: 1374
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.766e1

QD
type: SiteQuality
SIO_000300: 2.64e0

FS
type: SiteQuality
SIO_000300: 1.154e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.721e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.817e0

DP
type: SiteQuality
SIO_000300: 2.32021e6

VQSLOD
type: SiteQuality
SIO_000300: 2.62e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.34e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.735e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.267e0

GenotypeDepth
all individuals: 1883
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variant carriers: 0

GenotypeDepth
all individuals: 5429
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variant carriers: 5

GenotypeDepth
all individuals: 9685
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variant carriers: 14

GenotypeDepth
all individuals: 1904
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variant carriers: 36

GenotypeDepth
all individuals: 3853
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variant carriers: 1

GenotypeDepth
all individuals: 1316
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variant carriers: 0

GenotypeDepth
all individuals: 355
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GenotypeDepth
all individuals: 896
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GenotypeDepth
all individuals: 9646
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variant carriers: 39

GenotypeDepth
all individuals: 2617
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variant carriers: 1

GenotypeDepth
all individuals: 380
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variant carriers: 0

GenotypeDepth
all individuals: 1795
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GenotypeQuality
all individuals: 216
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GenotypeQuality
all individuals: 429
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variant carriers: 9

GenotypeQuality
all individuals: 83
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variant carriers: 11

GenotypeQuality
all individuals: 1239
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GenotypeQuality
all individuals: 888
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variant carriers: 8

GenotypeQuality
all individuals: 2233
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variant carriers: 10

GenotypeQuality
all individuals: 875
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
all individuals: 50021
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GenotypeQuality
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variant carriers: 10

GenotypeQuality
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variant carriers: 11

GenotypeQuality
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variant carriers: 7

GenotypeQuality
all individuals: 18
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GenotypeQuality
all individuals: 1270
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variant carriers: 10

GenotypeQuality
all individuals: 352
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variant carriers: 15

GenotypeQuality
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variant carriers: 7

GenotypeQuality
all individuals: 255
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variant carriers: 10

GenotypeQuality
all individuals: 28
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variant carriers: 6

GenotypeQuality
all individuals: 15
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variant carriers: 3

GenotypeQuality
all individuals: 111
bin: 9.75e1
variant carriers: 54

Other
type: Population
allele count: 1
allele frequency: 1.041666666666667e-2
allele num: 96
num of homozygotes: 0

South Asian
type: Population
allele count: 27
allele frequency: 1.831750339213026e-2
allele num: 1474
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 119
allele frequency: 1.579925650557621e-2
allele num: 7532
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 6.769825918762089e-3
allele num: 1034
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 6
allele frequency: 8.356545961002786e-3
allele num: 718
num of homozygotes: 0

East Asian
type: Population
allele count: 9
allele frequency: 8.687258687258687e-3
allele num: 1036
num of homozygotes: 0

Latino
type: Population
allele count: 19
allele frequency: 1.264980026631158e-2
allele num: 1502
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.648e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.734e0

DP
type: SiteQuality
SIO_000300: 2.305375e6

QD
type: SiteQuality
SIO_000300: 4.31e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.73e-1

FS
type: SiteQuality
SIO_000300: 4.936e0

MQ
type: SiteQuality
SIO_000300: 5.805e1

MQRankSum
type: SiteQuality
SIO_000300: -1.735e0

VQSLOD
type: SiteQuality
SIO_000300: 2.67e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.146e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 397
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GenotypeDepth
all individuals: 258
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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
all individuals: 192
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GenotypeQuality
all individuals: 2280
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 144
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1018
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2096
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1432
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1866
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 7.633587786259542e-4
allele num: 1310
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9218
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.595e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.520000000000001e-2

FS
type: SiteQuality
SIO_000300: 1.5454e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.84e-1

DP
type: SiteQuality
SIO_000300: 1.980788e6

VQSLOD
type: SiteQuality
SIO_000300: -6.508e-1

QD
type: SiteQuality
SIO_000300: 5.600000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.73e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.775e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.13e-1

GenotypeDepth
all individuals: 10033
bin: 2.25e1
variant carriers: 87

GenotypeDepth
all individuals: 225
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variant carriers: 4

GenotypeDepth
all individuals: 1678
bin: 5.25e1
variant carriers: 42

GenotypeDepth
all individuals: 10363
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variant carriers: 114

GenotypeDepth
all individuals: 1275
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variant carriers: 24

GenotypeQuality
all individuals: 300
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variant carriers: 6

GenotypeQuality
all individuals: 2280
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GenotypeQuality
all individuals: 130
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GenotypeQuality
all individuals: 855
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GenotypeQuality
all individuals: 1014
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GenotypeQuality
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GenotypeQuality
all individuals: 1531
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variant carriers: 20

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 38
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GenotypeQuality
all individuals: 503
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GenotypeQuality
all individuals: 646
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variant carriers: 587

GenotypeQuality
all individuals: 110
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GenotypeQuality
all individuals: 23
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variant carriers: 8

Latino
type: Population
allele count: 38
allele frequency: 2.036441586280814e-2
allele num: 1866
num of homozygotes: 0

East Asian
type: Population
allele count: 44
allele frequency: 3.358778625954199e-2
allele num: 1310
num of homozygotes: 0

Other
type: Population
allele count: 8
allele frequency: 5.555555555555555e-2
allele num: 144
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 50
allele frequency: 4.911591355599214e-2
allele num: 1018
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 324
allele frequency: 3.51486222607941e-2
allele num: 9218
num of homozygotes: 0

South Asian
type: Population
allele count: 202
allele frequency: 9.637404580152671e-2
allele num: 2096
num of homozygotes: 0

African
type: Population
allele count: 61
allele frequency: 4.259776536312849e-2
allele num: 1432
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.520000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.508e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.13e-1

DP
type: SiteQuality
SIO_000300: 1.980788e6

FS
type: SiteQuality
SIO_000300: 1.5454e1

MQRankSum
type: SiteQuality
SIO_000300: -3.775e0

QD
type: SiteQuality
SIO_000300: 5.600000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.595e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.73e-1

GenotypeDepth
all individuals: 1643
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variant carriers: 40

GenotypeDepth
all individuals: 757
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GenotypeDepth
all individuals: 262
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GenotypeDepth
all individuals: 10455
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variant carriers: 162

GenotypeDepth
all individuals: 6789
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variant carriers: 70

GenotypeDepth
all individuals: 443
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GenotypeDepth
all individuals: 1254
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GenotypeDepth
all individuals: 220
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GenotypeDepth
all individuals: 3820
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variant carriers: 85

GenotypeQuality
all individuals: 2304
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GenotypeQuality
all individuals: 483
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variant carriers: 20

GenotypeQuality
all individuals: 118
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variant carriers: 20

GenotypeQuality
all individuals: 181
bin: 5.25e1
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GenotypeQuality
all individuals: 124
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GenotypeQuality
all individuals: 364
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GenotypeQuality
all individuals: 47251
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GenotypeQuality
all individuals: 66
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GenotypeQuality
all individuals: 326
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GenotypeQuality
all individuals: 3671
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GenotypeQuality
all individuals: 1035
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GenotypeQuality
all individuals: 536
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variant carriers: 473

GenotypeQuality
all individuals: 34
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variant carriers: 16

GenotypeQuality
all individuals: 562
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variant carriers: 19

GenotypeQuality
all individuals: 860
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GenotypeQuality
all individuals: 193
bin: 4.75e1
variant carriers: 16

GenotypeQuality
all individuals: 300
bin: 6.75e1
variant carriers: 19

GenotypeQuality
all individuals: 45
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variant carriers: 28

GenotypeQuality
all individuals: 44
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variant carriers: 21

GenotypeQuality
all individuals: 1531
bin: 6.25e1
variant carriers: 17

East Asian
type: Population
allele count: 61
allele frequency: 4.505169867060561e-2
allele num: 1354
num of homozygotes: 0

Latino
type: Population
allele count: 64
allele frequency: 3.404255319148936e-2
allele num: 1880
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 46
allele frequency: 4.527559055118111e-2
allele num: 1016
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 446
allele frequency: 4.69177361666316e-2
allele num: 9506
num of homozygotes: 0

African
type: Population
allele count: 72
allele frequency: 5.049088359046283e-2
allele num: 1426
num of homozygotes: 0

South Asian
type: Population
allele count: 104
allele frequency: 5.597416576964478e-2
allele num: 1858
num of homozygotes: 0

Other
type: Population
allele count: 4
allele frequency: 3.03030303030303e-2
allele num: 132
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.849e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.223e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.379999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.89e-1

DP
type: SiteQuality
SIO_000300: 1.969238e6

BaseQRankSum
type: SiteQuality
SIO_000300: -9.71e-1

FS
type: SiteQuality
SIO_000300: 1.0648e1

MQ
type: SiteQuality
SIO_000300: 5.699e1

QD
type: SiteQuality
SIO_000300: 2.95e0

VQSLOD
type: SiteQuality
SIO_000300: -7.504e-1

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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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 300
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1426
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 7.385524372230429e-4
allele num: 1354
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1858
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1880
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9506
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1016
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -7.504e-1

QD
type: SiteQuality
SIO_000300: 2.95e0

MQRankSum
type: SiteQuality
SIO_000300: -2.849e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.89e-1

FS
type: SiteQuality
SIO_000300: 1.0648e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.379999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.223e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.71e-1

MQ
type: SiteQuality
SIO_000300: 5.699e1

DP
type: SiteQuality
SIO_000300: 1.969238e6

GenotypeDepth
all individuals: 1326
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variant carriers: 4

GenotypeDepth
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variant carriers: 169

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 5

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: 22

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 25

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 18

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 474

GenotypeQuality
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variant carriers: 19

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 24

GenotypeQuality
all individuals: 176
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variant carriers: 38

GenotypeQuality
all individuals: 29
bin: 8.75e1
variant carriers: 13

European (Non-Finnish)
type: Population
allele count: 446
allele frequency: 4.522409247617117e-2
allele num: 9862
num of homozygotes: 0

South Asian
type: Population
allele count: 104
allele frequency: 5.543710021321962e-2
allele num: 1876
num of homozygotes: 0

East Asian
type: Population
allele count: 61
allele frequency: 4.401154401154401e-2
allele num: 1386
num of homozygotes: 0

African
type: Population
allele count: 72
allele frequency: 4.891304347826087e-2
allele num: 1472
num of homozygotes: 0

Latino
type: Population
allele count: 64
allele frequency: 3.28879753340185e-2
allele num: 1946
num of homozygotes: 0

Other
type: Population
allele count: 4
allele frequency: 2.941176470588235e-2
allele num: 136
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 46
allele frequency: 4.397705544933078e-2
allele num: 1046
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e0

MQ
type: SiteQuality
SIO_000300: 5.705e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.256e0

DP
type: SiteQuality
SIO_000300: 1.959823e6

FS
type: SiteQuality
SIO_000300: 1.0805e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.29e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.834e0

VQSLOD
type: SiteQuality
SIO_000300: 5.46e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.547e-1

QD
type: SiteQuality
SIO_000300: 3.05e0

GenotypeDepth
all individuals: 494
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variant carriers: 0

GenotypeDepth
all individuals: 1231
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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
all individuals: 1137
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GenotypeQuality
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GenotypeQuality
all individuals: 246
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GenotypeQuality
all individuals: 4524
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 70
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GenotypeQuality
all individuals: 18
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 144
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1958
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 7.320644216691069e-4
allele num: 1366
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1048
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1836
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9914
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.417e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.296e0

QD
type: SiteQuality
SIO_000300: 1.899e1

DP
type: SiteQuality
SIO_000300: 1.929818e6

FS
type: SiteQuality
SIO_000300: 1.558e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.8e-2

MQ
type: SiteQuality
SIO_000300: 5.996e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1566
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10996
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15712
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8290
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62832
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.084363478638039e-4
allele num: 9222
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 8.87e-1

QD
type: SiteQuality
SIO_000300: 6.46e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e0

DP
type: SiteQuality
SIO_000300: 1.854123e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.5e0

VQSLOD
type: SiteQuality
SIO_000300: -1.137e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.22e-1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 400
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variant carriers: 0

African
type: Population
allele count: 6
allele frequency: 2.824858757062147e-3
allele num: 2124
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2308
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13536
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1576
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2014
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2718
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.79e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.471e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.086e-1

MQ
type: SiteQuality
SIO_000300: 5.945e1

FS
type: SiteQuality
SIO_000300: 5.205e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.44e-1

DP
type: SiteQuality
SIO_000300: 1.814815e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.83e0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
all individuals: 3716
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GenotypeQuality
all individuals: 2725
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6388
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.222195062331948e-4
allele num: 8182
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61596
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15390
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10866
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9090
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.603e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

DP
type: SiteQuality
SIO_000300: 1.692315e6

MQRankSum
type: SiteQuality
SIO_000300: -7.8e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
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SIO_000300: 7.64e-1

FS
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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SIO_000300: 6.98e-1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
allele num: 14994
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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num of homozygotes: 0

Other
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num of homozygotes: 0

Latino
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allele frequency: 9.354536950420954e-5
allele num: 10690
num of homozygotes: 0

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

East Asian
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QD
type: SiteQuality
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DP
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VQSLOD
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MQ
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MQRankSum
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ReadPosRankSum
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FS
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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 frequency: 4.101722723543889e-4
allele num: 2438
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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

East Asian
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allele frequency: 0.0e0
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MQ
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SIO_000300: 5.625e1

MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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QD
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FS
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -1.13e-1

DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 252
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

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

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

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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VQSLOD
type: SiteQuality
SIO_000300: 4.13e-1

ClippingRankSum
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QD
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MQRankSum
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FS
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BaseQRankSum
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DP
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 5.79e1

InbreedingCoeff
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SIO_000300: -1.718e-1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 3430
num of homozygotes: 0

European (Non-Finnish)
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allele count: 75
allele frequency: 4.88408439697838e-3
allele num: 15356
num of homozygotes: 0

East Asian
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African
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Other
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European (Finnish)
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allele count: 1
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allele num: 2300
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South Asian
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allele num: 2958
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InbreedingCoeff
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FS
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ClippingRankSum
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MQ
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VQSLOD
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MQRankSum
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BaseQRankSum
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DP
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QD
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

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

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

East Asian
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num of homozygotes: 0

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

Other
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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

South Asian
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East Asian
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European (Finnish)
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European (Non-Finnish)
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MQ
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BaseQRankSum
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InbreedingCoeff
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DP
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QD
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ClippingRankSum
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FS
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ReadPosRankSum
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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European (Non-Finnish)
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allele frequency: 1.719572170443993e-5
allele num: 58154
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

Other
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QD
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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MQ
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VQSLOD
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ReadPosRankSum
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FS
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele num: 15680
num of homozygotes: 0

European (Finnish)
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Latino
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Other
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East Asian
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African
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European (Non-Finnish)
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ClippingRankSum
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BaseQRankSum
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QD
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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MQ
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MQRankSum
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 59862
num of homozygotes: 0

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

Other
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South Asian
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FS
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VQSLOD
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DP
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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MQ
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BaseQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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European (Finnish)
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South Asian
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African
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European (Non-Finnish)
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ReadPosRankSum
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DP
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MQRankSum
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InbreedingCoeff
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QD
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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MQ
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FS
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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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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
all individuals: 836
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.628120893561104e-4
allele num: 15220
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.182011030971574e-4
allele num: 9428
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 5.247966413014956e-4
allele num: 7622
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 9.83671060397403e-5
allele num: 10166
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.321155762205248e-4
allele num: 6022
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 23
allele frequency: 4.021822760019584e-4
allele num: 57188
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.979e0

VQSLOD
type: SiteQuality
SIO_000300: -3.031e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.53e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.64e-2

DP
type: SiteQuality
SIO_000300: 1.656898e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.24e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2068
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15876
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8242
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61684
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9914
num of homozygotes: 0

Latino
type: Population
allele count: 29
allele frequency: 2.672318466642094e-3
allele num: 10852
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.07e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

DP
type: SiteQuality
SIO_000300: 1.706973e6

VQSLOD
type: SiteQuality
SIO_000300: 4.81e0

QD
type: SiteQuality
SIO_000300: 1.544e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11262
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16376
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65936
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16333178222429e-4
allele num: 8596
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.136582e6

MQ
type: SiteQuality
SIO_000300: 5.828e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.693e0

QD
type: SiteQuality
SIO_000300: 1.364e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.81e-1

GenotypeDepth
all individuals: 1946
bin: 5.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 10353
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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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variant carriers: 1

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3628
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GenotypeQuality
all individuals: 2014
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11338
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.010959894014212e-5
allele num: 66424
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-1

FS
type: SiteQuality
SIO_000300: 3.914e0

QD
type: SiteQuality
SIO_000300: 9.16e0

MQ
type: SiteQuality
SIO_000300: 5.317e1

MQRankSum
type: SiteQuality
SIO_000300: 3.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

DP
type: SiteQuality
SIO_000300: 2.152213e6

VQSLOD
type: SiteQuality
SIO_000300: -1.379e0

GenotypeDepth
all individuals: 5348
bin: 4.25e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11340
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06501698204755e-5
allele num: 16488
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66444
num of homozygotes: 0

BaseQRankSum
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SIO_000300: -2.58e-1

MQ
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SIO_000300: 5.468e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.86e-1

ClippingRankSum
type: SiteQuality
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DP
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FS
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VQSLOD
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

QD
type: SiteQuality
SIO_000300: 7.2e-1

MQRankSum
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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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GenotypeQuality
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variant carriers: 0

African
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allele count: 1
allele frequency: 9.671179883945841e-5
allele num: 10340
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11362
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.504302304591131e-5
allele num: 66476
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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FS
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QD
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MQ
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3885
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2908
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17673
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5642
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2896
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3633
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2015
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21638
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504302304591131e-5
allele num: 66476
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11362
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.685e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.202e0

FS
type: SiteQuality
SIO_000300: 2.017e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.36e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 6.74e0

MQ
type: SiteQuality
SIO_000300: 5.522e1

MQRankSum
type: SiteQuality
SIO_000300: -3.505e0

DP
type: SiteQuality
SIO_000300: 2.154289e6

GenotypeDepth
all individuals: 3725
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 232
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10371
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 16254
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 55
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 121
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9475
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6019
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3885
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5640
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21642
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 62
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2906
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2897
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17671
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2017
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3632
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504166541319455e-5
allele num: 66482
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11362
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.533e0

QD
type: SiteQuality
SIO_000300: 7.63e0

MQRankSum
type: SiteQuality
SIO_000300: 1.64e0

MQ
type: SiteQuality
SIO_000300: 5.591e1

VQSLOD
type: SiteQuality
SIO_000300: -1.312e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.412e0

DP
type: SiteQuality
SIO_000300: 2.153907e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-1

GenotypeDepth
all individuals: 64
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 47
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2534
bin: 5.25e1
variant carriers: 2

GenotypeDepth
all individuals: 6021
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1387
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 503
bin: 9.75e1
variant carriers: 2