6-136600863-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600863
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600862
    reference: chr 6
allele count: 2
allele frequency: 7.998080460689434e-5
allele num: 25006
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.104+37delA
  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.104+37delA
  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.104+37delA
  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.104+37delA
  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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.330delA
  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.104+37delA
  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.104+37delA
  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.104+37delA
  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.104+37delA
  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.104+37delA
  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.104+37delA
  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.104+37delA
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21454
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14541
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7078
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4063
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7125
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: AT
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD

http://identifiers.org/exac.variant/6-136600863-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600863
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600863
    reference: chr 6
allele count: 1
allele frequency: 3.999040230344717e-5
allele num: 25006
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.104+38T>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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.331T>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.104+38T>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.104+38T>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.104+38T>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.104+38T>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.104+38T>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.104+38T>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.104+38T>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.104+38T>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.104+38T>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.104+38T>G
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14541
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21454
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7078
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7125
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

6-136600866-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600866
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600866
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 70668
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.104+35A>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.104+35A>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.104+35A>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.104+35A>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.104+35A>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.104+35A>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.104+35A>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.104+35A>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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.328A>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.104+35A>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.104+35A>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.104+35A>G
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5769
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18793
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15496
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8585
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5512
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
reference allele: T
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

6-136600866-TAATTATTTTAAAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600866
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600853
    reference: chr 6
allele count: 2
allele frequency: 2.830135280466406e-5
allele num: 70668
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000528229
  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: 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: ENSP00000376159
  ensembl transcript: ENST00000392348
  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: ENSP00000431734
  ensembl transcript: ENST00000529826
  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: ENSP00000434826
  ensembl transcript: ENST00000527759
  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: 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: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8585
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15496
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18793
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5769
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5512
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6645
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: TAATTATTTTAAAA
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

6-136600875-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600875
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600875
    reference: chr 6
allele count: 1
allele frequency: 4.46548182548897e-5
allele num: 22394
alternate allele: A
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.104+26A>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.104+26A>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.104+26A>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.104+26A>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.104+26A>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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.319A>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.104+26A>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.104+26A>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.104+26A>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.104+26A>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.104+26A>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.104+26A>T
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7614
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15014
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14683
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

6-136600876-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600876
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600876
    reference: chr 6
allele count: 1
allele frequency: 4.797543657647284e-5
allele num: 20844
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.318T>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.104+25T>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.104+25T>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.104+25T>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.104+25T>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.104+25T>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.104+25T>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.104+25T>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.104+25T>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.104+25T>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.104+25T>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.104+25T>C
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14608
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14895
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3737
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2437
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

6-136600881-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600881
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600882
    reference: chr 6
allele count: 2
allele frequency: 8.448086508405846e-5
allele num: 23674
alternate allele: TG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.104+19_104+20insC
  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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.312_313insC
  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.104+19_104+20insC
  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.104+19_104+20insC
  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.104+19_104+20insC
  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.104+19_104+20insC
  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.104+19_104+20insC
  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.104+19_104+20insC
  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.104+19_104+20insC
  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.104+19_104+20insC
  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.104+19_104+20insC
  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.104+19_104+20insC
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11890
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13802
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9149
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12968
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4106
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD

6-136600882-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600882
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600882
    reference: chr 6
allele count: 29
allele frequency: 1.226008286124968e-3
allele num: 23654
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.312A>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.104+19A>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.104+19A>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.104+19A>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.104+19A>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.104+19A>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.104+19A>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.104+19A>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.104+19A>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.104+19A>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.104+19A>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.104+19A>T
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13615
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4176
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 12799
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2666
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9250
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11975
  bin: 1.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

6-136600883-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600883
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600883
    reference: chr 6
allele count: 1
allele frequency: 9.6237128284092e-6
allele num: 103910
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.104+18A>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.104+18A>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.104+18A>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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.311A>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.104+18A>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.104+18A>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.104+18A>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.104+18A>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.104+18A>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.104+18A>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.104+18A>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.104+18A>G
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4491
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7240
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7605
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12319
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9837
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12358
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

6-136600883-T-TCTGG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600883
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600887
    reference: chr 6
allele count: 2
allele frequency: 1.92474256568184e-5
allele num: 103910
alternate allele: TCTGG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.104+17_104+18insCCAG
  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.104+17_104+18insCCAG
  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.104+17_104+18insCCAG
  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.104+17_104+18insCCAG
  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.104+17_104+18insCCAG
  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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.310_311insCCAG
  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.104+17_104+18insCCAG
  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.104+17_104+18insCCAG
  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.104+17_104+18insCCAG
  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.104+17_104+18insCCAG
  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.104+17_104+18insCCAG
  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.104+17_104+18insCCAG
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12358
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12319
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7605
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9837
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum

6-136600885-A-ACG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600885
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600887
    reference: chr 6
allele count: 2
allele frequency: 7.22700007227e-5
allele num: 27674
alternate allele: ACG
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.104+15_104+16insCG
  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.104+15_104+16insCG
  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.104+15_104+16insCG
  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.104+15_104+16insCG
  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.104+15_104+16insCG
  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.104+15_104+16insCG
  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.104+15_104+16insCG
  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.104+15_104+16insCG
  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.104+15_104+16insCG
  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.104+15_104+16insCG
  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.104+15_104+16insCG
  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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.308_309insCG
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8243
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12268
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2812
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6420
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5200
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD

6-136600887-GCACATTAAATC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600887
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600876
    reference: chr 6
allele count: 2
allele frequency: 7.010164738871364e-5
allele num: 28530
alternate allele: G
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: 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: 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: ENSP00000433822
  ensembl transcript: ENST00000534269
  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: 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: 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: 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: ENST00000528229
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12027
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7716
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2899
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8245
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5340
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6019
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13148
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.104+3_104+13delGATTTAATGTG
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: GCACATTAAATC
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum

6-136600888-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600888
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600888
    reference: chr 6
allele count: 1
allele frequency: 3.446611980423244e-5
allele num: 29014
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.104+13G>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.104+13G>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.104+13G>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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.306G>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.104+13G>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.104+13G>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.104+13G>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.104+13G>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.104+13G>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.104+13G>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.104+13G>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.104+13G>A
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13281
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8302
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7557
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5824
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11973
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum

6-136600890-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600890
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600890
    reference: chr 6
allele count: 2
allele frequency: 7.051191651389085e-5
allele num: 28364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.104+11G>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.104+11G>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.104+11G>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.104+11G>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.104+11G>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.104+11G>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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.304G>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.104+11G>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.104+11G>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.104+11G>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.104+11G>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.104+11G>A
  variant of: http://identifiers.org/hgnc/16863
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11813
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5377
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7098
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5705
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

6-136600896-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600896
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600896
    reference: chr 6
allele count: 1
allele frequency: 3.702332469455757e-5
allele num: 27010
alternate allele: G
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.104+5T>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.104+5T>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.104+5T>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.104+5T>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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.298T>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.104+5T>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.104+5T>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.104+5T>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.104+5T>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.104+5T>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.104+5T>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.104+5T>C
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: splice region
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3691
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.104+5T>C
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-136600908-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600908
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600908
    reference: chr 6
allele count: 1
allele frequency: 8.36050497450046e-6
allele num: 119610
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.97C>G
  hgvsp: ENSP00000436216.1:p.Arg33Gly
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.97C>G
  hgvsp: ENSP00000433822.1:p.Arg33Gly
  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.97C>G
  hgvsp: ENSP00000435441.1:p.Arg33Gly
  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.97C>G
  hgvsp: ENSP00000434826.1:p.Arg33Gly
  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.97C>G
  hgvsp: ENSP00000436501.1:p.Arg33Gly
  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.97C>G
  hgvsp: ENSP00000433505.1:p.Arg33Gly
  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.97C>G
  hgvsp: ENSP00000431734.1:p.Arg33Gly
  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.97C>G
  hgvsp: ENSP00000229446.5:p.Arg33Gly
  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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.286C>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.97C>G
  hgvsp: ENSP00000435210.1:p.Arg33Gly
  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.97C>G
  hgvsp: ENSP00000376159.2:p.Arg33Gly
  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.97C>G
  hgvsp: ENSP00000436142.1:p.Arg33Gly
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15451
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12480
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg33Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

6-136600924-AGATCTT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600924
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600918
    reference: chr 6
allele count: 1
allele frequency: 8.300683976359652e-6
allele num: 120472
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.75_80delAAGATC
  hgvsp: ENSP00000435210.1:p.Arg26_Ser27del
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.75_80delAAGATC
  hgvsp: ENSP00000229446.5:p.Arg26_Ser27del
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.75_80delAAGATC
  hgvsp: ENSP00000436142.1:p.Arg26_Ser27del
  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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.264_269delAAGATC
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.75_80delAAGATC
  hgvsp: ENSP00000433822.1:p.Arg26_Ser27del
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.75_80delAAGATC
  hgvsp: ENSP00000433505.1:p.Arg26_Ser27del
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.75_80delAAGATC
  hgvsp: ENSP00000436216.1:p.Arg26_Ser27del
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.75_80delAAGATC
  hgvsp: ENSP00000435441.1:p.Arg26_Ser27del
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.75_80delAAGATC
  hgvsp: ENSP00000434826.1:p.Arg26_Ser27del
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.75_80delAAGATC
  hgvsp: ENSP00000376159.2:p.Arg26_Ser27del
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.75_80delAAGATC
  hgvsp: ENSP00000431734.1:p.Arg26_Ser27del
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.75_80delAAGATC
  hgvsp: ENSP00000436501.1:p.Arg26_Ser27del
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 19700
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12649
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17021
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg26_Ser27del
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: AGATCTT
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum

6-136600929-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600929
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600929
    reference: chr 6
allele count: 6
allele frequency: 4.976362279173924e-5
allele num: 120570
alternate allele: C
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.76A>G
  hgvsp: ENSP00000433505.1:p.Arg26Gly
  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.76A>G
  hgvsp: ENSP00000434826.1:p.Arg26Gly
  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.76A>G
  hgvsp: ENSP00000436142.1:p.Arg26Gly
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.76A>G
  hgvsp: ENSP00000433822.1:p.Arg26Gly
  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.76A>G
  hgvsp: ENSP00000435210.1:p.Arg26Gly
  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.76A>G
  hgvsp: ENSP00000436216.1:p.Arg26Gly
  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.76A>G
  hgvsp: ENSP00000431734.1:p.Arg26Gly
  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.76A>G
  hgvsp: ENSP00000376159.2:p.Arg26Gly
  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.76A>G
  hgvsp: ENSP00000229446.5:p.Arg26Gly
  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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.265A>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.76A>G
  hgvsp: ENSP00000435441.1:p.Arg26Gly
  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.76A>G
  hgvsp: ENSP00000436501.1:p.Arg26Gly
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4518
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12668
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg26Gly
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

6-136600933-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600933
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600933
    reference: chr 6
allele count: 1
allele frequency: 8.288437629506838e-6
allele num: 120650
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.72A>T
  hgvsp: ENSP00000434826.1:p.Arg24Ser
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.72A>T
  hgvsp: ENSP00000433822.1:p.Arg24Ser
  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.72A>T
  hgvsp: ENSP00000433505.1:p.Arg24Ser
  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.72A>T
  hgvsp: ENSP00000436142.1:p.Arg24Ser
  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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.261A>T
  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.72A>T
  hgvsp: ENSP00000435210.1:p.Arg24Ser
  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.72A>T
  hgvsp: ENSP00000229446.5:p.Arg24Ser
  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.72A>T
  hgvsp: ENSP00000431734.1:p.Arg24Ser
  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.72A>T
  hgvsp: ENSP00000436216.1:p.Arg24Ser
  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.72A>T
  hgvsp: ENSP00000435441.1:p.Arg24Ser
  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.72A>T
  hgvsp: ENSP00000376159.2:p.Arg24Ser
  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.72A>T
  hgvsp: ENSP00000436501.1:p.Arg24Ser
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17074
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19831
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg24Ser
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ

6-136600936-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600936
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600936
    reference: chr 6
allele count: 2
allele frequency: 1.656534199148542e-5
allele num: 120734
alternate allele: C
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.69A>G
  hgvsp: ENST00000530429.1:c.69A>G(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.69A>G
  hgvsp: ENST00000529826.1:c.69A>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.69A>G
  hgvsp: ENST00000527613.1:c.69A>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.69A>G
  hgvsp: ENST00000527759.1:c.69A>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.69A>G
  hgvsp: ENST00000392348.2:c.69A>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: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.69A>G
  hgvsp: ENST00000534269.1:c.69A>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: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.69A>G
  hgvsp: ENST00000532384.1:c.69A>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.69A>G
  hgvsp: ENST00000530767.1:c.69A>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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.258A>G
  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.69A>G
  hgvsp: ENST00000531224.1:c.69A>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.69A>G
  hgvsp: ENST00000353331.4:c.69A>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.69A>G
  hgvsp: ENST00000527536.1:c.69A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19856
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser23Ser
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

6-136600940-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600940
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600940
    reference: chr 6
allele count: 8
allele frequency: 6.623942239223673e-5
allele num: 120774
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.65G>A
  hgvsp: ENSP00000431734.1:p.Arg22Gln
  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.65G>A
  hgvsp: ENSP00000436216.1:p.Arg22Gln
  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.65G>A
  hgvsp: ENSP00000436501.1:p.Arg22Gln
  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.65G>A
  hgvsp: ENSP00000229446.5:p.Arg22Gln
  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.65G>A
  hgvsp: ENSP00000436142.1:p.Arg22Gln
  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.65G>A
  hgvsp: ENSP00000433505.1:p.Arg22Gln
  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.65G>A
  hgvsp: ENSP00000435210.1:p.Arg22Gln
  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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.254G>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.65G>A
  hgvsp: ENSP00000433822.1:p.Arg22Gln
  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.65G>A
  hgvsp: ENSP00000434826.1:p.Arg22Gln
  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.65G>A
  hgvsp: ENSP00000376159.2:p.Arg22Gln
  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.65G>A
  hgvsp: ENSP00000435441.1:p.Arg22Gln
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17090
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12704
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg22Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

6-136600941-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600941
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600941
    reference: chr 6
allele count: 4
allele frequency: 3.311422752785734e-5
allele num: 120794
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.64C>T
  hgvsp: ENSP00000431734.1:p.Arg22Ter
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.64C>T
  hgvsp: ENSP00000433505.1:p.Arg22Ter
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.64C>T
  hgvsp: ENSP00000433822.1:p.Arg22Ter
  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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.253C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.64C>T
  hgvsp: ENSP00000436216.1:p.Arg22Ter
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.64C>T
  hgvsp: ENSP00000229446.5:p.Arg22Ter
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.64C>T
  hgvsp: ENSP00000436501.1:p.Arg22Ter
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.64C>T
  hgvsp: ENSP00000434826.1:p.Arg22Ter
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.64C>T
  hgvsp: ENSP00000376159.2:p.Arg22Ter
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.64C>T
  hgvsp: ENSP00000435210.1:p.Arg22Ter
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.64C>T
  hgvsp: ENSP00000435441.1:p.Arg22Ter
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.64C>T
  hgvsp: ENSP00000436142.1:p.Arg22Ter
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4521
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Arg22Ter
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

6-136600945-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600945
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600945
    reference: chr 6
allele count: 2
allele frequency: 1.655355073663301e-5
allele num: 120820
alternate allele: G
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.60T>C
  hgvsp: ENST00000530429.1:c.60T>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: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.60T>C
  hgvsp: ENST00000534269.1:c.60T>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.60T>C
  hgvsp: ENST00000527759.1:c.60T>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.60T>C
  hgvsp: ENST00000527613.1:c.60T>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.60T>C
  hgvsp: ENST00000527536.1:c.60T>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.60T>C
  hgvsp: ENST00000532384.1:c.60T>C(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.60T>C
  hgvsp: ENST00000529826.1:c.60T>C(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.60T>C
  hgvsp: ENST00000353331.4:c.60T>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.60T>C
  hgvsp: ENST00000531224.1:c.60T>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.60T>C
  hgvsp: ENST00000530767.1:c.60T>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.60T>C
  hgvsp: ENST00000392348.2:c.60T>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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.249T>C
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 4523
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19923
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12706
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17096
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser20Ser
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: A
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-136600949-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600949
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600949
    reference: chr 6
allele count: 7252
allele frequency: 6.113640195582532e-2
allele num: 118620
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.56C>T
  hgvsp: ENSP00000435441.1:p.Ser19Phe
  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.56C>T
  hgvsp: ENSP00000229446.5:p.Ser19Phe
  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.56C>T
  hgvsp: ENSP00000436142.1:p.Ser19Phe
  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.56C>T
  hgvsp: ENSP00000436501.1:p.Ser19Phe
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.56C>T
  hgvsp: ENSP00000433822.1:p.Ser19Phe
  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.56C>T
  hgvsp: ENSP00000434826.1:p.Ser19Phe
  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.56C>T
  hgvsp: ENSP00000431734.1:p.Ser19Phe
  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.56C>T
  hgvsp: ENSP00000436216.1:p.Ser19Phe
  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.56C>T
  hgvsp: ENSP00000435210.1:p.Ser19Phe
  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.56C>T
  hgvsp: ENSP00000433505.1:p.Ser19Phe
  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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.245C>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.56C>T
  hgvsp: ENSP00000376159.2:p.Ser19Phe
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 6.75e1
  variant carriers: 670
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.75e1
  variant carriers: 343
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 4.25e1
  variant carriers: 427
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 9.75e1
  variant carriers: 1376
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.25e1
  variant carriers: 274
genotype depth: GenotypeDepth
  all individuals: 3828
  bin: 3.75e1
  variant carriers: 264
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 11211
  bin: 3.25e1
  variant carriers: 170
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 7.25e1
  variant carriers: 572
genotype depth: GenotypeDepth
  all individuals: 18251
  bin: 2.75e1
  variant carriers: 87
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 5.25e1
  variant carriers: 649
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 8.25e1
  variant carriers: 393
genotype quality: GenotypeQuality
hgvs: p.Ser19Phe
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

6-136600950-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600950
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600950
    reference: chr 6
allele count: 1
allele frequency: 8.274583788435442e-6
allele num: 120852
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.55T>A
  hgvsp: ENSP00000229446.5:p.Ser19Thr
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.55T>A
  hgvsp: ENSP00000433822.1:p.Ser19Thr
  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.55T>A
  hgvsp: ENSP00000436142.1:p.Ser19Thr
  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.55T>A
  hgvsp: ENSP00000435441.1:p.Ser19Thr
  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.55T>A
  hgvsp: ENSP00000434826.1:p.Ser19Thr
  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.55T>A
  hgvsp: ENSP00000376159.2:p.Ser19Thr
  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.55T>A
  hgvsp: ENSP00000431734.1:p.Ser19Thr
  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.55T>A
  hgvsp: ENSP00000433505.1:p.Ser19Thr
  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.55T>A
  hgvsp: ENSP00000435210.1:p.Ser19Thr
  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.55T>A
  hgvsp: ENSP00000436501.1:p.Ser19Thr
  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.55T>A
  hgvsp: ENSP00000436216.1:p.Ser19Thr
  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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.244T>A
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14019
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4363
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser19Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum

6-136600951-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600951
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600951
    reference: chr 6
allele count: 4
allele frequency: 3.309723969020984e-5
allele num: 120856
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.54G>C
  hgvsp: ENSP00000436501.1:p.Gln18His
  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.54G>C
  hgvsp: ENSP00000436142.1:p.Gln18His
  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.54G>C
  hgvsp: ENSP00000431734.1:p.Gln18His
  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.54G>C
  hgvsp: ENSP00000436216.1:p.Gln18His
  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.54G>C
  hgvsp: ENSP00000434826.1:p.Gln18His
  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.54G>C
  hgvsp: ENSP00000229446.5:p.Gln18His
  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.54G>C
  hgvsp: ENSP00000435210.1:p.Gln18His
  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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.243G>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.54G>C
  hgvsp: ENSP00000376159.2:p.Gln18His
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.54G>C
  hgvsp: ENSP00000433822.1:p.Gln18His
  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.54G>C
  hgvsp: ENSP00000433505.1:p.Gln18His
  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.54G>C
  hgvsp: ENSP00000435441.1:p.Gln18His
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14020
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4364
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln18His
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP

6-136600955-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600955
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600955
    reference: chr 6
allele count: 3
allele frequency: 2.482251898922703e-5
allele num: 120858
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.50C>T
  hgvsp: ENSP00000229446.5:p.Ser17Leu
  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.50C>T
  hgvsp: ENSP00000435210.1:p.Ser17Leu
  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.50C>T
  hgvsp: ENSP00000376159.2:p.Ser17Leu
  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.50C>T
  hgvsp: ENSP00000433505.1:p.Ser17Leu
  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.50C>T
  hgvsp: ENSP00000434826.1:p.Ser17Leu
  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.50C>T
  hgvsp: ENSP00000436501.1:p.Ser17Leu
  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.50C>T
  hgvsp: ENSP00000436142.1:p.Ser17Leu
  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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.239C>T
  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.50C>T
  hgvsp: ENSP00000431734.1:p.Ser17Leu
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.50C>T
  hgvsp: ENSP00000433822.1:p.Ser17Leu
  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.50C>T
  hgvsp: ENSP00000436216.1:p.Ser17Leu
  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.50C>T
  hgvsp: ENSP00000435441.1:p.Ser17Leu
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14019
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15442
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22026
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4368
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser17Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-136600957-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600957
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600957
    reference: chr 6
allele count: 1
allele frequency: 8.274446853227862e-6
allele num: 120854
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.48A>T
  hgvsp: ENSP00000431734.1:p.Arg16Ser
  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.48A>T
  hgvsp: ENSP00000436501.1:p.Arg16Ser
  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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.237A>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.48A>T
  hgvsp: ENSP00000433505.1:p.Arg16Ser
  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.48A>T
  hgvsp: ENSP00000229446.5:p.Arg16Ser
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.48A>T
  hgvsp: ENSP00000433822.1:p.Arg16Ser
  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.48A>T
  hgvsp: ENSP00000436216.1:p.Arg16Ser
  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.48A>T
  hgvsp: ENSP00000436142.1:p.Arg16Ser
  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.48A>T
  hgvsp: ENSP00000435210.1:p.Arg16Ser
  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.48A>T
  hgvsp: ENSP00000435441.1:p.Arg16Ser
  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.48A>T
  hgvsp: ENSP00000434826.1:p.Arg16Ser
  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.48A>T
  hgvsp: ENSP00000376159.2:p.Arg16Ser
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 15427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22037
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14018
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg16Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

6-136600958-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600958
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600958
    reference: chr 6
allele count: 1
allele frequency: 8.274994621253496e-6
allele num: 120846
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.47G>A
  hgvsp: ENSP00000436216.1:p.Arg16Lys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.47G>A
  hgvsp: ENSP00000433822.1:p.Arg16Lys
  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.47G>A
  hgvsp: ENSP00000435441.1:p.Arg16Lys
  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.47G>A
  hgvsp: ENSP00000434826.1:p.Arg16Lys
  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.47G>A
  hgvsp: ENSP00000436501.1:p.Arg16Lys
  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.47G>A
  hgvsp: ENSP00000435210.1:p.Arg16Lys
  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.47G>A
  hgvsp: ENSP00000433505.1:p.Arg16Lys
  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.47G>A
  hgvsp: ENSP00000431734.1:p.Arg16Lys
  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.47G>A
  hgvsp: ENSP00000436142.1:p.Arg16Lys
  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.47G>A
  hgvsp: ENSP00000229446.5:p.Arg16Lys
  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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.236G>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.47G>A
  hgvsp: ENSP00000376159.2:p.Arg16Lys
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15414
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4366
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14016
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg16Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum

6-136600961-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600961
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600961
    reference: chr 6
allele count: 3
allele frequency: 2.48245730173441e-5
allele num: 120848
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.44C>G
  hgvsp: ENSP00000436501.1:p.Ser15Cys
  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.44C>G
  hgvsp: ENSP00000435210.1:p.Ser15Cys
  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.44C>G
  hgvsp: ENSP00000229446.5:p.Ser15Cys
  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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.233C>G
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.44C>G
  hgvsp: ENSP00000433822.1:p.Ser15Cys
  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.44C>G
  hgvsp: ENSP00000436142.1:p.Ser15Cys
  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.44C>G
  hgvsp: ENSP00000434826.1:p.Ser15Cys
  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.44C>G
  hgvsp: ENSP00000433505.1:p.Ser15Cys
  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.44C>G
  hgvsp: ENSP00000431734.1:p.Ser15Cys
  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.44C>G
  hgvsp: ENSP00000436216.1:p.Ser15Cys
  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.44C>G
  hgvsp: ENSP00000376159.2:p.Ser15Cys
  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.44C>G
  hgvsp: ENSP00000435441.1:p.Ser15Cys
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14018
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser15Cys
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum

6-136600962-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600962
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600962
    reference: chr 6
allele count: 1
allele frequency: 8.274720728175424e-6
allele num: 120850
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.232T>A
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.43T>A
  hgvsp: ENSP00000433822.1:p.Ser15Thr
  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.43T>A
  hgvsp: ENSP00000435441.1:p.Ser15Thr
  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.43T>A
  hgvsp: ENSP00000435210.1:p.Ser15Thr
  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.43T>A
  hgvsp: ENSP00000436142.1:p.Ser15Thr
  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.43T>A
  hgvsp: ENSP00000436216.1:p.Ser15Thr
  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.43T>A
  hgvsp: ENSP00000229446.5:p.Ser15Thr
  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.43T>A
  hgvsp: ENSP00000434826.1:p.Ser15Thr
  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.43T>A
  hgvsp: ENSP00000376159.2:p.Ser15Thr
  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.43T>A
  hgvsp: ENSP00000433505.1:p.Ser15Thr
  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.43T>A
  hgvsp: ENSP00000436501.1:p.Ser15Thr
  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.43T>A
  hgvsp: ENSP00000431734.1:p.Ser15Thr
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 22040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15396
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14016
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser15Thr
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

6-136600964-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600964
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600964
    reference: chr 6
allele count: 2
allele frequency: 1.655218074981379e-5
allele num: 120830
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.41A>T
  hgvsp: ENSP00000435210.1:p.Lys14Met
  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.41A>T
  hgvsp: ENSP00000434826.1:p.Lys14Met
  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.41A>T
  hgvsp: ENSP00000436216.1:p.Lys14Met
  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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.230A>T
  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.41A>T
  hgvsp: ENSP00000431734.1:p.Lys14Met
  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.41A>T
  hgvsp: ENSP00000229446.5:p.Lys14Met
  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.41A>T
  hgvsp: ENSP00000436142.1:p.Lys14Met
  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.41A>T
  hgvsp: ENSP00000436501.1:p.Lys14Met
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.41A>T
  hgvsp: ENSP00000433822.1:p.Lys14Met
  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.41A>T
  hgvsp: ENSP00000435441.1:p.Lys14Met
  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.41A>T
  hgvsp: ENSP00000433505.1:p.Lys14Met
  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.41A>T
  hgvsp: ENSP00000376159.2:p.Lys14Met
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4364
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14020
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15364
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys14Met
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

6-136600966-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600966
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600966
    reference: chr 6
allele count: 1
allele frequency: 8.277186418792524e-6
allele num: 120814
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.39A>C
  hgvsp: ENST00000353331.4:c.39A>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.39A>C
  hgvsp: ENST00000532384.1:c.39A>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.39A>C
  hgvsp: ENST00000392348.2:c.39A>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.39A>C
  hgvsp: ENST00000531224.1:c.39A>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.39A>C
  hgvsp: ENST00000530767.1:c.39A>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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.228A>C
  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.39A>C
  hgvsp: ENST00000527613.1:c.39A>C(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.39A>C
  hgvsp: ENST00000529826.1:c.39A>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.39A>C
  hgvsp: ENST00000530429.1:c.39A>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.39A>C
  hgvsp: ENST00000527759.1:c.39A>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: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.39A>C
  hgvsp: ENST00000534269.1:c.39A>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.39A>C
  hgvsp: ENST00000527536.1:c.39A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15323
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4364
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22050
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14018
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser13Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: QD

6-136600970-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600970
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600970
    reference: chr 6
allele count: 2
allele frequency: 1.656095258599275e-5
allele num: 120766
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.35G>C
  hgvsp: ENSP00000431734.1:p.Arg12Thr
  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.35G>C
  hgvsp: ENSP00000229446.5:p.Arg12Thr
  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.35G>C
  hgvsp: ENSP00000436501.1:p.Arg12Thr
  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.35G>C
  hgvsp: ENSP00000433505.1:p.Arg12Thr
  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.35G>C
  hgvsp: ENSP00000434826.1:p.Arg12Thr
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.35G>C
  hgvsp: ENSP00000433822.1:p.Arg12Thr
  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.35G>C
  hgvsp: ENSP00000435441.1:p.Arg12Thr
  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.35G>C
  hgvsp: ENSP00000435210.1:p.Arg12Thr
  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.35G>C
  hgvsp: ENSP00000436142.1:p.Arg12Thr
  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.35G>C
  hgvsp: ENSP00000436216.1:p.Arg12Thr
  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.35G>C
  hgvsp: ENSP00000376159.2:p.Arg12Thr
  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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.224G>C
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15250
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14015
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg12Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

6-136600971-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600971
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600971
    reference: chr 6
allele count: 1
allele frequency: 8.281847845891375e-6
allele num: 120746
alternate allele: G
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.34A>C
  hgvsp: ENST00000532384.1:c.34A>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.34A>C
  hgvsp: ENST00000530767.1:c.34A>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.34A>C
  hgvsp: ENST00000392348.2:c.34A>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.34A>C
  hgvsp: ENST00000527613.1:c.34A>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.34A>C
  hgvsp: ENST00000530429.1:c.34A>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.34A>C
  hgvsp: ENST00000527536.1:c.34A>C(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.34A>C
  hgvsp: ENST00000529826.1:c.34A>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.34A>C
  hgvsp: ENST00000531224.1:c.34A>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.34A>C
  hgvsp: ENST00000527759.1:c.34A>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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.223A>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.34A>C
  hgvsp: ENST00000353331.4:c.34A>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: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.34A>C
  hgvsp: ENST00000534269.1:c.34A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15214
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22075
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14012
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg12Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

6-136600973-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600973
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600973
    reference: chr 6
allele count: 3
allele frequency: 2.485212982752622e-5
allele num: 120714
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.32C>T
  hgvsp: ENSP00000435210.1:p.Ser11Leu
  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.32C>T
  hgvsp: ENSP00000376159.2:p.Ser11Leu
  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.32C>T
  hgvsp: ENSP00000431734.1:p.Ser11Leu
  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.32C>T
  hgvsp: ENSP00000436216.1:p.Ser11Leu
  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.32C>T
  hgvsp: ENSP00000436501.1:p.Ser11Leu
  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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.221C>T
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.32C>T
  hgvsp: ENSP00000433822.1:p.Ser11Leu
  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.32C>T
  hgvsp: ENSP00000433505.1:p.Ser11Leu
  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.32C>T
  hgvsp: ENSP00000434826.1:p.Ser11Leu
  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.32C>T
  hgvsp: ENSP00000435441.1:p.Ser11Leu
  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.32C>T
  hgvsp: ENSP00000229446.5:p.Ser11Leu
  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.32C>T
  hgvsp: ENSP00000436142.1:p.Ser11Leu
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22075
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15174
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser11Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

6-136600975-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600975
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600975
    reference: chr 6
allele count: 1
allele frequency: 8.284455048546906e-6
allele num: 120708
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.30T>C
  hgvsp: ENST00000529826.1:c.30T>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.30T>C
  hgvsp: ENST00000527759.1:c.30T>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.30T>C
  hgvsp: ENST00000530767.1:c.30T>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.30T>C
  hgvsp: ENST00000527613.1:c.30T>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.30T>C
  hgvsp: ENST00000392348.2:c.30T>C(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.30T>C
  hgvsp: ENST00000353331.4:c.30T>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.30T>C
  hgvsp: ENST00000530429.1:c.30T>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.30T>C
  hgvsp: ENST00000527536.1:c.30T>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.30T>C
  hgvsp: ENST00000532384.1:c.30T>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.30T>C
  hgvsp: ENST00000531224.1:c.30T>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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.219T>C
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.30T>C
  hgvsp: ENST00000534269.1:c.30T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4358
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15171
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22066
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser10Ser
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

6-136600977-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600977
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600977
    reference: chr 6
allele count: 2
allele frequency: 1.657934876318058e-5
allele num: 120632
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.28T>A
  hgvsp: ENSP00000436501.1:p.Ser10Thr
  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.28T>A
  hgvsp: ENSP00000229446.5:p.Ser10Thr
  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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.217T>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.28T>A
  hgvsp: ENSP00000431734.1:p.Ser10Thr
  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.28T>A
  hgvsp: ENSP00000436216.1:p.Ser10Thr
  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.28T>A
  hgvsp: ENSP00000436142.1:p.Ser10Thr
  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.28T>A
  hgvsp: ENSP00000376159.2:p.Ser10Thr
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.28T>A
  hgvsp: ENSP00000433822.1:p.Ser10Thr
  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.28T>A
  hgvsp: ENSP00000434826.1:p.Ser10Thr
  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.28T>A
  hgvsp: ENSP00000433505.1:p.Ser10Thr
  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.28T>A
  hgvsp: ENSP00000435210.1:p.Ser10Thr
  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.28T>A
  hgvsp: ENSP00000435441.1:p.Ser10Thr
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13992
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4352
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15084
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22074
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser10Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/6-136600978-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600978
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600978
    reference: chr 6
allele count: 1
allele frequency: 8.289262089888757e-6
allele num: 120638
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.27T>G
  hgvsp: ENSP00000434826.1:p.His9Gln
  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.27T>G
  hgvsp: ENSP00000436216.1:p.His9Gln
  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.27T>G
  hgvsp: ENSP00000431734.1:p.His9Gln
  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.27T>G
  hgvsp: ENSP00000435210.1:p.His9Gln
  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.27T>G
  hgvsp: ENSP00000436501.1:p.His9Gln
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.27T>G
  hgvsp: ENSP00000433822.1:p.His9Gln
  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.27T>G
  hgvsp: ENSP00000433505.1:p.His9Gln
  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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.216T>G
  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.27T>G
  hgvsp: ENSP00000376159.2:p.His9Gln
  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.27T>G
  hgvsp: ENSP00000436142.1:p.His9Gln
  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.27T>G
  hgvsp: ENSP00000229446.5:p.His9Gln
  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.27T>G
  hgvsp: ENSP00000435441.1:p.His9Gln
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15083
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His9Gln
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

6-136600980-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600980
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600980
    reference: chr 6
allele count: 4
allele frequency: 3.317189676905725e-5
allele num: 120584
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  hgvsc: ENST00000392348.2:c.25C>T
  hgvsp: ENSP00000376159.2:p.His9Tyr
  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.25C>T
  hgvsp: ENSP00000436501.1:p.His9Tyr
  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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.214C>T
  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.25C>T
  hgvsp: ENSP00000434826.1:p.His9Tyr
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.25C>T
  hgvsp: ENSP00000433822.1:p.His9Tyr
  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.25C>T
  hgvsp: ENSP00000431734.1:p.His9Tyr
  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.25C>T
  hgvsp: ENSP00000435210.1:p.His9Tyr
  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.25C>T
  hgvsp: ENSP00000436142.1:p.His9Tyr
  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.25C>T
  hgvsp: ENSP00000436216.1:p.His9Tyr
  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.25C>T
  hgvsp: ENSP00000433505.1:p.His9Tyr
  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.25C>T
  hgvsp: ENSP00000229446.5:p.His9Tyr
  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.25C>T
  hgvsp: ENSP00000435441.1:p.His9Tyr
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4352
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15006
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22056
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.His9Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

6-136600984-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600984
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600984
    reference: chr 6
allele count: 1
allele frequency: 8.304820117596252e-6
allele num: 120412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.21A>G
  hgvsp: ENST00000527536.1:c.21A>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.21A>G
  hgvsp: ENST00000530767.1:c.21A>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.21A>G
  hgvsp: ENST00000531224.1:c.21A>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.21A>G
  hgvsp: ENST00000353331.4:c.21A>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: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.21A>G
  hgvsp: ENST00000534269.1:c.21A>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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.210A>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.21A>G
  hgvsp: ENST00000530429.1:c.21A>G(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.21A>G
  hgvsp: ENST00000529826.1:c.21A>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.21A>G
  hgvsp: ENST00000392348.2:c.21A>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.21A>G
  hgvsp: ENST00000527759.1:c.21A>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: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.21A>G
  hgvsp: ENST00000532384.1:c.21A>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.21A>G
  hgvsp: ENST00000527613.1:c.21A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13993
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14766
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg7Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-136600991-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600991
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600991
    reference: chr 6
allele count: 1
allele frequency: 8.345016356232058e-6
allele num: 119832
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.14A>G
  hgvsp: ENSP00000229446.5:p.Asn5Ser
  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.14A>G
  hgvsp: ENSP00000435441.1:p.Asn5Ser
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.14A>G
  hgvsp: ENSP00000433822.1:p.Asn5Ser
  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.14A>G
  hgvsp: ENSP00000434826.1:p.Asn5Ser
  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.14A>G
  hgvsp: ENSP00000433505.1:p.Asn5Ser
  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.14A>G
  hgvsp: ENSP00000436501.1:p.Asn5Ser
  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.14A>G
  hgvsp: ENSP00000431734.1:p.Asn5Ser
  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.14A>G
  hgvsp: ENSP00000436216.1:p.Asn5Ser
  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.14A>G
  hgvsp: ENSP00000376159.2:p.Asn5Ser
  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.14A>G
  hgvsp: ENSP00000435210.1:p.Asn5Ser
  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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.203A>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.14A>G
  hgvsp: ENSP00000436142.1:p.Asn5Ser
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4351
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13944
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21873
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14019
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn5Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

6-136600994-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600994
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600994
    reference: chr 6
allele count: 2
allele frequency: 1.67319211591875e-5
allele num: 119532
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.200C>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.11C>A
  hgvsp: ENSP00000436216.1:p.Ser4Tyr
  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.11C>A
  hgvsp: ENSP00000433505.1:p.Ser4Tyr
  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.11C>A
  hgvsp: ENSP00000229446.5:p.Ser4Tyr
  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.11C>A
  hgvsp: ENSP00000436501.1:p.Ser4Tyr
  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.11C>A
  hgvsp: ENSP00000435210.1:p.Ser4Tyr
  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.11C>A
  hgvsp: ENSP00000434826.1:p.Ser4Tyr
  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.11C>A
  hgvsp: ENSP00000436142.1:p.Ser4Tyr
  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.11C>A
  hgvsp: ENSP00000431734.1:p.Ser4Tyr
  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.11C>A
  hgvsp: ENSP00000376159.2:p.Ser4Tyr
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.11C>A
  hgvsp: ENSP00000433822.1:p.Ser4Tyr
  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.11C>A
  hgvsp: ENSP00000435441.1:p.Ser4Tyr
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13576
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21736
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13930
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser4Tyr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

6-136600997-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600997
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600997
    reference: chr 6
allele count: 38
allele frequency: 3.200970399447411e-4
allele num: 118714
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.8G>A
  hgvsp: ENSP00000229446.5:p.Arg3His
  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.8G>A
  hgvsp: ENSP00000435210.1:p.Arg3His
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.8G>A
  hgvsp: ENSP00000433822.1:p.Arg3His
  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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.197G>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.8G>A
  hgvsp: ENSP00000434826.1:p.Arg3His
  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.8G>A
  hgvsp: ENSP00000436142.1:p.Arg3His
  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.8G>A
  hgvsp: ENSP00000431734.1:p.Arg3His
  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.8G>A
  hgvsp: ENSP00000376159.2:p.Arg3His
  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.8G>A
  hgvsp: ENSP00000433505.1:p.Arg3His
  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.8G>A
  hgvsp: ENSP00000436501.1:p.Arg3His
  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.8G>A
  hgvsp: ENSP00000436216.1:p.Arg3His
  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.8G>A
  hgvsp: ENSP00000435441.1:p.Arg3His
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 13879
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 12367
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg3His
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP

6-136600998-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136600998
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600998
    reference: chr 6
allele count: 9
allele frequency: 7.58022403773267e-5
allele num: 118730
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.7C>T
  hgvsp: ENSP00000229446.5:p.Arg3Cys
  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.7C>T
  hgvsp: ENSP00000436142.1:p.Arg3Cys
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.7C>T
  hgvsp: ENSP00000433822.1:p.Arg3Cys
  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.7C>T
  hgvsp: ENSP00000435441.1:p.Arg3Cys
  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.7C>T
  hgvsp: ENSP00000436501.1:p.Arg3Cys
  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.7C>T
  hgvsp: ENSP00000436216.1:p.Arg3Cys
  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.7C>T
  hgvsp: ENSP00000433505.1:p.Arg3Cys
  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.7C>T
  hgvsp: ENSP00000376159.2:p.Arg3Cys
  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.7C>T
  hgvsp: ENSP00000434826.1:p.Arg3Cys
  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.7C>T
  hgvsp: ENSP00000435210.1:p.Arg3Cys
  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.7C>T
  hgvsp: ENSP00000431734.1:p.Arg3Cys
  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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.196C>T
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21460
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12311
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg3Cys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

http://identifiers.org/exac.variant/6-136601000-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136601000
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136601000
    reference: chr 6
allele count: 1
allele frequency: 8.460380040271409e-6
allele num: 118198
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.5G>T
  hgvsp: ENSP00000433822.1:p.Gly2Val
  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.5G>T
  hgvsp: ENSP00000436216.1:p.Gly2Val
  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.5G>T
  hgvsp: ENSP00000436142.1:p.Gly2Val
  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.5G>T
  hgvsp: ENSP00000229446.5:p.Gly2Val
  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.5G>T
  hgvsp: ENSP00000435210.1:p.Gly2Val
  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.5G>T
  hgvsp: ENSP00000431734.1:p.Gly2Val
  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.5G>T
  hgvsp: ENSP00000376159.2:p.Gly2Val
  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.5G>T
  hgvsp: ENSP00000436501.1:p.Gly2Val
  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.5G>T
  hgvsp: ENSP00000435441.1:p.Gly2Val
  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.5G>T
  hgvsp: ENSP00000434826.1:p.Gly2Val
  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.5G>T
  hgvsp: ENSP00000433505.1:p.Gly2Val
  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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.194G>T
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21113
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11578
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly2Val
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

6-136601003-ATTTCT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136601003
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136600998
    reference: chr 6
allele count: 15
allele frequency: 1.27968877968878e-4
allele num: 117216
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: coding_sequence_variant
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.-4_1delAGAAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: coding_sequence_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.-4_1delAGAAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: coding_sequence_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.-4_1delAGAAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: coding_sequence_variant
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.-4_1delAGAAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: coding_sequence_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.-4_1delAGAAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: coding_sequence_variant
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.-4_1delAGAAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: coding_sequence_variant
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.-4_1delAGAAA
  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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.186_190delAGAAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: coding_sequence_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.-4_1delAGAAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: coding_sequence_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.-4_1delAGAAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: coding_sequence_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.-4_1delAGAAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: coding_sequence_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000376159
  ensembl transcript: ENST00000392348
  gene symbol: BCLAF1
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: coding sequence
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4286
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3611
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13514
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10243
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20231
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: ATTTCT
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

6-136601004-TTTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136601004
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136601001
    reference: chr 6
allele count: 1
allele frequency: 8.563256777817739e-6
allele num: 116778
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.187_189delGAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435441
  ensembl transcript: ENST00000527536
  gene symbol: BCLAF1
  hgvsc: ENST00000527536.1:c.-3_-1delGAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.-3_-1delGAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433822
  ensembl transcript: ENST00000534269
  gene symbol: BCLAF1
  hgvsc: ENST00000534269.1:c.-3_-1delGAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436142
  ensembl transcript: ENST00000530429
  gene symbol: BCLAF1
  hgvsc: ENST00000530429.1:c.-3_-1delGAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.-3_-1delGAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.-3_-1delGAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000433505
  ensembl transcript: ENST00000532384
  gene symbol: BCLAF1
  hgvsc: ENST00000532384.1:c.-3_-1delGAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000431734
  ensembl transcript: ENST00000529826
  gene symbol: BCLAF1
  hgvsc: ENST00000529826.1:c.-3_-1delGAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000435210
  ensembl transcript: ENST00000531224
  gene symbol: BCLAF1
  hgvsc: ENST00000531224.1:c.-3_-1delGAA
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436216
  ensembl transcript: ENST00000527613
  gene symbol: BCLAF1
  hgvsc: ENST00000527613.1:c.-3_-1delGAA
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: 5' UTR
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2767
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4255
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4014
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9916
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19767
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13310
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
reference allele: TTTC
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum

6-136601027-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136601027
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136601027
    reference: chr 6
allele count: 1
allele frequency: 1.060557853430905e-5
allele num: 94290
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.-10-13A>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.-10-13A>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.-10-13A>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.-10-13A>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.-10-13A>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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.180-13A>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.-10-13A>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.-10-13A>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.-10-13A>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.-10-13A>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.-10-13A>G
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6936
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18545
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9325
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6848
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6371
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/6-136601032-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136601032
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136601032
    reference: chr 6
allele count: 2
allele frequency: 2.333286667599981e-5
allele num: 85716
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000434826
  ensembl transcript: ENST00000527759
  gene symbol: BCLAF1
  hgvsc: ENST00000527759.1:c.-10-18G>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.-10-18G>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.-10-18G>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.-10-18G>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.-10-18G>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.-10-18G>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.-10-18G>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.-10-18G>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.-10-18G>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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.180-18G>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.-10-18G>T
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6925
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21397
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7760
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8270
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4208
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6623
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/6-136601032-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136601032
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136601033
    reference: chr 6
allele count: 35
allele frequency: 4.083251668299967e-4
allele num: 85716
alternate allele: CA
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.-10-19dupT
  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.-10-19dupT
  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.-10-19dupT
  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.-10-19dupT
  variant of: http://identifiers.org/hgnc/16863
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl transcript: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.180-19dupT
  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.-10-19dupT
  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.-10-19dupT
  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.-10-19dupT
  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.-10-19dupT
  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.-10-19dupT
  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.-10-19dupT
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8270
  bin: 1.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 6623
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7760
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21397
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4208
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6925
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD

6-136601040-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136601040
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136601040
    reference: chr 6
allele count: 1
allele frequency: 1.283433441141742e-5
allele num: 77916
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000229446
  ensembl transcript: ENST00000353331
  gene symbol: BCLAF1
  hgvsc: ENST00000353331.4:c.-10-26C>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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.180-26C>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.-10-26C>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.-10-26C>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.-10-26C>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.-10-26C>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.-10-26C>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.-10-26C>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.-10-26C>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.-10-26C>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.-10-26C>T
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10832
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3652
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3956
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22427
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10093
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD

6-136601053-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136601053
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136601053
    reference: chr 6
allele count: 3
allele frequency: 5.155702206640545e-5
allele num: 58188
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000029363
  ensembl protein: ENSP00000436501
  ensembl transcript: ENST00000530767
  gene symbol: BCLAF1
  hgvsc: ENST00000530767.1:c.-10-39T>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.-10-39T>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.-10-39T>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.-10-39T>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.-10-39T>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.-10-39T>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.-10-39T>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.-10-39T>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.-10-39T>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.-10-39T>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: ENST00000528229
  gene symbol: BCLAF1
  hgvsc: ENST00000528229.1:n.180-39T>C
  variant of: http://identifiers.org/hgnc/16863
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18030
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5052
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3637
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19291
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8988
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD

6-136665338-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136665338
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136665338
    reference: chr 6
allele count: 1
allele frequency: 1.60426091699554e-5
allele num: 62334
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000445737
  ensembl transcript: ENST00000544465
  gene symbol: MAP7
  hgvsc: ENST00000544465.1:c.*28A>G
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000346581
  ensembl transcript: ENST00000354570
  gene symbol: MAP7
  hgvsc: ENST00000354570.3:c.*28A>G
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414879
  ensembl transcript: ENST00000432797
  gene symbol: MAP7
  hgvsc: ENST00000432797.2:c.*28A>G
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414712
  ensembl transcript: ENST00000454590
  gene symbol: MAP7
  hgvsc: ENST00000454590.1:c.*28A>G
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000400790
  ensembl transcript: ENST00000438100
  gene symbol: MAP7
  hgvsc: ENST00000438100.2:c.*28A>G
  variant of: http://identifiers.org/hgnc/6869
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5269
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13919
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23934
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9617
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 883
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3767
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 758
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24662
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 816
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4969
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4693
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1551
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD

6-136665348-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136665348
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136665348
    reference: chr 6
allele count: 1
allele frequency: 1.56416192204217e-5
allele num: 63932
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000445737
  ensembl transcript: ENST00000544465
  gene symbol: MAP7
  hgvsc: ENST00000544465.1:c.*18C>A
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414879
  ensembl transcript: ENST00000432797
  gene symbol: MAP7
  hgvsc: ENST00000432797.2:c.*18C>A
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414712
  ensembl transcript: ENST00000454590
  gene symbol: MAP7
  hgvsc: ENST00000454590.1:c.*18C>A
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000400790
  ensembl transcript: ENST00000438100
  gene symbol: MAP7
  hgvsc: ENST00000438100.2:c.*18C>A
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000346581
  ensembl transcript: ENST00000354570
  gene symbol: MAP7
  hgvsc: ENST00000354570.3:c.*18C>A
  variant of: http://identifiers.org/hgnc/6869
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 7.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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  bin: 9.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 5.75e1
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genotype quality: GenotypeQuality
  all individuals: 863
  bin: 6.75e1
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genotype quality: GenotypeQuality
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  bin: 4.25e1
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 297
  bin: 7.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 3958
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 452
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/6-136665351-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136665351
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136665351
    reference: chr 6
allele count: 1
allele frequency: 1.553953257086027e-5
allele num: 64352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000445737
  ensembl transcript: ENST00000544465
  gene symbol: MAP7
  hgvsc: ENST00000544465.1:c.*15G>T
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414879
  ensembl transcript: ENST00000432797
  gene symbol: MAP7
  hgvsc: ENST00000432797.2:c.*15G>T
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000400790
  ensembl transcript: ENST00000438100
  gene symbol: MAP7
  hgvsc: ENST00000438100.2:c.*15G>T
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414712
  ensembl transcript: ENST00000454590
  gene symbol: MAP7
  hgvsc: ENST00000454590.1:c.*15G>T
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000346581
  ensembl transcript: ENST00000354570
  gene symbol: MAP7
  hgvsc: ENST00000354570.3:c.*15G>T
  variant of: http://identifiers.org/hgnc/6869
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4012
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
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genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10561
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1985
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 289
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 24165
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 107
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 115
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 184
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 387
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genotype quality: GenotypeQuality
  all individuals: 296
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

6-136665378-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136665378
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136665378
    reference: chr 6
allele count: 1
allele frequency: 1.48720999405116e-5
allele num: 67240
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000400790
  ensembl transcript: ENST00000438100
  gene symbol: MAP7
  hgvsc: ENST00000438100.2:c.2195-2A>G
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414712
  ensembl transcript: ENST00000454590
  gene symbol: MAP7
  hgvsc: ENST00000454590.1:c.2306-2A>G
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000346581
  ensembl transcript: ENST00000354570
  gene symbol: MAP7
  hgvsc: ENST00000354570.3:c.2240-2A>G
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000445737
  ensembl transcript: ENST00000544465
  gene symbol: MAP7
  hgvsc: ENST00000544465.1:c.2195-2A>G
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414879
  ensembl transcript: ENST00000432797
  gene symbol: MAP7
  hgvsc: ENST00000432797.2:c.1802-2A>G
  variant of: http://identifiers.org/hgnc/6869
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23259
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 100
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9880
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: c.2306-2A>G
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: African
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

6-136665379-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136665379
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136665379
    reference: chr 6
allele count: 1
allele frequency: 1.493295104978646e-5
allele num: 66966
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000445737
  ensembl transcript: ENST00000544465
  gene symbol: MAP7
  hgvsc: ENST00000544465.1:c.2195-3T>C
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414879
  ensembl transcript: ENST00000432797
  gene symbol: MAP7
  hgvsc: ENST00000432797.2:c.1802-3T>C
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414712
  ensembl transcript: ENST00000454590
  gene symbol: MAP7
  hgvsc: ENST00000454590.1:c.2306-3T>C
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000346581
  ensembl transcript: ENST00000354570
  gene symbol: MAP7
  hgvsc: ENST00000354570.3:c.2240-3T>C
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000400790
  ensembl transcript: ENST00000438100
  gene symbol: MAP7
  hgvsc: ENST00000438100.2:c.2195-3T>C
  variant of: http://identifiers.org/hgnc/6869
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
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genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 3.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 1.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
hgvs: c.2306-3T>C
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-136665380-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136665380
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136665380
    reference: chr 6
allele count: 1
allele frequency: 1.493295104978646e-5
allele num: 66966
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414712
  ensembl transcript: ENST00000454590
  gene symbol: MAP7
  hgvsc: ENST00000454590.1:c.2306-4G>A
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000400790
  ensembl transcript: ENST00000438100
  gene symbol: MAP7
  hgvsc: ENST00000438100.2:c.2195-4G>A
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000445737
  ensembl transcript: ENST00000544465
  gene symbol: MAP7
  hgvsc: ENST00000544465.1:c.2195-4G>A
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414879
  ensembl transcript: ENST00000432797
  gene symbol: MAP7
  hgvsc: ENST00000432797.2:c.1802-4G>A
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000346581
  ensembl transcript: ENST00000354570
  gene symbol: MAP7
  hgvsc: ENST00000354570.3:c.2240-4G>A
  variant of: http://identifiers.org/hgnc/6869
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2601
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10524
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3680
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 907
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 979
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 916
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2540
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15684
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2696
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 875
  bin: 6.75e1
  variant carriers: 0
hgvs: c.2306-4G>A
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

6-136665382-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136665382
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136665382
    reference: chr 6
allele count: 1
allele frequency: 1.487254231238288e-5
allele num: 67238
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000400790
  ensembl transcript: ENST00000438100
  gene symbol: MAP7
  hgvsc: ENST00000438100.2:c.2195-6A>C
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414879
  ensembl transcript: ENST00000432797
  gene symbol: MAP7
  hgvsc: ENST00000432797.2:c.1802-6A>C
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000346581
  ensembl transcript: ENST00000354570
  gene symbol: MAP7
  hgvsc: ENST00000354570.3:c.2240-6A>C
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000445737
  ensembl transcript: ENST00000544465
  gene symbol: MAP7
  hgvsc: ENST00000544465.1:c.2195-6A>C
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414712
  ensembl transcript: ENST00000454590
  gene symbol: MAP7
  hgvsc: ENST00000454590.1:c.2306-6A>C
  variant of: http://identifiers.org/hgnc/6869
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10529
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15838
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2678
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 873
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 741
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 887
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3658
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 696
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2038
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 27233
  bin: 2.25e1
  variant carriers: 0
hgvs: c.2306-6A>C
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

6-136665383-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136665383
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136665383
    reference: chr 6
allele count: 8
allele frequency: 1.195064384093693e-4
allele num: 66942
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000445737
  ensembl transcript: ENST00000544465
  gene symbol: MAP7
  hgvsc: ENST00000544465.1:c.2195-7C>T
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000346581
  ensembl transcript: ENST00000354570
  gene symbol: MAP7
  hgvsc: ENST00000354570.3:c.2240-7C>T
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414879
  ensembl transcript: ENST00000432797
  gene symbol: MAP7
  hgvsc: ENST00000432797.2:c.1802-7C>T
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000400790
  ensembl transcript: ENST00000438100
  gene symbol: MAP7
  hgvsc: ENST00000438100.2:c.2195-7C>T
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414712
  ensembl transcript: ENST00000454590
  gene symbol: MAP7
  hgvsc: ENST00000454590.1:c.2306-7C>T
  variant of: http://identifiers.org/hgnc/6869
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11143
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14890
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23034
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2635
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3826
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 850
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 965
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2821
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2042
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 2709
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3816
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15042
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27195
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 1.25e1
  variant carriers: 0
hgvs: c.2306-7C>T
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

6-136665390-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136665390
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136665390
    reference: chr 6
allele count: 5
allele frequency: 7.47853659995812e-5
allele num: 66858
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000445737
  ensembl transcript: ENST00000544465
  gene symbol: MAP7
  hgvsc: ENST00000544465.1:c.2195-14G>C
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414879
  ensembl transcript: ENST00000432797
  gene symbol: MAP7
  hgvsc: ENST00000432797.2:c.1802-14G>C
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414712
  ensembl transcript: ENST00000454590
  gene symbol: MAP7
  hgvsc: ENST00000454590.1:c.2306-14G>C
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000346581
  ensembl transcript: ENST00000354570
  gene symbol: MAP7
  hgvsc: ENST00000354570.3:c.2240-14G>C
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000400790
  ensembl transcript: ENST00000438100
  gene symbol: MAP7
  hgvsc: ENST00000438100.2:c.2195-14G>C
  variant of: http://identifiers.org/hgnc/6869
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22825
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12245
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2653
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13610
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 836
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1163
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 576
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27681
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4107
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2999
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 673
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3027
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 801
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

6-136665392-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136665392
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136665392
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 66734
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000400790
  ensembl transcript: ENST00000438100
  gene symbol: MAP7
  hgvsc: ENST00000438100.2:c.2195-16C>A
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000346581
  ensembl transcript: ENST00000354570
  gene symbol: MAP7
  hgvsc: ENST00000354570.3:c.2240-16C>A
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414712
  ensembl transcript: ENST00000454590
  gene symbol: MAP7
  hgvsc: ENST00000454590.1:c.2306-16C>A
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000445737
  ensembl transcript: ENST00000544465
  gene symbol: MAP7
  hgvsc: ENST00000544465.1:c.2195-16C>A
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414879
  ensembl transcript: ENST00000432797
  gene symbol: MAP7
  hgvsc: ENST00000432797.2:c.1802-16C>A
  variant of: http://identifiers.org/hgnc/6869
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22710
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4197
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12953
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12752
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2602
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27749
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 844
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4247
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 705
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3105
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3174
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1263
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-136665410-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136665410
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136665410
    reference: chr 6
allele count: 2
allele frequency: 3.0970299482796e-5
allele num: 64578
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000400790
  ensembl transcript: ENST00000438100
  gene symbol: MAP7
  hgvsc: ENST00000438100.2:c.2195-34A>G
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000445737
  ensembl transcript: ENST00000544465
  gene symbol: MAP7
  hgvsc: ENST00000544465.1:c.2195-34A>G
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414879
  ensembl transcript: ENST00000432797
  gene symbol: MAP7
  hgvsc: ENST00000432797.2:c.1802-34A>G
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000346581
  ensembl transcript: ENST00000354570
  gene symbol: MAP7
  hgvsc: ENST00000354570.3:c.2240-34A>G
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414712
  ensembl transcript: ENST00000454590
  gene symbol: MAP7
  hgvsc: ENST00000454590.1:c.2306-34A>G
  variant of: http://identifiers.org/hgnc/6869
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6259
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21452
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7058
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16313
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4407
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5701
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23585
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6785
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2478
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2483
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 878
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1028
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4287
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4776
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3581
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-136665421-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136665421
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136665421
    reference: chr 6
allele count: 1
allele frequency: 1.633453119895459e-5
allele num: 61220
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414879
  ensembl transcript: ENST00000432797
  gene symbol: MAP7
  hgvsc: ENST00000432797.2:c.1802-45A>G
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414712
  ensembl transcript: ENST00000454590
  gene symbol: MAP7
  hgvsc: ENST00000454590.1:c.2306-45A>G
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000445737
  ensembl transcript: ENST00000544465
  gene symbol: MAP7
  hgvsc: ENST00000544465.1:c.2195-45A>G
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000346581
  ensembl transcript: ENST00000354570
  gene symbol: MAP7
  hgvsc: ENST00000354570.3:c.2240-45A>G
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000400790
  ensembl transcript: ENST00000438100
  gene symbol: MAP7
  hgvsc: ENST00000438100.2:c.2195-45A>G
  variant of: http://identifiers.org/hgnc/6869
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6469
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3514
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22732
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15170
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5222
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18594
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2261
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 752
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1470
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1836
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4054
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2035
  bin: 9.75e1
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genotype quality: GenotypeQuality
  all individuals: 4295
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7367
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/6-136666914-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136666914
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136666914
    reference: chr 6
allele count: 16
allele frequency: 1.350917779766629e-4
allele num: 118438
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414879
  ensembl transcript: ENST00000432797
  gene symbol: MAP7
  hgvsc: ENST00000432797.2:c.1801+80G>T
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000346581
  ensembl transcript: ENST00000354570
  gene symbol: MAP7
  hgvsc: ENST00000354570.3:c.2239+80G>T
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414712
  ensembl transcript: ENST00000454590
  gene symbol: MAP7
  hgvsc: ENST00000454590.1:c.2305+80G>T
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000445737
  ensembl transcript: ENST00000544465
  gene symbol: MAP7
  hgvsc: ENST00000544465.1:c.2194+80G>T
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000400790
  ensembl transcript: ENST00000438100
  gene symbol: MAP7
  hgvsc: ENST00000438100.2:c.2194+80G>T
  variant of: http://identifiers.org/hgnc/6869
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6093
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16927
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10668
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18700
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5210
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3474
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2712
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 994
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 754
  bin: 9.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 5587
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1169
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4550
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1144
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2312
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

6-136666916-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136666916
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136666916
    reference: chr 6
allele count: 1
allele frequency: 8.442380751371886e-6
allele num: 118450
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414712
  ensembl transcript: ENST00000454590
  gene symbol: MAP7
  hgvsc: ENST00000454590.1:c.2305+78C>T
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414879
  ensembl transcript: ENST00000432797
  gene symbol: MAP7
  hgvsc: ENST00000432797.2:c.1801+78C>T
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000445737
  ensembl transcript: ENST00000544465
  gene symbol: MAP7
  hgvsc: ENST00000544465.1:c.2194+78C>T
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000346581
  ensembl transcript: ENST00000354570
  gene symbol: MAP7
  hgvsc: ENST00000354570.3:c.2239+78C>T
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000400790
  ensembl transcript: ENST00000438100
  gene symbol: MAP7
  hgvsc: ENST00000438100.2:c.2194+78C>T
  variant of: http://identifiers.org/hgnc/6869
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19864
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5237
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9369
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6035
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17110
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1835
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 740
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2473
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1274
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5617
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2679
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1109
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2209
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ

6-136666917-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136666917
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136666917
    reference: chr 6
allele count: 4
allele frequency: 3.373136342170951e-5
allele num: 118584
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414712
  ensembl transcript: ENST00000454590
  gene symbol: MAP7
  hgvsc: ENST00000454590.1:c.2305+77A>G
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000445737
  ensembl transcript: ENST00000544465
  gene symbol: MAP7
  hgvsc: ENST00000544465.1:c.2194+77A>G
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000346581
  ensembl transcript: ENST00000354570
  gene symbol: MAP7
  hgvsc: ENST00000354570.3:c.2239+77A>G
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000400790
  ensembl transcript: ENST00000438100
  gene symbol: MAP7
  hgvsc: ENST00000438100.2:c.2194+77A>G
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414879
  ensembl transcript: ENST00000432797
  gene symbol: MAP7
  hgvsc: ENST00000432797.2:c.1801+77A>G
  variant of: http://identifiers.org/hgnc/6869
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8615
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20613
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5992
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5226
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17175
  bin: 2.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 5632
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1224
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2641
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 951
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3713
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2108
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1828
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1965
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 9.75e1
  variant carriers: 4
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

6-136666919-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136666919
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 136666919
    reference: chr 6
allele count: 35
allele frequency: 2.951444521275699e-4
allele num: 118586
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414879
  ensembl transcript: ENST00000432797
  gene symbol: MAP7
  hgvsc: ENST00000432797.2:c.1801+75C>T
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000346581
  ensembl transcript: ENST00000354570
  gene symbol: MAP7
  hgvsc: ENST00000354570.3:c.2239+75C>T
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000400790
  ensembl transcript: ENST00000438100
  gene symbol: MAP7
  hgvsc: ENST00000438100.2:c.2194+75C>T
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000414712
  ensembl transcript: ENST00000454590
  gene symbol: MAP7
  hgvsc: ENST00000454590.1:c.2305+75C>T
  variant of: http://identifiers.org/hgnc/6869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135525
  ensembl protein: ENSP00000445737
  ensembl transcript: ENST00000544465
  gene symbol: MAP7
  hgvsc: ENST00000544465.1:c.2194+75C>T
  variant of: http://identifiers.org/hgnc/6869
canonical: true
consequence: intron
filter: PASS
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 1046
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 216
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2182
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1125
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2371
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6145
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1020
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 244
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2126
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27746
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1846
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2017
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10012
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 250
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.607503607503608e-4
allele num: 2772
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1072
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5466
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12602
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1954
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.88e-2

QD
type: SiteQuality
SIO_000300: 1.863e1

MQRankSum
type: SiteQuality
SIO_000300: -1.734e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.21e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.56e-1

MQ
type: SiteQuality
SIO_000300: 5.414e1

DP
type: SiteQuality
SIO_000300: 7.36443e5

VQSLOD
type: SiteQuality
SIO_000300: 2.8e0

GenotypeDepth
all individuals: 61
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 56
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1020
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 225
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2371
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6145
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1125
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2017
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1846
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27746
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2126
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2182
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10012
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2772
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 7.935248373274083e-5
allele num: 12602
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5466
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1954
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1072
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 250
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.414e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.21e0

QD
type: SiteQuality
SIO_000300: 1.863e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.88e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.8e0

MQRankSum
type: SiteQuality
SIO_000300: -1.734e0

DP
type: SiteQuality
SIO_000300: 7.36443e5

GenotypeDepth
all individuals: 1407
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 83
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4047
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 696
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 932
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5223
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4192
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2011
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1713
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3417
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6645
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3729
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4587
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14602
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2185
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1667
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2081
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 285
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 662
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 765
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4072
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36858
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11592
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4002
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7462
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6064
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.896e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -9.330000000000001e-1

DP
type: SiteQuality
SIO_000300: 8.2528e5

ClippingRankSum
type: SiteQuality
SIO_000300: 5.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.22e-1

QD
type: SiteQuality
SIO_000300: 3.32e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.23e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.72e-2

GenotypeQuality
all individuals: 765
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14602
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4192
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2011
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3417
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2185
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4047
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3729
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 696
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 662
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4587
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1667
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 285
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2081
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1713
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5223
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 932
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36858
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

African
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num of homozygotes: 0

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

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

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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BaseQRankSum
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FS
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QD
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ReadPosRankSum
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DP
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MQ
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10624
num of homozygotes: 0

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

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 9.025270758122744e-4
allele num: 1108
num of homozygotes: 0

South Asian
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European (Finnish)
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Other
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African
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allele num: 2678
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Latino
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European (Non-Finnish)
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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VQSLOD
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FS
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InbreedingCoeff
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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European (Non-Finnish)
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European (Finnish)
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East Asian
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Latino
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South Asian
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FS
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BaseQRankSum
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MQRankSum
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VQSLOD
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ClippingRankSum
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MQ
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ReadPosRankSum
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DP
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InbreedingCoeff
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QD
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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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Other
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African
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European (Finnish)
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East Asian
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Latino
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European (Non-Finnish)
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BaseQRankSum
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FS
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MQRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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MQ
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DP
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VQSLOD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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European (Non-Finnish)
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East Asian
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European (Finnish)
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Latino
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InbreedingCoeff
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DP
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MQ
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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FS
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ClippingRankSum
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QD
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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African
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European (Non-Finnish)
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Other
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East Asian
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FS
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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DP
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MQRankSum
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QD
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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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European (Non-Finnish)
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Latino
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African
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East Asian
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European (Finnish)
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South Asian
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Other
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FS
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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QD
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DP
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InbreedingCoeff
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MQ
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MQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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Other
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European (Non-Finnish)
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East Asian
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European (Finnish)
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Latino
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QD
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MQ
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VQSLOD
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DP
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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FS
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BaseQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

Other
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Latino
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East Asian
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South Asian
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African
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European (Non-Finnish)
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InbreedingCoeff
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FS
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QD
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VQSLOD
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MQ
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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European (Non-Finnish)
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African
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European (Finnish)
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Other
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East Asian
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DP
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ClippingRankSum
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QD
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VQSLOD
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MQ
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FS
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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Latino
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East Asian
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African
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MQRankSum
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MQ
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ClippingRankSum
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ReadPosRankSum
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DP
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FS
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BaseQRankSum
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VQSLOD
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South Asian
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Latino
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East Asian
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ReadPosRankSum
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DP
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VQSLOD
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MQRankSum
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QD
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FS
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MQ
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BaseQRankSum
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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: 1988
bin: 8.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11348
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66348
num of homozygotes: 0

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

African
type: Population
allele count: 6
allele frequency: 5.799342741156003e-4
allele num: 10346
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.102e0

QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: 1.67e0

MQRankSum
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DP
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SIO_000300: 1.794288e6

InbreedingCoeff
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SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.22e-1

MQ
type: SiteQuality
SIO_000300: 5.373e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.38e-1

VQSLOD
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SIO_000300: -2.722e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1992
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.068697657482704e-5
allele num: 16478
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66396
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.0e-1

InbreedingCoeff
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SIO_000300: -1.0e-4

ReadPosRankSum
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BaseQRankSum
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QD
type: SiteQuality
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DP
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VQSLOD
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FS
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MQRankSum
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MQ
type: SiteQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7
bin: 1.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66440
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 4.99e1

VQSLOD
type: SiteQuality
SIO_000300: -3.983e0

QD
type: SiteQuality
SIO_000300: 4.05e0

ClippingRankSum
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SIO_000300: -8.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.4e0

MQRankSum
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SIO_000300: 3.49e0

FS
type: SiteQuality
SIO_000300: 1.6355e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.48e0

DP
type: SiteQuality
SIO_000300: 1.796869e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 18
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.009057262359703e-5
allele num: 66466
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.76056338028169e-4
allele num: 11360
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.63948332369385e-5
allele num: 10374
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159554730983302e-4
allele num: 8624
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.21300339640951e-4
allele num: 16488
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.55e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.417e0

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -8.76e-1

MQ
type: SiteQuality
SIO_000300: 5.277e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 3.238e0

DP
type: SiteQuality
SIO_000300: 1.798243e6

GenotypeDepth
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variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.512906913773392e-5
allele num: 66476
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.63948332369385e-5
allele num: 10374
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.174e1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
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QD
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MQRankSum
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.7231e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.93e-1

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503940323647958e-5
allele num: 66492
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11370
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.637625289128758e-5
allele num: 10376
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.237e1

QD
type: SiteQuality
SIO_000300: 1.45e0

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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SIO_000300: 3.12e0

VQSLOD
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FS
type: SiteQuality
SIO_000300: 3.1362e1

DP
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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SIO_000300: -4.39e-1

GenotypeDepth
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variant carriers: 736

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
all individuals: 442
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GenotypeQuality
all individuals: 254
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variant carriers: 139

Other
type: Population
allele count: 70
allele frequency: 7.918552036199095e-2
allele num: 884
num of homozygotes: 0

Latino
type: Population
allele count: 414
allele frequency: 3.690497414868961e-2
allele num: 11218
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4260
allele frequency: 6.532139352306182e-2
allele num: 65216
num of homozygotes: 0

European (Finnish)
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allele count: 596
allele frequency: 9.269051321928461e-2
allele num: 6430
num of homozygotes: 0

South Asian
type: Population
allele count: 644
allele frequency: 3.961126829868372e-2
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num of homozygotes: 0

African
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allele count: 541
allele frequency: 5.28526768268855e-2
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num of homozygotes: 0

East Asian
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allele count: 727
allele frequency: 8.677488660778229e-2
allele num: 8378
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.2e1

InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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QD
type: SiteQuality
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MQRankSum
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FS
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VQSLOD
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DP
type: SiteQuality
SIO_000300: 2.163616e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.664e0

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

European (Non-Finnish)
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allele num: 66514
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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East Asian
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African
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allele frequency: 3.854307188282906e-4
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European (Finnish)
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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ReadPosRankSum
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FS
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QD
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 4.510193036261952e-5
allele num: 66516
num of homozygotes: 0

Latino
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East Asian
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European (Finnish)
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Other
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African
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South Asian
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MQ
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VQSLOD
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BaseQRankSum
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MQRankSum
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QD
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FS
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InbreedingCoeff
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DP
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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European (Finnish)
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allele count: 0
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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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African
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South Asian
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Other
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Latino
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MQRankSum
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BaseQRankSum
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MQ
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DP
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FS
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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QD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66510
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Latino
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African
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Other
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East Asian
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South Asian
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European (Finnish)
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DP
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VQSLOD
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BaseQRankSum
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FS
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MQ
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QD
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Non-Finnish)
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African
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South Asian
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European (Finnish)
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Latino
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East Asian
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BaseQRankSum
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InbreedingCoeff
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MQ
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ClippingRankSum
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VQSLOD
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MQRankSum
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DP
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FS
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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European (Non-Finnish)
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

DP
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ReadPosRankSum
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ClippingRankSum
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MQ
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InbreedingCoeff
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SIO_000300: 0.0e0

BaseQRankSum
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FS
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MQRankSum
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QD
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SIO_000300: 5.600000000000001e-1

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11368
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.007518796992481e-5
allele num: 66500
num of homozygotes: 0

European (Finnish)
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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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Other
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MQRankSum
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MQ
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BaseQRankSum
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InbreedingCoeff
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FS
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QD
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ReadPosRankSum
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ClippingRankSum
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DP
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SIO_000300: 1.768984e6

VQSLOD
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SIO_000300: -4.265e0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

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

South Asian
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allele frequency: 6.065752759917505e-5
allele num: 16486
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66492
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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MQRankSum
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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MQ
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SIO_000300: 5.181e1

DP
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QD
type: SiteQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.009328919650918e-5
allele num: 66460
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

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

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

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

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

BaseQRankSum
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SIO_000300: -1.052e0

MQ
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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QD
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FS
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DP
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MQRankSum
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SIO_000300: -2.232e0

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66454
num of homozygotes: 0

African
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Latino
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num of homozygotes: 0

Other
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DP
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ReadPosRankSum
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MQRankSum
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MQ
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BaseQRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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QD
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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 count: 2
allele frequency: 3.010416039496658e-5
allele num: 66436
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66390
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
allele num: 902
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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allele num: 16462
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.765332e6

ReadPosRankSum
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SIO_000300: 1.1e0

BaseQRankSum
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SIO_000300: 1.57e0

FS
type: SiteQuality
SIO_000300: 9.69e-1

QD
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MQ
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InbreedingCoeff
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MQRankSum
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VQSLOD
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ClippingRankSum
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SIO_000300: -5.97e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.506160195198361e-5
allele num: 66394
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11344
num of homozygotes: 0

Other
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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

South Asian
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allele frequency: 0.0e0
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DP
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BaseQRankSum
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MQRankSum
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MQ
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InbreedingCoeff
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FS
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ReadPosRankSum
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SIO_000300: -3.51e-1

ClippingRankSum
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SIO_000300: 2.14e-1

QD
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.027909219687151e-5
allele num: 66358
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11344
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8606
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

MQRankSum
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SIO_000300: -2.844e0

ClippingRankSum
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SIO_000300: -5.570000000000001e-1

FS
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DP
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MQ
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BaseQRankSum
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SIO_000300: -1.717e0

VQSLOD
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SIO_000300: -1.914e0

QD
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SIO_000300: 1.41e0

InbreedingCoeff
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SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.75e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66262
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

Latino
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
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East Asian
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: -4.819e0

QD
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SIO_000300: 8.7e-1

FS
type: SiteQuality
SIO_000300: 8.646000000000001e0

VQSLOD
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MQ
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SIO_000300: 5.213e1

InbreedingCoeff
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SIO_000300: -2.0e-4

DP
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SIO_000300: 1.761131e6

BaseQRankSum
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SIO_000300: 4.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.44e-1

GenotypeDepth
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16320
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.517266492686776e-5
allele num: 65908
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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DP
type: SiteQuality
SIO_000300: 1.750289e6

QD
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InbreedingCoeff
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FS
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BaseQRankSum
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ClippingRankSum
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SIO_000300: 6.17e-1

MQRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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SIO_000300: -6.830000000000001e-1

GenotypeDepth
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65710
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South Asian
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East Asian
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allele frequency: 2.332633543270352e-4
allele num: 8574
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African
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Other
type: Population
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Latino
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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FS
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QD
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VQSLOD
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MQ
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DP
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ClippingRankSum
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BaseQRankSum
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GenotypeDepth
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variant carriers: 5

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 7
allele frequency: 4.332219334075999e-4
allele num: 16158
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 16
allele frequency: 1.877493546115935e-3
allele num: 8522
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Latino
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Other
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African
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allele count: 1
allele frequency: 9.788566953797964e-5
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num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.146251724666564e-4
allele num: 65230
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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QD
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FS
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ClippingRankSum
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MQRankSum
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MQ
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SIO_000300: 5.46e1

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

European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.065791894046232e-5
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East Asian
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South Asian
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Other
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FS
type: SiteQuality
SIO_000300: 9.9e-1

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

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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Other
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European (Finnish)
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South Asian
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East Asian
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VQSLOD
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BaseQRankSum
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DP
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QD
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InbreedingCoeff
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MQRankSum
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FS
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ReadPosRankSum
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MQ
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ClippingRankSum
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SIO_000300: -2.18e-1

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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Latino
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European (Finnish)
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European (Non-Finnish)
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East Asian
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South Asian
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FS
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SIO_000300: 8.88e-1

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

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

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

African
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num of homozygotes: 0

European (Non-Finnish)
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Other
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East Asian
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Latino
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European (Finnish)
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South Asian
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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DP
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FS
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MQ
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SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.223e1

GenotypeQuality
all individuals: 1641
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1162
bin: 6.75e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7733
bin: 7.5e0
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GenotypeQuality
all individuals: 925
bin: 1.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11642
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.456398919184476e-5
allele num: 40710
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7176
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 640
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5224
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4576
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7948
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

DP
type: SiteQuality
SIO_000300: 9.34901e5

ClippingRankSum
type: SiteQuality
SIO_000300: -4.05e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.37e-2

FS
type: SiteQuality
SIO_000300: 3.31e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.26e0

QD
type: SiteQuality
SIO_000300: 9.369999999999999e0

GenotypeQuality
all individuals: 13324
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 234
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variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 7.75e1
variant carriers: 1

South Asian
type: Population
allele count: 3
allele frequency: 3.03275374039628e-4
allele num: 9892
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2932
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6330
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 29660
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 548
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5544
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3282
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.76e0

DP
type: SiteQuality
SIO_000300: 7.85167e5

QD
type: SiteQuality
SIO_000300: 1.647e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.02e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.58e0

MQRankSum
type: SiteQuality
SIO_000300: -5.7e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.501e-1

GenotypeQuality
all individuals: 3059
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2040
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variant carriers: 1

GenotypeQuality
all individuals: 9602
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 480
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7144
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.240230704426155e-5
allele num: 30862
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7926
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6234
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5758
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3930
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.7e-3

DP
type: SiteQuality
SIO_000300: 8.73977e5

BaseQRankSum
type: SiteQuality
SIO_000300: 7.41e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.292e0

QD
type: SiteQuality
SIO_000300: 4.61e0

GenotypeQuality
all individuals: 1744
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3637
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variant carriers: 0

GenotypeQuality
all individuals: 2039
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variant carriers: 1

GenotypeQuality
all individuals: 778
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variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6298
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5890
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7498
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8046
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.155768745266347e-5
allele num: 31688
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4026
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 486
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 4.4e0

VQSLOD
type: SiteQuality
SIO_000300: -2.023e0

MQRankSum
type: SiteQuality
SIO_000300: -2.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.032e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.3e-3

FS
type: SiteQuality
SIO_000300: 2.044e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.4e-2

DP
type: SiteQuality
SIO_000300: 9.23856e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.81e-1

GenotypeQuality
all individuals: 192
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 134
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2039
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variant carriers: 1

GenotypeQuality
all individuals: 356
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variant carriers: 0

GenotypeQuality
all individuals: 698
bin: 1.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4042
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5910
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.134599711616826e-5
allele num: 31902
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 486
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8102
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6338
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.78e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.82e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.500000000000001e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

QD
type: SiteQuality
SIO_000300: 8.57e0

DP
type: SiteQuality
SIO_000300: 9.35928e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

GenotypeQuality
all individuals: 254
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2038
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variant carriers: 1

GenotypeQuality
all individuals: 369
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variant carriers: 0

GenotypeQuality
all individuals: 293
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variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4194
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.987928767778176e-5
allele num: 33468
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8088
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 504
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6184
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6444
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.889999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.900000000000001e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.44e-1

FS
type: SiteQuality
SIO_000300: 1.377e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.76e0

DP
type: SiteQuality
SIO_000300: 9.70768e5

VQSLOD
type: SiteQuality
SIO_000300: 5.06e-1

QD
type: SiteQuality
SIO_000300: 1.128e1

GenotypeQuality
all individuals: 973
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2038
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 989
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
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variant carriers: 0

GenotypeQuality
all individuals: 15277
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6416
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.244400199104032e-4
allele num: 8036
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4166
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6162
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33340
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.200000000000001e-3

QD
type: SiteQuality
SIO_000300: 1.464e1

MQ
type: SiteQuality
SIO_000300: 5.682e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e0

DP
type: SiteQuality
SIO_000300: 9.61017e5

VQSLOD
type: SiteQuality
SIO_000300: -1.004e0

FS
type: SiteQuality
SIO_000300: 2.632e0

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.89e-1

GenotypeQuality
all individuals: 189
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 7.75e1
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GenotypeQuality
all individuals: 27002
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2038
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 410
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 502
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6412
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4170
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.99868058054456e-5
allele num: 33348
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8028
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8338
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6168
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.925e1

MQRankSum
type: SiteQuality
SIO_000300: 1.92e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.75e0

DP
type: SiteQuality
SIO_000300: 9.62698e5

ClippingRankSum
type: SiteQuality
SIO_000300: -7.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.399999999999999e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e-1

QD
type: SiteQuality
SIO_000300: 8.390000000000001e0

GenotypeQuality
all individuals: 217
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16541
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2520
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6438
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8366
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4194
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33496
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6182
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 504
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.241002730206007e-4
allele num: 8058
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.850000000000001e-1

DP
type: SiteQuality
SIO_000300: 9.6428e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

QD
type: SiteQuality
SIO_000300: 2.74e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.900000000000001e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.91e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.161e0

GenotypeQuality
all individuals: 408
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 275
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 8.75e1
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GenotypeQuality
all individuals: 1008
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4172
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.998141152485459e-5
allele num: 33354
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 9.730781706130393e-4
allele num: 6166
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.25e-4
allele num: 8000
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6420
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 502
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.734e0

FS
type: SiteQuality
SIO_000300: 9.29e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.51e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.7e-1

DP
type: SiteQuality
SIO_000300: 9.55939e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 7.18e-1

QD
type: SiteQuality
SIO_000300: 1.168e1

GenotypeQuality
all individuals: 259
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 8.75e1
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GenotypeQuality
all individuals: 14447
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 7.75e1
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GenotypeQuality
all individuals: 2041
bin: 9.75e1
variant carriers: 5

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4184
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8334
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6150
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.198537783903638e-4
allele num: 33374
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.568873548791967e-4
allele num: 6374
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7932
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.42888e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.02e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.52e0

FS
type: SiteQuality
SIO_000300: 6.42e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.3e-1

QD
type: SiteQuality
SIO_000300: 1.03e1

GenotypeQuality
all individuals: 13852
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 789
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 127
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2038
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 236
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6140
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33278
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7916
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6380
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4180
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.105e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.5e-3

QD
type: SiteQuality
SIO_000300: 5.92e0

MQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

DP
type: SiteQuality
SIO_000300: 9.35514e5

ClippingRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

GenotypeQuality
all individuals: 364
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2038
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 126
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4140
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6172
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 496
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8184
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5970
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 6.206168931918326e-5
allele num: 32226
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7390
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.17e-1

DP
type: SiteQuality
SIO_000300: 8.4323e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.35e-2

QD
type: SiteQuality
SIO_000300: 1.24e1

FS
type: SiteQuality
SIO_000300: 1.395e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.24e0

MQRankSum
type: SiteQuality
SIO_000300: -1.07e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.06e-1

GenotypeQuality
all individuals: 129
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4143
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5895
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5920
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3974
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.485884101040119e-4
allele num: 6730
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5666
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7930
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30534
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.16815e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

QD
type: SiteQuality
SIO_000300: 1.742e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.78e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.548e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.58e-2

GenotypeQuality
all individuals: 1310
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3650
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29961
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1806
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10104
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11094
num of homozygotes: 0

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

South Asian
type: Population
allele count: 16
allele frequency: 9.92063492063492e-4
allele num: 16128
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.28e0

QD
type: SiteQuality
SIO_000300: 1.244e1

MQRankSum
type: SiteQuality
SIO_000300: 4.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.4e-2

FS
type: SiteQuality
SIO_000300: 8.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.375224e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.912e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.55e-1

GenotypeQuality
all individuals: 608
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 959
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3566
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32366
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4054
bin: 4.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10100
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.002520705797624e-5
allele num: 11108
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16138
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.66e-1

QD
type: SiteQuality
SIO_000300: 1.168e1

MQRankSum
type: SiteQuality
SIO_000300: -2.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.22e-1

DP
type: SiteQuality
SIO_000300: 1.382612e6

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.991e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 384
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3513
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33753
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1114
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16150
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.533083951677194e-5
allele num: 65228
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10098
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.700756211739287e-4
allele num: 11108
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.17e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.44e0

MQRankSum
type: SiteQuality
SIO_000300: 1.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

QD
type: SiteQuality
SIO_000300: 1.135e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.15e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.386761e6