14-65488702-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65488702
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65488702
    reference: chr 14
allele count: 1
allele frequency: 9.288500835965076e-5
allele num: 10766
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555372
  gene symbol: FNTB
  hgvsc: ENST00000555372.1:n.436C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.237-5469C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-15700G>C
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.480-5469C>G
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.375-5469C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.311-5469C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.579-5469C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.24+5457C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.477-5469C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*94-5469C>G
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.180-5469C>G
  variant of: http://identifiers.org/hgnc/3785
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: n.436C>G
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD

14-65488718-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65488718
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65488718
    reference: chr 14
allele count: 1
allele frequency: 9.291953168556031e-5
allele num: 10762
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.477-5453A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.311-5453A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*94-5453A>G
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.579-5453A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.237-5453A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555372
  gene symbol: FNTB
  hgvsc: ENST00000555372.1:n.452A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.180-5453A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.25-5453A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.375-5453A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-15716T>C
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.480-5453A>G
  variant of: http://identifiers.org/hgnc/42960
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2370
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: DP

14-65488744-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65488744
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65488744
    reference: chr 14
allele count: 7
allele frequency: 6.50315867707172e-4
allele num: 10764
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.180-5427A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.477-5427A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555372
  gene symbol: FNTB
  hgvsc: ENST00000555372.1:n.478A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*94-5427A>G
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-15742T>C
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.311-5427A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.579-5427A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.375-5427A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.25-5427A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.480-5427A>G
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.237-5427A>G
  variant of: http://identifiers.org/hgnc/3785
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum

14-65488745-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65488745
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65488745
    reference: chr 14
allele count: 1
allele frequency: 9.29022668153103e-5
allele num: 10764
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.579-5426A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.237-5426A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-15743T>C
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.375-5426A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*94-5426A>G
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.25-5426A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.477-5426A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555372
  gene symbol: FNTB
  hgvsc: ENST00000555372.1:n.479A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.311-5426A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.180-5426A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.480-5426A>G
  variant of: http://identifiers.org/hgnc/42960
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4977
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum

14-65488752-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65488752
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65488752
    reference: chr 14
allele count: 1
allele frequency: 9.29022668153103e-5
allele num: 10764
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.180-5419G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*94-5419G>A
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.480-5419G>A
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.477-5419G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.311-5419G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-15750C>T
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.579-5419G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555372
  gene symbol: FNTB
  hgvsc: ENST00000555372.1:n.486G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.375-5419G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.237-5419G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.25-5419G>A
  variant of: http://identifiers.org/hgnc/3785
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2561
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

14-65488769-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65488769
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65488769
    reference: chr 14
allele count: 1
allele frequency: 9.288500835965076e-5
allele num: 10766
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.180-5402G>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.477-5402G>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.375-5402G>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-15767C>A
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555372
  gene symbol: FNTB
  hgvsc: ENST00000555372.1:n.503G>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.237-5402G>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*94-5402G>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.25-5402G>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.579-5402G>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.480-5402G>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.311-5402G>T
  variant of: http://identifiers.org/hgnc/3785
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

14-65488773-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65488773
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65488773
    reference: chr 14
allele count: 1
allele frequency: 9.288500835965076e-5
allele num: 10766
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-15771T>A
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.375-5398A>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*94-5398A>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.579-5398A>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.477-5398A>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555372
  gene symbol: FNTB
  hgvsc: ENST00000555372.1:n.507A>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.25-5398A>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.311-5398A>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.480-5398A>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.180-5398A>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.237-5398A>T
  variant of: http://identifiers.org/hgnc/3785
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

14-65494122-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494122
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494122
    reference: chr 14
allele count: 3
allele frequency: 2.512184092850324e-5
allele num: 119418
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.477-49G>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.480-49G>C
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.18G>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*94-49G>C
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.237-49G>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.311-49G>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21120C>G
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.579-49G>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.375-49G>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.25-49G>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.180-49G>C
  variant of: http://identifiers.org/hgnc/3785
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26586
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7315
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12694
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 813
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

14-65494124-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494124
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494124
    reference: chr 14
allele count: 1
allele frequency: 8.385322331790435e-6
allele num: 119256
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.237-47C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.480-47C>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.477-47C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.25-47C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.180-47C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.579-47C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.20C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.375-47C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21122G>A
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.311-47C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*94-47C>T
  variant of: http://identifiers.org/hgnc/42960
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26606
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7424
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3425
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3013
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/14-65494125-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494125
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494125
    reference: chr 14
allele count: 1
allele frequency: 8.371142995864656e-6
allele num: 119458
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.375-46A>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.477-46A>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*94-46A>C
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.21A>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.311-46A>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.579-46A>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.480-46A>C
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.180-46A>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21123T>G
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.25-46A>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.237-46A>C
  variant of: http://identifiers.org/hgnc/3785
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7519
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3425
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1480
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26621
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9317
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

14-65494127-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494127
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494127
    reference: chr 14
allele count: 1
allele frequency: 8.372544751251695e-6
allele num: 119438
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.237-44G>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*94-44G>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.477-44G>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.25-44G>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.375-44G>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.23G>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.480-44G>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.180-44G>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.311-44G>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21125C>A
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.579-44G>T
  variant of: http://identifiers.org/hgnc/3785
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26632
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7689
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3424
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12711
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

14-65494130-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494130
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494130
    reference: chr 14
allele count: 2
allele frequency: 1.673024158468848e-5
allele num: 119544
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.375-41T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.480-41T>C
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.311-41T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.579-41T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.477-41T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.180-41T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21128A>G
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.26T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*94-41T>C
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.237-41T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.25-41T>C
  variant of: http://identifiers.org/hgnc/3785
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26656
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12716
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7933
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 874
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

14-65494130-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494130
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494130
    reference: chr 14
allele count: 1
allele frequency: 8.365120792344242e-6
allele num: 119544
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.375-41T>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.480-41T>G
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21128A>C
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.180-41T>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.579-41T>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.477-41T>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.25-41T>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*94-41T>G
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.26T>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.311-41T>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.237-41T>G
  variant of: http://identifiers.org/hgnc/3785
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12716
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26656
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7933
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

14-65494134-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494134
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494134
    reference: chr 14
allele count: 209
allele frequency: 1.747696218620909e-3
allele num: 119586
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*94-37C>G
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.311-37C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.480-37C>G
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.180-37C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.477-37C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.25-37C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.375-37C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21132G>C
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.30C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.579-37C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.237-37C>G
  variant of: http://identifiers.org/hgnc/3785
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 1.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8381
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12739
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 9.75e1
  variant carriers: 154
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26731
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 5368
  bin: 9.75e1
  variant carriers: 210
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

14-65494135-TCTGA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494135
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494131
    reference: chr 14
allele count: 1
allele frequency: 8.356033892073466e-6
allele num: 119674
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.237-33_237-30delGACT
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.477-33_477-30delGACT
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.180-33_180-30delGACT
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.34_37delGACT
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.480-33_480-30delGACT
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.311-33_311-30delGACT
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.375-33_375-30delGACT
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.25-33_25-30delGACT
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21137_172-21134delTCAG
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*94-33_*94-30delGACT
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.579-33_579-30delGACT
  variant of: http://identifiers.org/hgnc/3785
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26847
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8506
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3437
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: African
population: East Asian
reference allele: TCTGA
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD

http://identifiers.org/exac.variant/14-65494136-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494136
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494136
    reference: chr 14
allele count: 1
allele frequency: 8.358268835358821e-6
allele num: 119642
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*94-35C>A
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.237-35C>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21134G>T
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.477-35C>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.311-35C>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.579-35C>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.480-35C>A
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.32C>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.375-35C>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.180-35C>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.25-35C>A
  variant of: http://identifiers.org/hgnc/3785
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26863
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12795
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8613
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

14-65494143-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494143
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494143
    reference: chr 14
allele count: 1
allele frequency: 8.334861391255063e-6
allele num: 119978
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.477-28T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.39T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.375-28T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21141A>G
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*94-28T>C
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.311-28T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.237-28T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.480-28T>C
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.579-28T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.25-28T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.180-28T>C
  variant of: http://identifiers.org/hgnc/3785
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9334
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27012
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3447
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12852
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD

14-65494147-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494147
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494147
    reference: chr 14
allele count: 2
allele frequency: 1.664779916095092e-5
allele num: 120136
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.25-24T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*94-24T>C
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21145A>G
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.480-24T>C
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.579-24T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.43T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.311-24T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.477-24T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.375-24T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.237-24T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.180-24T>C
  variant of: http://identifiers.org/hgnc/3785
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12886
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9597
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27079
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD

14-65494151-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494151
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494151
    reference: chr 14
allele count: 1
allele frequency: 8.317114959162966e-6
allele num: 120234
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.375-20C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.25-20C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.237-20C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21149G>A
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.47C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.480-20C>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.579-20C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.477-20C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*94-20C>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.311-20C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.180-20C>T
  variant of: http://identifiers.org/hgnc/3785
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12929
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27246
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3454
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

14-65494156-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494156
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494156
    reference: chr 14
allele count: 1
allele frequency: 8.294212298657997e-6
allele num: 120566
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.477-15T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.237-15T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.579-15T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.480-15T>C
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.52T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.311-15T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*94-15T>C
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21154A>G
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.180-15T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.375-15T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.25-15T>C
  variant of: http://identifiers.org/hgnc/3785
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27379
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9904
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13020
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3457
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34822
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

14-65494158-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494158
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494158
    reference: chr 14
allele count: 1
allele frequency: 8.288025460814215e-6
allele num: 120656
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.480-13G>C
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*94-13G>C
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.311-13G>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.54G>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.579-13G>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.375-13G>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21156C>G
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.477-13G>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.237-13G>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.25-13G>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.180-13G>C
  variant of: http://identifiers.org/hgnc/3785
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13043
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD

14-65494161-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494161
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494161
    reference: chr 14
allele count: 1
allele frequency: 8.280202036929701e-6
allele num: 120770
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.375-10G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.180-10G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*94-10G>A
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.237-10G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.480-10G>A
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21159C>T
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.311-10G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.477-10G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.57G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.25-10G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.579-10G>A
  variant of: http://identifiers.org/hgnc/3785
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27501
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3471
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13078
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9984
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS

14-65494176-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494176
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494176
    reference: chr 14
allele count: 1
allele frequency: 8.25300409349003e-6
allele num: 121168
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.485G>A
  hgvsp: ENSP00000447121.1:p.Cys162Tyr
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*99G>A
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.380G>A
  hgvsp: ENSP00000246166.2:p.Cys127Tyr
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.72G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.30G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.242G>A
  hgvsp: ENSP00000443140.1:p.Cys81Tyr
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.482G>A
  hgvsp: ENSP00000406393.2:p.Cys161Tyr
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21174C>T
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.316G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.185G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.584G>A
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27713
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13182
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3487
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys127Tyr
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/14-65494179-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494179
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494179
    reference: chr 14
allele count: 1
allele frequency: 8.25000825000825e-6
allele num: 121212
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.587A>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*102A>C
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.75A>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.33A>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.383A>C
  hgvsp: ENSP00000246166.2:p.Gln128Pro
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.319A>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.188A>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.488A>C
  hgvsp: ENSP00000447121.1:p.Gln163Pro
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.485A>C
  hgvsp: ENSP00000406393.2:p.Gln162Pro
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.245A>C
  hgvsp: ENSP00000443140.1:p.Gln82Pro
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21177T>G
  variant of: http://identifiers.org/hgnc/6913
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27749
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10097
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13197
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3488
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln128Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD

14-65494183-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494183
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494183
    reference: chr 14
allele count: 1
allele frequency: 8.247014580721778e-6
allele num: 121256
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.37C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.249C>T
  hgvsp: ENST00000542227.1:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21181G>A
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*106C>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.492C>T
  hgvsp: ENST00000549987.1:c.492C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.79C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.387C>T
  hgvsp: ENST00000246166.2:c.387C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.591C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.192C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.323C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.489C>T
  hgvsp: ENST00000447296.2:c.489C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27786
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13204
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10114
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe129Phe
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ

14-65494192-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494192
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494192
    reference: chr 14
allele count: 1
allele frequency: 8.242935804015958e-6
allele num: 121316
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.498G>A
  hgvsp: ENST00000447296.2:c.498G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.88G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.332G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.46G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.396G>A
  hgvsp: ENST00000246166.2:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.258G>A
  hgvsp: ENST00000542227.1:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.501G>A
  hgvsp: ENST00000549987.1:c.501G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*115G>A
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.600G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.201G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21190C>T
  variant of: http://identifiers.org/hgnc/6913
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13215
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10105
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27863
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu132Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum

14-65494228-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494228
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494228
    reference: chr 14
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.432C>T
  hgvsp: ENST00000246166.2:c.432C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.237C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.368C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.534C>T
  hgvsp: ENST00000447296.2:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.537C>T
  hgvsp: ENST00000549987.1:c.537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.124C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*151C>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.636C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21226G>A
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.294C>T
  hgvsp: ENST00000542227.1:c.294C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.82C>T
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27923
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13230
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10115
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro144Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

14-65494234-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494234
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494234
    reference: chr 14
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.543G>T
  hgvsp: ENSP00000447121.1:p.Gln181His
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.438G>T
  hgvsp: ENSP00000246166.2:p.Gln146His
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.243G>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.88G>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21232C>A
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.130G>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.300G>T
  hgvsp: ENSP00000443140.1:p.Gln100His
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*157G>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.540G>T
  hgvsp: ENSP00000406393.2:p.Gln180His
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.374G>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.642G>T
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3494
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10113
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27931
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13225
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln146His
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD

14-65494235-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494235
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494235
    reference: chr 14
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21233A>G
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.89T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.301T>C
  hgvsp: ENSP00000443140.1:p.Tyr101His
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.544T>C
  hgvsp: ENSP00000447121.1:p.Tyr182His
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.643T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.439T>C
  hgvsp: ENSP00000246166.2:p.Tyr147His
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.541T>C
  hgvsp: ENSP00000406393.2:p.Tyr181His
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.131T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.375T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*158T>C
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.244T>C
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13242
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10127
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27968
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr147His
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/14-65494238-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494238
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494238
    reference: chr 14
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.544C>A
  hgvsp: ENSP00000406393.2:p.Pro182Thr
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.378C>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*161C>A
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21236G>T
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.547C>A
  hgvsp: ENSP00000447121.1:p.Pro183Thr
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.304C>A
  hgvsp: ENSP00000443140.1:p.Pro102Thr
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.92C>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.442C>A
  hgvsp: ENSP00000246166.2:p.Pro148Thr
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.646C>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.134C>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.247C>A
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27972
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10126
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3496
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13240
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro148Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

14-65494255-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494255
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494255
    reference: chr 14
allele count: 14
allele frequency: 1.153193522347243e-4
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.321A>G
  hgvsp: ENST00000542227.1:c.321A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.151A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*178A>G
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.459A>G
  hgvsp: ENST00000246166.2:c.459A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.663A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.109A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.264A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.561A>G
  hgvsp: ENST00000447296.2:c.561A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.564A>G
  hgvsp: ENST00000549987.1:c.564A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21253T>C
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.395A>G
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13238
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27975
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr153Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

14-65494257-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494257
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494257
    reference: chr 14
allele count: 18
allele frequency: 1.482677385875027e-4
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.397A>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.461A>T
  hgvsp: ENSP00000246166.2:p.Tyr154Phe
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.266A>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.323A>T
  hgvsp: ENSP00000443140.1:p.Tyr108Phe
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21255T>A
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*180A>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.563A>T
  hgvsp: ENSP00000406393.2:p.Tyr188Phe
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.566A>T
  hgvsp: ENSP00000447121.1:p.Tyr189Phe
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.111A>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.665A>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.153A>T
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10119
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13241
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr154Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/14-65494264-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494264
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494264
    reference: chr 14
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.330A>C
  hgvsp: ENST00000542227.1:c.330A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.160A>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.468A>C
  hgvsp: ENST00000246166.2:c.468A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.672A>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.404A>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.570A>C
  hgvsp: ENST00000447296.2:c.570A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21262T>G
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.573A>C
  hgvsp: ENST00000549987.1:c.573A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.273A>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.118A>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*187A>C
  variant of: http://identifiers.org/hgnc/42960
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10115
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3496
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13242
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27994
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala156Ala
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

14-65494267-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494267
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494267
    reference: chr 14
allele count: 8
allele frequency: 6.589785831960461e-5
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.163C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.675C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.276C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.121C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.471C>G
  hgvsp: ENST00000246166.2:c.471C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.333C>G
  hgvsp: ENST00000542227.1:c.333C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.573C>G
  hgvsp: ENST00000447296.2:c.573C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.407C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.576C>G
  hgvsp: ENST00000549987.1:c.576C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*190C>G
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21265G>C
  variant of: http://identifiers.org/hgnc/6913
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27997
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13245
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val157Val
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

14-65494273-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494273
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494273
    reference: chr 14
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21271T>C
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.339A>G
  hgvsp: ENST00000542227.1:c.339A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.477A>G
  hgvsp: ENST00000246166.2:c.477A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.579A>G
  hgvsp: ENST00000447296.2:c.579A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.413A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.169A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.582A>G
  hgvsp: ENST00000549987.1:c.582A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*196A>G
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.127A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.282A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.681A>G
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10085
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27992
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13249
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala159Ala
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

14-65494283-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494283
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494283
    reference: chr 14
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*206A>G
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.292A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.423A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.179A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.691A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.589A>G
  hgvsp: ENSP00000406393.2:p.Ile197Val
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.487A>G
  hgvsp: ENSP00000246166.2:p.Ile163Val
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.592A>G
  hgvsp: ENSP00000447121.1:p.Ile198Val
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.137A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.349A>G
  hgvsp: ENSP00000443140.1:p.Ile117Val
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21281T>C
  variant of: http://identifiers.org/hgnc/6913
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13234
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile163Val
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

14-65494291-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494291
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494291
    reference: chr 14
allele count: 2
allele frequency: 1.647935137272997e-5
allele num: 121364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.699C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.495C>T
  hgvsp: ENST00000246166.2:c.495C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.187C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*214C>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.597C>T
  hgvsp: ENST00000447296.2:c.597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21289G>A
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.431C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.300C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.145C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.357C>T
  hgvsp: ENST00000542227.1:c.357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.600C>T
  hgvsp: ENST00000549987.1:c.600C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/42960
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13216
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10041
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3485
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27990
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr165Thr
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

14-65494292-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494292
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494292
    reference: chr 14
allele count: 2
allele frequency: 1.648016612007449e-5
allele num: 121358
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*215G>A
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.432G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.601G>A
  hgvsp: ENSP00000447121.1:p.Glu201Lys
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.496G>A
  hgvsp: ENSP00000246166.2:p.Glu166Lys
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.700G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.188G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.598G>A
  hgvsp: ENSP00000406393.2:p.Glu200Lys
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.358G>A
  hgvsp: ENSP00000443140.1:p.Glu120Lys
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.146G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21290C>T
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.301G>A
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13213
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27990
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3481
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu166Lys
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

14-65494292-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494292
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494292
    reference: chr 14
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.598G>T
  hgvsp: ENSP00000406393.2:p.Glu200Ter
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.601G>T
  hgvsp: ENSP00000447121.1:p.Glu201Ter
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.301G>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.700G>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.358G>T
  hgvsp: ENSP00000443140.1:p.Glu120Ter
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21290C>A
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.432G>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*215G>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.188G>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.146G>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.496G>T
  hgvsp: ENSP00000246166.2:p.Glu166Ter
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27990
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3481
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13213
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu166Ter
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

14-65494316-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494316
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494316
    reference: chr 14
allele count: 1
allele frequency: 8.249872126982032e-6
allele num: 121214
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.170A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.212A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.382A>G
  hgvsp: ENSP00000443140.1:p.Arg128Gly
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.622A>G
  hgvsp: ENSP00000406393.2:p.Arg208Gly
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21314T>C
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*239A>G
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.625A>G
  hgvsp: ENSP00000447121.1:p.Arg209Gly
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.325A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.520A>G
  hgvsp: ENSP00000246166.2:p.Arg174Gly
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.456A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555742
  gene symbol: FNTB
  hgvsc: ENST00000555742.1:n.724A>G
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27693
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10015
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12948
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3423
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg209Gly
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS

14-65494327-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494327
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494327
    reference: chr 14
allele count: 2
allele frequency: 1.650927821435647e-5
allele num: 121144
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.521+10A>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.457+10A>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*240+10A>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.171+10A>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.326+10A>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.626+10A>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21325T>A
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.213+10A>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.383+10A>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.623+10A>T
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27259
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12587
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1525
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3096
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

14-65494347-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494347
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494347
    reference: chr 14
allele count: 1
allele frequency: 8.269246671628215e-6
allele num: 120930
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21345G>C
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.326+30C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.521+30C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*240+30C>G
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.383+30C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.623+30C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.213+30C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.171+30C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.457+30C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.626+30C>G
  variant of: http://identifiers.org/hgnc/42960
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11592
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10967
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25740
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8886
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 877
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

14-65494349-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494349
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494349
    reference: chr 14
allele count: 1
allele frequency: 8.268973158913126e-6
allele num: 120934
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.521+32A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.213+32A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.326+32A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.171+32A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.457+32A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.383+32A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.623+32A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.626+32A>G
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21347T>C
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*240+32A>G
  variant of: http://identifiers.org/hgnc/42960
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11487
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32427
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8915
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP

14-65494361-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494361
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494361
    reference: chr 14
allele count: 2
allele frequency: 1.657110661849998e-5
allele num: 120692
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.626+44C>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.457+44C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.521+44C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.171+44C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.326+44C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*240+44C>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.383+44C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21359G>A
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.213+44C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.623+44C>T
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2929
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24700
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10993
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11908
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 762
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1223
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2688
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

14-65494362-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494362
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494362
    reference: chr 14
allele count: 9
allele frequency: 7.454527382963921e-5
allele num: 120732
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.326+45G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.171+45G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.457+45G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.626+45G>A
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21360C>T
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.521+45G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.213+45G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.383+45G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*240+45G>A
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.623+45G>A
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24837
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12002
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10884
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31793
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1669
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1166
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

14-65494373-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494373
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494373
    reference: chr 14
allele count: 2
allele frequency: 1.656150113446283e-5
allele num: 120762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*241-43C>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.214-43C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.624-43C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.627-43C>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21371G>A
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.458-43C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.384-43C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.172-43C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.522-43C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.327-43C>T
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24652
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3070
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13033
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10500
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2498
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1010
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum

14-65494374-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494374
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494374
    reference: chr 14
allele count: 4
allele frequency: 3.31394674487581e-5
allele num: 120702
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.214-42G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.627-42G>A
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.522-42G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.327-42G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.384-42G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.458-42G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.172-42G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21372C>T
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*241-42G>A
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.624-42G>A
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13118
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24634
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3060
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10530
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2423
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1646
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 996
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 869
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

14-65494386-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494386
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494386
    reference: chr 14
allele count: 1
allele frequency: 8.274994621253496e-6
allele num: 120846
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.384-30G>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.458-30G>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21384C>G
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.172-30G>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.214-30G>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.522-30G>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*241-30G>C
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.627-30G>C
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.327-30G>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.624-30G>C
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14150
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24904
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10311
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2578
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8135
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum

14-65494387-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494387
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494387
    reference: chr 14
allele count: 1
allele frequency: 8.27417299640901e-6
allele num: 120858
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.384-29C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.458-29C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.627-29C>G
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.214-29C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*241-29C>G
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.624-29C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.327-29C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.172-29C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.522-29C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21385G>C
  variant of: http://identifiers.org/hgnc/6913
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24982
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10305
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14114
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4963
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

14-65494395-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494395
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494395
    reference: chr 14
allele count: 1
allele frequency: 8.269520202437855e-6
allele num: 120926
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.522-21A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.172-21A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21393T>C
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.214-21A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.627-21A>G
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*241-21A>G
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.384-21A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.624-21A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.327-21A>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.458-21A>G
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10292
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14701
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25270
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2575
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD

14-65494397-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494397
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494397
    reference: chr 14
allele count: 29
allele frequency: 2.397328219033133e-4
allele num: 120968
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.458-19C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*241-19C>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.327-19C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.214-19C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.627-19C>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.522-19C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21395G>A
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.172-19C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.624-19C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.384-19C>T
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10297
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14799
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25335
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2575
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

14-65494398-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494398
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494398
    reference: chr 14
allele count: 6
allele frequency: 4.95949743759299e-5
allele num: 120980
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21396A>T
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.172-18T>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.627-18T>A
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.214-18T>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.522-18T>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*241-18T>A
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.384-18T>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.458-18T>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.624-18T>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.327-18T>A
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25395
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14834
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3012
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10299
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum

14-65494401-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494401
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494401
    reference: chr 14
allele count: 1
allele frequency: 8.264189613566494e-6
allele num: 121004
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21399A>C
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.627-15T>G
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.384-15T>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.172-15T>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.327-15T>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*241-15T>G
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.522-15T>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.458-15T>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.624-15T>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.214-15T>G
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10287
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3006
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25508
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14923
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

14-65494404-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494404
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494404
    reference: chr 14
allele count: 1
allele frequency: 8.263370132874991e-6
allele num: 121016
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.214-12C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*241-12C>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.458-12C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.327-12C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21402G>A
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.384-12C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.624-12C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.522-12C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.627-12C>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.172-12C>T
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10319
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15046
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3010
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

14-65494406-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494406
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494406
    reference: chr 14
allele count: 1
allele frequency: 8.261595148791329e-6
allele num: 121042
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.627-10T>C
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.458-10T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.522-10T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*241-10T>C
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.624-10T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.384-10T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.327-10T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21404A>G
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.214-10T>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.172-10T>C
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10328
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25633
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3005
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 659
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD

14-65494411-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494411
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494411
    reference: chr 14
allele count: 2
allele frequency: 1.651855033202286e-5
allele num: 121076
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.172-5C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.627-5C>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.522-5C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.214-5C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*241-5C>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.458-5C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.327-5C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.624-5C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21409G>A
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.384-5C>T
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10335
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15298
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3008
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25690
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 2.75e1
  variant carriers: 0
hgvs: c.522-5C>T
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

14-65494440-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494440
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494440
    reference: chr 14
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*265C>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.408C>T
  hgvsp: ENST00000542227.1:c.408C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.351C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21438G>A
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.651C>T
  hgvsp: ENST00000549987.1:c.651C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.546C>T
  hgvsp: ENST00000246166.2:c.546C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.648C>T
  hgvsp: ENST00000447296.2:c.648C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.238C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.196C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.482C>T
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26070
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3004
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10377
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15488
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Tyr217Tyr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

14-65494443-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494443
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494443
    reference: chr 14
allele count: 1
allele frequency: 8.243887157672586e-6
allele num: 121302
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.411C>G
  hgvsp: ENST00000542227.1:c.411C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.654C>G
  hgvsp: ENST00000549987.1:c.654C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.549C>G
  hgvsp: ENST00000246166.2:c.549C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21441G>C
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.651C>G
  hgvsp: ENST00000447296.2:c.651C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.354C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*268C>G
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.241C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.485C>G
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.199C>G
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26114
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser218Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/14-65494454-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494454
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494454
    reference: chr 14
allele count: 2
allele frequency: 1.648559982854976e-5
allele num: 121318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.365C>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.252C>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.422C>A
  hgvsp: ENSP00000443140.1:p.Pro141His
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.665C>A
  hgvsp: ENSP00000447121.1:p.Pro222His
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.662C>A
  hgvsp: ENSP00000406393.2:p.Pro221His
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*279C>A
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21452G>T
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.560C>A
  hgvsp: ENSP00000246166.2:p.Pro187His
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.210C>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.496C>A
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26146
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3007
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro222His
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

14-65494458-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494458
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494458
    reference: chr 14
allele count: 4
allele frequency: 3.296902560044838e-5
allele num: 121326
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.669C>T
  hgvsp: ENST00000549987.1:c.669C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*283C>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.214C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.500C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.426C>T
  hgvsp: ENST00000542227.1:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21456G>A
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.666C>T
  hgvsp: ENST00000447296.2:c.666C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.564C>T
  hgvsp: ENST00000246166.2:c.564C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.369C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.256C>T
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10375
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15467
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26155
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2530
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp223Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

14-65494459-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494459
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494459
    reference: chr 14
allele count: 2
allele frequency: 1.648424106554134e-5
allele num: 121328
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.501G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.257G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.427G>A
  hgvsp: ENSP00000443140.1:p.Gly143Ser
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.215G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21457C>T
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.370G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.667G>A
  hgvsp: ENSP00000406393.2:p.Gly223Ser
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.565G>A
  hgvsp: ENSP00000246166.2:p.Gly189Ser
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*284G>A
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.670G>A
  hgvsp: ENSP00000447121.1:p.Gly224Ser
  variant of: http://identifiers.org/hgnc/42960
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26158
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly224Ser
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

14-65494479-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494479
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494479
    reference: chr 14
allele count: 1
allele frequency: 8.248375070111188e-6
allele num: 121236
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.585C>T
  hgvsp: ENST00000246166.2:c.585C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.277C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.687C>T
  hgvsp: ENST00000447296.2:c.687C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.447C>T
  hgvsp: ENST00000542227.1:c.447C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*304C>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.390C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.690C>T
  hgvsp: ENST00000549987.1:c.690C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.521C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21477G>A
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.235C>T
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10361
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15331
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26141
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38898
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val230Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

14-65494488-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494488
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494488
    reference: chr 14
allele count: 10
allele frequency: 8.254230293025175e-5
allele num: 121150
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.699G>A
  hgvsp: ENST00000549987.1:c.699G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21486C>T
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.530G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.696G>A
  hgvsp: ENST00000447296.2:c.696G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.286G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.594G>A
  hgvsp: ENST00000246166.2:c.594G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.239+5G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.456G>A
  hgvsp: ENST00000542227.1:c.456G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.399G>A
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*313G>A
  variant of: http://identifiers.org/hgnc/42960
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2997
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15120
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26111
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1600
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
hgvs: n.239+5G>A
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD

14-65494489-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494489
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494489
    reference: chr 14
allele count: 1
allele frequency: 8.256274768824306e-6
allele num: 121120
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.595G>C
  hgvsp: ENSP00000246166.2:p.Val199Leu
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21487C>G
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.697G>C
  hgvsp: ENSP00000406393.2:p.Val233Leu
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.457G>C
  hgvsp: ENSP00000443140.1:p.Val153Leu
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.700G>C
  hgvsp: ENSP00000447121.1:p.Val234Leu
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.239+6G>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.531G>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000555618
  gene symbol: FNTB
  hgvsc: ENST00000555618.1:n.287G>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.400G>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*314G>C
  variant of: http://identifiers.org/hgnc/42960
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2990
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10327
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15074
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26083
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val199Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

14-65494518-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494518
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494518
    reference: chr 14
allele count: 1
allele frequency: 8.356452852893003e-6
allele num: 119668
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.541+19A>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.239+35A>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.605+19A>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21516T>A
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.710+19A>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.707+19A>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.410+19A>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*324+19A>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.467+19A>T
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9360
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2767
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3596
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23575
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1523
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1076
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 966
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6899
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

14-65494520-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494520
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494520
    reference: chr 14
allele count: 1
allele frequency: 8.400961069946402e-6
allele num: 119034
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21518C>A
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.541+21G>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.467+21G>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.710+21G>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.410+21G>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.605+21G>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.239+37G>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*324+21G>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.707+21G>T
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13356
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9173
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23409
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3888
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2179
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2693
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2254
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6789
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1052
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

14-65494521-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494521
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494521
    reference: chr 14
allele count: 1
allele frequency: 8.354498061756449e-6
allele num: 119696
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.467+22C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.707+22C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.710+22C>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21519G>A
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.541+22C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.605+22C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.410+22C>T
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*324+22C>T
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.239+38C>T
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13163
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4216
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23305
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2183
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1068
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33078
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

14-65494523-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65494523
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 65494523
    reference: chr 14
allele count: 1
allele frequency: 8.356033892073466e-6
allele num: 119674
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000449668
  ensembl transcript: ENST00000552941
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000552941.1:c.*324+24G>C
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125952
  ensembl protein: ENSP00000342482
  ensembl transcript: ENST00000341653
  gene symbol: MAX
  hgvsc: ENST00000341653.2:c.172-21521C>G
  variant of: http://identifiers.org/hgnc/6913
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125954
  ensembl protein: ENSP00000447121
  ensembl transcript: ENST00000549987
  gene symbol: CHURC1-FNTB
  hgvsc: ENST00000549987.1:c.710+24G>C
  variant of: http://identifiers.org/hgnc/42960
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000443140
  ensembl transcript: ENST00000542227
  gene symbol: FNTB
  hgvsc: ENST00000542227.1:c.467+24G>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000406393
  ensembl transcript: ENST00000447296
  gene symbol: FNTB
  hgvsc: ENST00000447296.2:c.707+24G>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl protein: ENSP00000246166
  ensembl transcript: ENST00000246166
  gene symbol: FNTB
  hgvsc: ENST00000246166.2:c.605+24G>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554334
  gene symbol: FNTB
  hgvsc: ENST00000554334.1:n.410+24G>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000556709
  gene symbol: FNTB
  hgvsc: ENST00000556709.1:n.239+40G>C
  variant of: http://identifiers.org/hgnc/3785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000257365
  ensembl transcript: ENST00000554210
  gene symbol: FNTB
  hgvsc: ENST00000554210.1:n.541+24G>C
  variant of: http://identifiers.org/hgnc/3785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22678
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4836
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8913
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2747
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12836
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2254
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 783
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP

GenotypeQuality
all individuals: 1
bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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African
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MQRankSum
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BaseQRankSum
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MQ
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DP
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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FS
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ReadPosRankSum
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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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European (Non-Finnish)
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Latino
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South Asian
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East Asian
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European (Finnish)
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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QD
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MQ
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DP
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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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East Asian
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African
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Latino
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Other
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European (Non-Finnish)
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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MQ
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VQSLOD
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QD
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FS
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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African
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East Asian
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Other
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European (Finnish)
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ClippingRankSum
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QD
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VQSLOD
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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DP
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FS
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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Latino
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South Asian
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East Asian
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European (Non-Finnish)
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European (Finnish)
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QD
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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MQ
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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FS
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DP
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South Asian
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European (Finnish)
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African
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Latino
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European (Non-Finnish)
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QD
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MQRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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VQSLOD
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MQ
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DP
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ReadPosRankSum
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European (Finnish)
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QD
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VQSLOD
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InbreedingCoeff
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DP
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East Asian
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allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.985e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.34e-1

QD
type: SiteQuality
SIO_000300: 1.477e1

MQRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.11e-1

FS
type: SiteQuality
SIO_000300: 2.703e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.536e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.1e-3

DP
type: SiteQuality
SIO_000300: 1.900003e6

VQSLOD
type: SiteQuality
SIO_000300: 1.43e0

GenotypeQuality
all individuals: 2954
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66112
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15022
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.706e0

FS
type: SiteQuality
SIO_000300: 2.191e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.04e0

VQSLOD
type: SiteQuality
SIO_000300: 8.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.637e0

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

DP
type: SiteQuality
SIO_000300: 1.900841e6

MQ
type: SiteQuality
SIO_000300: 5.914e1

QD
type: SiteQuality
SIO_000300: 1.205e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511441613010489e-5
allele num: 66162
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15166
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -4.553e-1

BaseQRankSum
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SIO_000300: 5.22e0

MQRankSum
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SIO_000300: -1.596e0

FS
type: SiteQuality
SIO_000300: 1.69e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.534e0

DP
type: SiteQuality
SIO_000300: 1.901421e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.58e0

QD
type: SiteQuality
SIO_000300: 1.366e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 2961
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15176
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66136
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.902588e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

QD
type: SiteQuality
SIO_000300: 1.183e1

VQSLOD
type: SiteQuality
SIO_000300: -1.714e0

MQRankSum
type: SiteQuality
SIO_000300: -5.99e-1

FS
type: SiteQuality
SIO_000300: 2.814e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.983e0

MQ
type: SiteQuality
SIO_000300: 5.851e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.28e-1

GenotypeQuality
all individuals: 720
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15228
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66186
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.28e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.582e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

MQRankSum
type: SiteQuality
SIO_000300: 1.56e0

FS
type: SiteQuality
SIO_000300: 1.0745e1

QD
type: SiteQuality
SIO_000300: 1.287e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

DP
type: SiteQuality
SIO_000300: 1.904499e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.41e-1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.566850538481745e-5
allele num: 15228
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66186
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.977e1

MQRankSum
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QD
type: SiteQuality
SIO_000300: 1.287e1

DP
type: SiteQuality
SIO_000300: 1.904499e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

FS
type: SiteQuality
SIO_000300: 1.0745e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.41e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.582e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 7
allele frequency: 1.058361052313275e-3
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 8
allele frequency: 6.915629322268327e-4
allele num: 11568
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 9.620935154897056e-4
allele num: 10394
num of homozygotes: 0

South Asian
type: Population
allele count: 27
allele frequency: 1.769331585845347e-3
allele num: 15260
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 156
allele frequency: 2.356495468277946e-3
allele num: 66200
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.111111111111111e-3
allele num: 900
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.914035e6

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.97e1

FS
type: SiteQuality
SIO_000300: 1.485e0

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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SIO_000300: 1.81e0

MQRankSum
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SIO_000300: 1.46e-1

QD
type: SiteQuality
SIO_000300: 1.444e1

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510072181450273e-5
allele num: 66222
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15320
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 3.752e0

BaseQRankSum
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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MQ
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DP
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VQSLOD
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SIO_000300: 1.26e0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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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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South Asian
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allele frequency: 6.529972574115189e-5
allele num: 15314
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

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

East Asian
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allele frequency: 0.0e0
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ClippingRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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MQRankSum
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QD
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FS
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ReadPosRankSum
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DP
type: SiteQuality
SIO_000300: 1.896823e6

BaseQRankSum
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SIO_000300: -2.608e0

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

African
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allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

South Asian
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allele frequency: 6.433350488934638e-5
allele num: 15544
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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FS
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MQ
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MQRankSum
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InbreedingCoeff
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QD
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DP
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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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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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South Asian
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allele frequency: 1.278118609406953e-4
allele num: 15648
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DP
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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FS
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BaseQRankSum
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QD
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SIO_000300: 1.302e1

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.506750241080039e-5
allele num: 66368
num of homozygotes: 0

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

East Asian
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VQSLOD
type: SiteQuality
SIO_000300: 3.43e-1

ReadPosRankSum
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SIO_000300: 1.93e-1

MQ
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BaseQRankSum
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MQRankSum
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DP
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FS
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SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: -3.86e-1

InbreedingCoeff
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SIO_000300: 0.0e0

QD
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SIO_000300: 1.168e1

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

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

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

European (Non-Finnish)
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allele frequency: 1.504890895410083e-5
allele num: 66450
num of homozygotes: 0

Other
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allele num: 904
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Latino
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South Asian
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DP
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QD
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ReadPosRankSum
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VQSLOD
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FS
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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allele num: 16028
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African
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Other
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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DP
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MQ
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MQRankSum
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InbreedingCoeff
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FS
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ReadPosRankSum
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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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East Asian
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num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

European (Non-Finnish)
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Latino
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African
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South Asian
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Other
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InbreedingCoeff
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MQ
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ReadPosRankSum
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ClippingRankSum
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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South Asian
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European (Non-Finnish)
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allele num: 66612
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East Asian
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Latino
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MQ
type: SiteQuality
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QD
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BaseQRankSum
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DP
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MQRankSum
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SIO_000300: -2.31e-1

ClippingRankSum
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VQSLOD
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InbreedingCoeff
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SIO_000300: 1.0e-4

FS
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SIO_000300: 6.32e-1

ReadPosRankSum
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SIO_000300: 6.57e-1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66632
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 908
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

East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

BaseQRankSum
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SIO_000300: 1.94e0

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

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

InbreedingCoeff
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FS
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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VQSLOD
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QD
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DP
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SIO_000300: 1.935412e6

MQ
type: SiteQuality
SIO_000300: 5.983e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

FS
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SIO_000300: 5.287e0

BaseQRankSum
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ReadPosRankSum
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VQSLOD
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DP
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QD
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InbreedingCoeff
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SIO_000300: 0.0e0

ClippingRankSum
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MQ
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MQRankSum
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SIO_000300: -1.1e-2

GenotypeQuality
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variant carriers: 0

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

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

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele num: 16512
num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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African
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South Asian
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num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

European (Finnish)
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DP
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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QD
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MQRankSum
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FS
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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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variant carriers: 0

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

Latino
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num of homozygotes: 0

European (Finnish)
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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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South Asian
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VQSLOD
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InbreedingCoeff
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DP
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MQRankSum
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ReadPosRankSum
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MQ
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QD
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FS
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 14

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 903
bin: 9.25e1
variant carriers: 0

East Asian
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allele count: 14
allele frequency: 1.618122977346278e-3
allele num: 8652
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

BaseQRankSum
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SIO_000300: 4.22e0

DP
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SIO_000300: 1.934092e6

FS
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SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.0e-3

InbreedingCoeff
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SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.56e-1

QD
type: SiteQuality
SIO_000300: 1.523e1

MQ
type: SiteQuality
SIO_000300: 5.963e1

VQSLOD
type: SiteQuality
SIO_000300: 5.78e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.51e-1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 18

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

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

East Asian
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allele count: 18
allele frequency: 2.079963022879593e-3
allele num: 8654
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.933128e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.29e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.77e-1

QD
type: SiteQuality
SIO_000300: 1.417e1

VQSLOD
type: SiteQuality
SIO_000300: 3.93e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

GenotypeQuality
all individuals: 1900
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.765e-1

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -5.261e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.01e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.79e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.373e0

DP
type: SiteQuality
SIO_000300: 1.931461e6

GenotypeQuality
all individuals: 9944
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 8

GenotypeQuality
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GenotypeQuality
all individuals: 3239
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GenotypeQuality
all individuals: 3201
bin: 7.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.31107002542177e-4
allele num: 8654
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.991458114790949e-5
allele num: 66730
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.43e-1

DP
type: SiteQuality
SIO_000300: 1.931346e6

VQSLOD
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SIO_000300: 5.51e0

QD
type: SiteQuality
SIO_000300: 1.471e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.22e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.4e-1

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 762
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variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.367e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.45e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.930657e6

MQRankSum
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SIO_000300: 2.83e0

BaseQRankSum
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SIO_000300: 1.54e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.1e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

QD
type: SiteQuality
SIO_000300: 1.899e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 1.076e0

ClippingRankSum
type: SiteQuality
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VQSLOD
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DP
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
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MQ
type: SiteQuality
SIO_000300: 5.982e1

MQRankSum
type: SiteQuality
SIO_000300: -9.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.97e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.09e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

Latino
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allele count: 2
allele frequency: 1.728608470181504e-4
allele num: 11570
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
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MQ
type: SiteQuality
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QD
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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VQSLOD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 23
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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: 10406
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

QD
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SIO_000300: 1.273e1

ClippingRankSum
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SIO_000300: -4.25e-1

MQRankSum
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SIO_000300: 7.61e-1

VQSLOD
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SIO_000300: 3.84e-1

MQ
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SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 5.39e-1

DP
type: SiteQuality
SIO_000300: 1.928797e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.157e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

Latino
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allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 7.61e-1

VQSLOD
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BaseQRankSum
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DP
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QD
type: SiteQuality
SIO_000300: 1.273e1

FS
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SIO_000300: 5.39e-1

MQ
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SIO_000300: 6.0e1

ReadPosRankSum
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InbreedingCoeff
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SIO_000300: 2.0e-4

ClippingRankSum
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SIO_000300: -4.25e-1

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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bin: 9.75e1
variant carriers: 1

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

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

South Asian
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allele frequency: 6.059871530723549e-5
allele num: 16502
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VQSLOD
type: SiteQuality
SIO_000300: 1.49e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
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MQRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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BaseQRankSum
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SIO_000300: -2.451e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.64e-1

FS
type: SiteQuality
SIO_000300: 1.043e0

GenotypeQuality
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variant carriers: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.73190162798753e-4
allele num: 11548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66602
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

InbreedingCoeff
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SIO_000300: 0.0e0

VQSLOD
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SIO_000300: 6.7e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
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DP
type: SiteQuality
SIO_000300: 1.904044e6

ReadPosRankSum
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SIO_000300: 2.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.91e-1

QD
type: SiteQuality
SIO_000300: 1.403e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.28e-1

GenotypeQuality
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variant carriers: 0

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.50407604608489e-5
allele num: 66486
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8568
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African
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South Asian
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MQ
type: SiteQuality
SIO_000300: 5.924e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

DP
type: SiteQuality
SIO_000300: 1.870974e6

ReadPosRankSum
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FS
type: SiteQuality
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MQRankSum
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QD
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
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allele num: 66494
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
allele num: 16492
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
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MQRankSum
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FS
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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QD
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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num of homozygotes: 0

African
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Other
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.01313727853441e-5
allele num: 66376
num of homozygotes: 0

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

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

Latino
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African
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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South Asian
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allele num: 16468
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ReadPosRankSum
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MQ
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MQRankSum
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FS
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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DP
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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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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
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
allele num: 11510
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: 1
allele frequency: 9.628345850182938e-5
allele num: 10386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505842669557885e-5
allele num: 66408
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.367e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.09e-1

FS
type: SiteQuality
SIO_000300: 3.507e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.25e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.2e0

DP
type: SiteQuality
SIO_000300: 1.848561e6

VQSLOD
type: SiteQuality
SIO_000300: -4.443e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -8.48e-1

GenotypeQuality
all individuals: 889
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 4

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.635767970707265e-5
allele num: 10378
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)
type: Population
allele count: 3
allele frequency: 4.519569736961041e-5
allele num: 66378
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.63e-1

DP
type: SiteQuality
SIO_000300: 1.849358e6

VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

QD
type: SiteQuality
SIO_000300: 1.103e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.41e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.1e-2

MQ
type: SiteQuality
SIO_000300: 5.933e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.1e-2

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8524
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66458
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.674531575294934e-5
allele num: 11528
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.335e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

DP
type: SiteQuality
SIO_000300: 1.853691e6

QD
type: SiteQuality
SIO_000300: 1.378e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

GenotypeQuality
all individuals: 421
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 34741
bin: 6.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8524
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66476
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.97e-1

QD
type: SiteQuality
SIO_000300: 2.807e1

VQSLOD
type: SiteQuality
SIO_000300: -2.995e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.24e-1

MQ
type: SiteQuality
SIO_000300: 5.93e1

MQRankSum
type: SiteQuality
SIO_000300: 5.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.72e-1

DP
type: SiteQuality
SIO_000300: 1.854207e6

GenotypeQuality
all individuals: 416
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variant carriers: 0

GenotypeQuality
all individuals: 398
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 182
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66514
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.171508903467666e-4
allele num: 8536
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.47e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.09e0

MQ
type: SiteQuality
SIO_000300: 5.931e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.6e-2

QD
type: SiteQuality
SIO_000300: 1.743e1

DP
type: SiteQuality
SIO_000300: 1.860965e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -8.267e-1

GenotypeQuality
all individuals: 4989
bin: 9.75e1
variant carriers: 29

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502810255177181e-5
allele num: 66542
num of homozygotes: 0

Other
type: Population
allele count: 4
allele frequency: 4.424778761061947e-3
allele num: 904
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8540
num of homozygotes: 0

South Asian
type: Population
allele count: 21
allele frequency: 1.273035887487876e-3
allele num: 16496
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.601005722212589e-4
allele num: 11534
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.6e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.1e-2

DP
type: SiteQuality
SIO_000300: 1.863124e6

MQRankSum
type: SiteQuality
SIO_000300: -1.69e-1

QD
type: SiteQuality
SIO_000300: 1.389e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.32e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4967
bin: 9.75e1
variant carriers: 6

Latino
type: Population
allele count: 6
allele frequency: 5.198405822214521e-4
allele num: 11542
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8546
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: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66544
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.029e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e-1

DP
type: SiteQuality
SIO_000300: 1.863345e6

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

MQ
type: SiteQuality
SIO_000300: 5.95e1

QD
type: SiteQuality
SIO_000300: 1.361e1

BaseQRankSum
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SIO_000300: -2.452e0

MQRankSum
type: SiteQuality
SIO_000300: 9.3e-2

GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66550
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.168770453482936e-4
allele num: 8556
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
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FS
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -2.0e-4

MQ
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SIO_000300: 5.75e1

ClippingRankSum
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BaseQRankSum
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QD
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ReadPosRankSum
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 2555
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.063545961678389e-5
allele num: 16492
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
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
allele num: 904
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66550
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.867465e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.04e-1

FS
type: SiteQuality
SIO_000300: 1.038e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.226e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.15e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.66e-1

QD
type: SiteQuality
SIO_000300: 3.297e1

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66560
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.166588894073728e-4
allele num: 8572
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 5.393e0

BaseQRankSum
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SIO_000300: 1.66e0

VQSLOD
type: SiteQuality
SIO_000300: 6.81e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.19e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.78e-1

DP
type: SiteQuality
SIO_000300: 1.868664e6

QD
type: SiteQuality
SIO_000300: 1.228e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.523461304082876e-4
allele num: 6564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501636784094663e-5
allele num: 66594
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.8e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.74e-1

DP
type: SiteQuality
SIO_000300: 1.870717e6

QD
type: SiteQuality
SIO_000300: 1.446e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.91e-1

FS
type: SiteQuality
SIO_000300: 5.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.409e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8270
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variant carriers: 0

GenotypeQuality
all individuals: 1628
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.653513326410523e-5
allele num: 11556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66704
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.55e-1

FS
type: SiteQuality
SIO_000300: 4.79e-1

DP
type: SiteQuality
SIO_000300: 1.878095e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.92e1

VQSLOD
type: SiteQuality
SIO_000300: 5.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.757e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.55e-1

QD
type: SiteQuality
SIO_000300: 1.01e1

GenotypeQuality
all individuals: 8270
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variant carriers: 0

GenotypeQuality
all individuals: 38849
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variant carriers: 0

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

GenotypeQuality
all individuals: 4
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.939e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.66e-1

DP
type: SiteQuality
SIO_000300: 1.87862e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.958e1

QD
type: SiteQuality
SIO_000300: 8.4e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.95e-1

FS
type: SiteQuality
SIO_000300: 1.2227e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.15e-1

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49902563333833e-5
allele num: 66710
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.879209e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.705e0

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 6.28e-1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498935755613514e-5
allele num: 66714
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

Latino
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allele count: 3
allele frequency: 2.594706798131811e-4
allele num: 11562
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
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South Asian
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allele num: 16504
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MQRankSum
type: SiteQuality
SIO_000300: 7.75e-1

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 4.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.48e-1

QD
type: SiteQuality
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ReadPosRankSum
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SIO_000300: 7.06e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4958
bin: 9.75e1
variant carriers: 2

Latino
type: Population
allele count: 2
allele frequency: 1.730103806228374e-4
allele num: 11560
num of homozygotes: 0

South Asian
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Other
type: Population
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66716
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.55e0

FS
type: SiteQuality
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InbreedingCoeff
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DP
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VQSLOD
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ReadPosRankSum
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MQRankSum
type: SiteQuality
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MQ
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ClippingRankSum
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QD
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SIO_000300: 2.189e1

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

European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.499565126113427e-5
allele num: 66686
num of homozygotes: 0

South Asian
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QD
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FS
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6554
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East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.500015000150001e-4
allele num: 66666
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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DP
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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FS
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MQ
type: SiteQuality
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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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European (Finnish)
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allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10388
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66652
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East Asian
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South Asian
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allele num: 16456
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Other
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MQ
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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DP
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MQRankSum
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QD
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FS
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele num: 16288
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65976
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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QD
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
type: SiteQuality
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BaseQRankSum
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MQRankSum
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FS
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SIO_000300: 0.0e0

MQ
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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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Latino
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num of homozygotes: 0

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

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