3-58129322-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58129322
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58129322
    reference: chr 3
allele count: 52
allele frequency: 4.29383009644603e-4
allele num: 121104
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5407A>T
  hgvsp: ENSP00000349819.4:p.Met1803Leu
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4867A>T
  hgvsp: ENSP00000414532.2:p.Met1623Leu
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5407A>T
  hgvsp: ENSP00000295956.4:p.Met1803Leu
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5374A>T
  hgvsp: ENSP00000415599.2:p.Met1792Leu
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5335A>T
  hgvsp: ENSP00000351339.3:p.Met1779Leu
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4828A>T
  hgvsp: ENSP00000418510.1:p.Met1610Leu
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5500A>T
  hgvsp: ENSP00000420213.1:p.Met1834Leu
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1675A>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5407A>T
  hgvsp: ENSP00000232447.7:p.Met1803Leu
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13915
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11236
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4323
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2460
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3284
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Met1834Leu
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD

3-58129324-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58129324
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58129324
    reference: chr 3
allele count: 2
allele frequency: 1.65169133192389e-5
allele num: 121088
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5502G>T
  hgvsp: ENSP00000420213.1:p.Met1834Ile
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5409G>T
  hgvsp: ENSP00000232447.7:p.Met1803Ile
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5409G>T
  hgvsp: ENSP00000349819.4:p.Met1803Ile
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5337G>T
  hgvsp: ENSP00000351339.3:p.Met1779Ile
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1677G>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4869G>T
  hgvsp: ENSP00000414532.2:p.Met1623Ile
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5409G>T
  hgvsp: ENSP00000295956.4:p.Met1803Ile
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4830G>T
  hgvsp: ENSP00000418510.1:p.Met1610Ile
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5376G>T
  hgvsp: ENSP00000415599.2:p.Met1792Ile
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11311
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21662
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13808
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4351
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1904
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1053
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1319
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Met1834Ile
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

3-58129325-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58129325
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58129325
    reference: chr 3
allele count: 3
allele frequency: 2.477659767760691e-5
allele num: 121082
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5410G>C
  hgvsp: ENSP00000232447.7:p.Gly1804Arg
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4831G>C
  hgvsp: ENSP00000418510.1:p.Gly1611Arg
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4870G>C
  hgvsp: ENSP00000414532.2:p.Gly1624Arg
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5377G>C
  hgvsp: ENSP00000415599.2:p.Gly1793Arg
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5410G>C
  hgvsp: ENSP00000349819.4:p.Gly1804Arg
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1678G>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5338G>C
  hgvsp: ENSP00000351339.3:p.Gly1780Arg
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5410G>C
  hgvsp: ENSP00000295956.4:p.Gly1804Arg
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5503G>C
  hgvsp: ENSP00000420213.1:p.Gly1835Arg
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13767
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1901
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4345
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29962
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2473
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3282
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly1835Arg
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

3-58129326-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58129326
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58129326
    reference: chr 3
allele count: 29
allele frequency: 2.418238521705775e-4
allele num: 119922
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5411G>C
  hgvsp: ENSP00000232447.7:p.Gly1804Ala
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5411G>C
  hgvsp: ENSP00000295956.4:p.Gly1804Ala
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5504G>C
  hgvsp: ENSP00000420213.1:p.Gly1835Ala
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4832G>C
  hgvsp: ENSP00000418510.1:p.Gly1611Ala
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4871G>C
  hgvsp: ENSP00000414532.2:p.Gly1624Ala
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5339G>C
  hgvsp: ENSP00000351339.3:p.Gly1780Ala
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5411G>C
  hgvsp: ENSP00000349819.4:p.Gly1804Ala
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1679G>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5378G>C
  hgvsp: ENSP00000415599.2:p.Gly1793Ala
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 21491
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1949
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13703
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11237
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4364
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2359
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 2.5e0
  variant carriers: 2
hgvs: p.Gly1835Ala
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

3-58129329-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58129329
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58129329
    reference: chr 3
allele count: 1
allele frequency: 8.262141216517673e-6
allele num: 121034
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5381G>A
  hgvsp: ENSP00000415599.2:p.Ser1794Asn
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4835G>A
  hgvsp: ENSP00000418510.1:p.Ser1612Asn
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1682G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5414G>A
  hgvsp: ENSP00000349819.4:p.Ser1805Asn
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5507G>A
  hgvsp: ENSP00000420213.1:p.Ser1836Asn
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5342G>A
  hgvsp: ENSP00000351339.3:p.Ser1781Asn
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5414G>A
  hgvsp: ENSP00000295956.4:p.Ser1805Asn
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5414G>A
  hgvsp: ENSP00000232447.7:p.Ser1805Asn
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4874G>A
  hgvsp: ENSP00000414532.2:p.Ser1625Asn
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1811
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13698
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21959
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4286
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1018
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8011
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9337
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser1836Asn
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

3-58129336-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58129336
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58129336
    reference: chr 3
allele count: 1
allele frequency: 8.270204108637402e-6
allele num: 120916
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5421C>T
  hgvsp: ENST00000357272.4:c.5421C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5349C>T
  hgvsp: ENST00000358537.3:c.5349C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1689C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5421C>T
  hgvsp: ENST00000348383.5:c.5421C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4842C>T
  hgvsp: ENST00000493452.1:c.4842C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5421C>T
  hgvsp: ENST00000295956.4:c.5421C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5388C>T
  hgvsp: ENST00000429972.2:c.5388C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5514C>T
  hgvsp: ENST00000490882.1:c.5514C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4881C>T
  hgvsp: ENST00000419752.2:c.4881C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4283
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21848
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11349
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3193
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ile1838Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD

3-58129339-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58129339
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58129339
    reference: chr 3
allele count: 1
allele frequency: 8.272803984182399e-6
allele num: 120878
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5424T>G
  hgvsp: ENST00000348383.5:c.5424T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1692T>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4845T>G
  hgvsp: ENST00000493452.1:c.4845T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5391T>G
  hgvsp: ENST00000429972.2:c.5391T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5352T>G
  hgvsp: ENST00000358537.3:c.5352T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5517T>G
  hgvsp: ENST00000490882.1:c.5517T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4884T>G
  hgvsp: ENST00000419752.2:c.4884T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5424T>G
  hgvsp: ENST00000357272.4:c.5424T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5424T>G
  hgvsp: ENST00000295956.4:c.5424T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4271
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11333
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8008
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
hgvs: c.5517T>G
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum

3-58129348-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58129348
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58129348
    reference: chr 3
allele count: 1
allele frequency: 8.284455048546906e-6
allele num: 120708
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4846+8G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1693+8G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5425+8G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5392+8G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4885+8G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5353+8G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5425+8G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5425+8G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5518+8G>A
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4276
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11234
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21454
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12888
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1024
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8005
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1006
  bin: 8.75e1
  variant carriers: 0
hgvs: c.5518+8G>A
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

3-58129354-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58129354
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58129354
    reference: chr 3
allele count: 1
allele frequency: 8.297515723792297e-6
allele num: 120518
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5425+14G>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4846+14G>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5392+14G>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5425+14G>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1693+14G>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5425+14G>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4885+14G>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5518+14G>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5353+14G>T
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11020
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4232
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20673
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 643
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27480
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8397
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD

3-58129365-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58129365
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58129365
    reference: chr 3
allele count: 2
allele frequency: 1.661736847352853e-5
allele num: 120356
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4885+25A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5425+25A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5392+25A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5353+25A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5518+25A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5425+25A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5425+25A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4846+25A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1693+25A>G
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11852
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10593
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3028
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2103
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26914
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

3-58129368-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58129368
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58129368
    reference: chr 3
allele count: 1
allele frequency: 8.314901967305805e-6
allele num: 120266
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5353+28G>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4846+28G>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5425+28G>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4885+28G>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5425+28G>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5425+28G>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5392+28G>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1693+28G>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5518+28G>T
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3371
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19138
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7994
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 25893
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2288
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD

3-58129373-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58129373
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58129373
    reference: chr 3
allele count: 1
allele frequency: 8.327088017320342e-6
allele num: 120090
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4885+33A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1693+33A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5425+33A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5518+33A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5425+33A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5425+33A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4846+33A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5353+33A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5392+33A>G
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4145
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3805
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10491
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4934
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18087
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10250
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2268
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 983
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2722
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1217
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3319
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD

3-58129373-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58129373
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58129373
    reference: chr 3
allele count: 4
allele frequency: 3.330835206928137e-5
allele num: 120090
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5425+33A>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5425+33A>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4885+33A>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5518+33A>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5353+33A>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4846+33A>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5425+33A>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1693+33A>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5392+33A>T
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18087
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4145
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3805
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4934
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10250
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10491
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2176
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 778
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7993
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1386
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3319
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2722
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD

3-58129389-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58129389
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58129389
    reference: chr 3
allele count: 26
allele frequency: 2.1969108054213e-4
allele num: 118348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5353+49C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1693+49C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5425+49C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5425+49C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4846+49C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5518+49C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4885+49C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5425+49C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5392+49C>T
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3897
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13192
  bin: 2.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 13678
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3700
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8080
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8775
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3499
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5581
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2435
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4191
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum

3-58129390-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58129390
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58129390
    reference: chr 3
allele count: 2
allele frequency: 1.687421956734501e-5
allele num: 118524
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4885+50G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5353+50G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5425+50G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1693+50G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5425+50G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5425+50G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4846+50G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5518+50G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5392+50G>A
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13144
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8738
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13879
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7956
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3501
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7983
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3138
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1913
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

3-58129392-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58129392
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58129392
    reference: chr 3
allele count: 1
allele frequency: 8.46811753747142e-6
allele num: 118090
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5425+52G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1693+52G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4846+52G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5392+52G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5518+52G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5425+52G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5353+52G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5425+52G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4885+52G>A
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13881
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8710
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3961
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7860
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2550
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3511
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2403
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

3-58131597-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131597
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131597
    reference: chr 3
allele count: 3
allele frequency: 2.470966147763776e-5
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5426-51C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5393-51C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4847-51C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4886-51C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5519-51C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5426-51C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5426-51C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5354-51C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1694-51C>T
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13291
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4867
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18993
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3652
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17411
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7583
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2141
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

3-58131598-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131598
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131598
    reference: chr 3
allele count: 346
allele frequency: 2.849847623754221e-3
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4847-50G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5426-50G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4886-50G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5354-50G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5426-50G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1694-50G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5393-50G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5426-50G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5519-50G>A
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13290
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4865
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 7.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 8.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 18999
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 7.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 8.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 6018
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3651
  bin: 9.75e1
  variant carriers: 225
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 6.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 9.25e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 3
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

3-58131606-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131606
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131606
    reference: chr 3
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5426-42C>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5393-42C>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4847-42C>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1694-42C>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5426-42C>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5426-42C>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5354-42C>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4886-42C>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5519-42C>G
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6053
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19095
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13367
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1536
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

3-58131608-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131608
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131608
    reference: chr 3
allele count: 235
allele frequency: 1.935558264421968e-3
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5426-40T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4847-40T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5393-40T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5354-40T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4886-40T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5426-40T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1694-40T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5426-40T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5519-40T>C
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6053
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13367
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 8.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 9.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 4890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 9.75e1
  variant carriers: 194
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3362
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1536
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 1
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD

http://identifiers.org/exac.variant/3-58131609-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131609
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131609
    reference: chr 3
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5519-39A>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4886-39A>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1694-39A>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5426-39A>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5426-39A>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5426-39A>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4847-39A>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5393-39A>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5354-39A>C
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19165
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4917
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6072
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13440
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3306
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3262
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16989
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum

3-58131613-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131613
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131613
    reference: chr 3
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5426-35A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1694-35A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4847-35A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5354-35A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5519-35A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5393-35A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5426-35A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4886-35A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5426-35A>G
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19167
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3305
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6072
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4915
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13442
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21067
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ

3-58131617-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131617
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131617
    reference: chr 3
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5426-31C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5354-31C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5426-31C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5426-31C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1694-31C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5519-31C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5393-31C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4847-31C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4886-31C>T
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19167
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4916
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6072
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4657
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21069
  bin: 6.25e1
  variant carriers: 0
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: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: VQSLOD

3-58131631-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131631
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131631
    reference: chr 3
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5426-17G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5426-17G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4847-17G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5354-17G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5426-17G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5393-17G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4886-17G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1694-17G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5519-17G>A
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6072
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4916
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19168
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3305
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2152
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7656
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

3-58131631-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131631
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131631
    reference: chr 3
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5426-17G>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5426-17G>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5354-17G>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5519-17G>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4886-17G>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4847-17G>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5426-17G>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1694-17G>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5393-17G>T
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19168
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6072
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3305
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4916
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1544
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3376
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

3-58131632-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131632
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131632
    reference: chr 3
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5426-16T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1694-16T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5426-16T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4886-16T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5393-16T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5426-16T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4847-16T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5519-16T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5354-16T>C
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6073
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4916
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19169
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3305
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2152
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3264
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4657
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3377
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

3-58131637-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131637
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131637
    reference: chr 3
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5426-11C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5393-11C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5354-11C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5426-11C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4847-11C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1694-11C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5426-11C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5519-11C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4886-11C>T
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19169
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4916
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6073
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2152
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7655
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3265
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS

3-58131638-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131638
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131638
    reference: chr 3
allele count: 626
allele frequency: 5.155997759694264e-3
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5426-10G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5519-10G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4847-10G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5426-10G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5426-10G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1694-10G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5354-10G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5393-10G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4886-10G>A
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4915
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19170
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6071
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3379
  bin: 9.75e1
  variant carriers: 597
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1544
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 16
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD

3-58131641-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131641
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131641
    reference: chr 3
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5354-7A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1694-7A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5519-7A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4847-7A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4886-7A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5426-7A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5426-7A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5393-7A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5426-7A>G
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13610
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19436
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2794
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2163
  bin: 9.25e1
  variant carriers: 0
hgvs: c.5519-7A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD

3-58131657-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131657
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131657
    reference: chr 3
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5363T>C
  hgvsp: ENSP00000351339.3:p.Leu1788Pro
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5402T>C
  hgvsp: ENSP00000415599.2:p.Leu1801Pro
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5435T>C
  hgvsp: ENSP00000295956.4:p.Leu1812Pro
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4895T>C
  hgvsp: ENSP00000414532.2:p.Leu1632Pro
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4856T>C
  hgvsp: ENSP00000418510.1:p.Leu1619Pro
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5435T>C
  hgvsp: ENSP00000349819.4:p.Leu1812Pro
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5435T>C
  hgvsp: ENSP00000232447.7:p.Leu1812Pro
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5528T>C
  hgvsp: ENSP00000420213.1:p.Leu1843Pro
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1703T>C
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19437
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6121
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13610
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2794
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16427
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Leu1843Pro
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

3-58131658-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131658
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131658
    reference: chr 3
allele count: 2
allele frequency: 1.647283629295292e-5
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5364C>T
  hgvsp: ENST00000358537.3:c.5364C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5436C>T
  hgvsp: ENST00000295956.4:c.5436C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5436C>T
  hgvsp: ENST00000348383.5:c.5436C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5436C>T
  hgvsp: ENST00000357272.4:c.5436C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5529C>T
  hgvsp: ENST00000490882.1:c.5529C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5403C>T
  hgvsp: ENST00000429972.2:c.5403C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1704C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4857C>T
  hgvsp: ENST00000493452.1:c.4857C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4896C>T
  hgvsp: ENST00000419752.2:c.4896C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13610
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19439
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6121
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2794
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7750
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu1843Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

3-58131658-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131658
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131658
    reference: chr 3
allele count: 2
allele frequency: 1.647283629295292e-5
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5436C>G
  hgvsp: ENST00000357272.4:c.5436C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4896C>G
  hgvsp: ENST00000419752.2:c.4896C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5436C>G
  hgvsp: ENST00000295956.4:c.5436C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5364C>G
  hgvsp: ENST00000358537.3:c.5364C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5529C>G
  hgvsp: ENST00000490882.1:c.5529C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4857C>G
  hgvsp: ENST00000493452.1:c.4857C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5403C>G
  hgvsp: ENST00000429972.2:c.5403C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1704C>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5436C>G
  hgvsp: ENST00000348383.5:c.5436C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13610
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6121
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19439
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2794
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4712
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu1843Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

3-58131659-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131659
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131659
    reference: chr 3
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5437C>T
  hgvsp: ENSP00000349819.4:p.Gln1813Ter
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5404C>T
  hgvsp: ENSP00000415599.2:p.Gln1802Ter
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5437C>T
  hgvsp: ENSP00000295956.4:p.Gln1813Ter
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5437C>T
  hgvsp: ENSP00000232447.7:p.Gln1813Ter
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4897C>T
  hgvsp: ENSP00000414532.2:p.Gln1633Ter
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5365C>T
  hgvsp: ENSP00000351339.3:p.Gln1789Ter
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5530C>T
  hgvsp: ENSP00000420213.1:p.Gln1844Ter
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4858C>T
  hgvsp: ENSP00000418510.1:p.Gln1620Ter
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1705C>T
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2791
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13610
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19442
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gln1844Ter
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

3-58131667-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131667
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131667
    reference: chr 3
allele count: 85
allele frequency: 7.000955424504991e-4
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5445C>T
  hgvsp: ENST00000348383.5:c.5445C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5412C>T
  hgvsp: ENST00000429972.2:c.5412C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5445C>T
  hgvsp: ENST00000357272.4:c.5445C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4905C>T
  hgvsp: ENST00000419752.2:c.4905C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1713C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5373C>T
  hgvsp: ENST00000358537.3:c.5373C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5445C>T
  hgvsp: ENST00000295956.4:c.5445C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5538C>T
  hgvsp: ENST00000490882.1:c.5538C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4866C>T
  hgvsp: ENST00000493452.1:c.4866C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13609
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4985
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19444
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2798
  bin: 9.75e1
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3307
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7752
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Tyr1846Tyr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

3-58131670-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131670
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131670
    reference: chr 3
allele count: 3
allele frequency: 2.470925443942938e-5
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5376G>A
  hgvsp: ENST00000358537.3:c.5376G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5448G>A
  hgvsp: ENST00000357272.4:c.5448G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5448G>A
  hgvsp: ENST00000348383.5:c.5448G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1716G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5415G>A
  hgvsp: ENST00000429972.2:c.5415G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5448G>A
  hgvsp: ENST00000295956.4:c.5448G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5541G>A
  hgvsp: ENST00000490882.1:c.5541G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4869G>A
  hgvsp: ENST00000493452.1:c.4869G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4908G>A
  hgvsp: ENST00000419752.2:c.4908G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4993
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2717
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val1847Val
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

3-58131677-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131677
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131677
    reference: chr 3
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5455C>T
  hgvsp: ENSP00000232447.7:p.Pro1819Ser
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4876C>T
  hgvsp: ENSP00000418510.1:p.Pro1626Ser
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5383C>T
  hgvsp: ENSP00000351339.3:p.Pro1795Ser
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5455C>T
  hgvsp: ENSP00000349819.4:p.Pro1819Ser
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5422C>T
  hgvsp: ENSP00000415599.2:p.Pro1808Ser
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4915C>T
  hgvsp: ENSP00000414532.2:p.Pro1639Ser
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5455C>T
  hgvsp: ENSP00000295956.4:p.Pro1819Ser
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5548C>T
  hgvsp: ENSP00000420213.1:p.Pro1850Ser
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1723C>T
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6130
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4993
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2716
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3418
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4718
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro1850Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

3-58131687-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131687
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131687
    reference: chr 3
allele count: 3
allele frequency: 2.470925443942938e-5
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5465G>A
  hgvsp: ENSP00000232447.7:p.Gly1822Glu
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5432G>A
  hgvsp: ENSP00000415599.2:p.Gly1811Glu
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5465G>A
  hgvsp: ENSP00000295956.4:p.Gly1822Glu
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4925G>A
  hgvsp: ENSP00000414532.2:p.Gly1642Glu
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5393G>A
  hgvsp: ENSP00000351339.3:p.Gly1798Glu
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5465G>A
  hgvsp: ENSP00000349819.4:p.Gly1822Glu
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4886G>A
  hgvsp: ENSP00000418510.1:p.Gly1629Glu
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1733G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5558G>A
  hgvsp: ENSP00000420213.1:p.Gly1853Glu
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4993
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6130
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2715
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2164
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly1853Glu
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD

3-58131703-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131703
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131703
    reference: chr 3
allele count: 3
allele frequency: 2.470925443942938e-5
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5409C>T
  hgvsp: ENST00000358537.3:c.5409C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5481C>T
  hgvsp: ENST00000295956.4:c.5481C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5481C>T
  hgvsp: ENST00000348383.5:c.5481C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1749C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5481C>T
  hgvsp: ENST00000357272.4:c.5481C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4902C>T
  hgvsp: ENST00000493452.1:c.4902C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4941C>T
  hgvsp: ENST00000419752.2:c.4941C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5574C>T
  hgvsp: ENST00000490882.1:c.5574C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5448C>T
  hgvsp: ENST00000429972.2:c.5448C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4994
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Tyr1858Tyr
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

3-58131716-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131716
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131716
    reference: chr 3
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5461G>A
  hgvsp: ENSP00000415599.2:p.Val1821Met
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5494G>A
  hgvsp: ENSP00000349819.4:p.Val1832Met
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4915G>A
  hgvsp: ENSP00000418510.1:p.Val1639Met
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5422G>A
  hgvsp: ENSP00000351339.3:p.Val1808Met
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5494G>A
  hgvsp: ENSP00000295956.4:p.Val1832Met
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5494G>A
  hgvsp: ENSP00000232447.7:p.Val1832Met
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5587G>A
  hgvsp: ENSP00000420213.1:p.Val1863Met
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4954G>A
  hgvsp: ENSP00000414532.2:p.Val1652Met
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1762G>A
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2712
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4994
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19496
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val1863Met
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

3-58131728-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131728
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131728
    reference: chr 3
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5506G>A
  hgvsp: ENSP00000232447.7:p.Ala1836Thr
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5473G>A
  hgvsp: ENSP00000415599.2:p.Ala1825Thr
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5506G>A
  hgvsp: ENSP00000295956.4:p.Ala1836Thr
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5434G>A
  hgvsp: ENSP00000351339.3:p.Ala1812Thr
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5506G>A
  hgvsp: ENSP00000349819.4:p.Ala1836Thr
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4927G>A
  hgvsp: ENSP00000418510.1:p.Ala1643Thr
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4966G>A
  hgvsp: ENSP00000414532.2:p.Ala1656Thr
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5599G>A
  hgvsp: ENSP00000420213.1:p.Ala1867Thr
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1774G>A
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3299
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6132
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala1867Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum

3-58131732-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131732
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131732
    reference: chr 3
allele count: 2
allele frequency: 1.647310765175851e-5
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5510A>G
  hgvsp: ENSP00000232447.7:p.Asn1837Ser
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5510A>G
  hgvsp: ENSP00000295956.4:p.Asn1837Ser
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1778A>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5510A>G
  hgvsp: ENSP00000349819.4:p.Asn1837Ser
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5603A>G
  hgvsp: ENSP00000420213.1:p.Asn1868Ser
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5438A>G
  hgvsp: ENSP00000351339.3:p.Asn1813Ser
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4970A>G
  hgvsp: ENSP00000414532.2:p.Asn1657Ser
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5477A>G
  hgvsp: ENSP00000415599.2:p.Asn1826Ser
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4931A>G
  hgvsp: ENSP00000418510.1:p.Asn1644Ser
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6132
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2710
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4997
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asn1868Ser
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP

3-58131742-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131742
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131742
    reference: chr 3
allele count: 3
allele frequency: 2.471047559428694e-5
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5487C>T
  hgvsp: ENST00000429972.2:c.5487C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4980C>T
  hgvsp: ENST00000419752.2:c.4980C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4941C>T
  hgvsp: ENST00000493452.1:c.4941C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5448C>T
  hgvsp: ENST00000358537.3:c.5448C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5520C>T
  hgvsp: ENST00000348383.5:c.5520C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5613C>T
  hgvsp: ENST00000490882.1:c.5613C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5520C>T
  hgvsp: ENST00000357272.4:c.5520C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5520C>T
  hgvsp: ENST00000295956.4:c.5520C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1788C>T
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3298
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6133
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2710
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3417
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala1871Ala
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff

3-58131743-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131743
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131743
    reference: chr 3
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5521A>G
  hgvsp: ENSP00000295956.4:p.Thr1841Ala
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5614A>G
  hgvsp: ENSP00000420213.1:p.Thr1872Ala
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5449A>G
  hgvsp: ENSP00000351339.3:p.Thr1817Ala
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4981A>G
  hgvsp: ENSP00000414532.2:p.Thr1661Ala
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5488A>G
  hgvsp: ENSP00000415599.2:p.Thr1830Ala
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5521A>G
  hgvsp: ENSP00000349819.4:p.Thr1841Ala
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5521A>G
  hgvsp: ENSP00000232447.7:p.Thr1841Ala
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4942A>G
  hgvsp: ENSP00000418510.1:p.Thr1648Ala
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1789A>G
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13625
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3298
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6134
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19493
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16324
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3313
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1556
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr1872Ala
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

3-58131745-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131745
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131745
    reference: chr 3
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5490C>T
  hgvsp: ENST00000429972.2:c.5490C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5616C>T
  hgvsp: ENST00000490882.1:c.5616C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5523C>T
  hgvsp: ENST00000295956.4:c.5523C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4944C>T
  hgvsp: ENST00000493452.1:c.4944C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5523C>T
  hgvsp: ENST00000348383.5:c.5523C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5451C>T
  hgvsp: ENST00000358537.3:c.5451C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5523C>T
  hgvsp: ENST00000357272.4:c.5523C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4983C>T
  hgvsp: ENST00000419752.2:c.4983C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1791C>T
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6134
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3298
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2163
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7767
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr1872Thr
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS

3-58131748-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131748
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131748
    reference: chr 3
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5619C>T
  hgvsp: ENST00000490882.1:c.5619C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5454C>T
  hgvsp: ENST00000358537.3:c.5454C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5526C>T
  hgvsp: ENST00000295956.4:c.5526C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1794C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4947C>T
  hgvsp: ENST00000493452.1:c.4947C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5493C>T
  hgvsp: ENST00000429972.2:c.5493C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5526C>T
  hgvsp: ENST00000357272.4:c.5526C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5526C>T
  hgvsp: ENST00000348383.5:c.5526C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4986C>T
  hgvsp: ENST00000419752.2:c.4986C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4998
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3298
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6134
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4717
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Phe1873Phe
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

3-58131754-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131754
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131754
    reference: chr 3
allele count: 76
allele frequency: 6.260709107684196e-4
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5532C>T
  hgvsp: ENST00000357272.4:c.5532C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4992C>T
  hgvsp: ENST00000419752.2:c.4992C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5625C>T
  hgvsp: ENST00000490882.1:c.5625C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5460C>T
  hgvsp: ENST00000358537.3:c.5460C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4953C>T
  hgvsp: ENST00000493452.1:c.4953C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5499C>T
  hgvsp: ENST00000429972.2:c.5499C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1800C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5532C>T
  hgvsp: ENST00000295956.4:c.5532C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5532C>T
  hgvsp: ENST00000348383.5:c.5532C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6135
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 9.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13619
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 7.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3296
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile1875Ile
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

3-58131755-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131755
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131755
    reference: chr 3
allele count: 3
allele frequency: 2.47137325974133e-5
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5533G>A
  hgvsp: ENSP00000349819.4:p.Val1845Ile
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5533G>A
  hgvsp: ENSP00000295956.4:p.Val1845Ile
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5533G>A
  hgvsp: ENSP00000232447.7:p.Val1845Ile
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.4993G>A
  hgvsp: ENSP00000414532.2:p.Val1665Ile
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5500G>A
  hgvsp: ENSP00000415599.2:p.Val1834Ile
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5461G>A
  hgvsp: ENSP00000351339.3:p.Val1821Ile
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4954G>A
  hgvsp: ENSP00000418510.1:p.Val1652Ile
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5626G>A
  hgvsp: ENSP00000420213.1:p.Val1876Ile
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1801G>A
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13642
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2698
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4997
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1553
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2166
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val1876Ile
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD

3-58131770-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131770
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131770
    reference: chr 3
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: T
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: stop_gained
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5548G>T
  hgvsp: ENSP00000232447.7:p.Gly1850Ter
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: stop_gained
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5548G>T
  hgvsp: ENSP00000295956.4:p.Gly1850Ter
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: stop_gained
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5476G>T
  hgvsp: ENSP00000351339.3:p.Gly1826Ter
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: stop_gained
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4969G>T
  hgvsp: ENSP00000418510.1:p.Gly1657Ter
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: stop_gained
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5548G>T
  hgvsp: ENSP00000349819.4:p.Gly1850Ter
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: stop_gained
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.5008G>T
  hgvsp: ENSP00000414532.2:p.Gly1670Ter
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  clinical significance: pathogenic
  consequence: stop_gained
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5641G>T
  hgvsp: ENSP00000420213.1:p.Gly1881Ter
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1816G>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: stop_gained
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5515G>T
  hgvsp: ENSP00000415599.2:p.Gly1839Ter
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13616
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6132
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5021
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19498
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7753
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly1881Ter
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: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

3-58131782-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131782
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131782
    reference: chr 3
allele count: 1
allele frequency: 8.244159013339049e-6
allele num: 121298
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5554+6G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5521+6G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1822+6G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5554+6G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5554+6G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5647+6G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5482+6G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4975+6G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.5014+6G>A
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13548
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5026
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19444
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4691
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
hgvs: c.5647+6G>A
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

3-58131786-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131786
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131786
    reference: chr 3
allele count: 1
allele frequency: 8.247694769311978e-6
allele num: 121246
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5554+10G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5482+10G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5554+10G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5554+10G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5647+10G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1822+10G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5521+10G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4975+10G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.5014+10G>A
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19345
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6091
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4683
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21243
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1543
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

3-58131790-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131790
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131790
    reference: chr 3
allele count: 1
allele frequency: 8.257638315441784e-6
allele num: 121100
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5554+14T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5554+14T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5554+14T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4975+14T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5482+14T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5521+14T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1822+14T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5647+14T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.5014+14T>C
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5954
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3240
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19134
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3163
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7265
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: T
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

3-58131792-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131792
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131792
    reference: chr 3
allele count: 1
allele frequency: 8.258183860205463e-6
allele num: 121092
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5554+16C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5521+16C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5554+16C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5482+16C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1822+16C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4975+16C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5647+16C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.5014+16C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5554+16C>T
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 19168
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3235
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5156
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1984
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12974
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5928
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3369
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1537
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

3-58131792-CGT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131792
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131790
    reference: chr 3
allele count: 1
allele frequency: 8.258183860205463e-6
allele num: 121092
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5482+19_5482+20delGT
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5554+19_5554+20delGT
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5554+19_5554+20delGT
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.5014+19_5014+20delGT
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1822+19_1822+20delGT
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5521+19_5521+20delGT
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5647+19_5647+20delGT
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4975+19_4975+20delGT
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5554+19_5554+20delGT
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3235
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1984
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19168
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5928
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5156
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12974
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2149
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4597
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3369
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3154
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: CGT
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

3-58131793-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131793
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131793
    reference: chr 3
allele count: 6
allele frequency: 4.954664816925135e-5
allele num: 121098
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5554+17G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5647+17G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1822+17G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5554+17G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4975+17G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5482+17G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5554+17G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5521+17G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.5014+17G>A
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19193
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1982
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5912
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3227
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5200
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12929
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4591
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1537
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7230
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20891
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum

3-58131800-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131800
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131800
    reference: chr 3
allele count: 1
allele frequency: 8.262687356435807e-6
allele num: 121026
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5482+24T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5521+24T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5554+24T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1822+24T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5554+24T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5647+24T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5554+24T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4975+24T>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.5014+24T>C
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18609
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5345
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5804
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3355
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4557
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum

3-58131802-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131802
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131802
    reference: chr 3
allele count: 1
allele frequency: 8.271298593879239e-6
allele num: 120900
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5482+26C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5554+26C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5554+26C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5554+26C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5521+26C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.5014+26C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4975+26C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1822+26C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5647+26C>T
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5748
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3205
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18359
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5392
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12075
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 638
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 804
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19470
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

3-58131805-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131805
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131805
    reference: chr 3
allele count: 1
allele frequency: 8.267605866693123e-6
allele num: 120954
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5482+29C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4975+29C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5647+29C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5521+29C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5554+29C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1822+29C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5554+29C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5554+29C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.5014+29C>T
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11340
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5716
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17745
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5619
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 968
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1036
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16163
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD

3-58131815-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131815
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131815
    reference: chr 3
allele count: 1
allele frequency: 8.279516476237788e-6
allele num: 120780
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5647+39C>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5521+39C>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.5014+39C>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5554+39C>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4975+39C>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5554+39C>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5482+39C>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5554+39C>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1822+39C>G
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5248
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5482
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10059
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6209
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6082
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2814
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 821
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/3-58131823-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131823
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131823
    reference: chr 3
allele count: 1
allele frequency: 8.291048983517394e-6
allele num: 120612
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5647+47A>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5554+47A>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4975+47A>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.5014+47A>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5521+47A>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1822+47A>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5554+47A>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5554+47A>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5482+47A>C
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9091
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6337
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3085
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12125
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3116
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2057
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1181
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5666
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2687
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
reference allele: A
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

3-58131825-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131825
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131825
    reference: chr 3
allele count: 1
allele frequency: 8.303165166561494e-6
allele num: 120436
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5482+49G>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4975+49G>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5554+49G>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5554+49G>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1822+49G>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5647+49G>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5554+49G>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5521+49G>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.5014+49G>C
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11635
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6334
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9845
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3086
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 967
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3107
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2056
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9483
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2719
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

3-58131828-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58131828
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58131828
    reference: chr 3
allele count: 2
allele frequency: 1.663091020971578e-5
allele num: 120258
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1822+52G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4975+52G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5521+52G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.5014+52G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5554+52G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5647+52G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5554+52G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5482+52G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5554+52G>A
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3082
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8657
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10334
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5393
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2194
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6301
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2142
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3767
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4088
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2639
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2078
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2738
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: G
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/3-58132505-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58132505
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58132505
    reference: chr 3
allele count: 1
allele frequency: 8.271298593879239e-6
allele num: 120900
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5522-42A>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000491408
  gene symbol: FLNB
  hgvsc: ENST00000491408.1:n.101A>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5555-42A>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.5015-42A>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5483-42A>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1823-42A>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5555-42A>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4976-42A>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5648-42A>C
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5555-42A>C
  variant of: http://identifiers.org/hgnc/3755
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13133
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4763
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12658
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 581
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10353
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2922
  bin: 8.25e1
  variant carriers: 0
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: A
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

3-58132508-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58132508
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58132508
    reference: chr 3
allele count: 2
allele frequency: 1.65371258475277e-5
allele num: 120940
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5648-39C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5555-39C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.5015-39C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5555-39C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000491408
  gene symbol: FLNB
  hgvsc: ENST00000491408.1:n.104C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5522-39C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5483-39C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5555-39C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4976-39C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1823-39C>T
  variant of: http://identifiers.org/hgnc/3755
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4774
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13628
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21283
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12738
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10413
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4353
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

http://identifiers.org/exac.variant/3-58132512-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58132512
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58132512
    reference: chr 3
allele count: 1
allele frequency: 8.263779852904718e-6
allele num: 121010
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5522-35C>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5483-35C>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4976-35C>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5555-35C>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.5015-35C>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5555-35C>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5648-35C>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000491408
  gene symbol: FLNB
  hgvsc: ENST00000491408.1:n.108C>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1823-35C>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5555-35C>A
  variant of: http://identifiers.org/hgnc/3755
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12807
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21515
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4774
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2282
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14039
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10477
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3624
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/3-58132521-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58132521
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58132521
    reference: chr 3
allele count: 1
allele frequency: 8.253549026081216e-6
allele num: 121160
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1823-26C>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5555-26C>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5555-26C>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5555-26C>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5648-26C>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000491408
  gene symbol: FLNB
  hgvsc: ENST00000491408.1:n.117C>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4976-26C>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5522-26C>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5483-26C>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.5015-26C>A
  variant of: http://identifiers.org/hgnc/3755
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14402
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21938
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12899
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4773
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3664
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

3-58132526-CAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58132526
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58132524
    reference: chr 3
allele count: 1
allele frequency: 8.248647221855616e-6
allele num: 121232
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5483-20_5483-19delAT
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4976-20_4976-19delAT
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000491408
  gene symbol: FLNB
  hgvsc: ENST00000491408.1:n.123_124delAT
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1823-20_1823-19delAT
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5555-20_5555-19delAT
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.5015-20_5015-19delAT
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5555-20_5555-19delAT
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5522-20_5522-19delAT
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5555-20_5555-19delAT
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5648-20_5648-19delAT
  variant of: http://identifiers.org/hgnc/3755
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14398
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12948
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22091
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
reference allele: CAT
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

3-58132537-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58132537
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58132537
    reference: chr 3
allele count: 1
allele frequency: 8.24347940778844e-6
allele num: 121308
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5555-10C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4976-10C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000491408
  gene symbol: FLNB
  hgvsc: ENST00000491408.1:n.133C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1823-10C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5555-10C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5648-10C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.5015-10C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5555-10C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5483-10C>T
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5522-10C>T
  variant of: http://identifiers.org/hgnc/3755
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22294
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12960
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4778
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14343
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10682
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

3-58132543-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58132543
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58132543
    reference: chr 3
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4976-4G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5555-4G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5483-4G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5555-4G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5522-4G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000491408
  gene symbol: FLNB
  hgvsc: ENST00000491408.1:n.139G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5648-4G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5555-4G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.5015-4G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1823-4G>A
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22350
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14325
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4777
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12975
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5718
  bin: 9.75e1
  variant carriers: 1
hgvs: c.5648-4G>A
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

3-58132548-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58132548
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58132548
    reference: chr 3
allele count: 2
allele frequency: 1.648206751054852e-5
allele num: 121344
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5649T>A
  hgvsp: ENST00000490882.1:c.5649T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5556T>A
  hgvsp: ENST00000295956.4:c.5556T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5556T>A
  hgvsp: ENST00000357272.4:c.5556T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.5016T>A
  hgvsp: ENST00000419752.2:c.5016T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5523T>A
  hgvsp: ENST00000429972.2:c.5523T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000491408
  gene symbol: FLNB
  hgvsc: ENST00000491408.1:n.144T>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1824T>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4977T>A
  hgvsp: ENST00000493452.1:c.4977T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5556T>A
  hgvsp: ENST00000348383.5:c.5556T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5484T>A
  hgvsp: ENST00000358537.3:c.5484T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12985
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14291
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22380
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4783
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.5649T>A
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD

3-58132552-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58132552
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58132552
    reference: chr 3
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.5560C>G
  hgvsp: ENSP00000232447.7:p.Leu1854Val
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.5527C>G
  hgvsp: ENSP00000415599.2:p.Leu1843Val
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.5488C>G
  hgvsp: ENSP00000351339.3:p.Leu1830Val
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.5560C>G
  hgvsp: ENSP00000349819.4:p.Leu1854Val
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000491408
  gene symbol: FLNB
  hgvsc: ENST00000491408.1:n.148C>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.5653C>G
  hgvsp: ENSP00000420213.1:p.Leu1885Val
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.5560C>G
  hgvsp: ENSP00000295956.4:p.Leu1854Val
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.4981C>G
  hgvsp: ENSP00000418510.1:p.Leu1661Val
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000136068
  ensembl transcript: ENST00000481470
  gene symbol: FLNB
  hgvsc: ENST00000481470.1:n.1828C>G
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.5020C>G
  hgvsp: ENSP00000414532.2:p.Leu1674Val
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12997
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14282
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu1885Val
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 1051
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1298
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3746
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9245
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8270
bin: 9.75e1
variant carriers: 52

GenotypeQuality
all individuals: 29790
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 45
allele frequency: 5.210745715609078e-3
allele num: 8636
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.650646593321752e-5
allele num: 10362
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501907422426482e-5
allele num: 66582
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: 11546
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.033244358165494e-4
allele num: 16484
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 1.097e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

VQSLOD
type: SiteQuality
SIO_000300: 4.43e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e0

DP
type: SiteQuality
SIO_000300: 1.983287e6

MQRankSum
type: SiteQuality
SIO_000300: 2.18e-1

QD
type: SiteQuality
SIO_000300: 1.25e1

GenotypeQuality
all individuals: 133
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8248
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3285
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2472
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9304
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3767
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29994
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 5.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66578
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.213297743266198e-4
allele num: 16484
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.061e0

QD
type: SiteQuality
SIO_000300: 1.145e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.9e-2

DP
type: SiteQuality
SIO_000300: 1.984032e6

VQSLOD
type: SiteQuality
SIO_000300: -1.793e0

FS
type: SiteQuality
SIO_000300: 1.3711e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.986e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.599999999999999e-2

GenotypeQuality
all individuals: 85
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 69
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1053
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1319
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9300
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3768
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8251
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 377
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.004175804368072e-5
allele num: 66574
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.654373431164318e-5
allele num: 10358
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: 11544
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.56e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.68e0

FS
type: SiteQuality
SIO_000300: 3.595e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.77e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.93e-1

DP
type: SiteQuality
SIO_000300: 1.983719e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.429e0

QD
type: SiteQuality
SIO_000300: 1.051e1

GenotypeQuality
all individuals: 70
bin: 1.25e1
variant carriers: 5

GenotypeQuality
all individuals: 242
bin: 2.75e1
variant carriers: 5

GenotypeQuality
all individuals: 81
bin: 1.75e1
variant carriers: 6

GenotypeQuality
all individuals: 237
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 83
bin: 7.5e0
variant carriers: 5

GenotypeQuality
all individuals: 254
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3161
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 8995
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 197
bin: 4.25e1
variant carriers: 4

GenotypeQuality
all individuals: 7999
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1010
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 299
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 29528
bin: 6.25e1
variant carriers: 3

GenotypeQuality
all individuals: 3617
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1242
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 7
allele frequency: 6.903353057199211e-4
allele num: 10140
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.708097928436911e-4
allele num: 6372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 18
allele frequency: 2.729588741962877e-4
allele num: 65944
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.689607229753215e-5
allele num: 11508
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.9102e1

MQRankSum
type: SiteQuality
SIO_000300: 1.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.912e0

MQ
type: SiteQuality
SIO_000300: 5.892e1

VQSLOD
type: SiteQuality
SIO_000300: -3.996e1

DP
type: SiteQuality
SIO_000300: 1.993111e6

QD
type: SiteQuality
SIO_000300: 2.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.582e0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2386
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3685
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3213
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30590
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1245
bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.665511265164645e-5
allele num: 11540
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.104e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.977857e6

MQRankSum
type: SiteQuality
SIO_000300: -2.52e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.298e0

FS
type: SiteQuality
SIO_000300: 2.365e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.13e-1

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

GenotypeQuality
all individuals: 159
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9266
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3671
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30138
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1242
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8011
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1016
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2388
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66488
num of homozygotes: 0

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

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

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

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

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.522533495736906e-4
allele num: 6568
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.973452e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.88e-1

QD
type: SiteQuality
SIO_000300: 8.09e0

MQRankSum
type: SiteQuality
SIO_000300: -1.364e0

VQSLOD
type: SiteQuality
SIO_000300: -9.842e-1

GenotypeQuality
all individuals: 1240
bin: 9.25e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 1015
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6560
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: 1
allele frequency: 1.504392827055001e-5
allele num: 66472
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.246e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -6.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

FS
type: SiteQuality
SIO_000300: 1.032e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

VQSLOD
type: SiteQuality
SIO_000300: 5.22e-1

DP
type: SiteQuality
SIO_000300: 1.971757e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.71e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.48e0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66372
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.11e-1

MQ
type: SiteQuality
SIO_000300: 5.876e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.415e1

FS
type: SiteQuality
SIO_000300: 3.962e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.754e0

DP
type: SiteQuality
SIO_000300: 1.960222e6

VQSLOD
type: SiteQuality
SIO_000300: 2.38e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.070000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.599999999999999e-2

GenotypeQuality
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bin: 9.25e1
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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8001
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 1
allele frequency: 9.74089226573154e-5
allele num: 10266
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66276
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16428
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: -5.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.69e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.853e0

FS
type: SiteQuality
SIO_000300: 3.848e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.938541e6

QD
type: SiteQuality
SIO_000300: 1.235e1

VQSLOD
type: SiteQuality
SIO_000300: 5.94e-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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variant carriers: 2

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: 17
bin: 1.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16424
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6528
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.021695775669306e-5
allele num: 66188
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.55e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.94e0

QD
type: SiteQuality
SIO_000300: 1.4e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.34e0

DP
type: SiteQuality
SIO_000300: 1.915747e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

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
all individuals: 2829
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.093845216331505e-5
allele num: 16410
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66142
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.003e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.318e0

VQSLOD
type: SiteQuality
SIO_000300: -1.449e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

DP
type: SiteQuality
SIO_000300: 1.904453e6

QD
type: SiteQuality
SIO_000300: 1.233e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7.5e0
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66044
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.097560975609756e-5
allele num: 16400
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6480
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10190
num of homozygotes: 0

Other
type: Population
allele count: 0
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allele num: 890
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.47e0

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.139999999999999e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.88251e6

QD
type: SiteQuality
SIO_000300: 9.140000000000001e0

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: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.542426261280358e-5
allele num: 66044
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10190
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6480
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.097560975609756e-5
allele num: 16400
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0

MQRankSum
type: SiteQuality
SIO_000300: 2.76e-1

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.88251e6

QD
type: SiteQuality
SIO_000300: 9.140000000000001e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 26

GenotypeQuality
all individuals: 1904
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GenotypeQuality
all individuals: 1214
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 20
allele frequency: 2.015722636565209e-3
allele num: 9922
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11354
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.798464491362764e-4
allele num: 6252
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16302
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.339181286549708e-4
allele num: 8550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.536239899222663e-5
allele num: 65094
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.799579e6

VQSLOD
type: SiteQuality
SIO_000300: 2.37e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.87e0

FS
type: SiteQuality
SIO_000300: 9.409999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.83e-1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.206e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.21e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2432
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 972
bin: 8.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9972
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.227897838899803e-4
allele num: 16288
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6304
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11366
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65170
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.79e-1

DP
type: SiteQuality
SIO_000300: 1.797989e6

FS
type: SiteQuality
SIO_000300: 1.2961e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.66e0

QD
type: SiteQuality
SIO_000300: 1.18e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.4e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.882e0

GenotypeQuality
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bin: 7.25e1
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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
all individuals: 600
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.539930395146139e-5
allele num: 64938
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16290
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9896
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11328
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6230
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.54e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.106e1

VQSLOD
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SIO_000300: -2.6e0

BaseQRankSum
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SIO_000300: -3.908e0

DP
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SIO_000300: 1.797263e6

FS
type: SiteQuality
SIO_000300: 1.9014e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.67e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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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variant carriers: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.023888720895071e-4
allele num: 6614
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.88e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

MQRankSum
type: SiteQuality
SIO_000300: 2.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.253e0

QD
type: SiteQuality
SIO_000300: 1.144e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e-1

DP
type: SiteQuality
SIO_000300: 2.529996e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.31e-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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variant carriers: 0

Other
type: Population
allele count: 4
allele frequency: 4.405286343612335e-3
allele num: 908
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.239854633555421e-4
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 76
allele frequency: 1.138747377884327e-3
allele num: 66740
num of homozygotes: 0

African
type: Population
allele count: 226
allele frequency: 2.171823947722468e-2
allele num: 10406
num of homozygotes: 3

Latino
type: Population
allele count: 31
allele frequency: 2.677491794783209e-3
allele num: 11578
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.023888720895071e-4
allele num: 6614
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.62e-1

DP
type: SiteQuality
SIO_000300: 2.530113e6

MQRankSum
type: SiteQuality
SIO_000300: 2.77e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.54e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.85e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.25e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.81e-1

QD
type: SiteQuality
SIO_000300: 1.363e1

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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variant carriers: 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: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

African
type: Population
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: 6614
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.505074e6

FS
type: SiteQuality
SIO_000300: 5.064e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.352e1

MQRankSum
type: SiteQuality
SIO_000300: 7.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.58e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

VQSLOD
type: SiteQuality
SIO_000300: 6.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.938e0

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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South Asian
type: Population
allele count: 10
allele frequency: 6.056201550387597e-4
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 177
allele frequency: 2.652082709020078e-3
allele num: 66740
num of homozygotes: 1

Latino
type: Population
allele count: 37
allele frequency: 3.195716013128347e-3
allele num: 11578
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

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

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

African
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allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.23e-1

MQ
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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QD
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DP
type: SiteQuality
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VQSLOD
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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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East Asian
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allele num: 8654
num of homozygotes: 0

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

African
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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
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

Other
type: Population
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ClippingRankSum
type: SiteQuality
SIO_000300: -7.26e-1

MQ
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
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FS
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BaseQRankSum
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QD
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MQRankSum
type: SiteQuality
SIO_000300: 9.6e-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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Latino
type: Population
allele count: 0
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num of homozygotes: 0

East Asian
type: Population
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allele frequency: 1.155535012710885e-4
allele num: 8654
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African
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South Asian
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Other
type: Population
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European (Non-Finnish)
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European (Finnish)
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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QD
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MQRankSum
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InbreedingCoeff
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DP
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FS
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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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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 0
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South Asian
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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FS
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QD
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MQ
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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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European (Non-Finnish)
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allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.498351813005694e-5
allele num: 66740
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South Asian
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African
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Other
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ClippingRankSum
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SIO_000300: -6.26e-1

MQ
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BaseQRankSum
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MQRankSum
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FS
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ReadPosRankSum
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QD
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InbreedingCoeff
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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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African
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allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66740
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South Asian
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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Latino
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Other
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InbreedingCoeff
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DP
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VQSLOD
type: SiteQuality
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BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.934e1

MQRankSum
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ReadPosRankSum
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QD
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ClippingRankSum
type: SiteQuality
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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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African
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East Asian
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allele num: 8654
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South Asian
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Latino
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allele frequency: 4.698566246329245e-2
allele num: 11578
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European (Finnish)
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allele frequency: 0.0e0
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Other
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European (Non-Finnish)
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allele count: 68
allele frequency: 1.018879232843872e-3
allele num: 66740
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ReadPosRankSum
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MQRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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FS
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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 (Non-Finnish)
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African
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European (Finnish)
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South Asian
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East Asian
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Other
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Latino
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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DP
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MQ
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BaseQRankSum
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FS
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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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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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Other
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South Asian
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FS
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InbreedingCoeff
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ReadPosRankSum
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DP
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QD
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VQSLOD
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66740
num of homozygotes: 0

African
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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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BaseQRankSum
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FS
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VQSLOD
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InbreedingCoeff
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MQRankSum
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MQ
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ClippingRankSum
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ReadPosRankSum
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DP
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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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European (Non-Finnish)
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ReadPosRankSum
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QD
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FS
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DP
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VQSLOD
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MQ
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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East Asian
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African
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European (Finnish)
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DP
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VQSLOD
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QD
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FS
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InbreedingCoeff
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MQ
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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European (Non-Finnish)
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European (Finnish)
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South Asian
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African
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FS
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MQRankSum
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VQSLOD
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QD
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BaseQRankSum
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MQ
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DP
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African
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European (Finnish)
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East Asian
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European (Non-Finnish)
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South Asian
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VQSLOD
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MQRankSum
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QD
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DP
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ClippingRankSum
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MQ
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FS
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InbreedingCoeff
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BaseQRankSum
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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African
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Other
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InbreedingCoeff
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BaseQRankSum
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MQ
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MQRankSum
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DP
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ClippingRankSum
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ReadPosRankSum
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FS
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VQSLOD
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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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East Asian
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European (Non-Finnish)
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African
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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MQ
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DP
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FS
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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FS
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MQ
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QD
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VQSLOD
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DP
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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FS
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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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Latino
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Other
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South Asian
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African
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European (Finnish)
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East Asian
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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South Asian
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African
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East Asian
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Other
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Latino
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ReadPosRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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MQRankSum
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MQ
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VQSLOD
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QD
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BaseQRankSum
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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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African
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European (Non-Finnish)
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European (Finnish)
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East Asian
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South Asian
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Other
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VQSLOD
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ReadPosRankSum
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FS
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MQRankSum
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DP
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QD
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ClippingRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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Other
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East Asian
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European (Non-Finnish)
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European (Finnish)
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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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VQSLOD
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MQ
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ClippingRankSum
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QD
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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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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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Latino
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European (Finnish)
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European (Non-Finnish)
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East Asian
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African
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BaseQRankSum
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ClippingRankSum
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QD
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VQSLOD
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InbreedingCoeff
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DP
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ReadPosRankSum
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MQRankSum
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MQ
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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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European (Finnish)
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Latino
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African
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South Asian
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East Asian
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European (Non-Finnish)
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Other
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MQRankSum
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QD
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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FS
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MQ
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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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European (Finnish)
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Latino
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Other
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African
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European (Non-Finnish)
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South Asian
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East Asian
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MQRankSum
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DP
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MQ
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QD
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FS
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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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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East Asian
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South Asian
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African
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European (Non-Finnish)
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European (Finnish)
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MQRankSum
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MQ
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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FS
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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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European (Finnish)
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.498890820792613e-5
allele num: 66716
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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African
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South Asian
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East Asian
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VQSLOD
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MQRankSum
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ReadPosRankSum
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FS
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DP
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QD
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MQ
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BaseQRankSum
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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Latino
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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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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
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African
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allele frequency: 0.0e0
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East Asian
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FS
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VQSLOD
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InbreedingCoeff
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DP
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QD
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MQ
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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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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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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South Asian
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Latino
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allele num: 11546
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East Asian
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European (Finnish)
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European (Non-Finnish)
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FS
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QD
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DP
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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allele num: 66598
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Latino
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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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Other
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East Asian
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QD
type: SiteQuality
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FS
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BaseQRankSum
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InbreedingCoeff
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MQ
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DP
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ClippingRankSum
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MQRankSum
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VQSLOD
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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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East Asian
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allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66594
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African
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allele count: 1
allele frequency: 9.63020030816641e-5
allele num: 10384
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Latino
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allele frequency: 0.0e0
allele num: 11520
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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MQRankSum
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QD
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BaseQRankSum
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ReadPosRankSum
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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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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Other
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European (Finnish)
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Latino
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South Asian
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European (Non-Finnish)
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MQRankSum
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VQSLOD
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DP
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QD
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FS
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ClippingRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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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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Latino
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African
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East Asian
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South Asian
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Other
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European (Non-Finnish)
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European (Finnish)
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MQ
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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DP
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VQSLOD
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QD
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InbreedingCoeff
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FS
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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European (Finnish)
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African
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South Asian
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European (Non-Finnish)
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Other
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ReadPosRankSum
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QD
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InbreedingCoeff
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FS
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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DP
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MQ
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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African
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Latino
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South Asian
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European (Finnish)
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European (Non-Finnish)
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allele num: 66482
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ClippingRankSum
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DP
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MQRankSum
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InbreedingCoeff
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QD
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FS
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ReadPosRankSum
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VQSLOD
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MQ
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BaseQRankSum
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

Other
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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: 11504
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66500
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.261e0

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.505e0

DP
type: SiteQuality
SIO_000300: 2.339862e6

FS
type: SiteQuality
SIO_000300: 7.15e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

QD
type: SiteQuality
SIO_000300: 1.113e1

VQSLOD
type: SiteQuality
SIO_000300: 3.98e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66418
num of homozygotes: 0

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.167406023815083e-4
allele num: 8566
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.39e0

DP
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VQSLOD
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SIO_000300: -1.131e-1

MQRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
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ReadPosRankSum
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SIO_000300: -1.077e0

InbreedingCoeff
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SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.231e1

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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variant carriers: 0

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

Other
type: Population
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: 6572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66336
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16434
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.654373431164318e-5
allele num: 10358
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.558e0

QD
type: SiteQuality
SIO_000300: 2.777e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e0

ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
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VQSLOD
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BaseQRankSum
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SIO_000300: -1.883e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

DP
type: SiteQuality
SIO_000300: 2.258917e6

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10352
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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66252
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.732099196646873e-5
allele num: 11452
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8486
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.878e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -4.41e-1

InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -4.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.449e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.669999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.253503e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.023431594860166e-5
allele num: 66150
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16424
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11434
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.631e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.26e-1

ClippingRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.72e-1

DP
type: SiteQuality
SIO_000300: 2.249925e6

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.617e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

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

African
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
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num of homozygotes: 0

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

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

South Asian
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allele count: 1
allele frequency: 6.09979260705136e-5
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66526
num of homozygotes: 0

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

East Asian
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South Asian
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allele frequency: 1.218917601170161e-4
allele num: 16408
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
type: Population
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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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ClippingRankSum
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ReadPosRankSum
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QD
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FS
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BaseQRankSum
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DP
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MQRankSum
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MQ
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InbreedingCoeff
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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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East Asian
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allele frequency: 1.162250116225012e-4
allele num: 8604
num of homozygotes: 0

South Asian
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African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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Latino
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Other
type: Population
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European (Non-Finnish)
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MQ
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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FS
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MQRankSum
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DP
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VQSLOD
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InbreedingCoeff
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50073536032656e-5
allele num: 66634
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 2.78e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.584e0

QD
type: SiteQuality
SIO_000300: 1.188e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.17e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.5e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.5e-2

DP
type: SiteQuality
SIO_000300: 1.83204e6

GenotypeQuality
all individuals: 61
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2939
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3679
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30023
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500060002400096e-5
allele num: 66664
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.009e0

MQRankSum
type: SiteQuality
SIO_000300: -4.29e-1

MQ
type: SiteQuality
SIO_000300: 5.895e1

VQSLOD
type: SiteQuality
SIO_000300: 9.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e-1

DP
type: SiteQuality
SIO_000300: 1.834835e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.8e0

QD
type: SiteQuality
SIO_000300: 1.109e1

GenotypeQuality
all individuals: 5717
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2941
bin: 8.25e1
variant carriers: 0

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
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: 16476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499205421126803e-5
allele num: 66702
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.17e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.69e-1

FS
type: SiteQuality
SIO_000300: 7.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.51e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

DP
type: SiteQuality
SIO_000300: 1.838108e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.147e0

QD
type: SiteQuality
SIO_000300: 2.384e1

GenotypeQuality
all individuals: 4405
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10692
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30247
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1582
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

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

African
type: Population
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: 6608
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 6.19e0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.331e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.039e0

DP
type: SiteQuality
SIO_000300: 1.8389e6

QD
type: SiteQuality
SIO_000300: 1.063e1

MQ
type: SiteQuality
SIO_000300: 5.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.436e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.55e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeDepth
all individuals: 44
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5719
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10691
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1216
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1581
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2947
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30234
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997512064986062e-5
allele num: 66722
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: 906
num of homozygotes: 0

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.340000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.839588e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.53e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.191e0

QD
type: SiteQuality
SIO_000300: 1.175e1