3-58088047-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58088047
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58088047
    reference: chr 3
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.1463G>A
  hgvsp: ENSP00000295956.4:p.Gly488Asp
  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.1463G>A
  hgvsp: ENSP00000232447.7:p.Gly488Asp
  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.1463G>A
  hgvsp: ENSP00000349819.4:p.Gly488Asp
  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.1463G>A
  hgvsp: ENSP00000351339.3:p.Gly488Asp
  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.956G>A
  hgvsp: ENSP00000414532.2:p.Gly319Asp
  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.1463G>A
  hgvsp: ENSP00000420213.1:p.Gly488Asp
  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.1463G>A
  hgvsp: ENSP00000415599.2:p.Gly488Asp
  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.956G>A
  hgvsp: ENSP00000418510.1:p.Gly319Asp
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4731
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8835
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6479
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9290
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5042
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10060
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2645
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly488Asp
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/3-58088051-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58088051
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58088051
    reference: chr 3
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.1467A>C
  hgvsp: ENST00000348383.5:c.1467A>C(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.1467A>C
  hgvsp: ENST00000357272.4:c.1467A>C(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.1467A>C
  hgvsp: ENST00000429972.2:c.1467A>C(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.960A>C
  hgvsp: ENST00000419752.2:c.960A>C(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.1467A>C
  hgvsp: ENST00000490882.1:c.1467A>C(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.960A>C
  hgvsp: ENST00000493452.1:c.960A>C(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.1467A>C
  hgvsp: ENST00000295956.4:c.1467A>C(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.1467A>C
  hgvsp: ENST00000358537.3:c.1467A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9290
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4730
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10061
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8834
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5042
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6479
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1742
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val489Val
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

3-58088056-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58088056
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58088056
    reference: chr 3
allele count: 81
allele frequency: 6.671828410457474e-4
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.1472T>C
  hgvsp: ENSP00000349819.4:p.Met491Thr
  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.1472T>C
  hgvsp: ENSP00000420213.1:p.Met491Thr
  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.1472T>C
  hgvsp: ENSP00000351339.3:p.Met491Thr
  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.965T>C
  hgvsp: ENSP00000418510.1:p.Met322Thr
  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.1472T>C
  hgvsp: ENSP00000295956.4:p.Met491Thr
  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.1472T>C
  hgvsp: ENSP00000232447.7:p.Met491Thr
  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.965T>C
  hgvsp: ENSP00000414532.2:p.Met322Thr
  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.1472T>C
  hgvsp: ENSP00000415599.2:p.Met491Thr
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8823
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10049
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4719
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.75e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6460
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Met491Thr
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/3-58088058-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58088058
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58088058
    reference: chr 3
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.1474A>C
  hgvsp: ENSP00000349819.4:p.Lys492Gln
  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.1474A>C
  hgvsp: ENSP00000351339.3:p.Lys492Gln
  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.1474A>C
  hgvsp: ENSP00000232447.7:p.Lys492Gln
  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.967A>C
  hgvsp: ENSP00000414532.2:p.Lys323Gln
  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.1474A>C
  hgvsp: ENSP00000415599.2:p.Lys492Gln
  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.1474A>C
  hgvsp: ENSP00000295956.4:p.Lys492Gln
  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.1474A>C
  hgvsp: ENSP00000420213.1:p.Lys492Gln
  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.967A>C
  hgvsp: ENSP00000418510.1:p.Lys323Gln
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10054
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8827
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2637
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3420
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Lys492Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

3-58088062-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58088062
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58088062
    reference: chr 3
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.1478G>T
  hgvsp: ENSP00000415599.2:p.Gly493Val
  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.1478G>T
  hgvsp: ENSP00000232447.7:p.Gly493Val
  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.1478G>T
  hgvsp: ENSP00000295956.4:p.Gly493Val
  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.1478G>T
  hgvsp: ENSP00000349819.4:p.Gly493Val
  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.1478G>T
  hgvsp: ENSP00000351339.3:p.Gly493Val
  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.1478G>T
  hgvsp: ENSP00000420213.1:p.Gly493Val
  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.971G>T
  hgvsp: ENSP00000414532.2:p.Gly324Val
  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.971G>T
  hgvsp: ENSP00000418510.1:p.Gly324Val
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8825
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10054
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9282
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2277
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1738
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly493Val
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP

3-58088078-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58088078
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58088078
    reference: chr 3
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
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.1483+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.1483+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.1483+11C>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.1483+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.1483+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.976+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.1483+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.976+11C>T
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6453
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10054
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4682
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2633
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4502
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2277
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

3-58088085-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58088085
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58088085
    reference: chr 3
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.976+18T>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.1483+18T>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.976+18T>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.1483+18T>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.1483+18T>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.1483+18T>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.1483+18T>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.1483+18T>C
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10054
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6449
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4669
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8823
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39488
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4487
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1736
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2629
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2278
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
reference allele: T
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

3-58088092-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58088092
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58088092
    reference: chr 3
allele count: 2
allele frequency: 1.647582173160887e-5
allele num: 121390
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.1483+25C>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.1483+25C>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.1483+25C>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.976+25C>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.1483+25C>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.1483+25C>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.976+25C>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.1483+25C>T
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8824
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6437
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10055
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4654
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2279
  bin: 8.75e1
  variant carriers: 0
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: 29
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

3-58088095-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58088095
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58088095
    reference: chr 3
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.1483+28A>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.1483+28A>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.976+28A>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.976+28A>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.1483+28A>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.1483+28A>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.1483+28A>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.1483+28A>G
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10053
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6439
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4641
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7250
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2894
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3668
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

3-58088098-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58088098
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58088098
    reference: chr 3
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.1483+31T>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.976+31T>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.1483+31T>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.976+31T>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.1483+31T>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.1483+31T>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.1483+31T>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.1483+31T>G
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4617
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10053
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7251
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6436
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9286
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2279
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39490
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1731
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: African
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

3-58088102-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58088102
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58088102
    reference: chr 3
allele count: 1109
allele frequency: 9.136294734067093e-3
allele num: 121384
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.1483+35G>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.1483+35G>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.1483+35G>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.1483+35G>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.1483+35G>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.1483+35G>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.976+35G>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.976+35G>A
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4972
  bin: 5.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 6.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 6.75e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6304
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 8.25e1
  variant carriers: 116
genotype depth: GenotypeDepth
  all individuals: 9114
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 96
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 7.25e1
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 4519
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 9.75e1
  variant carriers: 402
genotype depth: GenotypeDepth
  all individuals: 8685
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 9852
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 8.75e1
  variant carriers: 93
genotype depth: GenotypeDepth
  all individuals: 3332
  bin: 5.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 93
genotype depth: GenotypeDepth
  all individuals: 7145
  bin: 4.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1705
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39857
  bin: 9.75e1
  variant carriers: 1102
num of homozygotes: 6
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD

3-58088110-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58088110
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58088110
    reference: chr 3
allele count: 2
allele frequency: 1.647772211969417e-5
allele num: 121376
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.976+43T>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.1483+43T>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.1483+43T>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.1483+43T>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.1483+43T>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.1483+43T>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.1483+43T>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.976+43T>A
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9137
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4511
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5020
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7189
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9871
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3616
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

3-58088118-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58088118
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58088118
    reference: chr 3
allele count: 49
allele frequency: 4.037241492955426e-4
allele num: 121370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.1483+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.1483+51C>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.1483+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.1483+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.1483+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.976+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.1483+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.976+51C>T
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8696
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9868
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6314
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 8.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 5013
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7188
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 6.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 4113
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2849
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1709
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

3-58089636-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089636
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089635
    reference: chr 3
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
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.1484-46delT
  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.977-46delT
  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.1484-46delT
  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.1484-46delT
  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.977-46delT
  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.1484-46delT
  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.1484-46delT
  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.1484-46delT
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10876
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2316
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5799
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7707
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24410
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2484
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4770
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3885
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
reference allele: AT
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD

3-58089643-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089643
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089643
    reference: chr 3
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
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.1484-43G>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.1484-43G>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.977-43G>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.1484-43G>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.1484-43G>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.1484-43G>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.1484-43G>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.977-43G>T
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10917
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7708
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5799
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5947
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4468
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3043
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

3-58089645-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089645
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089645
    reference: chr 3
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
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.1484-41C>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.1484-41C>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.1484-41C>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.1484-41C>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.1484-41C>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.1484-41C>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.977-41C>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.977-41C>T
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10938
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5799
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7705
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3879
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2483
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

3-58089653-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089653
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089653
    reference: chr 3
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
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.977-33G>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.1484-33G>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.977-33G>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.1484-33G>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.1484-33G>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.1484-33G>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.1484-33G>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.1484-33G>A
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7707
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10970
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2432
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5800
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11633
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9547
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4464
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24406
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

3-58089668-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089668
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089668
    reference: chr 3
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.1484-18T>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.1484-18T>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.977-18T>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.1484-18T>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.1484-18T>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.1484-18T>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.977-18T>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.1484-18T>A
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9545
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2466
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5799
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7708
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4466
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3878
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5952
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: T
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

3-58089673-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089673
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089673
    reference: chr 3
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
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.1484-13T>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.977-13T>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.977-13T>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.1484-13T>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.1484-13T>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.1484-13T>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.1484-13T>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.1484-13T>C
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7707
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11642
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10988
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5799
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5949
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
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: 3046
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3878
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff

3-58089682-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089682
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089682
    reference: chr 3
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
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.1484-4A>T
  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.1484-4A>T
  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.977-4A>T
  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.1484-4A>T
  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.977-4A>T
  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.1484-4A>T
  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.1484-4A>T
  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.1484-4A>T
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9547
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7708
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5799
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10991
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2484
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11645
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4466
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5953
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
hgvs: c.1484-4A>T
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP

3-58089688-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089688
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089688
    reference: chr 3
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.1486G>T
  hgvsp: ENSP00000420213.1:p.Gly496Cys
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.979G>T
  hgvsp: ENSP00000418510.1:p.Gly327Cys
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.1486G>T
  hgvsp: ENSP00000351339.3:p.Gly496Cys
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.1486G>T
  hgvsp: ENSP00000295956.4:p.Gly496Cys
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.1486G>T
  hgvsp: ENSP00000349819.4:p.Gly496Cys
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.1486G>T
  hgvsp: ENSP00000415599.2:p.Gly496Cys
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.979G>T
  hgvsp: ENSP00000414532.2:p.Gly327Cys
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.1486G>T
  hgvsp: ENSP00000232447.7:p.Gly496Cys
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11649
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7708
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10999
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5799
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2484
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3050
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly496Cys
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP

3-58089718-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089718
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089718
    reference: chr 3
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.1009T>C
  hgvsp: ENSP00000414532.2:p.Phe337Leu
  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.1516T>C
  hgvsp: ENSP00000415599.2:p.Phe506Leu
  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.1516T>C
  hgvsp: ENSP00000232447.7:p.Phe506Leu
  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.1009T>C
  hgvsp: ENSP00000418510.1:p.Phe337Leu
  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.1516T>C
  hgvsp: ENSP00000295956.4:p.Phe506Leu
  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.1516T>C
  hgvsp: ENSP00000420213.1:p.Phe506Leu
  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.1516T>C
  hgvsp: ENSP00000349819.4:p.Phe506Leu
  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.1516T>C
  hgvsp: ENSP00000351339.3:p.Phe506Leu
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11019
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9547
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11646
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7707
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5798
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4171
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Phe506Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/3-58089721-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089721
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089721
    reference: chr 3
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
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.1519C>A
  hgvsp: ENSP00000349819.4:p.Leu507Met
  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.1519C>A
  hgvsp: ENSP00000232447.7:p.Leu507Met
  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.1519C>A
  hgvsp: ENSP00000415599.2:p.Leu507Met
  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.1519C>A
  hgvsp: ENSP00000351339.3:p.Leu507Met
  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.1519C>A
  hgvsp: ENSP00000295956.4:p.Leu507Met
  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.1012C>A
  hgvsp: ENSP00000418510.1:p.Leu338Met
  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.1519C>A
  hgvsp: ENSP00000420213.1:p.Leu507Met
  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.1012C>A
  hgvsp: ENSP00000414532.2:p.Leu338Met
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11646
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2466
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11018
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7707
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9546
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5798
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3878
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu507Met
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

3-58089724-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089724
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089724
    reference: chr 3
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.1522G>A
  hgvsp: ENSP00000420213.1:p.Asp508Asn
  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.1015G>A
  hgvsp: ENSP00000414532.2:p.Asp339Asn
  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.1522G>A
  hgvsp: ENSP00000349819.4:p.Asp508Asn
  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.1522G>A
  hgvsp: ENSP00000351339.3:p.Asp508Asn
  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.1522G>A
  hgvsp: ENSP00000295956.4:p.Asp508Asn
  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.1522G>A
  hgvsp: ENSP00000415599.2:p.Asp508Asn
  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.1522G>A
  hgvsp: ENSP00000232447.7:p.Asp508Asn
  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.1015G>A
  hgvsp: ENSP00000418510.1:p.Asp339Asn
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5798
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2890
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9547
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11017
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2466
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7707
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11646
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 24399
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5955
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asp508Asn
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD

3-58089727-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089727
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089727
    reference: chr 3
allele count: 2
allele frequency: 1.647582173160887e-5
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.1525G>A
  hgvsp: ENSP00000351339.3:p.Gly509Arg
  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.1525G>A
  hgvsp: ENSP00000349819.4:p.Gly509Arg
  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.1525G>A
  hgvsp: ENSP00000415599.2:p.Gly509Arg
  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.1525G>A
  hgvsp: ENSP00000295956.4:p.Gly509Arg
  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.1018G>A
  hgvsp: ENSP00000414532.2:p.Gly340Arg
  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.1525G>A
  hgvsp: ENSP00000420213.1:p.Gly509Arg
  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.1018G>A
  hgvsp: ENSP00000418510.1:p.Gly340Arg
  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.1525G>A
  hgvsp: ENSP00000232447.7:p.Gly509Arg
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11012
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11652
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2468
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2890
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9545
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7707
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5799
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24398
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly509Arg
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: African
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

3-58089735-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089735
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089735
    reference: chr 3
allele count: 8
allele frequency: 6.590763045591603e-5
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.1533C>T
  hgvsp: ENST00000295956.4:c.1533C>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.1533C>T
  hgvsp: ENST00000357272.4:c.1533C>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.1533C>T
  hgvsp: ENST00000348383.5:c.1533C>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.1533C>T
  hgvsp: ENST00000429972.2:c.1533C>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.1026C>T
  hgvsp: ENST00000493452.1:c.1026C>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.1533C>T
  hgvsp: ENST00000490882.1:c.1533C>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.1533C>T
  hgvsp: ENST00000358537.3:c.1533C>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.1026C>T
  hgvsp: ENST00000419752.2:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9545
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11021
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5799
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2889
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11662
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3045
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Tyr511Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum

3-58089736-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089736
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089736
    reference: chr 3
allele count: 56
allele frequency: 4.613762193514369e-4
allele num: 121376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.1534G>A
  hgvsp: ENSP00000295956.4:p.Ala512Thr
  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.1534G>A
  hgvsp: ENSP00000232447.7:p.Ala512Thr
  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.1534G>A
  hgvsp: ENSP00000349819.4:p.Ala512Thr
  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.1027G>A
  hgvsp: ENSP00000418510.1:p.Ala343Thr
  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.1534G>A
  hgvsp: ENSP00000415599.2:p.Ala512Thr
  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.1534G>A
  hgvsp: ENSP00000420213.1:p.Ala512Thr
  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.1027G>A
  hgvsp: ENSP00000414532.2:p.Ala343Thr
  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.1534G>A
  hgvsp: ENSP00000351339.3:p.Ala512Thr
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7707
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5799
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11020
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11642
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9545
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 9.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4171
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2468
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2890
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4463
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala512Thr
num of homozygotes: 2
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

3-58089741-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089741
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089741
    reference: chr 3
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
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.1539C>T
  hgvsp: ENST00000357272.4:c.1539C>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.1539C>T
  hgvsp: ENST00000348383.5:c.1539C>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.1032C>T
  hgvsp: ENST00000419752.2:c.1032C>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.1539C>T
  hgvsp: ENST00000295956.4:c.1539C>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.1032C>T
  hgvsp: ENST00000493452.1:c.1032C>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.1539C>T
  hgvsp: ENST00000358537.3:c.1539C>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.1539C>T
  hgvsp: ENST00000429972.2:c.1539C>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.1539C>T
  hgvsp: ENST00000490882.1:c.1539C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5800
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11644
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4174
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7720
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11022
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4468
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11655
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Phe513Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum

3-58089742-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089742
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089742
    reference: chr 3
allele count: 9
allele frequency: 7.41534151767323e-5
allele num: 121370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.1033G>A
  hgvsp: ENSP00000418510.1:p.Glu345Lys
  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.1540G>A
  hgvsp: ENSP00000351339.3:p.Glu514Lys
  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.1540G>A
  hgvsp: ENSP00000420213.1:p.Glu514Lys
  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.1540G>A
  hgvsp: ENSP00000415599.2:p.Glu514Lys
  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.1540G>A
  hgvsp: ENSP00000295956.4:p.Glu514Lys
  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.1540G>A
  hgvsp: ENSP00000349819.4:p.Glu514Lys
  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.1033G>A
  hgvsp: ENSP00000414532.2:p.Glu345Lys
  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.1540G>A
  hgvsp: ENSP00000232447.7:p.Glu514Lys
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7721
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11643
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11028
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4174
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5799
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2468
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2483
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4764
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4468
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu514Lys
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

3-58089744-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089744
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089744
    reference: chr 3
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
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.1542G>T
  hgvsp: ENSP00000232447.7:p.Glu514Asp
  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.1542G>T
  hgvsp: ENSP00000420213.1:p.Glu514Asp
  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.1035G>T
  hgvsp: ENSP00000414532.2:p.Glu345Asp
  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.1035G>T
  hgvsp: ENSP00000418510.1:p.Glu345Asp
  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.1542G>T
  hgvsp: ENSP00000295956.4:p.Glu514Asp
  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.1542G>T
  hgvsp: ENSP00000351339.3:p.Glu514Asp
  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.1542G>T
  hgvsp: ENSP00000415599.2:p.Glu514Asp
  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.1542G>T
  hgvsp: ENSP00000349819.4:p.Glu514Asp
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5801
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11018
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4174
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7724
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11650
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu514Asp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP

3-58089760-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089760
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089760
    reference: chr 3
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.1558C>T
  hgvsp: ENSP00000295956.4:p.Pro520Ser
  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.1558C>T
  hgvsp: ENSP00000349819.4:p.Pro520Ser
  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.1558C>T
  hgvsp: ENSP00000420213.1:p.Pro520Ser
  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.1558C>T
  hgvsp: ENSP00000415599.2:p.Pro520Ser
  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.1051C>T
  hgvsp: ENSP00000418510.1:p.Pro351Ser
  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.1051C>T
  hgvsp: ENSP00000414532.2:p.Pro351Ser
  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.1558C>T
  hgvsp: ENSP00000351339.3:p.Pro520Ser
  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.1558C>T
  hgvsp: ENSP00000232447.7:p.Pro520Ser
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10994
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5801
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9537
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4752
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro520Ser
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

3-58089761-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089761
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089761
    reference: chr 3
allele count: 307
allele frequency: 2.530456141507723e-3
allele num: 121322
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.1559C>T
  hgvsp: ENSP00000232447.7:p.Pro520Leu
  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.1559C>T
  hgvsp: ENSP00000349819.4:p.Pro520Leu
  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.1559C>T
  hgvsp: ENSP00000415599.2:p.Pro520Leu
  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.1559C>T
  hgvsp: ENSP00000295956.4:p.Pro520Leu
  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.1052C>T
  hgvsp: ENSP00000414532.2:p.Pro351Leu
  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.1052C>T
  hgvsp: ENSP00000418510.1:p.Pro351Leu
  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.1559C>T
  hgvsp: ENSP00000351339.3:p.Pro520Leu
  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.1559C>T
  hgvsp: ENSP00000420213.1:p.Pro520Leu
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2890
  bin: 5.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 11613
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 7716
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 6.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9533
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 6.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 4166
  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 10986
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 7.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.75e1
  variant carriers: 108
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 5801
  bin: 4.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5913
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro520Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ

3-58089762-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089762
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089762
    reference: chr 3
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.1053G>A
  hgvsp: ENST00000493452.1:c.1053G>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.1053G>A
  hgvsp: ENST00000419752.2:c.1053G>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.1560G>A
  hgvsp: ENST00000357272.4:c.1560G>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.1560G>A
  hgvsp: ENST00000490882.1:c.1560G>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.1560G>A
  hgvsp: ENST00000295956.4:c.1560G>A(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.1560G>A
  hgvsp: ENST00000358537.3:c.1560G>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.1560G>A
  hgvsp: ENST00000348383.5:c.1560G>A(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.1560G>A
  hgvsp: ENST00000429972.2:c.1560G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11674
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9565
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2887
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11054
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4175
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5821
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7743
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4765
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3898
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24160
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro520Pro
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum

3-58089770-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089770
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089770
    reference: chr 3
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.1061A>G
  hgvsp: ENSP00000418510.1:p.Tyr354Cys
  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.1061A>G
  hgvsp: ENSP00000414532.2:p.Tyr354Cys
  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.1568A>G
  hgvsp: ENSP00000349819.4:p.Tyr523Cys
  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.1568A>G
  hgvsp: ENSP00000232447.7:p.Tyr523Cys
  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.1568A>G
  hgvsp: ENSP00000415599.2:p.Tyr523Cys
  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.1568A>G
  hgvsp: ENSP00000351339.3:p.Tyr523Cys
  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.1568A>G
  hgvsp: ENSP00000295956.4:p.Tyr523Cys
  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.1568A>G
  hgvsp: ENSP00000420213.1:p.Tyr523Cys
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7737
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2887
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11029
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11665
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5819
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9562
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4174
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11647
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Tyr523Cys
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

3-58089773-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089773
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089773
    reference: chr 3
allele count: 1
allele frequency: 8.244838730954422e-6
allele num: 121288
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.1571G>C
  hgvsp: ENSP00000415599.2:p.Ser524Thr
  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.1571G>C
  hgvsp: ENSP00000295956.4:p.Ser524Thr
  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.1571G>C
  hgvsp: ENSP00000351339.3:p.Ser524Thr
  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.1064G>C
  hgvsp: ENSP00000418510.1:p.Ser355Thr
  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.1571G>C
  hgvsp: ENSP00000349819.4:p.Ser524Thr
  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.1571G>C
  hgvsp: ENSP00000420213.1:p.Ser524Thr
  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.1064G>C
  hgvsp: ENSP00000414532.2:p.Ser355Thr
  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.1571G>C
  hgvsp: ENSP00000232447.7:p.Ser524Thr
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9558
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11671
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7735
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4175
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11019
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5820
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4473
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3048
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5940
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser524Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum

3-58089783-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089783
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089783
    reference: chr 3
allele count: 3
allele frequency: 2.475288371095233e-5
allele num: 121198
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.1581C>T
  hgvsp: ENST00000358537.3:c.1581C>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.1581C>T
  hgvsp: ENST00000357272.4:c.1581C>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.1581C>T
  hgvsp: ENST00000429972.2:c.1581C>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.1581C>T
  hgvsp: ENST00000348383.5:c.1581C>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.1074C>T
  hgvsp: ENST00000419752.2:c.1074C>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.1581C>T
  hgvsp: ENST00000490882.1:c.1581C>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.1074C>T
  hgvsp: ENST00000493452.1:c.1074C>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.1581C>T
  hgvsp: ENST00000295956.4:c.1581C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7732
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4174
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5818
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9543
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2483
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5908
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ile527Ile
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

3-58089787-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089787
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089788
    reference: chr 3
allele count: 16
allele frequency: 1.321527686005022e-4
allele num: 121072
alternate allele: TG
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.1592dupG
  hgvsp: ENSP00000415599.2:p.His532ThrfsTer9
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.1085dupG
  hgvsp: ENSP00000418510.1:p.His363ThrfsTer9
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.1592dupG
  hgvsp: ENSP00000349819.4:p.His532ThrfsTer9
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.1592dupG
  hgvsp: ENSP00000232447.7:p.His532ThrfsTer9
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.1592dupG
  hgvsp: ENSP00000420213.1:p.His532ThrfsTer9
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.1085dupG
  hgvsp: ENSP00000414532.2:p.His363ThrfsTer9
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.1592dupG
  hgvsp: ENSP00000351339.3:p.His532ThrfsTer9
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.1592dupG
  hgvsp: ENSP00000295956.4:p.His532ThrfsTer9
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 5820
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10917
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9540
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7734
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11572
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4166
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2897
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4454
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5881
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 2.25e1
  variant carriers: 1
hgvs: p.His532ThrfsTer9
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

3-58089787-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089787
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089786
    reference: chr 3
allele count: 1
allele frequency: 8.259548037531387e-6
allele num: 121072
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.1592delG
  hgvsp: ENSP00000232447.7:p.Gly531AspfsTer42
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.1592delG
  hgvsp: ENSP00000295956.4:p.Gly531AspfsTer42
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000349819
  ensembl transcript: ENST00000357272
  gene symbol: FLNB
  hgvsc: ENST00000357272.4:c.1592delG
  hgvsp: ENSP00000349819.4:p.Gly531AspfsTer42
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000414532
  ensembl transcript: ENST00000419752
  gene symbol: FLNB
  hgvsc: ENST00000419752.2:c.1085delG
  hgvsp: ENSP00000414532.2:p.Gly362AspfsTer42
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000420213
  ensembl transcript: ENST00000490882
  gene symbol: FLNB
  hgvsc: ENST00000490882.1:c.1592delG
  hgvsp: ENSP00000420213.1:p.Gly531AspfsTer42
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.1085delG
  hgvsp: ENSP00000418510.1:p.Gly362AspfsTer42
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.1592delG
  hgvsp: ENSP00000351339.3:p.Gly531AspfsTer42
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.1592delG
  hgvsp: ENSP00000415599.2:p.Gly531AspfsTer42
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11572
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10917
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2897
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5820
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7734
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9540
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3886
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly531AspfsTer42
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: TG
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ

3-58089788-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089788
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089788
    reference: chr 3
allele count: 3
allele frequency: 2.479420807299415e-5
allele num: 120996
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.1586G>C
  hgvsp: ENSP00000232447.7:p.Trp529Ser
  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.1079G>C
  hgvsp: ENSP00000418510.1:p.Trp360Ser
  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.1079G>C
  hgvsp: ENSP00000414532.2:p.Trp360Ser
  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.1586G>C
  hgvsp: ENSP00000349819.4:p.Trp529Ser
  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.1586G>C
  hgvsp: ENSP00000351339.3:p.Trp529Ser
  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.1586G>C
  hgvsp: ENSP00000420213.1:p.Trp529Ser
  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.1586G>C
  hgvsp: ENSP00000295956.4:p.Trp529Ser
  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.1586G>C
  hgvsp: ENSP00000415599.2:p.Trp529Ser
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7735
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2896
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10904
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4162
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11578
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5822
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2488
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3017
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3883
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Trp529Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

3-58089788-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089788
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089788
    reference: chr 3
allele count: 1
allele frequency: 8.264736024331383e-6
allele num: 120996
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.1586G>T
  hgvsp: ENSP00000420213.1:p.Trp529Leu
  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.1586G>T
  hgvsp: ENSP00000232447.7:p.Trp529Leu
  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.1079G>T
  hgvsp: ENSP00000418510.1:p.Trp360Leu
  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.1586G>T
  hgvsp: ENSP00000295956.4:p.Trp529Leu
  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.1586G>T
  hgvsp: ENSP00000349819.4:p.Trp529Leu
  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.1586G>T
  hgvsp: ENSP00000351339.3:p.Trp529Leu
  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.1079G>T
  hgvsp: ENSP00000414532.2:p.Trp360Leu
  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.1586G>T
  hgvsp: ENSP00000415599.2:p.Trp529Leu
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2488
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11578
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10904
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2896
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7735
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5822
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4450
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3017
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11445
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5872
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Trp529Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

3-58089790-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089790
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089790
    reference: chr 3
allele count: 13
allele frequency: 1.073049938093273e-4
allele num: 121150
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.1588G>C
  hgvsp: ENSP00000295956.4:p.Gly530Arg
  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.1588G>C
  hgvsp: ENSP00000351339.3:p.Gly530Arg
  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.1588G>C
  hgvsp: ENSP00000415599.2:p.Gly530Arg
  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.1588G>C
  hgvsp: ENSP00000232447.7:p.Gly530Arg
  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.1588G>C
  hgvsp: ENSP00000420213.1:p.Gly530Arg
  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.1588G>C
  hgvsp: ENSP00000349819.4:p.Gly530Arg
  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.1081G>C
  hgvsp: ENSP00000418510.1:p.Gly361Arg
  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.1081G>C
  hgvsp: ENSP00000414532.2:p.Gly361Arg
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4146
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11565
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7728
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5816
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2494
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10946
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2875
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4467
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3031
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly530Arg
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

3-58089790-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089790
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089790
    reference: chr 3
allele count: 2
allele frequency: 1.650846058605035e-5
allele num: 121150
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.1081G>A
  hgvsp: ENSP00000418510.1:p.Gly361Arg
  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.1588G>A
  hgvsp: ENSP00000420213.1:p.Gly530Arg
  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.1588G>A
  hgvsp: ENSP00000349819.4:p.Gly530Arg
  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.1588G>A
  hgvsp: ENSP00000295956.4:p.Gly530Arg
  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.1588G>A
  hgvsp: ENSP00000351339.3:p.Gly530Arg
  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.1588G>A
  hgvsp: ENSP00000232447.7:p.Gly530Arg
  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.1588G>A
  hgvsp: ENSP00000415599.2:p.Gly530Arg
  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.1081G>A
  hgvsp: ENSP00000414532.2:p.Gly361Arg
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11565
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5816
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2494
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10946
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2875
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7728
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24079
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 11481
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gly530Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

3-58089790-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089790
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089790
    reference: chr 3
allele count: 6
allele frequency: 4.952538175815105e-5
allele num: 121150
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.1588G>T
  hgvsp: ENSP00000420213.1:p.Gly530Trp
  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.1588G>T
  hgvsp: ENSP00000351339.3:p.Gly530Trp
  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.1081G>T
  hgvsp: ENSP00000418510.1:p.Gly361Trp
  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.1588G>T
  hgvsp: ENSP00000349819.4:p.Gly530Trp
  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.1588G>T
  hgvsp: ENSP00000232447.7:p.Gly530Trp
  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.1588G>T
  hgvsp: ENSP00000415599.2:p.Gly530Trp
  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.1081G>T
  hgvsp: ENSP00000414532.2:p.Gly361Trp
  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.1588G>T
  hgvsp: ENSP00000295956.4:p.Gly530Trp
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7728
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5816
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2494
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11565
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2875
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10946
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4146
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3896
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11481
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly530Trp
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

3-58089792-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089792
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089792
    reference: chr 3
allele count: 13
allele frequency: 1.073227111367952e-4
allele num: 121130
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.1590G>A
  hgvsp: ENST00000295956.4:c.1590G>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.1083G>A
  hgvsp: ENST00000493452.1:c.1083G>A(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.1590G>A
  hgvsp: ENST00000429972.2:c.1590G>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.1590G>A
  hgvsp: ENST00000490882.1:c.1590G>A(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.1590G>A
  hgvsp: ENST00000358537.3:c.1590G>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.1590G>A
  hgvsp: ENST00000348383.5:c.1590G>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.1083G>A
  hgvsp: ENST00000419752.2:c.1083G>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.1590G>A
  hgvsp: ENST00000357272.4:c.1590G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4145
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7726
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11567
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10934
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5812
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2873
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4723
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly530Gly
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

3-58089810-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089810
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089810
    reference: chr 3
allele count: 1
allele frequency: 8.268562923763849e-6
allele num: 120940
alternate allele: A
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.1608G>A
  hgvsp: ENST00000429972.2:c.1608G>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.1608G>A
  hgvsp: ENST00000358537.3:c.1608G>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.1608G>A
  hgvsp: ENST00000295956.4:c.1608G>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.1608G>A
  hgvsp: ENST00000348383.5:c.1608G>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.1101G>A
  hgvsp: ENST00000419752.2:c.1101G>A(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.1608G>A
  hgvsp: ENST00000490882.1:c.1608G>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: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.1101G>A
  hgvsp: ENST00000493452.1:c.1101G>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.1608G>A
  hgvsp: ENST00000357272.4:c.1608G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5805
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9515
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11384
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2869
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10625
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7709
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5785
  bin: 6.75e1
  variant carriers: 0
hgvs: c.1608G>A
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum

3-58089817-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089817
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089817
    reference: chr 3
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
alternate allele: C
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.1103+5G>C
  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.1610+5G>C
  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.1610+5G>C
  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.1610+5G>C
  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.1610+5G>C
  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.1610+5G>C
  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.1103+5G>C
  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.1610+5G>C
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7699
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11180
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10195
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2325
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9485
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5801
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2867
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1032
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5654
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4430
  bin: 8.25e1
  variant carriers: 0
hgvs: c.1610+5G>C
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

3-58089818-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089818
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089818
    reference: chr 3
allele count: 1
allele frequency: 8.28239659427852e-6
allele num: 120738
alternate allele: C
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.1610+6G>C
  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.1610+6G>C
  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.1610+6G>C
  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.1103+6G>C
  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.1103+6G>C
  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.1610+6G>C
  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.1610+6G>C
  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.1610+6G>C
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9475
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7697
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2335
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11147
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5799
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2868
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10160
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4426
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2491
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 4.25e1
  variant carriers: 0
hgvs: c.1610+6G>C
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

3-58089818-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089818
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089818
    reference: chr 3
allele count: 1
allele frequency: 8.28239659427852e-6
allele num: 120738
alternate allele: T
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.1610+6G>T
  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.1610+6G>T
  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.1610+6G>T
  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.1103+6G>T
  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.1610+6G>T
  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.1610+6G>T
  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.1610+6G>T
  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.1103+6G>T
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9475
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7697
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2868
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5799
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2335
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11147
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
hgvs: c.1610+6G>T
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum

3-58089820-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089820
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089820
    reference: chr 3
allele count: 1
allele frequency: 8.283082632032337e-6
allele num: 120728
alternate allele: G
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.1103+8T>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.1610+8T>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.1610+8T>G
  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.1610+8T>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.1610+8T>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.1610+8T>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.1610+8T>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.1103+8T>G
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10144
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9462
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5799
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11089
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2866
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7689
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4139
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5626
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4421
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2943
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
hgvs: c.1610+8T>G
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP

3-58089824-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089824
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089824
    reference: chr 3
allele count: 1
allele frequency: 8.287338604080686e-6
allele num: 120666
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.1610+12G>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.1610+12G>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.1103+12G>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.1103+12G>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.1610+12G>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.1610+12G>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.1610+12G>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.1610+12G>A
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10937
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9440
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2453
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7682
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5797
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4138
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2936
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4411
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4619
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

3-58089827-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089827
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089827
    reference: chr 3
allele count: 1
allele frequency: 8.2917364554485e-6
allele num: 120602
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.1103+15G>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.1610+15G>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.1610+15G>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.1610+15G>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.1610+15G>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.1610+15G>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.1103+15G>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.1610+15G>A
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5791
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10829
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2492
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9427
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7674
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9757
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5475
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4398
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3881
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2918
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1222
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9795
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2482
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum

3-58089837-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089837
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089837
    reference: chr 3
allele count: 11
allele frequency: 9.137275098433373e-5
allele num: 120386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.1610+25C>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.1610+25C>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.1103+25C>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.1103+25C>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.1610+25C>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.1610+25C>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.1610+25C>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.1610+25C>G
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5789
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10430
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9354
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9080
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7643
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2868
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 617
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2480
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

3-58089845-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089845
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089845
    reference: chr 3
allele count: 2
allele frequency: 1.666500016665e-5
allele num: 120012
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.1610+33G>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.1103+33G>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.1610+33G>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.1103+33G>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.1610+33G>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.1610+33G>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.1610+33G>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.1610+33G>A
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5781
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9289
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7630
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8416
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10076
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4136
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 887
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1301
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4509
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7626
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2802
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

3-58089847-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089847
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089847
    reference: chr 3
allele count: 2
allele frequency: 1.666944490748458e-5
allele num: 119980
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.1610+35G>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.1103+35G>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.1610+35G>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.1610+35G>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.1610+35G>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.1103+35G>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.1610+35G>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.1610+35G>C
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10017
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5779
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9280
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7630
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4986
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3859
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2790
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 867
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7760
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum

3-58089848-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089848
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089848
    reference: chr 3
allele count: 1
allele frequency: 8.334166750008334e-6
allele num: 119988
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.1610+36G>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.1610+36G>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.1610+36G>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.1610+36G>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.1103+36G>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.1103+36G>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.1610+36G>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.1610+36G>A
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8370
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9981
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5779
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4135
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9274
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7622
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4491
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5004
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4332
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1303
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 741
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ

3-58089849-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089849
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089849
    reference: chr 3
allele count: 7
allele frequency: 5.837711617046118e-5
allele num: 119910
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.1610+37G>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.1610+37G>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.1610+37G>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.1103+37G>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.1610+37G>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.1610+37G>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.1610+37G>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.1103+37G>A
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9934
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7623
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8322
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9270
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5779
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3162
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4134
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23974
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4488
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 892
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7631
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

3-58089851-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089851
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089851
    reference: chr 3
allele count: 28103
allele frequency: 2.348806499063921e-1
allele num: 119648
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.1610+39G>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.1610+39G>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.1610+39G>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.1103+39G>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.1610+39G>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.1610+39G>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.1610+39G>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.1103+39G>A
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9852
  bin: 3.25e1
  variant carriers: 3079
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 3337
  bin: 2.25e1
  variant carriers: 1396
genotype depth: GenotypeDepth
  all individuals: 5780
  bin: 4.75e1
  variant carriers: 2704
genotype depth: GenotypeDepth
  all individuals: 9354
  bin: 3.75e1
  variant carriers: 3543
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.5e0
  variant carriers: 119
genotype depth: GenotypeDepth
  all individuals: 4072
  bin: 5.25e1
  variant carriers: 2098
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 6.25e1
  variant carriers: 1042
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 171
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 1.75e1
  variant carriers: 834
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 2861
  bin: 5.75e1
  variant carriers: 1560
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.75e1
  variant carriers: 301
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 1.25e1
  variant carriers: 473
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.75e1
  variant carriers: 115
genotype depth: GenotypeDepth
  all individuals: 7634
  bin: 4.25e1
  variant carriers: 3221
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 6.75e1
  variant carriers: 667
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 7.25e1
  variant carriers: 426
genotype depth: GenotypeDepth
  all individuals: 8049
  bin: 2.75e1
  variant carriers: 2340
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 3.75e1
  variant carriers: 42
genotype quality: GenotypeQuality
  all individuals: 5152
  bin: 6.25e1
  variant carriers: 133
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 1.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 2.75e1
  variant carriers: 25
genotype quality: GenotypeQuality
  all individuals: 2972
  bin: 7.75e1
  variant carriers: 179
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 1.25e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 34862
  bin: 9.75e1
  variant carriers: 22555
genotype quality: GenotypeQuality
  all individuals: 1697
  bin: 8.75e1
  variant carriers: 157
num of homozygotes: 4036
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

3-58089854-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089854
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089854
    reference: chr 3
allele count: 1
allele frequency: 8.397010664203544e-6
allele num: 119090
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.1610+42C>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.1610+42C>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.1103+42C>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.1610+42C>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.1610+42C>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.1103+42C>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.1610+42C>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.1610+42C>T
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3319
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4803
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8944
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9348
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7103
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1907
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5031
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10743
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20372
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4475
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6472
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1247
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1180
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1331
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

3-58089855-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089855
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089855
    reference: chr 3
allele count: 7
allele frequency: 5.876624466906209e-5
allele num: 119116
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.1610+43G>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.1610+43G>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.1103+43G>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.1610+43G>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.1610+43G>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.1103+43G>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.1610+43G>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.1610+43G>A
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7094
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3314
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10628
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5029
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4894
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8993
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9324
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2979
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 752
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5119
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 897
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1711
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6741
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

3-58089860-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089860
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089859
    reference: chr 3
allele count: 1
allele frequency: 8.397715821296607e-6
allele num: 119080
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.1610+51delG
  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.1610+51delG
  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.1610+51delG
  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.1610+51delG
  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.1103+51delG
  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.1610+51delG
  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.1610+51delG
  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.1103+51delG
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10290
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8871
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5022
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7082
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 892
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 749
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20366
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1263
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5125
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1332
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: AG
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

3-58089863-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089863
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089863
    reference: chr 3
allele count: 3
allele frequency: 2.520415364452062e-5
allele num: 119028
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000351339
  ensembl transcript: ENST00000358537
  gene symbol: FLNB
  hgvsc: ENST00000358537.3:c.1610+51G>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.1610+51G>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.1610+51G>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.1103+51G>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.1610+51G>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.1610+51G>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.1610+51G>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.1103+51G>A
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10117
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5755
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3265
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5020
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8781
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9230
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7080
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1823
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1798
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 911
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1196
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2441
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20366
  bin: 9.75e1
  variant carriers: 3
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

3-58089864-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58089864
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58089864
    reference: chr 3
allele count: 1
allele frequency: 8.40745909771149e-6
allele num: 118942
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.1610+52C>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.1103+52C>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.1610+52C>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.1610+52C>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.1610+52C>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.1610+52C>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.1610+52C>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.1103+52C>T
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3274
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10090
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8825
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5020
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5742
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7081
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1863
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2929
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20352
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1148
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1388
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum

3-58090760-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58090760
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58090760
    reference: chr 3
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
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.1611-47C>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.1611-47C>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.1104-47C>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.1611-47C>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.1611-47C>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.1611-47C>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.1611-47C>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.1104-47C>G
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5574
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8905
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3589
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3076
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9868
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7385
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6889
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4152
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8835
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2220
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

3-58090775-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58090775
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58090775
    reference: chr 3
allele count: 2
allele frequency: 1.647310765175851e-5
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000415599
  ensembl transcript: ENST00000429972
  gene symbol: FLNB
  hgvsc: ENST00000429972.2:c.1611-32C>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.1104-32C>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.1611-32C>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.1611-32C>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.1104-32C>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.1611-32C>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.1611-32C>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.1611-32C>G
  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: 2319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5573
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9868
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8908
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3076
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3591
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8851
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

3-58090776-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58090776
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58090776
    reference: chr 3
allele count: 9
allele frequency: 7.412898443291327e-5
allele num: 121410
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.1611-31T>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.1611-31T>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.1611-31T>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.1611-31T>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.1611-31T>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.1104-31T>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.1104-31T>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.1611-31T>C
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9868
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5573
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3591
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6893
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8909
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28669
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 2222
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3635
  bin: 9.25e1
  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: 0
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP

3-58090785-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58090785
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58090785
    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: ENSP00000232447
  ensembl transcript: ENST00000348383
  gene symbol: FLNB
  hgvsc: ENST00000348383.5:c.1611-22T>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.1611-22T>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.1104-22T>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.1611-22T>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.1611-22T>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.1611-22T>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.1104-22T>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.1611-22T>G
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6899
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3587
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8908
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9872
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5575
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3076
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5645
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4340
  bin: 8.25e1
  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: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8865
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4620
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/3-58090789-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58090789
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58090789
    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: ENSP00000295956
  ensembl transcript: ENST00000295956
  gene symbol: FLNB
  hgvsc: ENST00000295956.4:c.1611-18C>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.1611-18C>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.1611-18C>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.1611-18C>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.1611-18C>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.1611-18C>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.1104-18C>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.1104-18C>A
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3076
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9872
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5575
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8907
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8865
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  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: 5645
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

3-58090796-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58090796
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58090796
    reference: chr 3
allele count: 3
allele frequency: 2.470925443942938e-5
allele num: 121412
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.1611-11T>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.1104-11T>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.1611-11T>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.1611-11T>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.1611-11T>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.1611-11T>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.1104-11T>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.1611-11T>C
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5575
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3076
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3588
  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: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8907
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2713
  bin: 7.25e1
  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: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4620
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS

3-58090801-CTG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58090801
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58090799
    reference: chr 3
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
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.1611-4_1611-3delGT
  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.1104-4_1104-3delGT
  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.1611-4_1611-3delGT
  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.1611-4_1611-3delGT
  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.1611-4_1611-3delGT
  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.1611-4_1611-3delGT
  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.1611-4_1611-3delGT
  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.1104-4_1104-3delGT
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 9.75e1
  variant carriers: 1
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: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5576
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3076
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8908
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  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: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5646
  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: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
hgvs: c.1611-4_1611-3delGT
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: CTG
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

3-58090803-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58090803
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58090803
    reference: chr 3
allele count: 5312
allele frequency: 4.375257392307059e-2
allele num: 121410
alternate allele: A
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.1611-4G>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.1104-4G>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.1611-4G>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.1611-4G>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.1611-4G>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.1611-4G>A
  variant of: http://identifiers.org/hgnc/3755
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000136068
  ensembl protein: ENSP00000418510
  ensembl transcript: ENST00000493452
  gene symbol: FLNB
  hgvsc: ENST00000493452.1:c.1104-4G>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.1611-4G>A
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 7.75e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7311
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 7.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 8.25e1
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 9843
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 5.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 6882
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 6.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 6913
  bin: 9.75e1
  variant carriers: 4607
genotype depth: GenotypeDepth
  all individuals: 5439
  bin: 4.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8862
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 8.75e1
  variant carriers: 77
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 6.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 129
genotype depth: GenotypeDepth
  all individuals: 3940
  bin: 5.25e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 8856
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5640
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2707
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2210
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4608
  bin: 7.75e1
  variant carriers: 0
hgvs: c.1611-4G>A
num of homozygotes: 172
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

3-58090811-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58090811
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 58090811
    reference: chr 3
allele count: 8
allele frequency: 6.589134517181169e-5
allele num: 121412
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.1615T>C
  hgvsp: ENSP00000232447.7:p.Phe539Leu
  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.1615T>C
  hgvsp: ENSP00000415599.2:p.Phe539Leu
  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.1615T>C
  hgvsp: ENSP00000420213.1:p.Phe539Leu
  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.1615T>C
  hgvsp: ENSP00000351339.3:p.Phe539Leu
  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.1615T>C
  hgvsp: ENSP00000349819.4:p.Phe539Leu
  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.1615T>C
  hgvsp: ENSP00000295956.4:p.Phe539Leu
  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.1108T>C
  hgvsp: ENSP00000418510.1:p.Phe370Leu
  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.1108T>C
  hgvsp: ENSP00000414532.2:p.Phe370Leu
  variant of: http://identifiers.org/hgnc/3755
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9634
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4261
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10734
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7514
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5960
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 8.75e1
  variant carriers: 2
hgvs: p.Phe539Leu
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 1743
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3676
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4557
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2901
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39460
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3418
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2280
bin: 8.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.517496e6

QD
type: SiteQuality
SIO_000300: 1.593e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.317e0

VQSLOD
type: SiteQuality
SIO_000300: -2.081e-1

MQ
type: SiteQuality
SIO_000300: 5.877e1

FS
type: SiteQuality
SIO_000300: 1.912e0

MQRankSum
type: SiteQuality
SIO_000300: -2.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.599999999999999e-2

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

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 39460
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4560
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2901
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2644
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2280
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3419
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3676
bin: 9.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.2e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.517478e6

MQRankSum
type: SiteQuality
SIO_000300: 7.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.91e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.94e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.76e0

GenotypeQuality
all individuals: 1737
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2276
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3416
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2636
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4547
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2894
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3669
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39500
bin: 9.75e1
variant carriers: 81

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

African
type: Population
allele count: 79
allele frequency: 7.591773976551989e-3
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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -9.83e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.972e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-2

DP
type: SiteQuality
SIO_000300: 2.525083e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.25e0

QD
type: SiteQuality
SIO_000300: 1.228e1

GenotypeQuality
all individuals: 39488
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2896
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3669
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4544
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1739
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.946e1

MQRankSum
type: SiteQuality
SIO_000300: 9.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.38e0

QD
type: SiteQuality
SIO_000300: 1.605e1

DP
type: SiteQuality
SIO_000300: 2.520518e6

FS
type: SiteQuality
SIO_000300: 1.3938e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.73e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.928e0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2895
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2638
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3419
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39489
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
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

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -4.49e-1

QD
type: SiteQuality
SIO_000300: 7.34e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.19e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.153e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.186e0

DP
type: SiteQuality
SIO_000300: 2.520407e6

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3419
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3668
bin: 9.25e1
variant carriers: 0

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

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.87e0

MQ
type: SiteQuality
SIO_000300: 5.915e1

FS
type: SiteQuality
SIO_000300: 1.857e0

VQSLOD
type: SiteQuality
SIO_000300: -1.044e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.99e-1

QD
type: SiteQuality
SIO_000300: 1.209e1

DP
type: SiteQuality
SIO_000300: 2.520139e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.902e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.61e0

GenotypeQuality
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bin: 3.25e1
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: 4.25e1
variant carriers: 0

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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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 2.520098e6

FS
type: SiteQuality
SIO_000300: 1.4895e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.779e0

QD
type: SiteQuality
SIO_000300: 1.219e1

VQSLOD
type: SiteQuality
SIO_000300: -3.521e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.69e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.57e0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39488
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3668
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2894
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 2
allele frequency: 1.92270717169775e-4
allele num: 10402
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 2.519916e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.23e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.009e0

MQRankSum
type: SiteQuality
SIO_000300: 1.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.005e0

QD
type: SiteQuality
SIO_000300: 1.198e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4437
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2631
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.519766e6

MQRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.2e0

QD
type: SiteQuality
SIO_000300: 1.213e1

MQ
type: SiteQuality
SIO_000300: 5.943e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.63e-1

FS
type: SiteQuality
SIO_000300: 8.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e-2

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

GenotypeQuality
all individuals: 3668
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

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

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

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

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

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: 8652
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.341e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 3.071e0

VQSLOD
type: SiteQuality
SIO_000300: -1.467e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.421e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.102e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.62e-1

DP
type: SiteQuality
SIO_000300: 2.519713e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

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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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 35
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variant carriers: 0

GenotypeQuality
all individuals: 3354
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 5
allele frequency: 5.506607929515419e-3
allele num: 908
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 6
allele frequency: 9.071666162685213e-4
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 887
allele frequency: 1.329396600821318e-2
allele num: 66722
num of homozygotes: 6

South Asian
type: Population
allele count: 29
allele frequency: 1.756298449612403e-3
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 154
allele frequency: 1.3305685156385e-2
allele num: 11574
num of homozygotes: 0

African
type: Population
allele count: 28
allele frequency: 2.691790040376851e-3
allele num: 10402
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.4e0

FS
type: SiteQuality
SIO_000300: 2.386e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.403e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.65e-1

DP
type: SiteQuality
SIO_000300: 2.576802e6

QD
type: SiteQuality
SIO_000300: 1.263e1

GenotypeQuality
all individuals: 32
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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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variant carriers: 2

GenotypeQuality
all individuals: 2586
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GenotypeQuality
all individuals: 4
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variant carriers: 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: 11576
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.99805126667666e-5
allele num: 66710
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.17e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.74e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 2.555819e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.66e0

QD
type: SiteQuality
SIO_000300: 1.402e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

GenotypeQuality
all individuals: 33
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 46
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 49

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2254
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variant carriers: 0

GenotypeQuality
all individuals: 2575
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 10
allele frequency: 8.638562543192813e-4
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 38
allele frequency: 5.696297406685654e-4
allele num: 66710
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: 16512
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.945e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.9e-2

FS
type: SiteQuality
SIO_000300: 8.83e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.63e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.0e0

DP
type: SiteQuality
SIO_000300: 2.557952e6

QD
type: SiteQuality
SIO_000300: 1.316e1

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 3060
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variant carriers: 0

GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 28
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variant carriers: 0

GenotypeQuality
all individuals: 107
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GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 5956
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 119
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variant carriers: 0

GenotypeQuality
all individuals: 11231
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variant carriers: 0

GenotypeQuality
all individuals: 4474
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 3.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -7.19e-1

MQ
type: SiteQuality
SIO_000300: 6.066e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.97e-1

QD
type: SiteQuality
SIO_000300: 1.277e1

FS
type: SiteQuality
SIO_000300: 4.513e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

DP
type: SiteQuality
SIO_000300: 2.444331e6

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.0e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 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: 11578
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: 10390
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 5.969e0

DP
type: SiteQuality
SIO_000300: 2.44462e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQ
type: SiteQuality
SIO_000300: 5.987e1

MQRankSum
type: SiteQuality
SIO_000300: 1.0e-1

QD
type: SiteQuality
SIO_000300: 8.25e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.558e0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 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: 10392
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
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: 16512
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.31e-1

FS
type: SiteQuality
SIO_000300: 1.086e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.444841e6

QD
type: SiteQuality
SIO_000300: 1.609e1

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.515e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.373e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.79e-1

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
all individuals: 23
bin: 3.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 2.92e0

MQRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

FS
type: SiteQuality
SIO_000300: 6.061e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.157e0

VQSLOD
type: SiteQuality
SIO_000300: -2.19e0

DP
type: SiteQuality
SIO_000300: 2.4454e6

MQ
type: SiteQuality
SIO_000300: 5.837e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 24404
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
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African
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European (Finnish)
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South Asian
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MQ
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FS
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ReadPosRankSum
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QD
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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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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Other
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European (Non-Finnish)
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European (Finnish)
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African
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Latino
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South Asian
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DP
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ReadPosRankSum
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MQ
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VQSLOD
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BaseQRankSum
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QD
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MQRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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South Asian
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European (Finnish)
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European (Non-Finnish)
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FS
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InbreedingCoeff
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QD
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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African
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European (Non-Finnish)
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European (Finnish)
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East Asian
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MQRankSum
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InbreedingCoeff
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MQ
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FS
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ReadPosRankSum
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VQSLOD
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QD
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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Other
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African
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European (Finnish)
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South Asian
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MQRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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BaseQRankSum
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MQ
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VQSLOD
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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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Latino
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European (Non-Finnish)
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European (Finnish)
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African
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Other
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South Asian
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DP
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InbreedingCoeff
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FS
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BaseQRankSum
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QD
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MQRankSum
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ClippingRankSum
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MQ
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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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African
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European (Non-Finnish)
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East Asian
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South Asian
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Other
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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DP
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MQRankSum
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ClippingRankSum
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FS
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MQ
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BaseQRankSum
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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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East Asian
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European (Finnish)
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South Asian
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African
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DP
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ReadPosRankSum
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MQ
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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FS
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QD
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MQRankSum
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BaseQRankSum
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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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European (Finnish)
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Other
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BaseQRankSum
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QD
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DP
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQ
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FS
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GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 54

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11662
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 46
allele frequency: 6.894071098854984e-4
allele num: 66724
num of homozygotes: 1

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.202643171806168e-3
allele num: 908
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 8
allele frequency: 1.209555488358028e-3
allele num: 6614
num of homozygotes: 1

MQ
type: SiteQuality
SIO_000300: 5.963e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-1

DP
type: SiteQuality
SIO_000300: 2.446122e6

VQSLOD
type: SiteQuality
SIO_000300: 4.14e0

FS
type: SiteQuality
SIO_000300: 5.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.71e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.01e-2

QD
type: SiteQuality
SIO_000300: 1.352e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.855e0

GenotypeQuality
all individuals: 24361
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3044
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.406e0

DP
type: SiteQuality
SIO_000300: 2.44246e6

MQ
type: SiteQuality
SIO_000300: 5.923e1

VQSLOD
type: SiteQuality
SIO_000300: -7.18e-1

QD
type: SiteQuality
SIO_000300: 1.424e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.35e0

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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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variant carriers: 9

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: 5
bin: 5.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.348920863309352e-4
allele num: 66720
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 4.41e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.77e-1

QD
type: SiteQuality
SIO_000300: 1.288e1

DP
type: SiteQuality
SIO_000300: 2.442532e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.138e0

MQRankSum
type: SiteQuality
SIO_000300: 2.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 1.122e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

GenotypeQuality
all individuals: 4467
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11666
bin: 6.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -4.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.311e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 8.808e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.826e0

VQSLOD
type: SiteQuality
SIO_000300: -2.642e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

QD
type: SiteQuality
SIO_000300: 1.472e1

DP
type: SiteQuality
SIO_000300: 2.441914e6

GenotypeQuality
all individuals: 24343
bin: 9.75e1
variant carriers: 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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66686
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.503e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.41e-1

QD
type: SiteQuality
SIO_000300: 3.211e1

MQRankSum
type: SiteQuality
SIO_000300: 4.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.87e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.4402e6

GenotypeQuality
all individuals: 3037
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 30
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 11
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2480
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variant carriers: 0

GenotypeQuality
all individuals: 24350
bin: 9.75e1
variant carriers: 307

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 41
allele frequency: 6.200846944948578e-3
allele num: 6612
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.816860465116279e-4
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 32
allele frequency: 2.764817694833247e-3
allele num: 11574
num of homozygotes: 0

African
type: Population
allele count: 12
allele frequency: 1.155624036979969e-3
allele num: 10384
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 218
allele frequency: 3.269248072943223e-3
allele num: 66682
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.440777e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.0e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.61e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.42e-1

QD
type: SiteQuality
SIO_000300: 1.39e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.08e0

FS
type: SiteQuality
SIO_000300: 5.49e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 71
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GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66686
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -6.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.07e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.8e-2

DP
type: SiteQuality
SIO_000300: 2.426274e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 3.855e0

VQSLOD
type: SiteQuality
SIO_000300: 9.92e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.38e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.89e0

GenotypeQuality
all individuals: 3897
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 14
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GenotypeQuality
all individuals: 13
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3051
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variant carriers: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
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: 66670
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.15e-1

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 9.59e-1

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

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.425208e6

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 24
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66660
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

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

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

FS
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SIO_000300: 0.0e0

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 5.07e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.629999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.42e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.814e0

DP
type: SiteQuality
SIO_000300: 2.424797e6

MQRankSum
type: SiteQuality
SIO_000300: -4.56e-1

GenotypeQuality
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bin: 2.75e1
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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bin: 9.75e1
variant carriers: 3

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66610
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.471418653089562e-4
allele num: 8642
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.085e0

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -4.867e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.299999999999999e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.47e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.94e-1

DP
type: SiteQuality
SIO_000300: 2.421856e6

MQ
type: SiteQuality
SIO_000300: 5.949e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.0e-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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bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 11
allele frequency: 1.653687723623681e-4
allele num: 66518
num of homozygotes: 0

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

African
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allele count: 3
allele frequency: 2.905850445563735e-4
allele num: 10324
num of homozygotes: 0

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

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

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

East Asian
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allele count: 1
allele frequency: 1.157675387821255e-4
allele num: 8638
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.212e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.03e-1

MQ
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SIO_000300: 5.932e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
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SIO_000300: 2.420741e6

QD
type: SiteQuality
SIO_000300: 1.56e0

FS
type: SiteQuality
SIO_000300: 1.612e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-2

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503352476021528e-5
allele num: 66518
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-2

QD
type: SiteQuality
SIO_000300: 1.56e0

VQSLOD
type: SiteQuality
SIO_000300: -1.212e-1

FS
type: SiteQuality
SIO_000300: 1.612e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.95e-1

InbreedingCoeff
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SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.03e-1

DP
type: SiteQuality
SIO_000300: 2.420741e6

MQ
type: SiteQuality
SIO_000300: 5.932e1

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10306
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.513450081242101e-5
allele num: 66468
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -8.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

FS
type: SiteQuality
SIO_000300: 1.983e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.768e0

MQRankSum
type: SiteQuality
SIO_000300: -7.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.81e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.74e0

DP
type: SiteQuality
SIO_000300: 2.420589e6

QD
type: SiteQuality
SIO_000300: 1.349e1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10306
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66468
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.81e-1

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.981e1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.983e0

BaseQRankSum
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SIO_000300: -1.768e0

DP
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.74e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.25e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 13

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.728907330567082e-4
allele num: 11568
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501997656883655e-5
allele num: 66578
num of homozygotes: 0

South Asian
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allele count: 8
allele frequency: 4.845548152634767e-4
allele num: 16510
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.67305088024763e-5
allele num: 10338
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-3

MQ
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BaseQRankSum
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DP
type: SiteQuality
SIO_000300: 2.416178e6

ReadPosRankSum
type: SiteQuality
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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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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8642
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: 11568
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501997656883655e-5
allele num: 66578
num of homozygotes: 0

South Asian
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allele frequency: 6.056935190793458e-5
allele num: 16510
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Other
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BaseQRankSum
type: SiteQuality
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QD
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MQRankSum
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MQ
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VQSLOD
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FS
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DP
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.67305088024763e-5
allele num: 10338
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 5
allele frequency: 7.509988284418276e-5
allele num: 66578
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.93e0

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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VQSLOD
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QD
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DP
type: SiteQuality
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InbreedingCoeff
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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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bin: 9.75e1
variant carriers: 12

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3027
bin: 7.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
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: 13
allele frequency: 1.123789764868603e-3
allele num: 11568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66566
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.1e-1

DP
type: SiteQuality
SIO_000300: 2.414732e6

QD
type: SiteQuality
SIO_000300: 1.257e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.7e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.15e-1

FS
type: SiteQuality
SIO_000300: 5.35e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.95e-1

MQ
type: SiteQuality
SIO_000300: 5.929e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 7.5e-1

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

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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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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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10276
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: 6594
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: 66462
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.403468e6

FS
type: SiteQuality
SIO_000300: 2.306e0

QD
type: SiteQuality
SIO_000300: 2.104e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.14e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.133e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.348e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.773260359655981e-5
allele num: 10232
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66346
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.866e0

FS
type: SiteQuality
SIO_000300: 6.59e0

MQRankSum
type: SiteQuality
SIO_000300: 2.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.12e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

QD
type: SiteQuality
SIO_000300: 1.248e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 8.090000000000001e-1

DP
type: SiteQuality
SIO_000300: 2.391241e6

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 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: 11560
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
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: 10226
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507658907248824e-5
allele num: 66328
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.56e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.196e0

DP
type: SiteQuality
SIO_000300: 2.389819e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.27e-1

FS
type: SiteQuality
SIO_000300: 7.62e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.293e1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 24017
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
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: 10226
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66328
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

QD
type: SiteQuality
SIO_000300: 1.293e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.27e-1

DP
type: SiteQuality
SIO_000300: 2.389819e6

MQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.56e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

FS
type: SiteQuality
SIO_000300: 7.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.196e0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66328
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10222
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -2.521e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.39e0

MQ
type: SiteQuality
SIO_000300: 5.88e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.79e0

MQRankSum
type: SiteQuality
SIO_000300: -1.366e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

QD
type: SiteQuality
SIO_000300: 1.132e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.167e0

DP
type: SiteQuality
SIO_000300: 2.388262e6

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10204
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66286
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.381872e6

VQSLOD
type: SiteQuality
SIO_000300: -1.689e0

QD
type: SiteQuality
SIO_000300: 2.16e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -9.5e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.03e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.581e0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 173
bin: 4.75e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66254
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.879999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

DP
type: SiteQuality
SIO_000300: 2.377851e6

VQSLOD
type: SiteQuality
SIO_000300: -4.604e-1

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.926e0

FS
type: SiteQuality
SIO_000300: 6.03e0

MQ
type: SiteQuality
SIO_000300: 5.905e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.44e-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: 11

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.360544217687075e-4
allele num: 66150
num of homozygotes: 0

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

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

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

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.04228780042592e-4
allele num: 6574
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.92e-1

MQ
type: SiteQuality
SIO_000300: 5.901e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

QD
type: SiteQuality
SIO_000300: 1.266e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.5e-2

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.361673e6

FS
type: SiteQuality
SIO_000300: 3.001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.63e0

VQSLOD
type: SiteQuality
SIO_000300: 1.35e-1

GenotypeQuality
all individuals: 2471
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 737
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4991
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9968
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65948
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.323420074349442e-4
allele num: 8608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.456e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -3.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.302e0

QD
type: SiteQuality
SIO_000300: 2.677e1

FS
type: SiteQuality
SIO_000300: 1.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.9e-2

DP
type: SiteQuality
SIO_000300: 2.34743e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.38e-1

GenotypeQuality
all individuals: 586
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1312
bin: 2.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4491
bin: 7.75e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 896
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23970
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 468
bin: 4.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.004621257785815e-4
allele num: 9954
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65930
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.346233e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.35e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.552e0

QD
type: SiteQuality
SIO_000300: 1.103e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.41e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.28e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQRankSum
type: SiteQuality
SIO_000300: 1.4e0

GenotypeQuality
all individuals: 910
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2794
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23969
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3860
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
all individuals: 2474
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7705
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variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
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: 1
allele frequency: 1.002807862013638e-4
allele num: 9972
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65914
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.05e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.86e-1

FS
type: SiteQuality
SIO_000300: 5.457e0

VQSLOD
type: SiteQuality
SIO_000300: 2.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.26e-1

QD
type: SiteQuality
SIO_000300: 1.027e1

MQRankSum
type: SiteQuality
SIO_000300: -6.830000000000001e-1

DP
type: SiteQuality
SIO_000300: 2.345128e6

MQ
type: SiteQuality
SIO_000300: 5.954e1

GenotypeQuality
all individuals: 1262
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2472
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 152
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variant carriers: 0

GenotypeQuality
all individuals: 151
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GenotypeQuality
all individuals: 4334
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3861
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GenotypeQuality
all individuals: 223
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GenotypeQuality
all individuals: 918
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5001
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65864
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.246026931942254e-4
allele num: 16486
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9954
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

DP
type: SiteQuality
SIO_000300: 2.343955e6

FS
type: SiteQuality
SIO_000300: 7.345e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.46e-1

MQ
type: SiteQuality
SIO_000300: 5.92e1

VQSLOD
type: SiteQuality
SIO_000300: -4.044e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.07e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.474e0

QD
type: SiteQuality
SIO_000300: 1.429e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.33e-1

GenotypeQuality
all individuals: 909
bin: 2.25e1
variant carriers: 32

GenotypeQuality
all individuals: 102
bin: 2.5e0
variant carriers: 14

GenotypeQuality
all individuals: 701
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variant carriers: 55

GenotypeQuality
all individuals: 155
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variant carriers: 14

GenotypeQuality
all individuals: 439
bin: 4.25e1
variant carriers: 51

GenotypeQuality
all individuals: 3532
bin: 6.75e1
variant carriers: 131

GenotypeQuality
all individuals: 421
bin: 5.25e1
variant carriers: 101

GenotypeQuality
all individuals: 2012
bin: 7.25e1
variant carriers: 120

GenotypeQuality
all individuals: 630
bin: 4.75e1
variant carriers: 74

GenotypeQuality
all individuals: 2450
bin: 9.25e1
variant carriers: 201

GenotypeQuality
all individuals: 293
bin: 5.75e1
variant carriers: 74

GenotypeQuality
all individuals: 2924
bin: 8.25e1
variant carriers: 246

Latino
type: Population
allele count: 1473
allele frequency: 1.279756733275413e-1
allele num: 11510
num of homozygotes: 116

South Asian
type: Population
allele count: 3310
allele frequency: 2.012647452268029e-1
allele num: 16446
num of homozygotes: 386

African
type: Population
allele count: 780
allele frequency: 7.870837537840565e-2
allele num: 9910
num of homozygotes: 36

Other
type: Population
allele count: 236
allele frequency: 2.645739910313901e-1
allele num: 892
num of homozygotes: 32

East Asian
type: Population
allele count: 197
allele frequency: 2.292296951361415e-2
allele num: 8594
num of homozygotes: 2

European (Non-Finnish)
type: Population
allele count: 20528
allele frequency: 3.121654501216545e-1
allele num: 65760
num of homozygotes: 3306

European (Finnish)
type: Population
allele count: 1579
allele frequency: 2.415850673194614e-1
allele num: 6536
num of homozygotes: 158

QD
type: SiteQuality
SIO_000300: 1.602e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.61e-1

DP
type: SiteQuality
SIO_000300: 2.330185e6

FS
type: SiteQuality
SIO_000300: 8.43e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.42e0

MQRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.23e-2

MQ
type: SiteQuality
SIO_000300: 5.958e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.88e0

GenotypeQuality
all individuals: 750
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2446
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1578
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variant carriers: 0

GenotypeQuality
all individuals: 184
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variant carriers: 0

GenotypeQuality
all individuals: 1713
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variant carriers: 0

GenotypeQuality
all individuals: 890
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variant carriers: 0

GenotypeQuality
all individuals: 2985
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variant carriers: 0

GenotypeQuality
all individuals: 4689
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variant carriers: 0

GenotypeQuality
all individuals: 909
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3755
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5137
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9756
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.529519730804527e-5
allele num: 65380
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.923e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

DP
type: SiteQuality
SIO_000300: 2.166796e6

MQRankSum
type: SiteQuality
SIO_000300: 3.0e-2

QD
type: SiteQuality
SIO_000300: 6.51e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -5.664e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.66e-1

GenotypeQuality
all individuals: 4477
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
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variant carriers: 0

GenotypeQuality
all individuals: 1553
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variant carriers: 0

GenotypeQuality
all individuals: 46
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4693
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variant carriers: 0

GenotypeQuality
all individuals: 2443
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variant carriers: 0

GenotypeQuality
all individuals: 3758
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variant carriers: 0

GenotypeQuality
all individuals: 1327
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variant carriers: 0

GenotypeQuality
all individuals: 20376
bin: 9.75e1
variant carriers: 7

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.059226627508566e-5
allele num: 65376
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.436350347179924e-4
allele num: 16418
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9764
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.45e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

QD
type: SiteQuality
SIO_000300: 1.554e1

MQRankSum
type: SiteQuality
SIO_000300: 2.15e-1

MQ
type: SiteQuality
SIO_000300: 5.937e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.92e-1

DP
type: SiteQuality
SIO_000300: 2.165017e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-2

GenotypeQuality
all individuals: 4695
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 437
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variant carriers: 0

GenotypeQuality
all individuals: 294
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variant carriers: 0

GenotypeQuality
all individuals: 188
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variant carriers: 0

GenotypeQuality
all individuals: 6946
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2443
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3768
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4474
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variant carriers: 0

GenotypeQuality
all individuals: 1188
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1535
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2977
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1775
bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.026061974143238e-4
allele num: 9746
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16414
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65366
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.38e0

FS
type: SiteQuality
SIO_000300: 5.883e0

MQRankSum
type: SiteQuality
SIO_000300: -2.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

MQ
type: SiteQuality
SIO_000300: 6.065e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.639999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.159233e6

QD
type: SiteQuality
SIO_000300: 2.108e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.39e-1

GenotypeQuality
all individuals: 5995
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1090
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GenotypeQuality
all individuals: 1232
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variant carriers: 0

GenotypeQuality
all individuals: 5063
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GenotypeQuality
all individuals: 2964
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GenotypeQuality
all individuals: 4473
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GenotypeQuality
all individuals: 1354
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GenotypeQuality
all individuals: 175
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variant carriers: 0

GenotypeQuality
all individuals: 4702
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variant carriers: 0

GenotypeQuality
all individuals: 753
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GenotypeQuality
all individuals: 3772
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
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: 65342
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 2.060156571899464e-4
allele num: 9708
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.676036786395974e-5
allele num: 11526
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 7.38e-1

FS
type: SiteQuality
SIO_000300: 3.031e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.471e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.81e-1

QD
type: SiteQuality
SIO_000300: 8.539999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -3.953e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.8e-1

DP
type: SiteQuality
SIO_000300: 2.156757e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 3763
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1262
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 754
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variant carriers: 0

GenotypeQuality
all individuals: 4648
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16374
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.164958061509786e-4
allele num: 8584
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9738
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65308
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.115e1

MQ
type: SiteQuality
SIO_000300: 5.944e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.45e0

VQSLOD
type: SiteQuality
SIO_000300: 7.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e-1

DP
type: SiteQuality
SIO_000300: 2.156615e6

FS
type: SiteQuality
SIO_000300: 5.535e0

MQRankSum
type: SiteQuality
SIO_000300: 4.38e-1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
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: 3.00215e6

FS
type: SiteQuality
SIO_000300: 1.04e0

QD
type: SiteQuality
SIO_000300: 1.497e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.496e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

MQRankSum
type: SiteQuality
SIO_000300: -5.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e0

VQSLOD
type: SiteQuality
SIO_000300: 7.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4619
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
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: 2
allele frequency: 2.31107002542177e-4
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

VQSLOD
type: SiteQuality
SIO_000300: 9.84e-1

QD
type: SiteQuality
SIO_000300: 1.433e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.7e-2

DP
type: SiteQuality
SIO_000300: 3.002411e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.94e-1

FS
type: SiteQuality
SIO_000300: 3.423e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

GenotypeQuality
all individuals: 2
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1
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variant carriers: 0

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

African
type: Population
allele count: 7
allele frequency: 6.726888333653661e-4
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727712508638562e-4
allele num: 11576
num of homozygotes: 0

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

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.51e-1

QD
type: SiteQuality
SIO_000300: 1.324e1

MQRankSum
type: SiteQuality
SIO_000300: 5.679999999999999e-1

DP
type: SiteQuality
SIO_000300: 3.002476e6

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

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28665
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2222
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variant carriers: 0

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

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

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

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.95e0

DP
type: SiteQuality
SIO_000300: 3.001906e6

MQRankSum
type: SiteQuality
SIO_000300: 6.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 8.179999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.15e-1

FS
type: SiteQuality
SIO_000300: 1.204e0

MQ
type: SiteQuality
SIO_000300: 5.955e1

QD
type: SiteQuality
SIO_000300: 1.112e1

GenotypeQuality
all individuals: 4341
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2222
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3634
bin: 9.25e1
variant carriers: 0

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

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

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 3.001759e6

VQSLOD
type: SiteQuality
SIO_000300: -9.202e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.932e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

FS
type: SiteQuality
SIO_000300: 1.2213e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.56e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-1

QD
type: SiteQuality
SIO_000300: 8.640000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.5e-2

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2222
bin: 8.75e1
variant carriers: 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

East Asian
type: Population
allele count: 3
allele frequency: 3.466605038132656e-4
allele num: 8654
num of homozygotes: 0

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

DP
type: SiteQuality
SIO_000300: 3.001926e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e0

MQRankSum
type: SiteQuality
SIO_000300: -2.0e-3

QD
type: SiteQuality
SIO_000300: 1.203e1

MQ
type: SiteQuality
SIO_000300: 5.95e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.038e0

FS
type: SiteQuality
SIO_000300: 1.136e0

GenotypeQuality
all individuals: 2222
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2713
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28664
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 0
bin: 5.25e1
variant carriers: 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: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.00168e6

MQ
type: SiteQuality
SIO_000300: 6.027e1

FS
type: SiteQuality
SIO_000300: 1.871e0

MQRankSum
type: SiteQuality
SIO_000300: 4.76e-1

QD
type: SiteQuality
SIO_000300: 1.135e1

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.69e0

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

GenotypeQuality
all individuals: 0
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 28734
bin: 9.75e1
variant carriers: 5138

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 4330
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

European (Finnish)
type: Population
allele count: 291
allele frequency: 4.399758088902329e-2
allele num: 6614
num of homozygotes: 7

European (Non-Finnish)
type: Population
allele count: 4091
allele frequency: 6.129757267006293e-2
allele num: 66740
num of homozygotes: 148

Other
type: Population
allele count: 37
allele frequency: 4.074889867841409e-2
allele num: 908
num of homozygotes: 1

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

Latino
type: Population
allele count: 262
allele frequency: 2.263303386316517e-2
allele num: 11576
num of homozygotes: 5

African
type: Population
allele count: 113
allele frequency: 1.085911973861234e-2
allele num: 10406
num of homozygotes: 2

South Asian
type: Population
allele count: 518
allele frequency: 3.137112403100775e-2
allele num: 16512
num of homozygotes: 9

MQRankSum
type: SiteQuality
SIO_000300: 1.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.28e-2

FS
type: SiteQuality
SIO_000300: 1.809e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

VQSLOD
type: SiteQuality
SIO_000300: 3.78e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.968e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.78e-1

QD
type: SiteQuality
SIO_000300: 1.239e1

DP
type: SiteQuality
SIO_000300: 3.315786e6