X-153577253-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577253
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577253
    reference: chr 0
allele count: 1
allele frequency: 1.19019281123542e-5
allele num: 84020
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*6049C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7884C>T
  hgvsp: ENST00000422373.1:c.7884C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7884C>T
  hgvsp: ENST00000360319.4:c.7884C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7788C>T
  hgvsp: ENST00000344736.4:c.7788C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7908C>T
  hgvsp: ENST00000369850.3:c.7908C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-55C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2307C>T
  hgvsp: ENST00000369856.3:c.2307C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.5137C>T
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30008
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4786
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21563
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 829
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2134
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 4.75e1
  variant carriers: 0
hgvs: p.His2636His
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

X-153577259-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577259
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577259
    reference: chr 0
allele count: 1
allele frequency: 1.182116935007211e-5
allele num: 84594
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7878C>T
  hgvsp: ENST00000422373.1:c.7878C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7902C>T
  hgvsp: ENST00000369850.3:c.7902C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2301C>T
  hgvsp: ENST00000369856.3:c.2301C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7878C>T
  hgvsp: ENST00000360319.4:c.7878C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7782C>T
  hgvsp: ENST00000344736.4:c.7782C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.5131C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*6043C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-61C>T
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4851
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30385
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21797
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48760
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp2634Asp
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

X-153577261-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577261
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577261
    reference: chr 0
allele count: 1
allele frequency: 1.179287003077939e-5
allele num: 84797
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7876G>T
  hgvsp: ENSP00000353467.4:p.Asp2626Tyr
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-63G>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7900G>T
  hgvsp: ENSP00000358866.3:p.Asp2634Tyr
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2299G>T
  hgvsp: ENSP00000358872.3:p.Asp767Tyr
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*6041G>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7876G>T
  hgvsp: ENSP00000416926.1:p.Asp2626Tyr
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.5129G>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7780G>T
  hgvsp: ENSP00000358863.3:p.Asp2594Tyr
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30547
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21880
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 844
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48995
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6073
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asp2634Tyr
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: C
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

X-153577271-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577271
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577271
    reference: chr 0
allele count: 2
allele frequency: 2.341125378969671e-5
allele num: 85429
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7866C>G
  hgvsp: ENST00000360319.4:c.7866C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7770C>G
  hgvsp: ENST00000344736.4:c.7770C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2289C>G
  hgvsp: ENST00000369856.3:c.2289C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7890C>G
  hgvsp: ENST00000369850.3:c.7890C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.5119C>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-73C>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7866C>G
  hgvsp: ENST00000422373.1:c.7866C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*6031C>G
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22120
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4923
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30928
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1027
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6146
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49618
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val2630Val
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

X-153577281-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577281
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577281
    reference: chr 0
allele count: 1
allele frequency: 1.166058372882146e-5
allele num: 85759
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7856C>A
  hgvsp: ENSP00000416926.1:p.Thr2619Lys
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2279C>A
  hgvsp: ENSP00000358872.3:p.Thr760Lys
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-83C>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*6021C>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7856C>A
  hgvsp: ENSP00000353467.4:p.Thr2619Lys
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7880C>A
  hgvsp: ENSP00000358866.3:p.Thr2627Lys
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7760C>A
  hgvsp: ENSP00000358863.3:p.Thr2587Lys
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.5109C>A
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31143
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4942
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 798
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr2627Lys
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD

X-153577283-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577283
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577283
    reference: chr 0
allele count: 1
allele frequency: 1.165596260767195e-5
allele num: 85793
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-85C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7878C>T
  hgvsp: ENST00000369850.3:c.7878C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2277C>T
  hgvsp: ENST00000369856.3:c.2277C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.5107C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7854C>T
  hgvsp: ENST00000422373.1:c.7854C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7758C>T
  hgvsp: ENST00000344736.4:c.7758C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7854C>T
  hgvsp: ENST00000360319.4:c.7854C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*6019C>T
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22242
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4943
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31143
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49965
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 786
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Tyr2626Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

X-153577295-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577295
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577295
    reference: chr 0
allele count: 1
allele frequency: 1.163480668768688e-5
allele num: 85949
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.907C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*6007C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.1021C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7842C>T
  hgvsp: ENST00000422373.1:c.7842C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.5095C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2265C>T
  hgvsp: ENST00000369856.3:c.2265C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7842C>T
  hgvsp: ENST00000360319.4:c.7842C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7746C>T
  hgvsp: ENST00000344736.4:c.7746C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7866C>T
  hgvsp: ENST00000369850.3:c.7866C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-97C>T
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4958
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6165
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asp2622Asp
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
reference allele: G
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum

X-153577299-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577299
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577299
    reference: chr 0
allele count: 1
allele frequency: 1.163115287987345e-5
allele num: 85976
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2261A>G
  hgvsp: ENSP00000358872.3:p.Lys754Arg
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7838A>G
  hgvsp: ENSP00000416926.1:p.Lys2613Arg
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.5091A>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*6003A>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7742A>G
  hgvsp: ENSP00000358863.3:p.Lys2581Arg
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.903A>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7862A>G
  hgvsp: ENSP00000358866.3:p.Lys2621Arg
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.1017A>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-101A>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7838A>G
  hgvsp: ENSP00000353467.4:p.Lys2613Arg
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4956
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31090
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 862
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Lys2621Arg
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

X-153577313-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577313
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577313
    reference: chr 0
allele count: 6
allele frequency: 6.982752601075344e-5
allele num: 85926
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7848G>C
  hgvsp: ENST00000369850.3:c.7848G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.1003G>C
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7728G>C
  hgvsp: ENST00000344736.4:c.7728G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7824G>C
  hgvsp: ENST00000360319.4:c.7824G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2247G>C
  hgvsp: ENST00000369856.3:c.2247G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7824G>C
  hgvsp: ENST00000422373.1:c.7824G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-115G>C
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5989G>C
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.889G>C
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.5077G>C
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4954
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30763
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val2616Val
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP

X-153577324-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577324
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577324
    reference: chr 0
allele count: 1
allele frequency: 1.167337885951088e-5
allele num: 85665
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.5066C>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-126C>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7813C>G
  hgvsp: ENSP00000353467.4:p.Leu2605Val
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2236C>G
  hgvsp: ENSP00000358872.3:p.Leu746Val
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7837C>G
  hgvsp: ENSP00000358866.3:p.Leu2613Val
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7813C>G
  hgvsp: ENSP00000416926.1:p.Leu2605Val
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.992C>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7717C>G
  hgvsp: ENSP00000358863.3:p.Leu2573Val
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5978C>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.878C>G
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4937
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30217
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 834
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu2613Val
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

X-153577325-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577325
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577325
    reference: chr 0
allele count: 4
allele frequency: 4.67284260697889e-5
allele num: 85601
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7812G>A
  hgvsp: ENST00000422373.1:c.7812G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.991G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2235G>A
  hgvsp: ENST00000369856.3:c.2235G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-127G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.5065G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.877G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5977G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7716G>A
  hgvsp: ENST00000344736.4:c.7716G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7836G>A
  hgvsp: ENST00000369850.3:c.7836G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7812G>A
  hgvsp: ENST00000360319.4:c.7812G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4947
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22293
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30094
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 832
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg2612Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD

X-153577326-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577326
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577326
    reference: chr 0
allele count: 3
allele frequency: 3.510948307137758e-5
allele num: 85447
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7811G>A
  hgvsp: ENSP00000416926.1:p.Arg2604Gln
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5976G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2234G>A
  hgvsp: ENSP00000358872.3:p.Arg745Gln
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-128G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.990G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7811G>A
  hgvsp: ENSP00000353467.4:p.Arg2604Gln
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7715G>A
  hgvsp: ENSP00000358863.3:p.Arg2572Gln
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7835G>A
  hgvsp: ENSP00000358866.3:p.Arg2612Gln
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.5064G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.876G>A
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22245
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4958
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29734
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1744
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg2612Gln
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS

X-153577327-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577327
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577327
    reference: chr 0
allele count: 5
allele frequency: 5.851443551124063e-5
allele num: 85449
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7810C>T
  hgvsp: ENSP00000416926.1:p.Arg2604Trp
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2233C>T
  hgvsp: ENSP00000358872.3:p.Arg745Trp
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7810C>T
  hgvsp: ENSP00000353467.4:p.Arg2604Trp
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-129C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7834C>T
  hgvsp: ENSP00000358866.3:p.Arg2612Trp
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.989C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5975C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.5063C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7714C>T
  hgvsp: ENSP00000358863.3:p.Arg2572Trp
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.875C>T
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22261
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29735
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4951
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 9.25e1
  variant carriers: 1
hgvs: p.Arg2612Trp
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

X-153577337-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577337
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577337
    reference: chr 0
allele count: 2
allele frequency: 2.357211889776772e-5
allele num: 84846
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7824C>T
  hgvsp: ENST00000369850.3:c.7824C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7704C>T
  hgvsp: ENST00000344736.4:c.7704C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5965C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-139C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.5053C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7800C>T
  hgvsp: ENST00000422373.1:c.7800C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.979C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7800C>T
  hgvsp: ENST00000360319.4:c.7800C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2223C>T
  hgvsp: ENST00000369856.3:c.2223C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.865C>T
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28764
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21993
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4906
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 7.5e0
  variant carriers: 0
hgvs: p.His2608His
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD

X-153577339-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577339
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577339
    reference: chr 0
allele count: 14
allele frequency: 1.65611876737446e-4
allele num: 84535
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7798C>T
  hgvsp: ENSP00000353467.4:p.His2600Tyr
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.863C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.5051C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7798C>T
  hgvsp: ENSP00000416926.1:p.His2600Tyr
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5963C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7702C>T
  hgvsp: ENSP00000358863.3:p.His2568Tyr
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2221C>T
  hgvsp: ENSP00000358872.3:p.His741Tyr
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.977C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7822C>T
  hgvsp: ENSP00000358866.3:p.His2608Tyr
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-141C>T
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21804
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28333
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4885
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
hgvs: p.His2608Tyr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

X-153577358-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577358
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577358
    reference: chr 0
allele count: 5
allele frequency: 6.213186867808237e-5
allele num: 80474
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7803C>T
  hgvsp: ENST00000369850.3:c.7803C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2202C>T
  hgvsp: ENST00000369856.3:c.2202C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5944C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7779C>T
  hgvsp: ENST00000422373.1:c.7779C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.844C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-160C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.958C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.5032C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7779C>T
  hgvsp: ENST00000360319.4:c.7779C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7683C>T
  hgvsp: ENST00000344736.4:c.7683C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19562
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5471
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22700
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4567
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5524
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38784
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Cys2601Cys
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS

X-153577363-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577363
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577363
    reference: chr 0
allele count: 1
allele frequency: 1.270971021860702e-5
allele num: 78680
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.839C>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7774C>A
  hgvsp: ENSP00000353467.4:p.Pro2592Thr
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7798C>A
  hgvsp: ENSP00000358866.3:p.Pro2600Thr
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.953C>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2197C>A
  hgvsp: ENSP00000358872.3:p.Pro733Thr
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.5027C>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-165C>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7678C>A
  hgvsp: ENSP00000358863.3:p.Pro2560Thr
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5939C>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7774C>A
  hgvsp: ENSP00000416926.1:p.Pro2592Thr
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6958
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20532
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18363
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4354
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1114
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro2600Thr
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ

X-153577365-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577365
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577365
    reference: chr 0
allele count: 1
allele frequency: 1.275770565421515e-5
allele num: 78384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5937C>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2195C>A
  hgvsp: ENSP00000358872.3:p.Thr732Asn
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7796C>A
  hgvsp: ENSP00000358866.3:p.Thr2599Asn
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7772C>A
  hgvsp: ENSP00000353467.4:p.Thr2591Asn
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.951C>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-167C>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7676C>A
  hgvsp: ENSP00000358863.3:p.Thr2559Asn
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.837C>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7772C>A
  hgvsp: ENSP00000416926.1:p.Thr2591Asn
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.5025C>A
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7539
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18147
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4280
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr2599Asn
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

X-153577366-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577366
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577366
    reference: chr 0
allele count: 1
allele frequency: 1.279819801371967e-5
allele num: 78136
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7771A>T
  hgvsp: ENSP00000416926.1:p.Thr2591Ser
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7771A>T
  hgvsp: ENSP00000353467.4:p.Thr2591Ser
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.5024A>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7795A>T
  hgvsp: ENSP00000358866.3:p.Thr2599Ser
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.950A>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5936A>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2194A>T
  hgvsp: ENSP00000358872.3:p.Thr732Ser
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.836A>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-168A>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7675A>T
  hgvsp: ENSP00000358863.3:p.Thr2559Ser
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17906
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7425
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7832
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1651
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4239
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19974
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1162
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Thr2599Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

X-153577367-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577367
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577367
    reference: chr 0
allele count: 1
allele frequency: 1.285247924324602e-5
allele num: 77806
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7770G>A
  hgvsp: ENST00000422373.1:c.7770G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7770G>A
  hgvsp: ENST00000360319.4:c.7770G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7794G>A
  hgvsp: ENST00000369850.3:c.7794G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2193G>A
  hgvsp: ENST00000369856.3:c.2193G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.5023G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.949G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.835G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7674G>A
  hgvsp: ENST00000344736.4:c.7674G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5935G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-169G>A
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19580
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7679
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17677
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 688
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg2598Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

X-153577385-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577385
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577385
    reference: chr 0
allele count: 1
allele frequency: 1.428387778714165e-5
allele num: 70009
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-187G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7752G>A
  hgvsp: ENST00000360319.4:c.7752G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7752G>A
  hgvsp: ENST00000422373.1:c.7752G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7776G>A
  hgvsp: ENST00000369850.3:c.7776G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.5005G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7656G>A
  hgvsp: ENST00000344736.4:c.7656G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.931G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.817G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2175G>A
  hgvsp: ENST00000369856.3:c.2175G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5917G>A
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13862
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12889
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12511
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Val2592Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

X-153577385-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577385
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577385
    reference: chr 0
allele count: 1
allele frequency: 1.428387778714165e-5
allele num: 70009
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.5005G>C
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7656G>C
  hgvsp: ENST00000344736.4:c.7656G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.931G>C
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7752G>C
  hgvsp: ENST00000422373.1:c.7752G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2175G>C
  hgvsp: ENST00000369856.3:c.2175G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.817G>C
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-187G>C
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7776G>C
  hgvsp: ENST00000369850.3:c.7776G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7752G>C
  hgvsp: ENST00000360319.4:c.7752G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5917G>C
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13862
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12511
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12889
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 716
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val2592Val
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum

X-153577400-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577400
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577400
    reference: chr 0
allele count: 1
allele frequency: 1.646009250571988e-5
allele num: 60753
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7761C>T
  hgvsp: ENST00000369850.3:c.7761C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7737C>T
  hgvsp: ENST00000422373.1:c.7737C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2160C>T
  hgvsp: ENST00000369856.3:c.2160C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.802C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5902C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7737C>T
  hgvsp: ENST00000360319.4:c.7737C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4990C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7641C>T
  hgvsp: ENST00000344736.4:c.7641C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-202C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.916C>T
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7787
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5030
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15897
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17738
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8955
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2245
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14972
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asn2587Asn
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

X-153577407-G-GCTTTGCTGCAGTCTACTGTGA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577407
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577428
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 55678
alternate allele: GCTTTGCTGCAGTCTACTGTGA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7567
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5591
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16865
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17916
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7882
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1717
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2430
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 9.75e1
  variant carriers: 0
hgvs: c.7757-4_7757-3insTCACAGTAGACTGCAGCAAAG
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

X-153577426-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577426
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577426
    reference: chr 0
allele count: 1
allele frequency: 2.762278327164245e-5
allele num: 36202
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7757-22C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2156-22C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7733-22C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7637-22C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-228C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7733-22C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.798-22C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5898-22C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4986-22C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.912-22C>T
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12099
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18677
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16990
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

X-153577429-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577429
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577429
    reference: chr 0
allele count: 1
allele frequency: 2.75626360905157e-5
allele num: 36281
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.912-25G>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4986-25G>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.798-25G>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7637-25G>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5898-25G>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7757-25G>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2156-25G>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-231G>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7733-25G>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7733-25G>T
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18916
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2415
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11822
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2561
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3213
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

X-153577437-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577437
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577437
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 30697
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4986-33G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7637-33G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7757-33G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.912-33G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.798-33G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5898-33G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7733-33G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2156-33G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-239G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7733-33G>A
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21078
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8898
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17992
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4773
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

X-153577440-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577440
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577440
    reference: chr 0
allele count: 1
allele frequency: 3.628842036506151e-5
allele num: 27557
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.798-36G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5898-36G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7733-36G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2156-36G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7637-36G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7757-36G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4986-36G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.912-36G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7733-36G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-242G>A
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18656
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21552
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7431
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD

X-153577446-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577446
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577446
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 26414
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7733-42A>C
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.798-42A>C
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7733-42A>C
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4986-42A>C
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7637-42A>C
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7757-42A>C
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2156-42A>C
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-248A>C
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.912-42A>C
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5898-42A>C
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 21852
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6627
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19175
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1121
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1746
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5854
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
reference allele: T
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

X-153577452-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577452
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577452
    reference: chr 0
allele count: 2
allele frequency: 8.056719303899453e-5
allele num: 24824
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7733-48G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.798-48G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5898-48G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7637-48G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7733-48G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.912-48G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2156-48G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-254G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7757-48G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4986-48G>A
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19694
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4452
  bin: 2.25e1
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genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1663
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
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genotype depth: GenotypeDepth
  all individuals: 653
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genotype depth: GenotypeDepth
  all individuals: 22022
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5871
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  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
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genotype depth: GenotypeDepth
  all individuals: 2456
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1197
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

X-153577453-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577453
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577453
    reference: chr 0
allele count: 1
allele frequency: 4.028521935301938e-5
allele num: 24823
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5898-49C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4986-49C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7757-49C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.798-49C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7637-49C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2156-49C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7733-49C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.912-49C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-255C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7733-49C>T
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2432
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5878
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22060
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19704
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4446
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3708
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5605
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: African
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

X-153577679-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577679
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577679
    reference: chr 0
allele count: 1
allele frequency: 1.18058179070646e-5
allele num: 84704
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.911+51A>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7732+51A>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7732+51A>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7636+51A>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4985+51A>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7756+51A>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.797+51A>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2155+51A>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-481A>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5897+51A>G
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3624
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4758
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  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 1.25e1
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genotype depth: GenotypeDepth
  all individuals: 2696
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1894
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6046
  bin: 2.25e1
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genotype depth: GenotypeDepth
  all individuals: 778
  bin: 9.25e1
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genotype depth: GenotypeDepth
  all individuals: 14051
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8504
  bin: 3.25e1
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genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 639
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

X-153577682-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577682
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577682
    reference: chr 0
allele count: 1
allele frequency: 1.180916391119509e-5
allele num: 84680
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7756+48G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7732+48G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.911+48G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2155+48G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7636+48G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.797+48G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7732+48G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5897+48G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4985+48G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-484G>A
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8509
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4763
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2696
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14046
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3936
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3624
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6207
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1546
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22727
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 649
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

X-153577689-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577689
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577689
    reference: chr 0
allele count: 1
allele frequency: 1.181111662296553e-5
allele num: 84666
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7756+41G>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5897+41G>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7636+41G>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2155+41G>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4985+41G>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.911+41G>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7732+41G>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7732+41G>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.797+41G>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-491G>T
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8552
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14173
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4765
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum

X-153577702-AGGTGGGCC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577702
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577694
    reference: chr 0
allele count: 1
allele frequency: 1.180665423032421e-5
allele num: 84698
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8617
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7261
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14373
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3631
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2698
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4765
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1725
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22733
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5888
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1290
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: AGGTGGGCC
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: MQ

X-153577710-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577710
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577710
    reference: chr 0
allele count: 6
allele frequency: 7.083323495384034e-5
allele num: 84706
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5897+20G>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2155+20G>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7756+20G>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4985+20G>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.797+20G>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-512G>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7636+20G>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7732+20G>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7732+20G>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.911+20G>T
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3638
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8696
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14571
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7272
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3938
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4789
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17798
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

X-153577710-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577710
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577710
    reference: chr 0
allele count: 8
allele frequency: 9.444431327178712e-5
allele num: 84706
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4985+20G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7636+20G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7756+20G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.911+20G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2155+20G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5897+20G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7732+20G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-512G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.797+20G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7732+20G>A
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3638
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3938
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7272
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14571
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4789
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8696
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1210
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17798
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff

X-153577711-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577711
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577711
    reference: chr 0
allele count: 7
allele frequency: 8.248491704374058e-5
allele num: 84864
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-513C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4985+19C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5897+19C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.797+19C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.911+19C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7732+19C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7636+19C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7732+19C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7756+19C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2155+19C>T
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3937
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4795
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7282
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8711
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1732
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3658
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1568
  bin: 9.25e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

X-153577713-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577713
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577713
    reference: chr 0
allele count: 1
allele frequency: 1.177038336138608e-5
allele num: 84959
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4985+17C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7636+17C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7732+17C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7756+17C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-515C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5897+17C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.911+17C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2155+17C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.797+17C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7732+17C>T
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3936
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3639
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8706
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14733
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
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genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 1.25e1
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genotype depth: GenotypeDepth
  all individuals: 320
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7360
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genotype depth: GenotypeDepth
  all individuals: 334
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genotype depth: GenotypeDepth
  all individuals: 4792
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genotype depth: GenotypeDepth
  all individuals: 1137
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 9.25e1
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genotype depth: GenotypeDepth
  all individuals: 997
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22738
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2092
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2741
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD

X-153577718-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577718
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577718
    reference: chr 0
allele count: 1
allele frequency: 1.175889560452482e-5
allele num: 85042
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5897+12G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-520G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7732+12G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2155+12G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7756+12G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4985+12G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.911+12G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7732+12G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.797+12G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7636+12G>A
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4797
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8740
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3639
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14824
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3937
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18324
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2104
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5995
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

X-153577719-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577719
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577719
    reference: chr 0
allele count: 27520
allele frequency: 3.221388521462267e-1
allele num: 85429
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.797+11C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7756+11C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7732+11C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-521C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7732+11C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2155+11C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4985+11C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.911+11C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5897+11C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7636+11C>T
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 2.5e0
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 4.25e1
  variant carriers: 805
genotype depth: GenotypeDepth
  all individuals: 10055
  bin: 9.75e1
  variant carriers: 9858
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 1.25e1
  variant carriers: 386
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 4.75e1
  variant carriers: 979
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 7.25e1
  variant carriers: 1182
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 5.75e1
  variant carriers: 1204
genotype depth: GenotypeDepth
  all individuals: 13920
  bin: 2.75e1
  variant carriers: 481
genotype depth: GenotypeDepth
  all individuals: 3604
  bin: 3.75e1
  variant carriers: 609
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 8.25e1
  variant carriers: 936
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 5.25e1
  variant carriers: 1108
genotype depth: GenotypeDepth
  all individuals: 6520
  bin: 2.25e1
  variant carriers: 390
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 7.75e1
  variant carriers: 1047
genotype depth: GenotypeDepth
  all individuals: 7648
  bin: 3.25e1
  variant carriers: 539
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 7.5e0
  variant carriers: 199
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 8.75e1
  variant carriers: 857
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 1.75e1
  variant carriers: 402
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 9.25e1
  variant carriers: 787
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 6.75e1
  variant carriers: 1138
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 6.25e1
  variant carriers: 1248
genotype quality: GenotypeQuality
  all individuals: 26683
  bin: 9.75e1
  variant carriers: 22377
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.75e1
  variant carriers: 67
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 3.25e1
  variant carriers: 95
num of homozygotes: 3631
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

X-153577722-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577722
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577722
    reference: chr 0
allele count: 47
allele frequency: 5.49347795595867e-4
allele num: 85556
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.911+8A>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.797+8A>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7756+8A>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7636+8A>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7732+8A>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2155+8A>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7732+8A>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4985+8A>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-524A>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5897+8A>G
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 22046
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12157
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8984
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 9.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5333
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1029
  bin: 2.25e1
  variant carriers: 0
hgvs: c.7756+8A>G
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

X-153577723-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577723
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577723
    reference: chr 0
allele count: 1
allele frequency: 1.168060552259029e-5
allele num: 85612
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.797+7A>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7636+7A>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7732+7A>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5897+7A>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-525A>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7732+7A>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7756+7A>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.911+7A>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2155+7A>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4985+7A>T
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5341
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22063
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12162
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 4.75e1
  variant carriers: 0
hgvs: c.7756+7A>T
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

X-153577748-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577748
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577748
    reference: chr 0
allele count: 1
allele frequency: 1.164130801736883e-5
allele num: 85901
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-550G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7714G>A
  hgvsp: ENSP00000353467.4:p.Val2572Ile
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2137G>A
  hgvsp: ENSP00000358872.3:p.Val713Ile
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5879G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7618G>A
  hgvsp: ENSP00000358863.3:p.Val2540Ile
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.893G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7714G>A
  hgvsp: ENSP00000416926.1:p.Val2572Ile
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7738G>A
  hgvsp: ENSP00000358866.3:p.Val2580Ile
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.779G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4967G>A
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5347
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9554
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22258
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val2580Ile
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

X-153577761-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577761
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577761
    reference: chr 0
allele count: 3
allele frequency: 3.489224112864769e-5
allele num: 85979
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7725G>A
  hgvsp: ENST00000369850.3:c.7725G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7701G>A
  hgvsp: ENST00000422373.1:c.7701G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7605G>A
  hgvsp: ENST00000344736.4:c.7605G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.880G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5866G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-563G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2124G>A
  hgvsp: ENST00000369856.3:c.2124G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4954G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7701G>A
  hgvsp: ENST00000360319.4:c.7701G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.766G>A
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22373
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9494
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5348
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3415
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 840
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Lys2575Lys
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD

X-153577771-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577771
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577771
    reference: chr 0
allele count: 5
allele frequency: 5.813277525869085e-5
allele num: 86010
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4944T>C
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.756T>C
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5856T>C
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7691T>C
  hgvsp: ENSP00000353467.4:p.Val2564Ala
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7691T>C
  hgvsp: ENSP00000416926.1:p.Val2564Ala
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7595T>C
  hgvsp: ENSP00000358863.3:p.Val2532Ala
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7715T>C
  hgvsp: ENSP00000358866.3:p.Val2572Ala
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2114T>C
  hgvsp: ENSP00000358872.3:p.Val705Ala
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-573T>C
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.870T>C
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9429
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12177
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22409
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5345
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28203
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2519
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Val2572Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: African
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum

X-153577772-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577772
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577772
    reference: chr 0
allele count: 1
allele frequency: 1.16266902300922e-5
allele num: 86009
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-574G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7690G>A
  hgvsp: ENSP00000416926.1:p.Val2564Ile
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.869G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5855G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.755G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2113G>A
  hgvsp: ENSP00000358872.3:p.Val705Ile
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4943G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7594G>A
  hgvsp: ENSP00000358863.3:p.Val2532Ile
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7690G>A
  hgvsp: ENSP00000353467.4:p.Val2564Ile
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7714G>A
  hgvsp: ENSP00000358866.3:p.Val2572Ile
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12179
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22410
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5343
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1694
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val2572Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

X-153577773-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577773
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577773
    reference: chr 0
allele count: 5
allele frequency: 5.812939603557519e-5
allele num: 86015
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-575C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.754C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2112C>T
  hgvsp: ENST00000369856.3:c.2112C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.868C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7689C>T
  hgvsp: ENST00000360319.4:c.7689C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7689C>T
  hgvsp: ENST00000422373.1:c.7689C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7713C>T
  hgvsp: ENST00000369850.3:c.7713C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5854C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7593C>T
  hgvsp: ENST00000344736.4:c.7593C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4942C>T
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12175
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3415
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3795
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Tyr2571Tyr
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: G
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

X-153577774-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577774
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577774
    reference: chr 0
allele count: 1
allele frequency: 1.162358192300539e-5
allele num: 86032
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7712A>T
  hgvsp: ENSP00000358866.3:p.Tyr2571Phe
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2111A>T
  hgvsp: ENSP00000358872.3:p.Tyr704Phe
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4941A>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7688A>T
  hgvsp: ENSP00000416926.1:p.Tyr2563Phe
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7688A>T
  hgvsp: ENSP00000353467.4:p.Tyr2563Phe
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7592A>T
  hgvsp: ENSP00000358863.3:p.Tyr2531Phe
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-576A>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5853A>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.753A>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.867A>T
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5342
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22445
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9445
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12170
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Tyr2571Phe
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

X-153577776-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577776
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577776
    reference: chr 0
allele count: 11
allele frequency: 1.278430552165777e-4
allele num: 86043
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4939C>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7590C>G
  hgvsp: ENST00000344736.4:c.7590C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7686C>G
  hgvsp: ENST00000422373.1:c.7686C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7710C>G
  hgvsp: ENST00000369850.3:c.7710C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-578C>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2109C>G
  hgvsp: ENST00000369856.3:c.2109C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.751C>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.865C>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5851C>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7686C>G
  hgvsp: ENST00000360319.4:c.7686C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9451
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12170
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5342
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 22447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala2570Ala
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

X-153577800-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577800
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577800
    reference: chr 0
allele count: 74
allele frequency: 8.602850566160571e-4
allele num: 86018
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2085C>T
  hgvsp: ENST00000369856.3:c.2085C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7566C>T
  hgvsp: ENST00000344736.4:c.7566C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-602C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7686C>T
  hgvsp: ENST00000369850.3:c.7686C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5827C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7662C>T
  hgvsp: ENST00000360319.4:c.7662C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7662C>T
  hgvsp: ENST00000422373.1:c.7662C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.841C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.727C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4915C>T
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9340
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3410
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5334
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12141
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 22411
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala2562Ala
num of homozygotes: 1
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

X-153577803-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577803
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577803
    reference: chr 0
allele count: 1
allele frequency: 1.162385214460072e-5
allele num: 86030
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.724G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-605G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7683G>A
  hgvsp: ENST00000369850.3:c.7683G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5824G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4912G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7659G>A
  hgvsp: ENST00000422373.1:c.7659G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.838G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7563G>A
  hgvsp: ENST00000344736.4:c.7563G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7659G>A
  hgvsp: ENST00000360319.4:c.7659G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2082G>A
  hgvsp: ENST00000369856.3:c.2082G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5342
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22457
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12141
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9318
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1421
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Val2561Val
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

X-153577817-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577817
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577817
    reference: chr 0
allele count: 1
allele frequency: 1.162466288477634e-5
allele num: 86024
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7645G>A
  hgvsp: ENSP00000353467.4:p.Ala2549Thr
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.824G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4898G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5810G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7549G>A
  hgvsp: ENSP00000358863.3:p.Ala2517Thr
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.710G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7669G>A
  hgvsp: ENSP00000358866.3:p.Ala2557Thr
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-619G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2068G>A
  hgvsp: ENSP00000358872.3:p.Ala690Thr
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7645G>A
  hgvsp: ENSP00000416926.1:p.Ala2549Thr
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5334
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22509
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3411
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9249
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8930
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ala2557Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

X-153577818-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577818
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577818
    reference: chr 0
allele count: 5
allele frequency: 5.811655856986772e-5
allele num: 86034
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7644C>T
  hgvsp: ENST00000422373.1:c.7644C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4897C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7644C>T
  hgvsp: ENST00000360319.4:c.7644C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7548C>T
  hgvsp: ENST00000344736.4:c.7548C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-620C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2067C>T
  hgvsp: ENST00000369856.3:c.2067C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7668C>T
  hgvsp: ENST00000369850.3:c.7668C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5809C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.709C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.823C>T
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22525
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5328
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9262
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp2556Asp
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

X-153577836-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577836
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577836
    reference: chr 0
allele count: 1
allele frequency: 1.161764022491752e-5
allele num: 86076
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.805G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.691G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2049G>A
  hgvsp: ENST00000369856.3:c.2049G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7626G>A
  hgvsp: ENST00000360319.4:c.7626G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5791G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7650G>A
  hgvsp: ENST00000369850.3:c.7650G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-638G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7530G>A
  hgvsp: ENST00000344736.4:c.7530G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7626G>A
  hgvsp: ENST00000422373.1:c.7626G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4879G>A
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5317
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9385
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12137
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22571
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1415
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro2550Pro
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

X-153577837-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577837
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577837
    reference: chr 0
allele count: 5
allele frequency: 5.808617665168043e-5
allele num: 86079
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.690C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4878C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7529C>T
  hgvsp: ENSP00000358863.3:p.Pro2510Leu
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2048C>T
  hgvsp: ENSP00000358872.3:p.Pro683Leu
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-639C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7625C>T
  hgvsp: ENSP00000353467.4:p.Pro2542Leu
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7625C>T
  hgvsp: ENSP00000416926.1:p.Pro2542Leu
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7649C>T
  hgvsp: ENSP00000358866.3:p.Pro2550Leu
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.804C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5790C>T
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12135
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22587
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1415
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 4.25e1
  variant carriers: 1
hgvs: p.Pro2550Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

X-153577856-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577856
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577856
    reference: chr 0
allele count: 1
allele frequency: 1.158869407006524e-5
allele num: 86291
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7606G>A
  hgvsp: ENSP00000353467.4:p.Ala2536Thr
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7510G>A
  hgvsp: ENSP00000358863.3:p.Ala2504Thr
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7630G>A
  hgvsp: ENSP00000358866.3:p.Ala2544Thr
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.671G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5771G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7606G>A
  hgvsp: ENSP00000416926.1:p.Ala2536Thr
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2029G>A
  hgvsp: ENSP00000358872.3:p.Ala677Thr
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.785G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-658G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4859G>A
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5311
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22798
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9639
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12179
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala2544Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

X-153577858-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577858
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577858
    reference: chr 0
allele count: 1
allele frequency: 1.15854718183398e-5
allele num: 86315
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.783G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5769G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4857G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2027G>A
  hgvsp: ENSP00000358872.3:p.Cys676Tyr
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7604G>A
  hgvsp: ENSP00000353467.4:p.Cys2535Tyr
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7628G>A
  hgvsp: ENSP00000358866.3:p.Cys2543Tyr
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7508G>A
  hgvsp: ENSP00000358863.3:p.Cys2503Tyr
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7604G>A
  hgvsp: ENSP00000416926.1:p.Cys2535Tyr
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.669G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-660G>A
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5309
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22826
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12176
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9665
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2504
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Cys2543Tyr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff

X-153577859-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577859
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577859
    reference: chr 0
allele count: 1
allele frequency: 1.158278797706608e-5
allele num: 86335
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7507T>A
  hgvsp: ENSP00000358863.3:p.Cys2503Ser
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-661T>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4856T>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.782T>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7627T>A
  hgvsp: ENSP00000358866.3:p.Cys2543Ser
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7603T>A
  hgvsp: ENSP00000416926.1:p.Cys2535Ser
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5768T>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7603T>A
  hgvsp: ENSP00000353467.4:p.Cys2535Ser
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.668T>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2026T>A
  hgvsp: ENSP00000358872.3:p.Cys676Ser
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5310
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12166
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3797
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Cys2543Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ

X-153577864-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577864
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577864
    reference: chr 0
allele count: 3
allele frequency: 3.472945752587345e-5
allele num: 86382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.777C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5763C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-666C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7502C>T
  hgvsp: ENSP00000358863.3:p.Ala2501Val
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7598C>T
  hgvsp: ENSP00000416926.1:p.Ala2533Val
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7622C>T
  hgvsp: ENSP00000358866.3:p.Ala2541Val
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7598C>T
  hgvsp: ENSP00000353467.4:p.Ala2533Val
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2021C>T
  hgvsp: ENSP00000358872.3:p.Ala674Val
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4851C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.663C>T
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5315
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12163
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22867
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9757
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala2541Val
num of homozygotes: 1
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

X-153577872-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577872
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577872
    reference: chr 0
allele count: 1
allele frequency: 1.156523951611038e-5
allele num: 86466
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.2013G>A
  hgvsp: ENST00000369856.3:c.2013G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7590G>A
  hgvsp: ENST00000360319.4:c.7590G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7590G>A
  hgvsp: ENST00000422373.1:c.7590G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-674G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7614G>A
  hgvsp: ENST00000369850.3:c.7614G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7494G>A
  hgvsp: ENST00000344736.4:c.7494G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5755G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.769G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4843G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.655G>A
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9822
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12158
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5314
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22901
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu2538Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP

X-153577890-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577890
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577890
    reference: chr 0
allele count: 12
allele frequency: 1.386978582739051e-4
allele num: 86519
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.1995A>G
  hgvsp: ENST00000369856.3:c.1995A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7572A>G
  hgvsp: ENST00000422373.1:c.7572A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4825A>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5737A>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7596A>G
  hgvsp: ENST00000369850.3:c.7596A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-692A>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.637A>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7476A>G
  hgvsp: ENST00000344736.4:c.7476A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.751A>G
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7572A>G
  hgvsp: ENST00000360319.4:c.7572A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5313
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9780
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12160
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22950
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1680
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser2532Ser
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

X-153577918-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577918
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577918
    reference: chr 0
allele count: 31
allele frequency: 3.58605372139833e-4
allele num: 86446
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-720G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7568G>A
  hgvsp: ENSP00000358866.3:p.Ser2523Asn
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7544G>A
  hgvsp: ENSP00000416926.1:p.Ser2515Asn
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7544G>A
  hgvsp: ENSP00000353467.4:p.Ser2515Asn
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.1967G>A
  hgvsp: ENSP00000358872.3:p.Ser656Asn
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.609G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5709G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4797G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7448G>A
  hgvsp: ENSP00000358863.3:p.Ser2483Asn
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.723G>A
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5315
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12148
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 9.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 22824
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser2523Asn
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum

X-153577922-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577922
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577922
    reference: chr 0
allele count: 3
allele frequency: 3.471097329569121e-5
allele num: 86428
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.719G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7444G>A
  hgvsp: ENSP00000358863.3:p.Val2482Ile
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7540G>A
  hgvsp: ENSP00000353467.4:p.Val2514Ile
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5705G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7540G>A
  hgvsp: ENSP00000416926.1:p.Val2514Ile
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.605G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4793G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7564G>A
  hgvsp: ENSP00000358866.3:p.Val2522Ile
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.1963G>A
  hgvsp: ENSP00000358872.3:p.Val655Ile
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-724G>A
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22826
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8920
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val2522Ile
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

X-153577923-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577923
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577923
    reference: chr 0
allele count: 3
allele frequency: 3.471298149798086e-5
allele num: 86423
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7443C>T
  hgvsp: ENST00000344736.4:c.7443C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4792C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7563C>T
  hgvsp: ENST00000369850.3:c.7563C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7539C>T
  hgvsp: ENST00000422373.1:c.7539C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-725C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.604C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7539C>T
  hgvsp: ENST00000360319.4:c.7539C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.718C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5704C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.1962C>T
  hgvsp: ENST00000369856.3:c.1962C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12145
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5317
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9581
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22841
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3404
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8929
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 3.75e1
  variant carriers: 1
hgvs: p.Leu2521Leu
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

X-153577927-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577927
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577927
    reference: chr 0
allele count: 2
allele frequency: 2.315297168391563e-5
allele num: 86382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7535G>A
  hgvsp: ENSP00000353467.4:p.Arg2512His
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-729G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7439G>A
  hgvsp: ENSP00000358863.3:p.Arg2480His
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7559G>A
  hgvsp: ENSP00000358866.3:p.Arg2520His
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.714G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7535G>A
  hgvsp: ENSP00000416926.1:p.Arg2512His
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4788G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.1958G>A
  hgvsp: ENSP00000358872.3:p.Arg653His
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5700G>A
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.600G>A
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12175
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22842
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5317
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9522
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg2520His
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

X-153577928-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577928
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577928
    reference: chr 0
allele count: 9
allele frequency: 1.040931749574953e-4
allele num: 86461
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.599C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7438C>T
  hgvsp: ENSP00000358863.3:p.Arg2480Cys
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7558C>T
  hgvsp: ENSP00000358866.3:p.Arg2520Cys
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5699C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.713C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7534C>T
  hgvsp: ENSP00000353467.4:p.Arg2512Cys
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.1957C>T
  hgvsp: ENSP00000358872.3:p.Arg653Cys
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7534C>T
  hgvsp: ENSP00000416926.1:p.Arg2512Cys
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-730C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4787C>T
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5315
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12171
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9522
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22899
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg2520Cys
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

X-153577931-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577931
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577931
    reference: chr 0
allele count: 5
allele frequency: 5.783623092850285e-5
allele num: 86451
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7435C>T
  hgvsp: ENSP00000358863.3:p.Pro2479Ser
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-733C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.596C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4784C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7555C>T
  hgvsp: ENSP00000358866.3:p.Pro2519Ser
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7531C>T
  hgvsp: ENSP00000416926.1:p.Pro2511Ser
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.710C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5696C>T
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7531C>T
  hgvsp: ENSP00000353467.4:p.Pro2511Ser
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.1954C>T
  hgvsp: ENSP00000358872.3:p.Pro652Ser
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 22899
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9514
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5307
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12152
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro2519Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

X-153577939-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24153577939
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24153577939
    reference: chr 0
allele count: 3
allele frequency: 3.472423172637306e-5
allele num: 86395
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358866
  ensembl transcript: ENST00000369850
  gene symbol: FLNA
  hgvsc: ENST00000369850.3:c.7553-6T>C
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358872
  ensembl transcript: ENST00000369856
  gene symbol: FLNA
  hgvsc: ENST00000369856.3:c.1952-6T>C
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000416926
  ensembl transcript: ENST00000422373
  gene symbol: FLNA
  hgvsc: ENST00000422373.1:c.7529-6T>C
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000408921
  ensembl transcript: ENST00000420627
  gene symbol: FLNA
  hgvsc: ENST00000420627.1:c.*5694-6T>C
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498491
  gene symbol: FLNA
  hgvsc: ENST00000498491.1:n.594-6T>C
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000498411
  gene symbol: FLNA
  hgvsc: ENST00000498411.1:n.68-741T>C
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000490936
  gene symbol: FLNA
  hgvsc: ENST00000490936.1:n.4782-6T>C
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000353467
  ensembl transcript: ENST00000360319
  gene symbol: FLNA
  hgvsc: ENST00000360319.4:c.7529-6T>C
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl transcript: ENST00000462590
  gene symbol: FLNA
  hgvsc: ENST00000462590.1:n.708-6T>C
  variant of: http://identifiers.org/hgnc/3754
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196924
  ensembl protein: ENSP00000358863
  ensembl transcript: ENST00000344736
  gene symbol: FLNA
  hgvsc: ENST00000344736.4:c.7433-6T>C
  variant of: http://identifiers.org/hgnc/3754
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5299
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9505
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22882
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12152
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8097
  bin: 9.75e1
  variant carriers: 3
hgvs: c.7553-6T>C
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: A
site quality: ReadPosRankSum

GenotypeQuality
all individuals: 99
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 356
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5971
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1125
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48223
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 2.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 593
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9198
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9214
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4470
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7588
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.154104646403722e-5
allele num: 46423
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.79e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.09e-1

QD
type: SiteQuality
SIO_000300: 1.105e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

DP
type: SiteQuality
SIO_000300: 1.451899e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.226e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.205e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

GenotypeQuality
all individuals: 844
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1640
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6053
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1155
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 595
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.144312211858046e-5
allele num: 46635
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9231
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7610
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4475
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9502
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.221e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.18e0

DP
type: SiteQuality
SIO_000300: 1.462553e6

MQ
type: SiteQuality
SIO_000300: 5.89e1

FS
type: SiteQuality
SIO_000300: 2.5288e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 7.33e-1

QD
type: SiteQuality
SIO_000300: 1.27e1

GenotypeQuality
all individuals: 66
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1158
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1450
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4474
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 596
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9613
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.310959622443629e-4
allele num: 7628
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46699
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9237
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.606e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.376e1

VQSLOD
type: SiteQuality
SIO_000300: -2.658e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.1e-3

DP
type: SiteQuality
SIO_000300: 1.467216e6

GenotypeQuality
all individuals: 100
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 856
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1172
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9883
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9246
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46967
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 605
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7688
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.046922608165753e-4
allele num: 6564
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4476
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.459e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.23e-1

MQ
type: SiteQuality
SIO_000300: 5.759e1

MQRankSum
type: SiteQuality
SIO_000300: 1.66e0

QD
type: SiteQuality
SIO_000300: 1.629e1

FS
type: SiteQuality
SIO_000300: 2.483e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.999999999999999e-3

DP
type: SiteQuality
SIO_000300: 1.477502e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.28e-1

GenotypeQuality
all individuals: 101
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 29
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1182
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49965
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6170
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 118
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9995
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.29366106080207e-4
allele num: 7730
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9259
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6577
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4483
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 609
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47106
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.482512e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.6e-3

QD
type: SiteQuality
SIO_000300: 2.762e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

GenotypeQuality
all individuals: 45
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1183
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 857
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 346
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6173
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.122151012266033e-5
allele num: 47122
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9260
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10006
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 609
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6579
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7737
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4480
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.983e1

DP
type: SiteQuality
SIO_000300: 1.483077e6

FS
type: SiteQuality
SIO_000300: 4.267e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.839e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.85e-1

QD
type: SiteQuality
SIO_000300: 1.143e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e0

VQSLOD
type: SiteQuality
SIO_000300: 7.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-2

GenotypeQuality
all individuals: 71
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 735
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1179
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 45
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 859
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.961151509114453e-5
allele num: 10039
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47195
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4471
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9263
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7778
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6591
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.48508e6

QD
type: SiteQuality
SIO_000300: 9.869999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.583e0

MQRankSum
type: SiteQuality
SIO_000300: 1.02e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.435e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.895e1

FS
type: SiteQuality
SIO_000300: 5.305e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.8e-1

GenotypeQuality
all individuals: 359
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 24
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.5e0
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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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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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1181
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variant carriers: 0

GenotypeQuality
all individuals: 50048
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10041
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47209
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 613
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4462
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.283367556468173e-4
allele num: 7792
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9265
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.629e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.200000000000001e-3

FS
type: SiteQuality
SIO_000300: 4.51e-1

DP
type: SiteQuality
SIO_000300: 1.485092e6

MQRankSum
type: SiteQuality
SIO_000300: 8.03e-1

MQ
type: SiteQuality
SIO_000300: 5.883e1

VQSLOD
type: SiteQuality
SIO_000300: -5.653e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.85e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.44e0

GenotypeQuality
all individuals: 923
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 96
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 9.75e1
variant carriers: 6

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 46
bin: 5.75e1
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GenotypeQuality
all individuals: 103
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 612
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4424
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7803
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9263
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 1.271240306792661e-4
allele num: 47198
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10036
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.55e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.742e-1

QD
type: SiteQuality
SIO_000300: 2.22e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.19e-2

FS
type: SiteQuality
SIO_000300: 2.107e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.045e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

DP
type: SiteQuality
SIO_000300: 1.482574e6

GenotypeQuality
all individuals: 344
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 262
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1165
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49144
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variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 114
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.125398512221041e-5
allele num: 47050
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7789
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6579
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10003
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9256
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 609
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4379
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e0

DP
type: SiteQuality
SIO_000300: 1.475016e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.122e1

VQSLOD
type: SiteQuality
SIO_000300: -3.184e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.24e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.93e-1

MQ
type: SiteQuality
SIO_000300: 5.918e1

GenotypeQuality
all individuals: 73
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 8.75e1
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GenotypeQuality
all individuals: 66
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variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.5e0
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GenotypeQuality
all individuals: 111
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variant carriers: 0

GenotypeQuality
all individuals: 1467
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variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
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GenotypeQuality
all individuals: 48969
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variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
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GenotypeQuality
all individuals: 360
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 103
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1166
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6107
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.285181853232232e-4
allele num: 7781
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.289377289377289e-4
allele num: 4368
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.252785574551331e-5
allele num: 47028
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9255
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 608
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9985
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.12e-1

FS
type: SiteQuality
SIO_000300: 5.905e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.748e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.599999999999999e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.061e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e0

MQ
type: SiteQuality
SIO_000300: 5.931e1

DP
type: SiteQuality
SIO_000300: 1.473841e6

QD
type: SiteQuality
SIO_000300: 1.301e1

VQSLOD
type: SiteQuality
SIO_000300: -2.231e-1

GenotypeQuality
all individuals: 201
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 341
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GenotypeQuality
all individuals: 261
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GenotypeQuality
all individuals: 199
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GenotypeQuality
all individuals: 1156
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 27
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 358
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variant carriers: 2

GenotypeQuality
all individuals: 232
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48340
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7771
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6565
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4344
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 607
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9248
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.259125175688913e-5
allele num: 46958
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.469103e6

MQRankSum
type: SiteQuality
SIO_000300: -7.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.871e0

QD
type: SiteQuality
SIO_000300: 1.888e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.61e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.889e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.57e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.03e-1

FS
type: SiteQuality
SIO_000300: 9.369e0

GenotypeQuality
all individuals: 1741
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 826
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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: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 193
bin: 3.25e1
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GenotypeQuality
all individuals: 200
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.25e1
variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
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variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 3
allele frequency: 4.571080298643913e-4
allele num: 6563
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4344
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 607
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.081314878892734e-4
allele num: 9248
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46967
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.287498390627012e-4
allele num: 7767
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9953
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.597e0

MQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

QD
type: SiteQuality
SIO_000300: 1.731e1

MQ
type: SiteQuality
SIO_000300: 5.941e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.84e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.495e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.22e-2

DP
type: SiteQuality
SIO_000300: 1.469374e6

BaseQRankSum
type: SiteQuality
SIO_000300: -8.21e-1

GenotypeQuality
all individuals: 819
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 8.25e1
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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
all individuals: 110
bin: 8.75e1
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GenotypeQuality
all individuals: 295
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
all individuals: 27
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variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1116
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4269
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9214
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7739
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6535
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.288532464190754e-5
allele num: 46636
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 596
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9857
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e0

MQRankSum
type: SiteQuality
SIO_000300: 1.64e0

VQSLOD
type: SiteQuality
SIO_000300: -1.067e0

DP
type: SiteQuality
SIO_000300: 1.453219e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.733e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

QD
type: SiteQuality
SIO_000300: 1.808e1

GenotypeQuality
all individuals: 341
bin: 8.25e1
variant carriers: 1

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 9.75e1
variant carriers: 11

GenotypeQuality
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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: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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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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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 341
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4232
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 593
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6509
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7724
num of homozygotes: 0

South Asian
type: Population
allele count: 14
allele frequency: 1.428717216042453e-3
allele num: 9799
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9196
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46482
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.315e0

QD
type: SiteQuality
SIO_000300: 2.075e1

DP
type: SiteQuality
SIO_000300: 1.444906e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.95e-2

FS
type: SiteQuality
SIO_000300: 1.288e0

MQRankSum
type: SiteQuality
SIO_000300: -4.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.32e-1

MQ
type: SiteQuality
SIO_000300: 5.915e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.72e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.508e0

GenotypeQuality
all individuals: 5181
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

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: 549
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.12637981527371e-4
allele num: 8878
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6245
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3821
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.234850118611171e-4
allele num: 9274
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.259070166719378e-5
allele num: 44266
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 544
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.854e1

DP
type: SiteQuality
SIO_000300: 1.337002e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.369e0

MQRankSum
type: SiteQuality
SIO_000300: -2.81e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.56e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.091e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.77e-1

FS
type: SiteQuality
SIO_000300: 2.547e0

GenotypeQuality
all individuals: 292
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 537
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9098
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7313
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6121
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3666
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.312352587522545e-5
allele num: 43246
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8699
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.28574e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.44e0

MQRankSum
type: SiteQuality
SIO_000300: -3.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.72e-1

QD
type: SiteQuality
SIO_000300: 2.035e1

FS
type: SiteQuality
SIO_000300: 3.513e0

VQSLOD
type: SiteQuality
SIO_000300: -6.3e-1

MQ
type: SiteQuality
SIO_000300: 5.9e1

GenotypeQuality
all individuals: 1145
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 927
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variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8682
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 536
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6106
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3637
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9061
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7294
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.321909538404384e-5
allele num: 43068
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.276997e6

QD
type: SiteQuality
SIO_000300: 1.809e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.699999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: -5.48e-1

FS
type: SiteQuality
SIO_000300: 7.504e0

MQRankSum
type: SiteQuality
SIO_000300: 1.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.571e0

GenotypeQuality
all individuals: 101
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 277
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GenotypeQuality
all individuals: 677
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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
all individuals: 4590
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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
all individuals: 70
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GenotypeQuality
all individuals: 270
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3615
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7279
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8660
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.106194690265487e-4
allele num: 9040
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 535
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6090
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42917
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.268348e6

VQSLOD
type: SiteQuality
SIO_000300: -1.594e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.176e0

MQRankSum
type: SiteQuality
SIO_000300: -7.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.28e-1

QD
type: SiteQuality
SIO_000300: 1.278e1

FS
type: SiteQuality
SIO_000300: 3.118e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

MQ
type: SiteQuality
SIO_000300: 5.764e1

GenotypeQuality
all individuals: 706
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
all individuals: 237
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7269
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3585
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8627
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.340440470896623e-5
allele num: 42727
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.76e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.34e-1

QD
type: SiteQuality
SIO_000300: 1.432e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.07e-1

DP
type: SiteQuality
SIO_000300: 1.259843e6

VQSLOD
type: SiteQuality
SIO_000300: -9.034e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.65e-1

MQ
type: SiteQuality
SIO_000300: 5.919e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
all individuals: 278
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3079
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8213
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5427
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 477
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7833
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.61151154288102e-5
allele num: 38292
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.78e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.071889e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.919999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.67e0

QD
type: SiteQuality
SIO_000300: 1.49e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3381
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5427
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.495215311004785e-4
allele num: 6688
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7833
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3079
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38292
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 477
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8213
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

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

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

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

Other
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East Asian
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QD
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ClippingRankSum
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DP
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ReadPosRankSum
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MQ
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BaseQRankSum
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FS
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MQRankSum
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InbreedingCoeff
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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Other
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South Asian
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European (Non-Finnish)
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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InbreedingCoeff
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VQSLOD
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DP
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MQ
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FS
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ClippingRankSum
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QD
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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Other
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African
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Latino
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European (Finnish)
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European (Non-Finnish)
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MQRankSum
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MQ
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ReadPosRankSum
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QD
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InbreedingCoeff
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DP
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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South Asian
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Other
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European (Non-Finnish)
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Latino
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East Asian
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QD
type: SiteQuality
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MQRankSum
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MQ
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FS
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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European (Non-Finnish)
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European (Finnish)
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East Asian
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Other
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South Asian
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FS
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InbreedingCoeff
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MQ
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QD
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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DP
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BaseQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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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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Latino
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Other
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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MQ
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FS
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ClippingRankSum
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QD
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DP
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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East Asian
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European (Finnish)
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Other
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African
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Latino
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DP
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FS
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QD
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MQ
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Non-Finnish)
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Latino
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European (Finnish)
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Other
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South Asian
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VQSLOD
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MQRankSum
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FS
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MQ
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ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.81e-2

QD
type: SiteQuality
SIO_000300: 2.325e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.16e0

DP
type: SiteQuality
SIO_000300: 4.90136e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e0

GenotypeQuality
all individuals: 1898
bin: 3.25e1
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: 4.25e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 1

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 541
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 7.444353457902182e-5
allele num: 13433
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5219
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 202
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1233
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1439
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2756
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.34e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.517e0

VQSLOD
type: SiteQuality
SIO_000300: -2.94e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.79e-2

QD
type: SiteQuality
SIO_000300: 1.533e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

DP
type: SiteQuality
SIO_000300: 4.90262e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 22728
bin: 9.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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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: 9.25e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4489
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.159034479780642e-5
allele num: 46317
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 604
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6573
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10001
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7440
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9280
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.66e0

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

VQSLOD
type: SiteQuality
SIO_000300: -1.964e0

QD
type: SiteQuality
SIO_000300: 2.518e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.5e-1

DP
type: SiteQuality
SIO_000300: 2.56337e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.801e1

FS
type: SiteQuality
SIO_000300: 2.245e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6573
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9998
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 605
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.344086021505376e-4
allele num: 7440
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4488
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46296
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9280
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.49e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.747e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

DP
type: SiteQuality
SIO_000300: 2.564e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.419999999999999e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

MQRankSum
type: SiteQuality
SIO_000300: 5.32e-1

QD
type: SiteQuality
SIO_000300: 1.422e1

GenotypeQuality
all individuals: 1203
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2694
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10007
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9277
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7422
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 607
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46290
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.521375323292256e-4
allele num: 6573
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4490
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.549e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.12e-1

FS
type: SiteQuality
SIO_000300: 3.992e0

MQRankSum
type: SiteQuality
SIO_000300: 2.67e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.82e-1

DP
type: SiteQuality
SIO_000300: 2.567858e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.125e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.58e-1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1209
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variant carriers: 0

GenotypeQuality
all individuals: 46
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variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.520912547528517e-4
allele num: 6575
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10021
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 605
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7432
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9285
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4497
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46283
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.417e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.05e0

MQRankSum
type: SiteQuality
SIO_000300: -3.063e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

DP
type: SiteQuality
SIO_000300: 2.576259e6

FS
type: SiteQuality
SIO_000300: 9.47e-1

QD
type: SiteQuality
SIO_000300: 5.79e0

MQ
type: SiteQuality
SIO_000300: 5.301e1

GenotypeQuality
all individuals: 183
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 404
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GenotypeQuality
all individuals: 158
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2071
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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: 5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 6
allele frequency: 9.131030284583778e-4
allele num: 6571
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10019
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46292
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4496
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9283
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7438
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 607
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.58248e6

FS
type: SiteQuality
SIO_000300: 2.622e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.8e-2

MQ
type: SiteQuality
SIO_000300: 5.954e1

VQSLOD
type: SiteQuality
SIO_000300: 1.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.226e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.67e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.74e-1

QD
type: SiteQuality
SIO_000300: 1.63e1

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: 7

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7438
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.512140326622311e-4
allele num: 46292
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.521838380763963e-4
allele num: 6571
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9283
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 607
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10019
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4496
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.63e1

MQRankSum
type: SiteQuality
SIO_000300: 5.74e-1

DP
type: SiteQuality
SIO_000300: 2.58248e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.226e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

FS
type: SiteQuality
SIO_000300: 2.622e0

VQSLOD
type: SiteQuality
SIO_000300: 1.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-2

GenotypeQuality
all individuals: 108
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1312
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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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GenotypeQuality
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GenotypeQuality
all individuals: 274
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GenotypeQuality
all individuals: 114
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GenotypeQuality
all individuals: 98
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 57
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variant carriers: 0

GenotypeQuality
all individuals: 2718
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.309880400818877e-5
allele num: 46405
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4499
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6573
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 3.996403237086622e-4
allele num: 10009
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.077005923532579e-4
allele num: 9285
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7488
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 605
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.600000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.62e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.75e-1

DP
type: SiteQuality
SIO_000300: 2.584923e6

VQSLOD
type: SiteQuality
SIO_000300: 2.29e0

QD
type: SiteQuality
SIO_000300: 2.966e1

GenotypeQuality
all individuals: 1218
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5984
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 328
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2839
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1575
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1353
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18159
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6577
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9289
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4501
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 607
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10035
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7503
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.152991581802915e-5
allele num: 46447
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.736e0

DP
type: SiteQuality
SIO_000300: 2.585903e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

FS
type: SiteQuality
SIO_000300: 4.898e0

QD
type: SiteQuality
SIO_000300: 1.269e1

GenotypeQuality
all individuals: 300
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2850
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 67
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1353
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1220
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22745
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2746
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7522
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 605
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4503
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6577
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10042
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.07654214662504e-4
allele num: 9289
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46504
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.789e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.589149e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.239e0

VQSLOD
type: SiteQuality
SIO_000300: 5.610000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.59e-1

QD
type: SiteQuality
SIO_000300: 1.02e1

GenotypeQuality
all individuals: 74
bin: 1.25e1
variant carriers: 33

GenotypeQuality
all individuals: 100
bin: 2.5e0
variant carriers: 12

GenotypeQuality
all individuals: 2390
bin: 7.75e1
variant carriers: 154

GenotypeQuality
all individuals: 1127
bin: 9.25e1
variant carriers: 202

GenotypeQuality
all individuals: 172
bin: 5.25e1
variant carriers: 111

GenotypeQuality
all individuals: 2419
bin: 7.25e1
variant carriers: 84

GenotypeQuality
all individuals: 879
bin: 2.25e1
variant carriers: 85

GenotypeQuality
all individuals: 94
bin: 1.75e1
variant carriers: 47

GenotypeQuality
all individuals: 211
bin: 3.75e1
variant carriers: 104

GenotypeQuality
all individuals: 1641
bin: 8.25e1
variant carriers: 196

GenotypeQuality
all individuals: 17136
bin: 6.25e1
variant carriers: 110

GenotypeQuality
all individuals: 919
bin: 8.75e1
variant carriers: 131

GenotypeQuality
all individuals: 206
bin: 7.5e0
variant carriers: 22

GenotypeQuality
all individuals: 5503
bin: 6.75e1
variant carriers: 133

GenotypeQuality
all individuals: 158
bin: 4.75e1
variant carriers: 91

GenotypeQuality
all individuals: 207
bin: 2.75e1
variant carriers: 57

GenotypeQuality
all individuals: 149
bin: 4.25e1
variant carriers: 68

South Asian
type: Population
allele count: 1306
allele frequency: 1.299243931555909e-1
allele num: 10052
num of homozygotes: 47

East Asian
type: Population
allele count: 1
allele frequency: 1.520681265206813e-4
allele num: 6576
num of homozygotes: 0

African
type: Population
allele count: 440
allele frequency: 5.818566516794499e-2
allele num: 7562
num of homozygotes: 12

Latino
type: Population
allele count: 1179
allele frequency: 1.270884984369947e-1
allele num: 9277
num of homozygotes: 62

European (Non-Finnish)
type: Population
allele count: 22568
allele frequency: 4.81522574037723e-1
allele num: 46868
num of homozygotes: 3296

Other
type: Population
allele count: 218
allele frequency: 3.591433278418452e-1
allele num: 607
num of homozygotes: 19

European (Finnish)
type: Population
allele count: 1808
allele frequency: 4.029418319589926e-1
allele num: 4487
num of homozygotes: 195

ClippingRankSum
type: SiteQuality
SIO_000300: -4.18e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.73e-1

DP
type: SiteQuality
SIO_000300: 3.32962e6

MQRankSum
type: SiteQuality
SIO_000300: 1.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.947e1

QD
type: SiteQuality
SIO_000300: 2.316e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.289e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.82e-1

GenotypeQuality
all individuals: 1427
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 164
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8931
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3810
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
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variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8270
bin: 9.75e1
variant carriers: 44

GenotypeQuality
all individuals: 84
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27401
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 198
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2534
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1702
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3811
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.213858755811379e-4
allele num: 4517
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9292
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6575
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 609
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 6.589351607801792e-4
allele num: 7588
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 32
allele frequency: 6.8211369982734e-4
allele num: 46913
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 8.944543828264759e-4
allele num: 10062
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.376e-1

DP
type: SiteQuality
SIO_000300: 1.905843e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.65e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.87e1

MQ
type: SiteQuality
SIO_000300: 5.967e1

VQSLOD
type: SiteQuality
SIO_000300: 6.12e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.74e0

GenotypeQuality
all individuals: 183
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1701
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8951
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27508
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3815
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 1024
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variant carriers: 0

GenotypeQuality
all individuals: 108
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variant carriers: 0

GenotypeQuality
all individuals: 8235
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3820
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
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variant carriers: 0

GenotypeQuality
all individuals: 1428
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 260
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2539
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9291
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4517
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10063
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.129834724825354e-5
allele num: 46952
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7603
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6577
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 609
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

FS
type: SiteQuality
SIO_000300: 9.755000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.05e0

QD
type: SiteQuality
SIO_000300: 1.558e1

MQRankSum
type: SiteQuality
SIO_000300: 1.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.9e-1

DP
type: SiteQuality
SIO_000300: 1.903784e6

VQSLOD
type: SiteQuality
SIO_000300: -8.626e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.0e-1

GenotypeQuality
all individuals: 28198
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8982
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2523
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3800
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 894
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variant carriers: 0

GenotypeQuality
all individuals: 177
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variant carriers: 0

GenotypeQuality
all individuals: 59
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variant carriers: 0

GenotypeQuality
all individuals: 1427
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1696
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3816
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8228
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 56
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 613
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.123457838744612e-5
allele num: 47093
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6579
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10082
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4522
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7716
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9296
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.51e0

MQ
type: SiteQuality
SIO_000300: 5.988e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

FS
type: SiteQuality
SIO_000300: 4.01e-1

QD
type: SiteQuality
SIO_000300: 1.238e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.872e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

DP
type: SiteQuality
SIO_000300: 1.911468e6

VQSLOD
type: SiteQuality
SIO_000300: 7.38e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.27e-1

GenotypeQuality
all individuals: 3816
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
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variant carriers: 0

GenotypeQuality
all individuals: 3798
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variant carriers: 0

GenotypeQuality
all individuals: 28250
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variant carriers: 0

GenotypeQuality
all individuals: 8226
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 8985
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variant carriers: 0

GenotypeQuality
all individuals: 176
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GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 157
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variant carriers: 0

GenotypeQuality
all individuals: 23
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GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2519
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1426
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1695
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 615
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.364292078577793e-5
allele num: 47138
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7741
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10087
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9294
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6583
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4521
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.74e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.797e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.281e0

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-1

DP
type: SiteQuality
SIO_000300: 1.913028e6

MQ
type: SiteQuality
SIO_000300: 5.967e1

FS
type: SiteQuality
SIO_000300: 5.052e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.76e-2

QD
type: SiteQuality
SIO_000300: 1.842e1

GenotypeQuality
all individuals: 1424
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 830
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
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GenotypeQuality
all individuals: 35
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variant carriers: 0

GenotypeQuality
all individuals: 14
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GenotypeQuality
all individuals: 1695
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 8977
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
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GenotypeQuality
all individuals: 29
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GenotypeQuality
all individuals: 89
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variant carriers: 0

GenotypeQuality
all individuals: 8224
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 121
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3796
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3821
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.121025728042081e-5
allele num: 47147
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9295
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 615
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.982553528945282e-4
allele num: 10088
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4521
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.037205770690964e-4
allele num: 6585
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7759
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.4e0

MQRankSum
type: SiteQuality
SIO_000300: 9.26e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.36e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.209e0

VQSLOD
type: SiteQuality
SIO_000300: -3.42e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.867e1

DP
type: SiteQuality
SIO_000300: 1.913244e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.66e0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8219
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2519
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.120890774125132e-5
allele num: 47150
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6585
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 615
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9297
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7756
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4520
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10086
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.84e-1

FS
type: SiteQuality
SIO_000300: 4.012e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 6.2e-2

QD
type: SiteQuality
SIO_000300: 1.595e1

MQ
type: SiteQuality
SIO_000300: 5.932e1

VQSLOD
type: SiteQuality
SIO_000300: -1.4e-1

DP
type: SiteQuality
SIO_000300: 1.913024e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.17e-1

GenotypeQuality
all individuals: 1695
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28275
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 824
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6585
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10086
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.060422896651185e-4
allele num: 47151
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 615
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9296
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4521
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7761
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.5392e1

MQ
type: SiteQuality
SIO_000300: 5.959e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.01e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.161e0

QD
type: SiteQuality
SIO_000300: 2.944e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.29e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.45e-1

DP
type: SiteQuality
SIO_000300: 1.913397e6

GenotypeQuality
all individuals: 25
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1425
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3794
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2518
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8215
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9296
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7761
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.911785112498761e-5
allele num: 10089
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6585
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 615
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47165
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4521
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.913177e6

QD
type: SiteQuality
SIO_000300: 3.361e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.800000000000001e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.71e-1

GenotypeQuality
all individuals: 104
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
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variant carriers: 0

GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 59
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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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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 27
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variant carriers: 0

GenotypeQuality
all individuals: 13
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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: 8220
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 22
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GenotypeQuality
all individuals: 1425
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2521
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8990
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4520
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6585
num of homozygotes: 0

South Asian
type: Population
allele count: 10
allele frequency: 9.910802775024777e-4
allele num: 10090
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.075384449940854e-4
allele num: 9299
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 615
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7764
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47170
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.86e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-3

FS
type: SiteQuality
SIO_000300: 1.739e0

DP
type: SiteQuality
SIO_000300: 1.913775e6

MQ
type: SiteQuality
SIO_000300: 5.978e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.3e0

QD
type: SiteQuality
SIO_000300: 2.113e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.745e0

GenotypeQuality
all individuals: 8946
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 109
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variant carriers: 0

GenotypeQuality
all individuals: 94
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variant carriers: 0

GenotypeQuality
all individuals: 2504
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variant carriers: 1

GenotypeQuality
all individuals: 45
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 141
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variant carriers: 0

GenotypeQuality
all individuals: 155
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GenotypeQuality
all individuals: 1422
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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: 70

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4522
num of homozygotes: 0

African
type: Population
allele count: 46
allele frequency: 5.91792100861958e-3
allele num: 7773
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 4.862236628849271e-3
allele num: 617
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6589
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 18
allele frequency: 3.819304462220713e-4
allele num: 47129
num of homozygotes: 0

Latino
type: Population
allele count: 7
allele frequency: 7.525263384218448e-4
allele num: 9302
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10086
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.49e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.233e0

QD
type: SiteQuality
SIO_000300: 1.774e1

MQRankSum
type: SiteQuality
SIO_000300: 2.83e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.497e-1

DP
type: SiteQuality
SIO_000300: 1.91302e6

VQSLOD
type: SiteQuality
SIO_000300: 5.35e0

GenotypeQuality
all individuals: 780
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
all individuals: 50
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variant carriers: 0

GenotypeQuality
all individuals: 81
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variant carriers: 0

GenotypeQuality
all individuals: 3798
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1689
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.916699722332408e-5
allele num: 10084
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9304
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 617
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6589
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47138
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7776
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4522
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.25e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

MQ
type: SiteQuality
SIO_000300: 5.878e1

QD
type: SiteQuality
SIO_000300: 3.147e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.200000000000001e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.4e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.059e0

DP
type: SiteQuality
SIO_000300: 1.908988e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e0

GenotypeQuality
all individuals: 230
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 767
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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
all individuals: 8162
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1419
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.074575542660649e-4
allele num: 9306
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4523
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7768
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10079
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47137
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.979e0

MQRankSum
type: SiteQuality
SIO_000300: -8.1e-2

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.403e1

MQ
type: SiteQuality
SIO_000300: 5.975e1

VQSLOD
type: SiteQuality
SIO_000300: 9.27e-1

FS
type: SiteQuality
SIO_000300: 2.841e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.909166e6

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 22
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GenotypeQuality
all individuals: 108
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 780
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GenotypeQuality
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GenotypeQuality
all individuals: 8943
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3788
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.28633907898122e-4
allele num: 7774
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.921619208254787e-5
allele num: 10079
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6593
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 6.363887062217603e-5
allele num: 47141
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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BaseQRankSum
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SIO_000300: 1.3e0

FS
type: SiteQuality
SIO_000300: 5.36e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.64e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.74e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.28e-1

QD
type: SiteQuality
SIO_000300: 1.806e1

DP
type: SiteQuality
SIO_000300: 1.909469e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.999999999999999e-3

GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 616
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.284851599640242e-4
allele num: 7783
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10076
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47175
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6595
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 9306
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -1.0e-4

BaseQRankSum
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FS
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VQSLOD
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DP
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MQRankSum
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SIO_000300: 7.3e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

QD
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SIO_000300: 2.404e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.88e-1

ReadPosRankSum
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SIO_000300: -6.28e-1

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6597
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9307
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 1.059838480615554e-4
allele num: 47177
num of homozygotes: 0

African
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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: 616
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10071
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VQSLOD
type: SiteQuality
SIO_000300: -4.33e-2

QD
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SIO_000300: 1.81e1

InbreedingCoeff
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SIO_000300: 3.15e-2

MQRankSum
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DP
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MQ
type: SiteQuality
SIO_000300: 5.951e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: -6.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.21e0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9307
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6599
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7814
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10081
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.111977021690004e-5
allele num: 47349
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 616
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.1e-1

QD
type: SiteQuality
SIO_000300: 2.751e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.18e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

FS
type: SiteQuality
SIO_000300: 1.202e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.133e0

VQSLOD
type: SiteQuality
SIO_000300: -1.555e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.941e0

DP
type: SiteQuality
SIO_000300: 1.916038e6

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10080
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4524
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 617
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9307
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7821
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.111174446344501e-5
allele num: 47367
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6599
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.16e1

FS
type: SiteQuality
SIO_000300: 9.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e-1

MQRankSum
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VQSLOD
type: SiteQuality
SIO_000300: -1.069e0

DP
type: SiteQuality
SIO_000300: 1.916629e6

BaseQRankSum
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SIO_000300: -1.732e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.03e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.110639734903649e-5
allele num: 47379
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 617
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9307
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10082
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7827
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4524
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.29e-2

QD
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.846e1

GenotypeQuality
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variant carriers: 0

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

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 4523
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9307
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 6.327512022272843e-5
allele num: 47412
num of homozygotes: 1

South Asian
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num of homozygotes: 0

East Asian
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num of homozygotes: 0

Other
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MQRankSum
type: SiteQuality
SIO_000300: 1.31e0

FS
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
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MQ
type: SiteQuality
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QD
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InbreedingCoeff
type: SiteQuality
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VQSLOD
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4524
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.273398701133325e-4
allele num: 7853
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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BaseQRankSum
type: SiteQuality
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FS
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VQSLOD
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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QD
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8144
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7859
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6599
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9309
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10086
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 2.104111433741531e-4
allele num: 47526
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 617
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 4.421843908910016e-4
allele num: 4523
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.184e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.360000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.81e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.6e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.82e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.68e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-2

DP
type: SiteQuality
SIO_000300: 1.92024e6

GenotypeQuality
all individuals: 33
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8932
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28833
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8138
bin: 9.75e1
variant carriers: 30

GenotypeQuality
all individuals: 1416
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3764
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
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variant carriers: 0

GenotypeQuality
all individuals: 1675
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3771
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2503
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 29
allele frequency: 4.395937547370016e-3
allele num: 6597
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.912767644726408e-5
allele num: 10088
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9306
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7856
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.106948716868232e-5
allele num: 47462
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4520
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 617
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.51e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.193e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.947e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.09e-1

DP
type: SiteQuality
SIO_000300: 1.917073e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.055e-1

QD
type: SiteQuality
SIO_000300: 1.586e1

MQ
type: SiteQuality
SIO_000300: 5.954e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.45e-1

GenotypeQuality
all individuals: 132
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3763
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variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8111
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3762
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variant carriers: 0

GenotypeQuality
all individuals: 509
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variant carriers: 0

GenotypeQuality
all individuals: 2498
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1417
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28753
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1676
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.909820632246556e-5
allele num: 10091
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.107836937734497e-5
allele num: 47442
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.27258844489692e-4
allele num: 7858
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9306
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6599
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.853e0

VQSLOD
type: SiteQuality
SIO_000300: 6.870000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.755e1

DP
type: SiteQuality
SIO_000300: 1.914208e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-2

MQ
type: SiteQuality
SIO_000300: 5.983e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.29e0

MQRankSum
type: SiteQuality
SIO_000300: 7.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.63e-1

GenotypeQuality
all individuals: 494
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1677
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28778
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8108
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 163
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3768
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1418
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3765
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2500
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.272426517368622e-4
allele num: 7859
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9305
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 615
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47435
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6599
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4516
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.981375074301565e-4
allele num: 10094
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.84e-1

MQ
type: SiteQuality
SIO_000300: 5.929e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.92e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.47e-1

FS
type: SiteQuality
SIO_000300: 9.75e-1

DP
type: SiteQuality
SIO_000300: 1.91396e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.421e0

VQSLOD
type: SiteQuality
SIO_000300: 2.34e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.9e-1

QD
type: SiteQuality
SIO_000300: 2.135e1

GenotypeQuality
all individuals: 3761
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2499
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variant carriers: 0

GenotypeQuality
all individuals: 490
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8910
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 62
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
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variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3761
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1416
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1675
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8108
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 28648
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.907856930545922e-5
allele num: 10093
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9303
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4513
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 615
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7847
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.109170674090947e-5
allele num: 47412
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6599
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.28e0

DP
type: SiteQuality
SIO_000300: 1.91412e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.36e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.33e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.503e0

FS
type: SiteQuality
SIO_000300: 7.547e0

QD
type: SiteQuality
SIO_000300: 2.135e1

GenotypeQuality
all individuals: 88
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3764
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2496
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variant carriers: 0

GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 85
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variant carriers: 0

GenotypeQuality
all individuals: 1416
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variant carriers: 0

GenotypeQuality
all individuals: 135
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variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 27
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GenotypeQuality
all individuals: 59
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variant carriers: 0

GenotypeQuality
all individuals: 33
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variant carriers: 0

GenotypeQuality
all individuals: 28883
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3762
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8938
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8109
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 1675
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9304
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7857
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 7.927070947284979e-4
allele num: 10092
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4513
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 615
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.106105600134791e-5
allele num: 47481
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6599
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.88e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.108e0

DP
type: SiteQuality
SIO_000300: 1.914626e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.33e-1

FS
type: SiteQuality
SIO_000300: 1.2485e1

QD
type: SiteQuality
SIO_000300: 2.854e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.041e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.19e-1

GenotypeQuality
all individuals: 8935
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1676
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
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variant carriers: 0

GenotypeQuality
all individuals: 563
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variant carriers: 0

GenotypeQuality
all individuals: 28832
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variant carriers: 0

GenotypeQuality
all individuals: 1415
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variant carriers: 0

GenotypeQuality
all individuals: 3766
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variant carriers: 0

GenotypeQuality
all individuals: 126
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variant carriers: 0

GenotypeQuality
all individuals: 60
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variant carriers: 0

GenotypeQuality
all individuals: 3760
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variant carriers: 0

GenotypeQuality
all individuals: 62
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variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 8101
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variant carriers: 5

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2495
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4512
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10095
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.053319008194822e-4
allele num: 47469
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6599
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7856
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9304
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 616
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.913745e6

MQRankSum
type: SiteQuality
SIO_000300: 2.74e-1

QD
type: SiteQuality
SIO_000300: 2.516e1

FS
type: SiteQuality
SIO_000300: 1.979e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e-2

MQ
type: SiteQuality
SIO_000300: 5.936e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.89e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.12e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.462e-1

GenotypeQuality
all individuals: 146
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 4.75e1
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GenotypeQuality
all individuals: 3756
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8926
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3768
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 3.25e1
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GenotypeQuality
all individuals: 28915
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
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GenotypeQuality
all individuals: 184
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1411
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2493
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1676
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10096
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9302
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.325644161430439e-5
allele num: 47426
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7848
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6599
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.54e-1