ClinVar Miner

List of variants in gene FLNB reported by GeneReviews

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Gene type:
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Total variants: 29
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HGVS dbSNP gnomAD frequency
NM_001457.4(FLNB):c.2452C>T (p.Arg818Ter) rs80356519 0.00001
NM_001457.4(FLNB):c.4819C>T (p.Arg1607Ter) rs80356520 0.00001
NM_001457.4(FLNB):c.1081G>A (p.Gly361Ser) rs80356509
NM_001457.4(FLNB):c.1088G>A (p.Gly363Glu) rs80356510
NM_001457.4(FLNB):c.1945C>T (p.Arg649Ter) rs80356517
NM_001457.4(FLNB):c.4292T>G (p.Leu1431Arg) rs80356511
NM_001457.4(FLNB):c.442T>A (p.Trp148Arg) rs80356493
NM_001457.4(FLNB):c.4713_4715del (p.Asn1571del) rs80356512
NM_001457.4(FLNB):c.4747_4749del (p.Asp1583del) rs80356498
NM_001457.4(FLNB):c.4756G>A (p.Gly1586Arg) rs80356513
NM_001457.4(FLNB):c.4775T>A (p.Val1592Asp) rs80356514
NM_001457.4(FLNB):c.4804T>C (p.Ser1602Pro) rs80356501
NM_001457.4(FLNB):c.4808C>T (p.Pro1603Leu) rs80356515
NM_001457.4(FLNB):c.482T>G (p.Phe161Cys) rs80356506
NM_001457.4(FLNB):c.4835G>A (p.Gly1612Asp) rs80356505
NM_001457.4(FLNB):c.4927G>T (p.Ala1643Ser) rs80356502
NM_001457.4(FLNB):c.502G>A (p.Gly168Ser) rs80356504
NM_001457.4(FLNB):c.5071G>A (p.Gly1691Ser) rs80356503
NM_001457.4(FLNB):c.512T>A (p.Leu171Gln) rs80356494
NM_001457.4(FLNB):c.542G>T (p.Gly181Val) rs80356495
NM_001457.4(FLNB):c.549C>G (p.Cys183Trp) rs80356496
NM_001457.4(FLNB):c.5500G>A (p.Gly1834Arg) rs80356516
NM_001457.4(FLNB):c.602C>T (p.Ala201Val) rs80356499
NM_001457.4(FLNB):c.608A>C (p.Gln203Pro) rs80356497
NM_001457.4(FLNB):c.629G>T (p.Gly210Val) rs80356500
NM_001457.4(FLNB):c.6408del (p.Ser2137fs) rs80356521
NM_001457.4(FLNB):c.679G>A (p.Glu227Lys) rs80356508
NM_001457.4(FLNB):c.700C>G (p.Leu234Val) rs80356507
NM_001457.4(FLNB):c.7029T>G (p.Tyr2343Ter) rs80356518

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