ClinVar Miner

List of variants in gene FLNC reported as likely pathogenic for cardiovascular disorder

Included ClinVar conditions (1435):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 118
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HGVS dbSNP gnomAD frequency
NM_001458.5(FLNC):c.4871C>T (p.Ser1624Leu) rs879255639 0.00003
NM_001458.5(FLNC):c.4636G>A (p.Gly1546Ser) rs774263134 0.00002
NM_001458.5(FLNC):c.1216G>A (p.Gly406Ser) rs1343684536 0.00001
NM_001458.5(FLNC):c.3791-1G>C rs781135153 0.00001
NM_001458.5(FLNC):c.4069G>A (p.Gly1357Arg) rs1218299104 0.00001
NM_001458.5(FLNC):c.4738-1G>A rs1808678197 0.00001
NM_001458.5(FLNC):c.5199+1G>T rs1465588989 0.00001
NC_000007.13:g.(?_128475370)_(128478867_?)del
NC_000007.13:g.(?_128480199)_(128481774_?)del
NM_001458.5(FLNC):c.1047+1G>A rs762493013
NM_001458.5(FLNC):c.1047+1G>T rs762493013
NM_001458.5(FLNC):c.1411+1G>T rs2128934545
NM_001458.5(FLNC):c.1548_1549+2del rs763330423
NM_001458.5(FLNC):c.1549+1G>A
NM_001458.5(FLNC):c.1549+2T>G rs111806457
NM_001458.5(FLNC):c.1676+1G>A rs111452612
NM_001458.5(FLNC):c.1714C>T (p.Gln572Ter)
NM_001458.5(FLNC):c.1814-1G>A
NM_001458.5(FLNC):c.2007+1G>A
NM_001458.5(FLNC):c.2265+1G>A rs1585157354
NM_001458.5(FLNC):c.2312del (p.Gly771fs)
NM_001458.5(FLNC):c.2504dup (p.Pro836fs) rs1554398705
NM_001458.5(FLNC):c.2550+1G>C
NM_001458.5(FLNC):c.2550+2T>C rs113972676
NM_001458.5(FLNC):c.2785_2786del (p.Thr929fs)
NM_001458.5(FLNC):c.2811+1G>T rs2128936028
NM_001458.5(FLNC):c.2929+2_2929+7del rs2128936119
NM_001458.5(FLNC):c.2971C>T (p.Arg991Ter) rs886037830
NM_001458.5(FLNC):c.3193-2A>G rs749889670
NM_001458.5(FLNC):c.3307_3313del (p.Cys1103fs) rs2128936386
NM_001458.5(FLNC):c.3343_3344insT (p.Gly1115fs)
NM_001458.5(FLNC):c.341T>C (p.Leu114Pro) rs1807864684
NM_001458.5(FLNC):c.3456_3457del (p.Val1152_Phe1153insTer)
NM_001458.5(FLNC):c.352+1G>T
NM_001458.5(FLNC):c.3547_3548delinsCT (p.Ala1183Leu) rs1131692185
NM_001458.5(FLNC):c.3557C>T (p.Ala1186Val) rs1114167361
NM_001458.5(FLNC):c.3581C>T (p.Ser1194Leu) rs773481064
NM_001458.5(FLNC):c.3636C>G (p.Tyr1212Ter)
NM_001458.5(FLNC):c.3694G>A (p.Gly1232Arg) rs754533053
NM_001458.5(FLNC):c.3790+1G>C
NM_001458.5(FLNC):c.3964+1G>A rs1808557594
NM_001458.5(FLNC):c.3964+1G>T rs1808557594
NM_001458.5(FLNC):c.4021C>T (p.Arg1341Ter) rs1562998062
NM_001458.5(FLNC):c.4127+1G>A
NM_001458.5(FLNC):c.4128-1G>C
NM_001458.5(FLNC):c.4128-2_4128-1del rs1808585056
NM_001458.5(FLNC):c.4172C>A (p.Ser1391Ter)
NM_001458.5(FLNC):c.4288+1G>A rs2128937065
NM_001458.5(FLNC):c.4288+1G>T
NM_001458.5(FLNC):c.4288+2T>G
NM_001458.5(FLNC):c.4346C>G (p.Ser1449Ter)
NM_001458.5(FLNC):c.4409dup (p.Ser1470fs)
NM_001458.5(FLNC):c.4457-1G>A rs1404524040
NM_001458.5(FLNC):c.4580+1G>A
NM_001458.5(FLNC):c.4581-2A>G
NM_001458.5(FLNC):c.4584dup (p.Phe1529fs)
NM_001458.5(FLNC):c.4637G>A (p.Gly1546Asp) rs1427917546
NM_001458.5(FLNC):c.46dup (p.Asp16fs)
NM_001458.5(FLNC):c.4702del (p.Asp1568fs)
NM_001458.5(FLNC):c.4738G>A (p.Asp1580Asn)
NM_001458.5(FLNC):c.4861A>T (p.Ile1621Phe) rs1808685364
NM_001458.5(FLNC):c.4920_4927+6del
NM_001458.5(FLNC):c.4926_4927insACGTCACA (p.Val1643fs) rs1402879259
NM_001458.5(FLNC):c.4927+2T>C
NM_001458.5(FLNC):c.4927+2T>G rs2128937680
NM_001458.5(FLNC):c.4928-1G>C
NM_001458.5(FLNC):c.4951+2T>C rs1585164316
NM_001458.5(FLNC):c.4952-2A>T rs774945928
NM_001458.5(FLNC):c.5199+1G>A
NM_001458.5(FLNC):c.5199+1G>C rs1465588989
NM_001458.5(FLNC):c.5398+1G>C rs1808761665
NM_001458.5(FLNC):c.5399-1G>A
NM_001458.5(FLNC):c.5399-2A>C rs2128938204
NM_001458.5(FLNC):c.539A>G (p.Asn180Ser) rs2128933682
NM_001458.5(FLNC):c.5503C>T (p.Gln1835Ter)
NM_001458.5(FLNC):c.5540-2A>G rs111477195
NM_001458.5(FLNC):c.5683G>C (p.Ala1895Pro) rs2128938435
NM_001458.5(FLNC):c.5685del (p.Val1896fs) rs1808809268
NM_001458.5(FLNC):c.5693del (p.Gly1898fs)
NM_001458.5(FLNC):c.5842+1G>A rs2128938502
NM_001458.5(FLNC):c.5842+2T>G rs2128938503
NM_001458.5(FLNC):c.5843-2A>G rs1808866340
NM_001458.5(FLNC):c.5897C>A (p.Ser1966Ter)
NM_001458.5(FLNC):c.6004+2T>C rs1808874360
NM_001458.5(FLNC):c.602-2A>C
NM_001458.5(FLNC):c.6023dup (p.Glu2009fs)
NM_001458.5(FLNC):c.6031G>A (p.Gly2011Arg) rs1554400962
NM_001458.5(FLNC):c.617G>A (p.Trp206Ter)
NM_001458.5(FLNC):c.6202_6208+11del
NM_001458.5(FLNC):c.6209-1G>C
NM_001458.5(FLNC):c.6362-1G>T rs1808924231
NM_001458.5(FLNC):c.6451G>A (p.Gly2151Ser) rs1563003159
NM_001458.5(FLNC):c.6569G>C (p.Arg2190Pro) rs762680314
NM_001458.5(FLNC):c.6742C>T (p.Gln2248Ter)
NM_001458.5(FLNC):c.6892C>T (p.Pro2298Ser) rs1554401403
NM_001458.5(FLNC):c.6958G>A (p.Gly2320Arg) rs867808948
NM_001458.5(FLNC):c.699+1G>A rs1562991776
NM_001458.5(FLNC):c.6997+1G>A
NM_001458.5(FLNC):c.6997+1G>T rs1585169973
NM_001458.5(FLNC):c.711del (p.Glu238fs)
NM_001458.5(FLNC):c.7180G>C (p.Asp2394His) rs1554401561
NM_001458.5(FLNC):c.7235_7236del (p.Thr2412fs)
NM_001458.5(FLNC):c.7384+2T>C rs112941619
NM_001458.5(FLNC):c.7385-1G>A rs1585171818
NM_001458.5(FLNC):c.7486del (p.Val2496fs)
NM_001458.5(FLNC):c.7559C>A (p.Thr2520Asn) rs1809086992
NM_001458.5(FLNC):c.7562-1G>A rs2128940335
NM_001458.5(FLNC):c.7581del (p.Ile2527fs)
NM_001458.5(FLNC):c.7750_7769dup (p.Lys2591fs) rs2128940399
NM_001458.5(FLNC):c.7780+1G>A rs1563005607
NM_001458.5(FLNC):c.7780+1G>C rs1563005607
NM_001458.5(FLNC):c.7780+1G>T
NM_001458.5(FLNC):c.7780+2T>A
NM_001458.5(FLNC):c.7780+2T>C rs1809110247
NM_001458.5(FLNC):c.7925del (p.Gly2642fs)
NM_001458.5(FLNC):c.850+1G>A rs1808146842
NM_001458.5(FLNC):c.850+1G>T rs1808146842
NM_001458.5(FLNC):c.893_908del (p.Phe298fs) rs1808153476

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