ClinVar Miner

List of variants in gene FLNC reported as uncertain significance for not provided

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Gene type:
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Total variants: 109
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HGVS dbSNP
NM_001458.4(FLNC):c.1082G>A (p.Arg361His) rs752888774
NM_001458.4(FLNC):c.1166G>A (p.Gly389Asp) rs763039506
NM_001458.4(FLNC):c.1197C>T (p.Asp399=) rs756546984
NM_001458.4(FLNC):c.1502C>T (p.Thr501Ile) rs794727967
NM_001458.4(FLNC):c.1505A>T (p.Lys502Met)
NM_001458.4(FLNC):c.1508G>A (p.Gly503Asp)
NM_001458.4(FLNC):c.1519G>A (p.Gly507Arg) rs189525930
NM_001458.4(FLNC):c.1528A>C (p.Lys510Gln) rs955475416
NM_001458.4(FLNC):c.1568T>C (p.Val523Ala) rs182845462
NM_001458.4(FLNC):c.1600G>A (p.Glu534Lys) rs201905890
NM_001458.4(FLNC):c.1645A>G (p.Ile549Val) rs547997371
NM_001458.4(FLNC):c.1657G>A (p.Gly553Ser) rs201572079
NM_001458.4(FLNC):c.1698C>T (p.Ser566=) rs112194548
NM_001458.4(FLNC):c.1802T>C (p.Val601Ala) rs763590899
NM_001458.4(FLNC):c.1813+11G>T rs138716837
NM_001458.4(FLNC):c.1936G>C (p.Asp646His) rs372668691
NM_001458.4(FLNC):c.2008-7C>T rs767576240
NM_001458.4(FLNC):c.2040C>T (p.Thr680=) rs368121231
NM_001458.4(FLNC):c.2130C>T (p.Asp710=) rs778781499
NM_001458.4(FLNC):c.2169C>G (p.Asp723Glu)
NM_001458.4(FLNC):c.2244C>A (p.Asn748Lys) rs752145129
NM_001458.4(FLNC):c.2293G>A (p.Glu765Lys) rs373798394
NM_001458.4(FLNC):c.2390-8C>G rs146063718
NM_001458.4(FLNC):c.2459A>T (p.Asp820Val) rs886044638
NM_001458.4(FLNC):c.2686G>A (p.Gly896Arg) rs200215903
NM_001458.4(FLNC):c.2703G>T (p.Lys901Asn) rs1554398845
NM_001458.4(FLNC):c.272A>C (p.Asn91Thr) rs886042565
NM_001458.4(FLNC):c.2733G>A (p.Lys911=)
NM_001458.4(FLNC):c.2930-5C>T rs371599113
NM_001458.4(FLNC):c.294G>A (p.Glu98=) rs201839252
NM_001458.4(FLNC):c.3005G>A (p.Arg1002Gln) rs202039743
NM_001458.4(FLNC):c.3054C>T (p.Gly1018=) rs769624093
NM_001458.4(FLNC):c.3133C>A (p.His1045Asn) rs201863231
NM_001458.4(FLNC):c.3242C>T (p.Ala1081Val) rs200169573
NM_001458.4(FLNC):c.3243G>A (p.Ala1081=) rs534482249
NM_001458.4(FLNC):c.3295G>A (p.Val1099Ile) rs759452636
NM_001458.4(FLNC):c.3372G>A (p.Thr1124=) rs556913973
NM_001458.4(FLNC):c.3458T>G (p.Phe1153Cys) rs138663492
NM_001458.4(FLNC):c.3464C>T (p.Pro1155Leu)
NM_001458.4(FLNC):c.3475C>T (p.Arg1159Trp) rs760500171
NM_001458.4(FLNC):c.3476G>A (p.Arg1159Gln) rs141199483
NM_001458.4(FLNC):c.3489G>C (p.Pro1163=) rs369853278
NM_001458.4(FLNC):c.3499C>T (p.Arg1167Cys)
NM_001458.4(FLNC):c.3799C>T (p.Arg1267Trp)
NM_001458.4(FLNC):c.3893C>T (p.Ala1298Val) rs1064796931
NM_001458.4(FLNC):c.3949A>G (p.Thr1317Ala)
NM_001458.4(FLNC):c.3966C>T (p.Gly1322=) rs200237564
NM_001458.4(FLNC):c.4009A>C (p.Lys1337Gln) rs1554399580
NM_001458.4(FLNC):c.4022G>A (p.Arg1341Gln) rs149641783
NM_001458.4(FLNC):c.4109G>A (p.Arg1370Gln)
NM_001458.4(FLNC):c.4133C>T (p.Ala1378Val) rs748008658
NM_001458.4(FLNC):c.4296G>A (p.Pro1432=) rs370827536
NM_001458.4(FLNC):c.4301G>A (p.Arg1434His) rs143623535
NM_001458.4(FLNC):c.4301G>T (p.Arg1434Leu) rs143623535
NM_001458.4(FLNC):c.4420C>T (p.Arg1474Trp) rs372454458
NM_001458.4(FLNC):c.4488T>C (p.Asn1496=) rs377258966
NM_001458.4(FLNC):c.4553A>G (p.Lys1518Arg) rs201635205
NM_001458.4(FLNC):c.4576C>T (p.Arg1526Cys) rs746275035
NM_001458.4(FLNC):c.457G>T (p.Asp153Tyr) rs1554397199
NM_001458.4(FLNC):c.4581-5T>A rs368660628
NM_001458.4(FLNC):c.4627C>T (p.Arg1543Trp) rs745648230
NM_001458.4(FLNC):c.4636G>A (p.Gly1546Ser) rs774263134
NM_001458.4(FLNC):c.469C>G (p.Arg157Gly) rs759739899
NM_001458.4(FLNC):c.4700G>T (p.Arg1567Leu) rs2291569
NM_001458.4(FLNC):c.4880G>A (p.Arg1627His) rs751592993
NM_001458.4(FLNC):c.4952G>A (p.Gly1651Asp) rs762493974
NM_001458.4(FLNC):c.4991C>T (p.Thr1664Met) rs780829334
NM_001458.4(FLNC):c.5132C>T (p.Pro1711Leu)
NM_001458.4(FLNC):c.5208C>A (p.Asp1736Glu) rs1291689149
NM_001458.4(FLNC):c.5375C>T (p.Ala1792Val) rs200233856
NM_001458.4(FLNC):c.5377G>A (p.Val1793Met) rs587780337
NM_001458.4(FLNC):c.5418G>A (p.Ser1806=) rs376078394
NM_001458.4(FLNC):c.5509G>C (p.Gly1837Arg) rs1131691565
NM_001458.4(FLNC):c.5579G>A (p.Arg1860His) rs1019973830
NM_001458.4(FLNC):c.5644A>G (p.Ile1882Val) rs184018403
NM_001458.4(FLNC):c.5651C>T (p.Thr1884Ile) rs1064796546
NM_001458.4(FLNC):c.5686G>A (p.Val1896Met) rs891651799
NM_001458.4(FLNC):c.5759C>T (p.Pro1920Leu) rs199714090
NM_001458.4(FLNC):c.5791C>T (p.Arg1931Cys) rs562155863
NM_001458.4(FLNC):c.5955G>A (p.Ser1985=)
NM_001458.4(FLNC):c.600C>T (p.Pro200=) rs202105410
NM_001458.4(FLNC):c.6199C>T (p.Arg2067Cys) rs754160175
NM_001458.4(FLNC):c.6200G>A (p.Arg2067His) rs776520014
NM_001458.4(FLNC):c.6390C>T (p.Gly2130=) rs746751083
NM_001458.4(FLNC):c.6405G>A (p.Lys2135=) rs886043826
NM_001458.4(FLNC):c.643G>A (p.Val215Met) rs754309921
NM_001458.4(FLNC):c.6441C>T (p.Ile2147=) rs762017885
NM_001458.4(FLNC):c.6485-8C>T rs369347947
NM_001458.4(FLNC):c.6572C>T (p.Thr2191Met) rs768329311
NM_001458.4(FLNC):c.6714C>T (p.Thr2238=) rs10268251
NM_001458.4(FLNC):c.6799G>A (p.Val2267Ile) rs758080422
NM_001458.4(FLNC):c.6808G>A (p.Glu2270Lys) rs202223616
NM_001458.4(FLNC):c.6817G>A (p.Ala2273Thr) rs372251350
NM_001458.4(FLNC):c.6895G>C (p.Gly2299Arg) rs756870838
NM_001458.4(FLNC):c.6958G>A (p.Gly2320Arg) rs867808948
NM_001458.4(FLNC):c.6998-5C>T rs139030003
NM_001458.4(FLNC):c.7108G>A (p.Gly2370Ser) rs201917318
NM_001458.4(FLNC):c.7133C>T (p.Pro2378Leu)
NM_001458.4(FLNC):c.7280C>T (p.Ala2427Val)
NM_001458.4(FLNC):c.7289C>T (p.Ala2430Val) rs200516164
NM_001458.4(FLNC):c.7291G>A (p.Val2431Met) rs572952653
NM_001458.4(FLNC):c.7382G>A (p.Ser2461Asn) rs550547714
NM_001458.4(FLNC):c.7560C>T (p.Thr2520=) rs527921534
NM_001458.4(FLNC):c.7784C>T (p.Pro2595Leu) rs756144972
NM_001458.4(FLNC):c.7834G>A (p.Glu2612Lys) rs1183050599
NM_001458.4(FLNC):c.7862G>A (p.Arg2621Gln) rs201636548
NM_001458.4(FLNC):c.8003T>C (p.Met2668Thr) rs200502811
NM_001458.4(FLNC):c.8070G>T (p.Arg2690=) rs373087529
NM_001458.4(FLNC):c.970-4A>G rs532143625

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