ClinVar Miner

Variants in gene FLNC with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 150
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HGVS dbSNP gnomAD frequency
NM_001458.5(FLNC):c.8003T>C (p.Met2668Thr) rs200502811 0.00291
NM_001458.5(FLNC):c.5644A>G (p.Ile1882Val) rs184018403 0.00160
NM_001458.5(FLNC):c.6714C>T (p.Thr2238=) rs10268251 0.00143
NM_001458.5(FLNC):c.7862G>A (p.Arg2621Gln) rs201636548 0.00131
NM_001458.5(FLNC):c.1813+11G>T rs138716837 0.00126
NM_001458.5(FLNC):c.6998-5C>T rs139030003 0.00106
NM_001458.5(FLNC):c.5418G>A (p.Ser1806=) rs376078394 0.00090
NM_001458.5(FLNC):c.1600G>A (p.Glu534Lys) rs201905890 0.00086
NM_001458.5(FLNC):c.4022G>A (p.Arg1341Gln) rs149641783 0.00068
NM_001458.5(FLNC):c.6808G>A (p.Glu2270Lys) rs202223616 0.00068
NM_001458.5(FLNC):c.4553A>G (p.Lys1518Arg) rs201635205 0.00061
NM_001458.5(FLNC):c.1519G>A (p.Gly507Arg) rs189525930 0.00060
NM_001458.5(FLNC):c.2390-8C>G rs146063718 0.00057
NM_001458.5(FLNC):c.3966C>T (p.Gly1322=) rs200237564 0.00045
NM_001458.5(FLNC):c.5954C>T (p.Ser1985Leu) rs200415625 0.00031
NM_001458.5(FLNC):c.1474A>G (p.Lys492Glu) rs118056738 0.00029
NM_001458.5(FLNC):c.5311C>G (p.Pro1771Ala) rs200001272 0.00026
NM_001458.5(FLNC):c.1757T>C (p.Val586Ala) rs374132023 0.00025
NM_001458.5(FLNC):c.2068T>C (p.Phe690Leu) rs200943714 0.00025
NM_001458.5(FLNC):c.2733G>A (p.Lys911=) rs374135903 0.00024
NM_001458.5(FLNC):c.5221G>A (p.Glu1741Lys) rs200792813 0.00024
NM_001458.5(FLNC):c.2635C>T (p.Arg879Cys) rs374983276 0.00021
NM_001458.5(FLNC):c.7499G>A (p.Ser2500Asn) rs371244800 0.00021
NM_001458.5(FLNC):c.1924G>A (p.Val642Ile) rs369387744 0.00019
NM_001458.5(FLNC):c.2296C>T (p.Arg766Trp) rs200215340 0.00019
NM_001458.5(FLNC):c.3938G>A (p.Arg1313Gln) rs199804244 0.00019
NM_001458.5(FLNC):c.7108G>A (p.Gly2370Ser) rs201917318 0.00018
NM_001458.5(FLNC):c.1081C>T (p.Arg361Cys) rs200206944 0.00016
NM_001458.5(FLNC):c.1108A>G (p.Met370Val) rs370406338 0.00016
NM_001458.5(FLNC):c.1166G>A (p.Gly389Asp) rs763039506 0.00016
NM_001458.5(FLNC):c.2163C>A (p.Asn721Lys) rs370539335 0.00016
NM_001458.5(FLNC):c.2747G>A (p.Arg916Gln) rs143720860 0.00016
NM_001458.5(FLNC):c.4763C>G (p.Ala1588Gly) rs148545460 0.00016
NM_001458.5(FLNC):c.3304C>T (p.Pro1102Ser) rs199707920 0.00015
NM_001458.5(FLNC):c.1259G>A (p.Arg420Gln) rs371410741 0.00014
NM_001458.5(FLNC):c.3242C>T (p.Ala1081Val) rs200169573 0.00014
NM_001458.5(FLNC):c.4367G>C (p.Gly1456Ala) rs775049569 0.00014
NM_001458.5(FLNC):c.5020G>A (p.Gly1674Ser) rs374124083 0.00014
NM_001458.5(FLNC):c.5432G>A (p.Arg1811Gln) rs369759751 0.00014
NM_001458.5(FLNC):c.2297G>A (p.Arg766Gln) rs369935650 0.00013
NM_001458.5(FLNC):c.1568T>C (p.Val523Ala) rs182845462 0.00012
NM_001458.5(FLNC):c.6689G>A (p.Arg2230His) rs376035195 0.00012
NM_001458.5(FLNC):c.3853G>A (p.Gly1285Ser) rs200928780 0.00011
NM_001458.5(FLNC):c.5500C>T (p.His1834Tyr) rs377141822 0.00011
NM_001458.5(FLNC):c.31G>A (p.Gly11Ser) rs370512642 0.00010
NM_001458.5(FLNC):c.7289C>T (p.Ala2430Val) rs200516164 0.00010
NM_001458.5(FLNC):c.1205C>T (p.Thr402Ile) rs374757755 0.00009
NM_001458.5(FLNC):c.1605C>T (p.Cys535=) rs199976790 0.00009
NM_001458.5(FLNC):c.1606G>A (p.Glu536Lys) rs141616435 0.00009
NM_001458.5(FLNC):c.1616C>T (p.Pro539Leu) rs375570393 0.00009
NM_001458.5(FLNC):c.1645A>G (p.Ile549Val) rs547997371 0.00009
NM_001458.5(FLNC):c.3623C>T (p.Ala1208Val) rs202184162 0.00009
NM_001458.5(FLNC):c.5410A>T (p.Met1804Leu) rs201949844 0.00009
NM_001458.5(FLNC):c.643G>A (p.Val215Met) rs754309921 0.00009
NM_001458.5(FLNC):c.970-5A>G rs199755800 0.00009
NM_001458.5(FLNC):c.2040C>T (p.Thr680=) rs368121231 0.00008
NM_001458.5(FLNC):c.3740C>T (p.Ala1247Val) rs775496136 0.00008
NM_001458.5(FLNC):c.4488T>C (p.Asn1496=) rs377258966 0.00008
NM_001458.5(FLNC):c.4651G>A (p.Ala1551Thr) rs565918031 0.00008
NM_001458.5(FLNC):c.5216C>T (p.Pro1739Leu) rs745650222 0.00008
NM_001458.5(FLNC):c.6817G>A (p.Ala2273Thr) rs372251350 0.00008
NM_001458.5(FLNC):c.1142G>A (p.Arg381His) rs776469396 0.00007
NM_001458.5(FLNC):c.3872G>A (p.Arg1291His) rs370042010 0.00007
NM_001458.5(FLNC):c.3887C>T (p.Ser1296Leu) rs747587140 0.00006
NM_001458.5(FLNC):c.5468C>T (p.Thr1823Met) rs140857707 0.00006
NM_001458.5(FLNC):c.5944C>T (p.Arg1982Cys) rs538779271 0.00006
NM_001458.5(FLNC):c.6134G>A (p.Arg2045Gln) rs747196571 0.00006
NM_001458.5(FLNC):c.7090C>T (p.Arg2364Cys) rs374973240 0.00006
NM_001458.5(FLNC):c.7366G>A (p.Val2456Ile) rs770796119 0.00006
NM_001458.5(FLNC):c.2041G>A (p.Gly681Ser) rs199705417 0.00005
NM_001458.5(FLNC):c.4092G>C (p.Leu1364Phe) rs768635501 0.00005
NM_001458.5(FLNC):c.6865G>A (p.Ala2289Thr) rs766740877 0.00005
NM_001458.5(FLNC):c.1261C>T (p.Arg421Trp) rs759075520 0.00004
NM_001458.5(FLNC):c.2450T>C (p.Ile817Thr) rs200653747 0.00004
NM_001458.5(FLNC):c.2737G>A (p.Glu913Lys) rs774707336 0.00004
NM_001458.5(FLNC):c.3133C>A (p.His1045Asn) rs201863231 0.00004
NM_001458.5(FLNC):c.3680C>T (p.Thr1227Ile) rs373573447 0.00004
NM_001458.5(FLNC):c.3722G>A (p.Arg1241His) rs370520806 0.00004
NM_001458.5(FLNC):c.4055G>A (p.Arg1352His) rs746731567 0.00004
NM_001458.5(FLNC):c.6390C>T (p.Gly2130=) rs746751083 0.00004
NM_001458.5(FLNC):c.7229G>A (p.Arg2410His) rs558239439 0.00004
NM_001458.5(FLNC):c.7256C>T (p.Thr2419Met) rs199768217 0.00004
NM_001458.5(FLNC):c.7560C>T (p.Thr2520=) rs527921534 0.00004
NM_001458.5(FLNC):c.7877G>A (p.Ser2626Asn) rs2639142 0.00004
NM_001458.5(FLNC):c.1471G>A (p.Val491Met) rs770264114 0.00003
NM_001458.5(FLNC):c.2930-5C>T rs371599113 0.00003
NM_001458.5(FLNC):c.4911C>G (p.Ser1637Arg) rs1469272964 0.00003
NM_001458.5(FLNC):c.5273G>A (p.Arg1758Gln) rs573984029 0.00003
NM_001458.5(FLNC):c.5377G>A (p.Val1793Met) rs587780337 0.00003
NM_001458.5(FLNC):c.5984G>A (p.Arg1995His) rs371508414 0.00003
NM_001458.5(FLNC):c.6040G>A (p.Val2014Met) rs772477251 0.00003
NM_001458.5(FLNC):c.6471C>T (p.Asn2157=) rs764877771 0.00003
NM_001458.5(FLNC):c.6595G>A (p.Gly2199Arg) rs368977589 0.00003
NM_001458.5(FLNC):c.6779A>G (p.Lys2260Arg) rs751019991 0.00003
NM_001458.5(FLNC):c.2008-7C>T rs767576240 0.00002
NM_001458.5(FLNC):c.2311G>A (p.Gly771Ser) rs1031265089 0.00002
NM_001458.5(FLNC):c.3022C>T (p.Arg1008Cys) rs757969015 0.00002
NM_001458.5(FLNC):c.3243G>A (p.Ala1081=) rs534482249 0.00002
NM_001458.5(FLNC):c.3295G>A (p.Val1099Ile) rs759452636 0.00002
NM_001458.5(FLNC):c.3372G>A (p.Thr1124=) rs556913973 0.00002
NM_001458.5(FLNC):c.3812C>G (p.Thr1271Ser) rs778997084 0.00002
NM_001458.5(FLNC):c.4073C>G (p.Pro1358Arg) rs769586047 0.00002
NM_001458.5(FLNC):c.4699C>T (p.Arg1567Trp) rs369842920 0.00002
NM_001458.5(FLNC):c.4705G>A (p.Ala1569Thr) rs768737324 0.00002
NM_001458.5(FLNC):c.5278G>A (p.Gly1760Ser) rs150986092 0.00002
NM_001458.5(FLNC):c.5375C>T (p.Ala1792Val) rs200233856 0.00002
NM_001458.5(FLNC):c.7228C>T (p.Arg2410Cys) rs750686083 0.00002
NM_001458.5(FLNC):c.7310G>A (p.Arg2437Gln) rs201762568 0.00002
NM_001458.5(FLNC):c.8070G>T (p.Arg2690=) rs373087529 0.00002
NM_001458.5(FLNC):c.1169A>G (p.Asn390Ser) rs188905854 0.00001
NM_001458.5(FLNC):c.1766C>T (p.Ser589Leu) rs780098760 0.00001
NM_001458.5(FLNC):c.2023C>T (p.Pro675Ser) rs1227192105 0.00001
NM_001458.5(FLNC):c.2287C>T (p.His763Tyr) rs1380984220 0.00001
NM_001458.5(FLNC):c.2389+4C>T rs1057523921 0.00001
NM_001458.5(FLNC):c.2424C>T (p.Gly808=) rs764991202 0.00001
NM_001458.5(FLNC):c.3054C>T (p.Gly1018=) rs769624093 0.00001
NM_001458.5(FLNC):c.3268G>T (p.Ala1090Ser) rs760158891 0.00001
NM_001458.5(FLNC):c.3476G>A (p.Arg1159Gln) rs141199483 0.00001
NM_001458.5(FLNC):c.4109G>A (p.Arg1370Gln) rs761881020 0.00001
NM_001458.5(FLNC):c.4172C>T (p.Ser1391Leu) rs755832014 0.00001
NM_001458.5(FLNC):c.470G>A (p.Arg157His) rs752919962 0.00001
NM_001458.5(FLNC):c.5272C>T (p.Arg1758Trp) rs369187211 0.00001
NM_001458.5(FLNC):c.5281G>A (p.Ala1761Thr) rs376023896 0.00001
NM_001458.5(FLNC):c.5458G>A (p.Gly1820Ser) rs763930207 0.00001
NM_001458.5(FLNC):c.5544C>T (p.Ser1848=) rs1350503435 0.00001
NM_001458.5(FLNC):c.5670G>A (p.Gly1890=) rs369881758 0.00001
NM_001458.5(FLNC):c.5935G>A (p.Ala1979Thr) rs766127245 0.00001
NM_001458.5(FLNC):c.5955G>A (p.Ser1985=) rs777895128 0.00001
NM_001458.5(FLNC):c.6441C>T (p.Ile2147=) rs762017885 0.00001
NM_001458.5(FLNC):c.6572C>T (p.Thr2191Met) rs768329311 0.00001
NM_001458.5(FLNC):c.6608G>A (p.Arg2203His) rs1063262 0.00001
NM_001458.5(FLNC):c.6878G>A (p.Arg2293His) rs1034483511 0.00001
NM_001458.5(FLNC):c.7328G>A (p.Arg2443Gln) rs370293647 0.00001
NM_001458.5(FLNC):c.8080G>A (p.Val2694Ile) rs765388755 0.00001
NM_001458.5(FLNC):c.851-5C>T rs758216356 0.00001
NM_001458.5(FLNC):c.1000C>T (p.Arg334Cys) rs372497581
NM_001458.5(FLNC):c.2062G>A (p.Ala688Thr) rs774194364
NM_001458.5(FLNC):c.2167G>A (p.Asp723Asn) rs375414341
NM_001458.5(FLNC):c.3055G>A (p.Gly1019Ser) rs200864007
NM_001458.5(FLNC):c.3055G>T (p.Gly1019Cys) rs200864007
NM_001458.5(FLNC):c.3114G>A (p.Val1038=) rs376516180
NM_001458.5(FLNC):c.3261C>T (p.Thr1087=) rs2128936369
NM_001458.5(FLNC):c.3489G>C (p.Pro1163=) rs369853278
NM_001458.5(FLNC):c.3711A>C (p.Lys1237Asn) rs758220780
NM_001458.5(FLNC):c.3799C>T (p.Arg1267Trp) rs371483562
NM_001458.5(FLNC):c.4301G>A (p.Arg1434His) rs143623535
NM_001458.5(FLNC):c.4301G>T (p.Arg1434Leu) rs143623535
NM_001458.5(FLNC):c.5363T>G (p.Val1788Gly) rs573899913
NM_001458.5(FLNC):c.6799G>A (p.Val2267Ile) rs758080422
NM_001458.5(FLNC):c.7609G>A (p.Ala2537Thr) rs201486752

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