ClinVar Miner

List of variants in gene FLNC reported as benign for Myofibrillar myopathy, filamin C-related; Myopathy, distal, 4; Cardiomyopathy, familial hypertrophic, 26; Dilated Cardiomyopathy, Dominant

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Gene type:
ClinVar version:
Total variants: 75
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HGVS dbSNP
NM_001458.4(FLNC):c.1374C>T (p.Pro458=) rs115140972
NM_001458.4(FLNC):c.1425C>T (p.Asn475=) rs143610360
NM_001458.4(FLNC):c.1518C>T (p.Ser506=) rs368101036
NM_001458.4(FLNC):c.1577G>A (p.Arg526Gln) rs34932223
NM_001458.4(FLNC):c.1614C>T (p.Tyr538=) rs76046880
NM_001458.4(FLNC):c.1698C>T (p.Ser566=) rs112194548
NM_001458.4(FLNC):c.1902G>A (p.Glu634=) rs12536635
NM_001458.4(FLNC):c.2078A>C (p.Asp693Ala) rs34972246
NM_001458.4(FLNC):c.2199C>G (p.Thr733=) rs200655185
NM_001458.4(FLNC):c.2390-8C>G rs146063718
NM_001458.4(FLNC):c.2390-9T>C rs368068407
NM_001458.4(FLNC):c.2501C>T (p.Thr834Met) rs75133741
NM_001458.4(FLNC):c.2568C>T (p.Pro856=) rs201611050
NM_001458.4(FLNC):c.2841C>T (p.Gly947=) rs547060988
NM_001458.4(FLNC):c.2889G>A (p.Pro963=) rs191892345
NM_001458.4(FLNC):c.3000T>C (p.Asp1000=) rs184454068
NM_001458.4(FLNC):c.3006G>A (p.Arg1002=) rs61737781
NM_001458.4(FLNC):c.3201T>G (p.Ala1067=) rs760214102
NM_001458.4(FLNC):c.3506A>G (p.Lys1169Arg) rs530742766
NM_001458.4(FLNC):c.352+10G>A rs79489893
NM_001458.4(FLNC):c.3621C>T (p.Asn1207=) rs117864464
NM_001458.4(FLNC):c.3624G>A (p.Ala1208=) rs35281128
NM_001458.4(FLNC):c.3721C>T (p.Arg1241Cys) rs146953558
NM_001458.4(FLNC):c.3757G>A (p.Val1253Ile) rs117366477
NM_001458.4(FLNC):c.3765C>A (p.Val1255=) rs556428588
NM_001458.4(FLNC):c.3838C>T (p.Leu1280=) rs34180031
NM_001458.4(FLNC):c.3852C>T (p.Gly1284=) rs111337293
NM_001458.4(FLNC):c.3861C>T (p.His1287=) rs375986462
NM_001458.4(FLNC):c.3964+9C>T rs200448727
NM_001458.4(FLNC):c.3966C>T (p.Gly1322=) rs200237564
NM_001458.4(FLNC):c.4022G>A (p.Arg1341Gln) rs149641783
NM_001458.4(FLNC):c.4140C>T (p.Thr1380=) rs183668401
NM_001458.4(FLNC):c.4161C>T (p.Ile1387=) rs200288149
NM_001458.4(FLNC):c.4289-4A>C rs140031589
NM_001458.4(FLNC):c.4302C>T (p.Arg1434=) rs114697352
NM_001458.4(FLNC):c.4404C>T (p.Asp1468=) rs2249128
NM_001458.4(FLNC):c.4581-5T>A rs368660628
NM_001458.4(FLNC):c.4737+9_4737+10del rs794727437
NM_001458.4(FLNC):c.4928-7T>C rs201957008
NM_001458.4(FLNC):c.4947C>T (p.Gly1649=) rs201069454
NM_001458.4(FLNC):c.5042C>G (p.Thr1681Arg) rs193159707
NM_001458.4(FLNC):c.5070C>T (p.Leu1690=) rs202027738
NM_001458.4(FLNC):c.5262C>T (p.Tyr1754=) rs369165766
NM_001458.4(FLNC):c.5418G>A (p.Ser1806=) rs376078394
NM_001458.4(FLNC):c.5578C>T (p.Arg1860Cys) rs181067717
NM_001458.4(FLNC):c.5592C>T (p.Ala1864=) rs117517372
NM_001458.4(FLNC):c.561C>T (p.Asp187=) rs149474376
NM_001458.4(FLNC):c.5763_5764inv (p.Ala1922Thr)
NM_001458.4(FLNC):c.5842+8G>A rs781168906
NM_001458.4(FLNC):c.5889G>A (p.Thr1963=) rs374743518
NM_001458.4(FLNC):c.5892C>T (p.Asp1964=) rs747546440
NM_001458.4(FLNC):c.5910C>T (p.Thr1970=) rs544613263
NM_001458.4(FLNC):c.597C>T (p.Ala199=) rs143942649
NM_001458.4(FLNC):c.6005-9T>C rs118124743
NM_001458.4(FLNC):c.6120C>T (p.Asp2040=) rs116974302
NM_001458.4(FLNC):c.6309C>T (p.Thr2103=) rs376992044
NM_001458.4(FLNC):c.6459C>T (p.Thr2153=) rs113618587
NM_001458.4(FLNC):c.6714C>T (p.Thr2238=) rs10268251
NM_001458.4(FLNC):c.6771A>G (p.Pro2257=) rs34422412
NM_001458.4(FLNC):c.6888C>T (p.His2296=) rs375259002
NM_001458.4(FLNC):c.6988G>A (p.Gly2330Ser) rs527248119
NM_001458.4(FLNC):c.6991G>A (p.Val2331Met) rs191288058
NM_001458.4(FLNC):c.6998-5C>T rs139030003
NM_001458.4(FLNC):c.7185C>T (p.Ser2395=) rs199880128
NM_001458.4(FLNC):c.7385-5C>T rs367793265
NM_001458.4(FLNC):c.7533C>T (p.Tyr2511=) rs376806697
NM_001458.4(FLNC):c.7545C>T (p.Leu2515=) rs369791058
NM_001458.4(FLNC):c.7614G>T (p.Leu2538Phe) rs180834558
NM_001458.4(FLNC):c.7780+10A>G rs201149834
NM_001458.4(FLNC):c.7990+9C>T rs566679569
NM_001458.4(FLNC):c.8003T>C (p.Met2668Thr) rs200502811
NM_001458.4(FLNC):c.8049C>T (p.Tyr2683=) rs183104951
NM_001458.4(FLNC):c.8118C>T (p.Leu2706=) rs28379666
NM_001458.4(FLNC):c.8121T>C (p.Ile2707=) rs28437296
NM_001458.4(FLNC):c.851-7C>A rs576908770

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