ClinVar Miner

List of variants in gene FLNC reported as likely benign by PreventionGenetics, part of Exact Sciences

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Gene type:
ClinVar version:
Total variants: 79
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HGVS dbSNP gnomAD frequency
NM_001458.5(FLNC):c.5578C>T (p.Arg1860Cys) rs181067717 0.00536
NM_001458.5(FLNC):c.1813+36G>A rs142756348 0.00482
NM_001458.5(FLNC):c.2122-27T>C rs117577125 0.00352
NM_001458.5(FLNC):c.7091G>A (p.Arg2364His) rs201672146 0.00173
NM_001458.5(FLNC):c.5644A>G (p.Ile1882Val) rs184018403 0.00160
NM_001458.5(FLNC):c.2389+12C>T rs370526829 0.00151
NM_001458.5(FLNC):c.2180G>A (p.Arg727His) rs200618242 0.00120
NM_001458.5(FLNC):c.4581-5T>A rs368660628 0.00111
NM_001458.5(FLNC):c.3000T>C (p.Asp1000=) rs184454068 0.00110
NM_001458.5(FLNC):c.5766G>A (p.Ala1922=) rs58914363 0.00108
NM_001458.5(FLNC):c.7185C>T (p.Ser2395=) rs199880128 0.00090
NM_001458.5(FLNC):c.1600G>A (p.Glu534Lys) rs201905890 0.00086
NM_001458.5(FLNC):c.7947C>T (p.Phe2649=) rs368849358 0.00083
NM_001458.5(FLNC):c.6175G>A (p.Val2059Met) rs201333104 0.00076
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.2390-8C>G rs146063718 0.00057
NM_001458.5(FLNC):c.5200-18C>T rs372184893 0.00052
NM_001458.5(FLNC):c.3966C>T (p.Gly1322=) rs200237564 0.00045
NM_001458.5(FLNC):c.5374G>A (p.Ala1792Thr) rs201348102 0.00028
NM_001458.5(FLNC):c.5220C>T (p.His1740=) rs369739871 0.00027
NM_001458.5(FLNC):c.1354G>A (p.Val452Met) rs192163925 0.00019
NM_001458.5(FLNC):c.5143G>A (p.Val1715Ile) rs200178370 0.00018
NM_001458.5(FLNC):c.1657G>A (p.Gly553Ser) rs201572079 0.00017
NM_001458.5(FLNC):c.1923C>T (p.His641=) rs375361259 0.00016
NM_001458.5(FLNC):c.3153G>A (p.Pro1051=) rs373694043 0.00015
NM_001458.5(FLNC):c.5020G>A (p.Gly1674Ser) rs374124083 0.00014
NM_001458.5(FLNC):c.5298+6G>A rs373553314 0.00014
NM_001458.5(FLNC):c.3090C>T (p.Pro1030=) rs760926290 0.00013
NM_001458.5(FLNC):c.5892C>T (p.Asp1964=) rs747546440 0.00011
NM_001458.5(FLNC):c.4952-9G>T rs747821376 0.00010
NM_001458.5(FLNC):c.1645A>G (p.Ile549Val) rs547997371 0.00009
NM_001458.5(FLNC):c.2292C>T (p.Pro764=) rs369916201 0.00009
NM_001458.5(FLNC):c.3972T>C (p.His1324=) rs201922688 0.00009
NM_001458.5(FLNC):c.4161C>T (p.Ile1387=) rs200288149 0.00009
NM_001458.5(FLNC):c.3740C>T (p.Ala1247Val) rs775496136 0.00008
NM_001458.5(FLNC):c.4459G>A (p.Val1487Met) rs750186463 0.00008
NM_001458.5(FLNC):c.4488T>C (p.Asn1496=) rs377258966 0.00008
NM_001458.5(FLNC):c.352+8C>G rs780084616 0.00006
NM_001458.5(FLNC):c.3927C>T (p.Asp1309=) rs761297336 0.00006
NM_001458.5(FLNC):c.5796C>T (p.Phe1932=) rs572337697 0.00006
NM_001458.5(FLNC):c.6987C>T (p.Ala2329=) rs771037016 0.00006
NM_001458.5(FLNC):c.1851A>G (p.Glu617=) rs199715890 0.00005
NM_001458.5(FLNC):c.2490C>T (p.Thr830=) rs777580254 0.00005
NM_001458.5(FLNC):c.3138G>A (p.Pro1046=) rs369739262 0.00005
NM_001458.5(FLNC):c.1242C>T (p.Ile414=) rs761922411 0.00004
NM_001458.5(FLNC):c.327C>G (p.Arg109=) rs750328194 0.00004
NM_001458.5(FLNC):c.1953C>T (p.Asp651=) rs554570268 0.00003
NM_001458.5(FLNC):c.2392G>A (p.Asp798Asn) rs778594252 0.00003
NM_001458.5(FLNC):c.2415C>T (p.Cys805=) rs376800693 0.00003
NM_001458.5(FLNC):c.2930-5C>T rs371599113 0.00003
NM_001458.5(FLNC):c.366C>T (p.Ile122=) rs369120591 0.00003
NM_001458.5(FLNC):c.4218C>T (p.Thr1406=) rs748827721 0.00003
NM_001458.5(FLNC):c.1976T>G (p.Leu659Arg) rs576402053 0.00002
NM_001458.5(FLNC):c.4662C>T (p.Ile1554=) rs374683306 0.00002
NM_001458.5(FLNC):c.2502G>A (p.Thr834=) rs984526805 0.00001
NM_001458.5(FLNC):c.2874G>A (p.Val958=) rs754046100 0.00001
NM_001458.5(FLNC):c.3867G>A (p.Thr1289=) rs886038485 0.00001
NM_001458.5(FLNC):c.4134G>A (p.Ala1378=) rs200942470 0.00001
NM_001458.5(FLNC):c.423C>T (p.Tyr141=) rs761354079 0.00001
NM_001458.5(FLNC):c.5043G>A (p.Thr1681=) rs200405579 0.00001
NM_001458.5(FLNC):c.5370C>T (p.Pro1790=) rs766344715 0.00001
NM_001458.5(FLNC):c.5685C>T (p.Ala1895=) rs1219372997 0.00001
NM_001458.5(FLNC):c.5787C>T (p.Ile1929=) rs377063332 0.00001
NM_001458.5(FLNC):c.5805G>A (p.Lys1935=) rs759262897 0.00001
NM_001458.5(FLNC):c.5814G>A (p.Pro1938=) rs752263141 0.00001
NM_001458.5(FLNC):c.6727+7A>G rs746982412 0.00001
NM_001458.5(FLNC):c.700-5C>T rs745442558 0.00001
NM_001458.5(FLNC):c.7146G>A (p.Glu2382=) rs779162678 0.00001
NM_001458.5(FLNC):c.-26_-9dup rs749265933
NM_001458.5(FLNC):c.1650G>A (p.Thr550=) rs754474889
NM_001458.5(FLNC):c.1761C>A (p.Gly587=)
NM_001458.5(FLNC):c.2199C>G (p.Thr733=) rs200655185
NM_001458.5(FLNC):c.2508A>G (p.Pro836=)
NM_001458.5(FLNC):c.2652C>T (p.Val884=) rs369714355
NM_001458.5(FLNC):c.3489G>C (p.Pro1163=) rs369853278
NM_001458.5(FLNC):c.4293C>T (p.Ser1431=) rs376429779
NM_001458.5(FLNC):c.6005-5C>T
NM_001458.5(FLNC):c.969+14G>T rs765545958

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