ClinVar Miner

List of variants in gene FLNC reported by Eurofins NTD LLC (GA)

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Gene type:
ClinVar version:
Total variants: 70
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HGVS dbSNP gnomAD frequency
NM_001458.5(FLNC):c.4404T>C (p.Asp1468=) rs2249128 0.99086
NM_001458.5(FLNC):c.3973C>T (p.Leu1325=) rs34373805 0.28610
NM_001458.5(FLNC):c.5763T>C (p.Thr1921=) rs3816884 0.18399
NM_001458.5(FLNC):c.4431G>A (p.Leu1477=) rs2291568 0.15512
NM_001458.5(FLNC):c.4289-4A>C rs140031589 0.00743
NM_001458.5(FLNC):c.3721C>T (p.Arg1241Cys) rs146953558 0.00728
NM_001458.5(FLNC):c.5578C>T (p.Arg1860Cys) rs181067717 0.00536
NM_001458.5(FLNC):c.1902G>A (p.Glu634=) rs12536635 0.00414
NM_001458.5(FLNC):c.1425C>T (p.Asn475=) rs143610360 0.00297
NM_001458.5(FLNC):c.2078A>C (p.Asp693Ala) rs34972246 0.00297
NM_001458.5(FLNC):c.8003T>C (p.Met2668Thr) rs200502811 0.00291
NM_001458.5(FLNC):c.4928-7T>C rs201957008 0.00286
NM_001458.5(FLNC):c.3006G>A (p.Arg1002=) rs61737781 0.00283
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.6991G>A (p.Val2331Met) rs191288058 0.00156
NM_001458.5(FLNC):c.6714C>T (p.Thr2238=) rs10268251 0.00143
NM_001458.5(FLNC):c.1577G>A (p.Arg526Gln) rs34932223 0.00138
NM_001458.5(FLNC):c.1698C>T (p.Ser566=) rs112194548 0.00137
NM_001458.5(FLNC):c.2501C>T (p.Thr834Met) rs75133741 0.00136
NM_001458.5(FLNC):c.6459C>T (p.Thr2153=) rs113618587 0.00135
NM_001458.5(FLNC):c.6005-9T>C rs118124743 0.00133
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.597C>T (p.Ala199=) rs143942649 0.00124
NM_001458.5(FLNC):c.4947C>T (p.Gly1649=) rs201069454 0.00119
NM_001458.5(FLNC):c.6309C>T (p.Thr2103=) rs376992044 0.00116
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.5592C>T (p.Ala1864=) rs117517372 0.00048
NM_001458.5(FLNC):c.3966C>T (p.Gly1322=) rs200237564 0.00045
NM_001458.5(FLNC):c.5764G>A (p.Ala1922Thr) rs202128602 0.00040
NM_001458.5(FLNC):c.2733G>A (p.Lys911=) rs374135903 0.00024
NM_001458.5(FLNC):c.7289C>T (p.Ala2430Val) rs200516164 0.00010
NM_001458.5(FLNC):c.2040C>T (p.Thr680=) rs368121231 0.00008
NM_001458.5(FLNC):c.4488T>C (p.Asn1496=) rs377258966 0.00008
NM_001458.5(FLNC):c.1505A>T (p.Lys502Met) rs780486915 0.00006
NM_001458.5(FLNC):c.3949A>G (p.Thr1317Ala) rs377555574 0.00004
NM_001458.5(FLNC):c.4880G>A (p.Arg1627His) rs751592993 0.00004
NM_001458.5(FLNC):c.7291G>A (p.Val2431Met) rs572952653 0.00003
NM_001458.5(FLNC):c.1976T>G (p.Leu659Arg) rs576402053 0.00002
NM_001458.5(FLNC):c.2008-7C>T rs767576240 0.00002
NM_001458.5(FLNC):c.3243G>A (p.Ala1081=) rs534482249 0.00002
NM_001458.5(FLNC):c.5375C>T (p.Ala1792Val) rs200233856 0.00002
NM_001458.5(FLNC):c.7382G>A (p.Ser2461Asn) rs550547714 0.00002
NM_001458.5(FLNC):c.8070G>T (p.Arg2690=) rs373087529 0.00002
NM_001458.5(FLNC):c.1197C>T (p.Asp399=) rs756546984 0.00001
NM_001458.5(FLNC):c.3054C>T (p.Gly1018=) rs769624093 0.00001
NM_001458.5(FLNC):c.3506A>G (p.Lys1169Arg) rs530742766 0.00001
NM_001458.5(FLNC):c.4133C>T (p.Ala1378Val) rs748008658 0.00001
NM_001458.5(FLNC):c.4576C>T (p.Arg1526Cys) rs746275035 0.00001
NM_001458.5(FLNC):c.4952G>A (p.Gly1651Asp) rs762493974 0.00001
NM_001458.5(FLNC):c.6441C>T (p.Ile2147=) rs762017885 0.00001
NM_001458.5(FLNC):c.6485-8C>T rs369347947 0.00001
NM_001458.5(FLNC):c.1502C>T (p.Thr501Ile) rs794727967
NM_001458.5(FLNC):c.2244C>A (p.Asn748Lys) rs752145129
NM_001458.5(FLNC):c.2459A>T (p.Asp820Val) rs886044638
NM_001458.5(FLNC):c.272A>C (p.Asn91Thr) rs886042565
NM_001458.5(FLNC):c.3489G>C (p.Pro1163=) rs369853278
NM_001458.5(FLNC):c.4009A>C (p.Lys1337Gln) rs1554399580
NM_001458.5(FLNC):c.4301G>A (p.Arg1434His) rs143623535
NM_001458.5(FLNC):c.4737+9_4737+10del rs794727437
NM_001458.5(FLNC):c.5042C>G (p.Thr1681Arg) rs193159707
NM_001458.5(FLNC):c.6405G>A (p.Lys2135=) rs886043826

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