ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 47
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HGVS dbSNP gnomAD frequency
NM_001458.5(FLNC):c.5398+16T>C rs13227216 0.32203
NM_001458.5(FLNC):c.3973C>T (p.Leu1325=) rs34373805 0.28610
NM_001458.5(FLNC):c.3297A>G (p.Val1099=) rs3734973 0.28603
NM_001458.5(FLNC):c.5763T>C (p.Thr1921=) rs3816884 0.18399
NM_001458.5(FLNC):c.2265+12C>G rs2291566 0.17192
NM_001458.5(FLNC):c.1814-28T>C rs2291565 0.16389
NM_001458.5(FLNC):c.7221C>T (p.Asp2407=) rs3816885 0.15729
NM_001458.5(FLNC):c.4431G>A (p.Leu1477=) rs2291568 0.15512
NM_001458.5(FLNC):c.1032C>T (p.Val344=) rs2291562 0.12206
NM_001458.5(FLNC):c.1458C>A (p.Pro486=) rs2291563 0.11830
NM_001458.5(FLNC):c.720T>C (p.Ile240=) rs2291560 0.11080
NM_001458.5(FLNC):c.795T>C (p.Gly265=) rs2291561 0.10971
NM_001458.5(FLNC):c.147C>T (p.His49=) rs3734972 0.09267
NM_001458.5(FLNC):c.4056C>T (p.Arg1352=) rs75770585 0.08775
NM_001458.5(FLNC):c.850+18G>A rs55907818 0.08058
NM_001458.5(FLNC):c.3624G>A (p.Ala1208=) rs35281128 0.06868
NM_001458.5(FLNC):c.4700G>A (p.Arg1567Gln) rs2291569 0.06258
NM_001458.5(FLNC):c.*1A>G rs114713626 0.05145
NM_001458.5(FLNC):c.3838C>T (p.Leu1280=) rs34180031 0.03419
NM_001458.5(FLNC):c.1614C>T (p.Tyr538=) rs76046880 0.02993
NM_001458.5(FLNC):c.2390-13C>T rs78086167 0.02800
NM_001458.5(FLNC):c.5669-12C>T rs79790270 0.02786
NM_001458.5(FLNC):c.6004+19G>A rs12530507 0.01231
NM_001458.5(FLNC):c.2266-14G>C rs75612085 0.01030
NM_001458.5(FLNC):c.2390-14C>T rs71581921 0.00843
NM_001458.5(FLNC):c.3721C>T (p.Arg1241Cys) rs146953558 0.00728
NM_001458.5(FLNC):c.6004+11G>A rs117653869 0.00719
NM_001458.5(FLNC):c.352+10G>A rs79489893 0.00639
NM_001458.5(FLNC):c.-12G>T rs199842696 0.00599
NM_001458.5(FLNC):c.1902G>A (p.Glu634=) rs12536635 0.00414
NM_001458.5(FLNC):c.1549+15C>A rs181134489 0.00403
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.4928-7T>C rs201957008 0.00286
NM_001458.5(FLNC):c.7780+10A>G rs201149834 0.00281
NM_001458.5(FLNC):c.2889G>A (p.Pro963=) rs191892345 0.00212
NM_001458.5(FLNC):c.2507C>A (p.Pro836Gln) rs199652368 0.00207
NM_001458.5(FLNC):c.2390-9T>C rs368068407 0.00168
NM_001458.5(FLNC):c.6714C>T (p.Thr2238=) rs10268251 0.00143
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.597C>T (p.Ala199=) rs143942649 0.00124
NM_001458.5(FLNC):c.4947C>T (p.Gly1649=) rs201069454 0.00119
NM_001458.5(FLNC):c.4022G>A (p.Arg1341Gln) rs149641783 0.00068
NM_001458.5(FLNC):c.3621C>T (p.Asn1207=) rs117864464 0.00063
NM_001458.5(FLNC):c.5592C>T (p.Ala1864=) rs117517372 0.00048

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