ClinVar Miner

List of variants in gene FLNC reported as benign by Athena Diagnostics Inc

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Gene type:
ClinVar version:
Total variants: 33
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HGVS dbSNP gnomAD frequency
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.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.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.8121T>C (p.Ile2707=) rs28437296 0.01520
NM_001458.5(FLNC):c.8118C>T (p.Leu2706=) rs28379666 0.01465
NM_001458.5(FLNC):c.4302C>T (p.Arg1434=) rs114697352 0.00988
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.7091G>A (p.Arg2364His) rs201672146 0.00173
NM_001458.5(FLNC):c.2390-9T>C rs368068407 0.00168
NM_001458.5(FLNC):c.5644A>G (p.Ile1882Val) rs184018403 0.00160
NM_001458.5(FLNC):c.597C>T (p.Ala199=) rs143942649 0.00124
NM_001458.5(FLNC):c.6175G>A (p.Val2059Met) rs201333104 0.00076
NM_001458.5(FLNC):c.5764G>A (p.Ala1922Thr) rs202128602 0.00040
NM_001458.5(FLNC):c.6120C>T (p.Asp2040=) rs116974302 0.00039
NM_001458.5(FLNC):c.2382G>A (p.Ala794=) rs536456072 0.00006
NM_001458.5(FLNC):c.6114C>T (p.Ile2038=) rs559639511 0.00006
NM_001458.5(FLNC):c.4140C>T (p.Thr1380=) rs183668401 0.00004
NM_001458.5(FLNC):c.4425G>A (p.Ala1475=) rs371971762 0.00003
NM_001458.5(FLNC):c.5427G>C (p.Thr1809=) rs774600814

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