ClinVar Miner

List of variants in gene FLNC reported as likely benign for Cardiomyopathy

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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_001458.5(FLNC):c.7947C>T (p.Phe2649=) rs368849358 0.00083
NM_001458.5(FLNC):c.1474A>G (p.Lys492Glu) rs118056738 0.00029
NM_001458.5(FLNC):c.5374G>A (p.Ala1792Thr) rs201348102 0.00028
NM_001458.5(FLNC):c.5367C>T (p.Ile1789=) rs377214486 0.00026
NM_001458.5(FLNC):c.1434C>T (p.Arg478=) rs201810745 0.00023
NM_001458.5(FLNC):c.6387C>T (p.Thr2129=) rs200182180 0.00017
NM_001458.5(FLNC):c.3153G>A (p.Pro1051=) rs373694043 0.00014
NM_001458.5(FLNC):c.600C>T (p.Pro200=) rs202105410 0.00013
NM_001458.5(FLNC):c.1568T>C (p.Val523Ala) rs182845462 0.00012
NM_001458.5(FLNC):c.5445C>T (p.Thr1815=) rs758995789 0.00010
NM_001458.5(FLNC):c.7256C>T (p.Thr2419Met) rs199768217 0.00007
NM_001458.5(FLNC):c.6864C>T (p.Val2288=) rs761269440 0.00005
NM_001458.5(FLNC):c.2907C>A (p.Ile969=) rs368059457 0.00004
NM_001458.5(FLNC):c.6048C>T (p.Ser2016=) rs369991887 0.00004
NM_001458.5(FLNC):c.6226C>T (p.Leu2076=) rs756921919 0.00004
NM_001458.5(FLNC):c.8145C>T (p.Val2715=) rs746842532 0.00004
NM_001458.5(FLNC):c.366C>T (p.Ile122=) rs369120591 0.00003
NM_001458.5(FLNC):c.5745C>T (p.Thr1915=) rs369449907 0.00002
NM_001458.5(FLNC):c.1470C>T (p.Arg490=) rs765212618 0.00001
NM_001458.5(FLNC):c.1797C>T (p.Thr599=) rs773793586 0.00001
NM_001458.5(FLNC):c.3600C>T (p.Ala1200=) rs777931249 0.00001
NM_001458.5(FLNC):c.4728C>T (p.Val1576=) rs1222823077 0.00001
NM_001458.5(FLNC):c.129G>A (p.Thr43=) rs2536605149
NM_001458.5(FLNC):c.3489G>C (p.Pro1163=) rs369853278

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