ClinVar Miner

List of variants in gene FLNC reported as benign for Cardiomyopathy

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Total variants: 43
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HGVS dbSNP gnomAD frequency
NM_001458.5(FLNC):c.*1A>G rs114713626 0.05145
NM_001458.5(FLNC):c.1374C>T (p.Pro458=) rs115140972 0.01421
NM_001458.5(FLNC):c.4302C>T (p.Arg1434=) rs114697352 0.00920
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.3852C>T (p.Gly1284=) rs111337293 0.00689
NM_001458.5(FLNC):c.5578C>T (p.Arg1860Cys) rs181067717 0.00525
NM_001458.5(FLNC):c.1902G>A (p.Glu634=) rs12536635 0.00414
NM_001458.5(FLNC):c.7780+10A>G rs201149834 0.00403
NM_001458.5(FLNC):c.6005-9T>C rs118124743 0.00344
NM_001458.5(FLNC):c.6459C>T (p.Thr2153=) rs113618587 0.00343
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.1425C>T (p.Asn475=) rs143610360 0.00277
NM_001458.5(FLNC):c.5592C>T (p.Ala1864=) rs117517372 0.00263
NM_001458.5(FLNC):c.2507C>A (p.Pro836Gln) rs199652368 0.00192
NM_001458.5(FLNC):c.561C>T (p.Asp187=) rs149474376 0.00177
NM_001458.5(FLNC):c.2390-9T>C rs368068407 0.00173
NM_001458.5(FLNC):c.7091G>A (p.Arg2364His) rs201672146 0.00173
NM_001458.5(FLNC):c.8049C>T (p.Tyr2683=) rs183104951 0.00163
NM_001458.5(FLNC):c.5644A>G (p.Ile1882Val) rs184018403 0.00151
NM_001458.5(FLNC):c.6714C>T (p.Thr2238=) rs10268251 0.00143
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.4947C>T (p.Gly1649=) rs201069454 0.00127
NM_001458.5(FLNC):c.597C>T (p.Ala199=) rs143942649 0.00125
NM_001458.5(FLNC):c.7862G>A (p.Arg2621Gln) rs201636548 0.00123
NM_001458.5(FLNC):c.6309C>T (p.Thr2103=) rs376992044 0.00111
NM_001458.5(FLNC):c.5766G>A (p.Ala1922=) rs58914363 0.00102
NM_001458.5(FLNC):c.3621C>T (p.Asn1207=) rs117864464 0.00094
NM_001458.5(FLNC):c.1600G>A (p.Glu534Lys) rs201905890 0.00079
NM_001458.5(FLNC):c.7990+9C>T rs566679569 0.00077
NM_001458.5(FLNC):c.6175G>A (p.Val2059Met) rs201333104 0.00076
NM_001458.5(FLNC):c.4022G>A (p.Arg1341Gln) rs149641783 0.00072
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.7545C>T (p.Leu2515=) rs369791058 0.00060
NM_001458.5(FLNC):c.2390-8C>G rs146063718 0.00057
NM_001458.5(FLNC):c.3757G>A (p.Val1253Ile) rs117366477 0.00051
NM_001458.5(FLNC):c.5764G>A (p.Ala1922Thr) rs202128602 0.00050
NM_001458.5(FLNC):c.2841C>T (p.Gly947=) rs547060988 0.00017
NM_001458.5(FLNC):c.2392G>A (p.Asp798Asn) rs778594252 0.00003
NM_001458.5(FLNC):c.5763_5764inv (p.Ala1922Thr)

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