ClinVar Miner

List of variants in gene FLNC reported by Center for Human Genetics, University of Leuven

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Gene type:
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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_001458.5(FLNC):c.5296T>C (p.Trp1766Arg) rs751650734 0.00015
NM_001458.5(FLNC):c.3499C>T (p.Arg1167Cys) rs766439553 0.00002
NM_001458.5(FLNC):c.1571A>G (p.Lys524Arg) rs753176255
NM_001458.5(FLNC):c.2405del (p.Gly802fs)
NM_001458.5(FLNC):c.3908dup (p.Tyr1303Ter)
NM_001458.5(FLNC):c.3943C>T (p.Gln1315Ter)
NM_001458.5(FLNC):c.4021C>T (p.Arg1341Ter) rs1562998062
NM_001458.5(FLNC):c.404G>A (p.Trp135Ter)
NM_001458.5(FLNC):c.4346C>G (p.Ser1449Ter)
NM_001458.5(FLNC):c.4581-2A>G
NM_001458.5(FLNC):c.4584dup (p.Phe1529fs)
NM_001458.5(FLNC):c.4708G>T (p.Gly1570Cys) rs1562999563
NM_001458.5(FLNC):c.5142C>A (p.Tyr1714Ter)
NM_001458.5(FLNC):c.5503C>T (p.Gln1835Ter)
NM_001458.5(FLNC):c.617G>A (p.Trp206Ter)
NM_001458.5(FLNC):c.6742C>T (p.Gln2248Ter)
NM_001458.5(FLNC):c.6907C>T (p.Gln2303Ter)
NM_001458.5(FLNC):c.6947A>G (p.Lys2316Arg) rs1563003855
NM_001458.5(FLNC):c.7316_7317del (p.Val2439fs)
NM_001458.5(FLNC):c.7427A>G (p.His2476Arg) rs1563005164
NM_001458.5(FLNC):c.7581del (p.Ile2527fs)

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