ClinVar Miner

List of variants in gene FLNC studied for Myofibrillar myopathy, filamin C-related

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Total variants: 9
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HGVS dbSNP
NM_001458.4(FLNC):c.1081C>T (p.Arg361Cys) rs200206944
NM_001458.4(FLNC):c.1199T>C (p.Ile400Thr) rs1562992604
NM_001458.4(FLNC):c.2789_2800del (p.Val930_Thr933del) rs1562995872
NM_001458.4(FLNC):c.4480C>T (p.Arg1494Trp) rs779079128
NM_001458.4(FLNC):c.4566G>T (p.Gln1522His) rs559667295
NM_001458.4(FLNC):c.6175G>A (p.Val2059Met) rs201333104
NM_001458.4(FLNC):c.7947C>T (p.Phe2649=) rs368849358
NM_001458.4(FLNC):c.8130G>A (p.Trp2710Ter) rs121909518
NM_001458.4(FLNC):c.904A>G (p.Thr302Ala) rs1410531577

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