ClinVar Miner

List of variants in gene FLNC reported as uncertain significance for Cardiomyopathy

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Total variants: 46
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HGVS dbSNP gnomAD frequency
NM_001458.5(FLNC):c.5954C>T (p.Ser1985Leu) rs200415625 0.00031
NM_001458.5(FLNC):c.2068T>C (p.Phe690Leu) rs200943714 0.00023
NM_001458.5(FLNC):c.4127+9C>T rs368729011 0.00019
NM_001458.5(FLNC):c.1166G>A (p.Gly389Asp) rs763039506 0.00016
NM_001458.5(FLNC):c.3304C>T (p.Pro1102Ser) rs199707920 0.00015
NM_001458.5(FLNC):c.970-4A>G rs532143625 0.00015
NM_001458.5(FLNC):c.4951+7G>A rs370501464 0.00009
NM_001458.5(FLNC):c.1886G>A (p.Arg629Gln) rs765173966 0.00007
NM_001458.5(FLNC):c.3209C>T (p.Pro1070Leu) rs370391049 0.00005
NM_001458.5(FLNC):c.7111G>A (p.Val2371Ile) rs552252122 0.00005
NM_001458.5(FLNC):c.140A>G (p.Asn47Ser) rs770861991 0.00004
NM_001458.5(FLNC):c.2842G>A (p.Gly948Arg) rs768103657 0.00004
NM_001458.5(FLNC):c.547C>T (p.Arg183Cys) rs369221655 0.00004
NM_001458.5(FLNC):c.6052C>T (p.Arg2018Cys) rs1335627502 0.00004
NM_001458.5(FLNC):c.3133C>A (p.His1045Asn) rs201863231 0.00003
NM_001458.5(FLNC):c.3376C>G (p.Pro1126Ala) rs748785077 0.00003
NM_001458.5(FLNC):c.4420C>T (p.Arg1474Trp) rs372454458 0.00003
NM_001458.5(FLNC):c.4970G>A (p.Arg1657Gln) rs374294752 0.00003
NM_001458.5(FLNC):c.5540-6C>G rs201335006 0.00003
NM_001458.5(FLNC):c.925G>A (p.Glu309Lys) rs781212262 0.00003
NM_001458.5(FLNC):c.3295G>A (p.Val1099Ile) rs759452636 0.00002
NM_001458.5(FLNC):c.6773C>T (p.Ser2258Leu) rs762051422 0.00002
NM_001458.5(FLNC):c.1042C>T (p.His348Tyr) rs2128934341 0.00001
NM_001458.5(FLNC):c.1468C>T (p.Arg490Cys) rs1422233407 0.00001
NM_001458.5(FLNC):c.2121+4G>A rs372098008 0.00001
NM_001458.5(FLNC):c.3381C>T (p.Gly1127=) rs1052000080 0.00001
NM_001458.5(FLNC):c.5272C>T (p.Arg1758Trp) rs369187211 0.00001
NM_001458.5(FLNC):c.5765C>T (p.Ala1922Val) rs377206490 0.00001
NM_001458.5(FLNC):c.5828C>T (p.Thr1943Ile) rs376413798 0.00001
NM_001458.5(FLNC):c.7072G>A (p.Glu2358Lys) rs370769744 0.00001
NM_001458.5(FLNC):c.7280C>T (p.Ala2427Val) rs1343869103 0.00001
NM_001458.5(FLNC):c.179T>C (p.Leu60Pro) rs1807855891
NM_001458.5(FLNC):c.2084G>A (p.Arg695His) rs766592492
NM_001458.5(FLNC):c.2168A>G (p.Asp723Gly) rs1808365040
NM_001458.5(FLNC):c.244A>C (p.Met82Leu) rs2128932209
NM_001458.5(FLNC):c.2641+5G>T rs2128935942
NM_001458.5(FLNC):c.271A>G (p.Asn91Asp) rs2536605615
NM_001458.5(FLNC):c.301_302delinsAA (p.Ser101Asn) rs2128932233
NM_001458.5(FLNC):c.3689A>G (p.Tyr1230Cys) rs863225116
NM_001458.5(FLNC):c.539A>G (p.Asn180Ser) rs2128933682
NM_001458.5(FLNC):c.6129G>C (p.Lys2043Asn) rs775167656
NM_001458.5(FLNC):c.7319T>C (p.Ile2440Thr) rs764628080
NM_001458.5(FLNC):c.7990+10G>A rs745488329
NM_001458.5(FLNC):c.850+4T>G rs368602593
NM_001458.5(FLNC):c.851-4G>A rs372747855
NM_001458.5(FLNC):c.883C>G (p.Pro295Ala) rs2536618934

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