ClinVar Miner

List of variants in gene FLNC reported as uncertain significance for Hypertrophic cardiomyopathy 26

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Total variants: 86
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HGVS dbSNP gnomAD frequency
NM_001458.5(FLNC):c.5284C>T (p.Arg1762Cys) rs201926772 0.00026
NM_001458.5(FLNC):c.2635C>T (p.Arg879Cys) rs374983276 0.00021
NM_001458.5(FLNC):c.5296T>C (p.Trp1766Arg) rs751650734 0.00015
NM_001458.5(FLNC):c.3242C>T (p.Ala1081Val) rs200169573 0.00014
NM_001458.5(FLNC):c.2297G>A (p.Arg766Gln) rs369935650 0.00013
NM_001458.5(FLNC):c.1102G>A (p.Val368Met) rs781718076 0.00010
NM_001458.5(FLNC):c.3623C>T (p.Ala1208Val) rs202184162 0.00009
NM_001458.5(FLNC):c.5888C>T (p.Thr1963Met) rs772580545 0.00009
NM_001458.5(FLNC):c.4991C>T (p.Thr1664Met) rs780829334 0.00006
NM_001458.5(FLNC):c.3790G>A (p.Gly1264Ser) rs201335143 0.00005
NM_001458.5(FLNC):c.517G>T (p.Val173Leu) rs376235207 0.00005
NM_001458.5(FLNC):c.6052C>T (p.Arg2018Cys) rs1335627502 0.00005
NM_001458.5(FLNC):c.1243G>A (p.Val415Met) rs369182765 0.00004
NM_001458.5(FLNC):c.2164G>A (p.Gly722Ser) rs762248114 0.00004
NM_001458.5(FLNC):c.7256C>T (p.Thr2419Met) rs199768217 0.00004
NM_001458.5(FLNC):c.6595G>A (p.Gly2199Arg) rs368977589 0.00003
NM_001458.5(FLNC):c.6779A>G (p.Lys2260Arg) rs751019991 0.00003
NM_001458.5(FLNC):c.1309C>T (p.Arg437Cys) rs374847180 0.00002
NM_001458.5(FLNC):c.5156G>A (p.Arg1719His) rs746777092 0.00002
NM_001458.5(FLNC):c.6041T>C (p.Val2014Ala) rs765064363 0.00002
NM_001458.5(FLNC):c.2081C>T (p.Ala694Val) rs1315847764 0.00001
NM_001458.5(FLNC):c.2278G>A (p.Glu760Lys) rs772574007 0.00001
NM_001458.5(FLNC):c.2599G>A (p.Ala867Thr) rs772127988 0.00001
NM_001458.5(FLNC):c.2811+4C>T rs146715204 0.00001
NM_001458.5(FLNC):c.2811+5G>A rs781538211 0.00001
NM_001458.5(FLNC):c.3475C>T (p.Arg1159Trp) rs760500171 0.00001
NM_001458.5(FLNC):c.352+3C>T rs750255204 0.00001
NM_001458.5(FLNC):c.4117G>A (p.Val1373Met) rs1159994552 0.00001
NM_001458.5(FLNC):c.4471G>A (p.Val1491Met) rs186904046 0.00001
NM_001458.5(FLNC):c.470G>A (p.Arg157His) rs752919962 0.00001
NM_001458.5(FLNC):c.5051C>T (p.Thr1684Met) rs1294213097 0.00001
NM_001458.5(FLNC):c.5191C>T (p.His1731Tyr) rs1255727604 0.00001
NM_001458.5(FLNC):c.5293C>T (p.His1765Tyr) rs1263073740 0.00001
NM_001458.5(FLNC):c.5828C>T (p.Thr1943Ile) rs376413798 0.00001
NM_001458.5(FLNC):c.6233T>C (p.Ile2078Thr) rs780762913 0.00001
NM_001458.5(FLNC):c.7198C>G (p.Pro2400Ala) rs1390223951 0.00001
NM_001458.5(FLNC):c.7201G>A (p.Val2401Met) rs868744958 0.00001
NM_001458.5(FLNC):c.7226G>A (p.Arg2409His) rs767279710 0.00001
NM_001458.5(FLNC):c.7795G>A (p.Gly2599Arg) rs1389561527 0.00001
NM_001458.5(FLNC):c.1372C>G (p.Pro458Ala)
NM_001458.5(FLNC):c.1549+3_1549+4insT
NM_001458.5(FLNC):c.1610A>G (p.Tyr537Cys)
NM_001458.5(FLNC):c.2092G>A (p.Gly698Ser) rs1461903090
NM_001458.5(FLNC):c.2212C>A (p.His738Asn)
NM_001458.5(FLNC):c.2485T>G (p.Phe829Val) rs758056957
NM_001458.5(FLNC):c.2554A>T (p.Ile852Phe)
NM_001458.5(FLNC):c.308C>A (p.Ala103Asp)
NM_001458.5(FLNC):c.3527T>G (p.Phe1176Cys)
NM_001458.5(FLNC):c.3548C>T (p.Ala1183Val)
NM_001458.5(FLNC):c.3694G>A (p.Gly1232Arg) rs754533053
NM_001458.5(FLNC):c.3799C>G (p.Arg1267Gly) rs371483562
NM_001458.5(FLNC):c.3967G>T (p.Val1323Leu)
NM_001458.5(FLNC):c.4040G>T (p.Gly1347Val)
NM_001458.5(FLNC):c.4112T>G (p.Phe1371Cys)
NM_001458.5(FLNC):c.4345T>C (p.Ser1449Pro)
NM_001458.5(FLNC):c.4425G>T (p.Ala1475=)
NM_001458.5(FLNC):c.4566G>T (p.Gln1522His) rs559667295
NM_001458.5(FLNC):c.4588A>C (p.Lys1530Gln)
NM_001458.5(FLNC):c.4966C>G (p.Pro1656Ala)
NM_001458.5(FLNC):c.4969C>G (p.Arg1657Gly) rs1563000044
NM_001458.5(FLNC):c.5194G>A (p.Val1732Met) rs374848954
NM_001458.5(FLNC):c.5287C>A (p.Pro1763Thr)
NM_001458.5(FLNC):c.5501A>C (p.His1834Pro)
NM_001458.5(FLNC):c.5969_5983del (p.Pro1990_Lys1994del)
NM_001458.5(FLNC):c.6149_6150dup (p.Leu2051fs)
NM_001458.5(FLNC):c.6208+8C>G
NM_001458.5(FLNC):c.6239G>A (p.Gly2080Asp) rs2128939083
NM_001458.5(FLNC):c.6429G>T (p.Gln2143His)
NM_001458.5(FLNC):c.6451G>C (p.Gly2151Arg)
NM_001458.5(FLNC):c.6589C>T (p.Arg2197Trp) rs1808943188
NM_001458.5(FLNC):c.6826G>A (p.Val2276Met) rs1207179287
NM_001458.5(FLNC):c.699+4C>T
NM_001458.5(FLNC):c.7087G>A (p.Asp2363Asn) rs1554401490
NM_001458.5(FLNC):c.7251+15T>G rs1585170629
NM_001458.5(FLNC):c.733G>A (p.Val245Met)
NM_001458.5(FLNC):c.7414G>A (p.Glu2472Lys) rs948675422
NM_001458.5(FLNC):c.7511A>G (p.Asp2504Gly) rs1585171977
NM_001458.5(FLNC):c.7588A>T (p.Thr2530Ser) rs760694025
NM_001458.5(FLNC):c.7627G>C (p.Asp2543His)
NM_001458.5(FLNC):c.7745A>G (p.His2582Arg)
NM_001458.5(FLNC):c.7780+1G>T
NM_001458.5(FLNC):c.7814A>G (p.Glu2605Gly)
NM_001458.5(FLNC):c.790C>G (p.Pro264Ala) rs1808143178
NM_001458.5(FLNC):c.791C>G (p.Pro264Arg)
NM_001458.5(FLNC):c.7921C>T (p.Arg2641Trp) rs750629528
NM_001458.5(FLNC):c.904A>G (p.Thr302Ala) rs1410531577

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