ClinVar Miner

List of variants in gene FLNC reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 53
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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.4097A>G (p.Asn1366Ser) rs185746835 0.00026
NM_001458.5(FLNC):c.2296C>T (p.Arg766Trp) rs200215340 0.00019
NM_001458.5(FLNC):c.4763C>G (p.Ala1588Gly) rs148545460 0.00016
NM_001458.5(FLNC):c.3242C>T (p.Ala1081Val) rs200169573 0.00014
NM_001458.5(FLNC):c.1568T>C (p.Val523Ala) rs182845462 0.00012
NM_001458.5(FLNC):c.1102G>A (p.Val368Met) rs781718076 0.00010
NM_001458.5(FLNC):c.7289C>T (p.Ala2430Val) rs200516164 0.00010
NM_001458.5(FLNC):c.1142G>A (p.Arg381His) rs776469396 0.00007
NM_001458.5(FLNC):c.3458T>G (p.Phe1153Cys) rs138663492 0.00006
NM_001458.5(FLNC):c.4991C>T (p.Thr1664Met) rs780829334 0.00006
NM_001458.5(FLNC):c.5071G>A (p.Asp1691Asn) rs777061037 0.00006
NM_001458.5(FLNC):c.7090C>T (p.Arg2364Cys) rs374973240 0.00006
NM_001458.5(FLNC):c.2272G>A (p.Val758Met) rs371418145 0.00005
NM_001458.5(FLNC):c.1082G>A (p.Arg361His) rs752888774 0.00004
NM_001458.5(FLNC):c.140A>G (p.Asn47Ser) rs770861991 0.00004
NM_001458.5(FLNC):c.4880G>A (p.Arg1627His) rs751592993 0.00004
NM_001458.5(FLNC):c.5945G>A (p.Arg1982His) rs375046429 0.00004
NM_001458.5(FLNC):c.7618G>C (p.Val2540Leu) rs746349463 0.00004
NM_001458.5(FLNC):c.2930-5C>T rs371599113 0.00003
NM_001458.5(FLNC):c.4420C>T (p.Arg1474Trp) rs372454458 0.00003
NM_001458.5(FLNC):c.6471C>T (p.Asn2157=) rs764877771 0.00003
NM_001458.5(FLNC):c.3295G>A (p.Val1099Ile) rs759452636 0.00002
NM_001458.5(FLNC):c.1898C>T (p.Thr633Met) rs1187790496 0.00001
NM_001458.5(FLNC):c.2065G>A (p.Glu689Lys) rs1446694237 0.00001
NM_001458.5(FLNC):c.2293G>A (p.Glu765Lys) rs373798394 0.00001
NM_001458.5(FLNC):c.2767A>C (p.Asn923His) rs1420123492 0.00001
NM_001458.5(FLNC):c.3067G>C (p.Ala1023Pro) rs376107866 0.00001
NM_001458.5(FLNC):c.3137C>T (p.Pro1046Leu) rs768820218 0.00001
NM_001458.5(FLNC):c.3428C>T (p.Ser1143Leu) rs756192123 0.00001
NM_001458.5(FLNC):c.3475C>T (p.Arg1159Trp) rs760500171 0.00001
NM_001458.5(FLNC):c.3793G>A (p.Val1265Ile) rs368102638 0.00001
NM_001458.5(FLNC):c.470G>A (p.Arg157His) rs752919962 0.00001
NM_001458.5(FLNC):c.5955G>A (p.Ser1985=) rs777895128 0.00001
NM_001458.5(FLNC):c.6388G>A (p.Gly2130Ser) rs375778608 0.00001
NM_001458.5(FLNC):c.7324G>T (p.Ala2442Ser) rs1160639957 0.00001
NM_001458.5(FLNC):c.7604C>T (p.Ser2535Leu) rs201895675 0.00001
NM_001458.5(FLNC):c.1693G>A (p.Val565Met)
NM_001458.5(FLNC):c.2084G>C (p.Arg695Pro) rs766592492
NM_001458.5(FLNC):c.2438C>T (p.Ala813Val) rs1585157948
NM_001458.5(FLNC):c.3202T>C (p.Tyr1068His)
NM_001458.5(FLNC):c.3261C>T (p.Thr1087=) rs2128936369
NM_001458.5(FLNC):c.4373G>C (p.Arg1458Thr)
NM_001458.5(FLNC):c.5413C>T (p.Pro1805Ser) rs1808775264
NM_001458.5(FLNC):c.5792G>T (p.Arg1931Leu) rs780685346
NM_001458.5(FLNC):c.6791C>T (p.Ala2264Val) rs2128939470
NM_001458.5(FLNC):c.6826G>A (p.Val2276Met) rs1207179287
NM_001458.5(FLNC):c.7187C>T (p.Pro2396Leu)
NM_001458.5(FLNC):c.719T>C (p.Ile240Thr) rs778626535
NM_001458.5(FLNC):c.7244G>C (p.Ser2415Thr)
NM_001458.5(FLNC):c.7291G>C (p.Val2431Leu) rs572952653
NM_001458.5(FLNC):c.7339C>T (p.Pro2447Ser)
NM_001458.5(FLNC):c.904A>G (p.Thr302Ala) rs1410531577

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