ClinVar Miner

List of variants in gene FLNC reported as uncertain significance by CeGaT Praxis fuer Humangenetik Tuebingen

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Gene type:
ClinVar version:
Total variants: 44
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HGVS dbSNP
NM_001458.4(FLNC):c.1001G>A (p.Arg334His) rs779347920
NM_001458.4(FLNC):c.1082G>A (p.Arg361His) rs752888774
NM_001458.4(FLNC):c.1102G>A (p.Val368Met) rs781718076
NM_001458.4(FLNC):c.1142G>A (p.Arg381His) rs776469396
NM_001458.4(FLNC):c.1365G>A (p.Ala455=) rs377345122
NM_001458.4(FLNC):c.1568T>C (p.Val523Ala) rs182845462
NM_001458.4(FLNC):c.1632G>A (p.Lys544=) rs566538377
NM_001458.4(FLNC):c.1657G>A (p.Gly553Ser) rs201572079
NM_001458.4(FLNC):c.2068T>C (p.Phe690Leu) rs200943714
NM_001458.4(FLNC):c.2272G>A (p.Val758Met) rs371418145
NM_001458.4(FLNC):c.2293G>A (p.Glu765Lys) rs373798394
NM_001458.4(FLNC):c.2438C>T (p.Ala813Val) rs1585157948
NM_001458.4(FLNC):c.2930-5C>T rs371599113
NM_001458.4(FLNC):c.294G>A (p.Glu98=) rs201839252
NM_001458.4(FLNC):c.3061G>T (p.Ala1021Ser)
NM_001458.4(FLNC):c.3242C>T (p.Ala1081Val) rs200169573
NM_001458.4(FLNC):c.3295G>A (p.Val1099Ile) rs759452636
NM_001458.4(FLNC):c.3458T>G (p.Phe1153Cys) rs138663492
NM_001458.4(FLNC):c.3475C>T (p.Arg1159Trp) rs760500171
NM_001458.4(FLNC):c.3476G>A (p.Arg1159Gln) rs141199483
NM_001458.4(FLNC):c.3793G>A (p.Val1265Ile) rs368102638
NM_001458.4(FLNC):c.3938G>A (p.Arg1313Gln) rs199804244
NM_001458.4(FLNC):c.3952G>T (p.Ala1318Ser) rs777939926
NM_001458.4(FLNC):c.4134G>A (p.Ala1378=) rs200942470
NM_001458.4(FLNC):c.4296G>A (p.Pro1432=) rs370827536
NM_001458.4(FLNC):c.4420C>T (p.Arg1474Trp) rs372454458
NM_001458.4(FLNC):c.4880G>A (p.Arg1627His) rs751592993
NM_001458.4(FLNC):c.4991C>T (p.Thr1664Met) rs780829334
NM_001458.4(FLNC):c.5071G>A (p.Asp1691Asn) rs777061037
NM_001458.4(FLNC):c.5284C>T (p.Arg1762Cys) rs201926772
NM_001458.4(FLNC):c.5398+6G>C rs746415033
NM_001458.4(FLNC):c.5413C>T (p.Pro1805Ser)
NM_001458.4(FLNC):c.5448C>A (p.Asp1816Glu) rs775336546
NM_001458.4(FLNC):c.5954C>T (p.Ser1985Leu) rs200415625
NM_001458.4(FLNC):c.5955G>A (p.Ser1985=) rs777895128
NM_001458.4(FLNC):c.6471C>T (p.Asn2157=) rs764877771
NM_001458.4(FLNC):c.6817G>A (p.Ala2273Thr) rs372251350
NM_001458.4(FLNC):c.7136-4C>T
NM_001458.4(FLNC):c.7289C>T (p.Ala2430Val) rs200516164
NM_001458.4(FLNC):c.7291G>C (p.Val2431Leu) rs572952653
NM_001458.4(FLNC):c.7618G>C (p.Val2540Leu) rs746349463
NM_001458.4(FLNC):c.7847A>G (p.Lys2616Arg) rs1585172975
NM_001458.4(FLNC):c.851-4G>A rs372747855
NM_001458.4(FLNC):c.904A>G (p.Thr302Ala) rs1410531577

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