ClinVar Miner

List of variants in gene FLNA reported as pathogenic for congenital nervous system disorder

Included ClinVar conditions (840):
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Gene type:
ClinVar version:
Total variants: 110
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HGVS dbSNP gnomAD frequency
NM_001110556.2(FLNA):c.1966C>T (p.Leu656Phe) rs137853311 0.00001
NM_001110556.2(FLNA):c.3557C>T (p.Ser1186Leu) rs137853312 0.00001
NM_001110556.2(FLNA):c.4726G>A (p.Gly1576Arg) rs797045044 0.00001
NC_000023.10:g.(?_153576900)_(153599729_?)del
NC_000023.10:g.(?_153592874)_(153593874_?)del
NC_000023.10:g.(?_153595748)_(153596947_?)del
NM_001110556.2(FLNA):c.1034G>A (p.Trp345Ter) rs2067763458
NM_001110556.2(FLNA):c.1062_1063del (p.His354fs)
NM_001110556.2(FLNA):c.1065G>A (p.Lys355=) rs1557179325
NM_001110556.2(FLNA):c.1087C>T (p.Gln363Ter) rs2067761804
NM_001110556.2(FLNA):c.1112_1113dup (p.Val372fs) rs2148118072
NM_001110556.2(FLNA):c.1119C>A (p.Tyr373Ter)
NM_001110556.2(FLNA):c.1133_1134del (p.Gln378fs) rs1603362871
NM_001110556.2(FLNA):c.1159C>T (p.Gln387Ter) rs2067760741
NM_001110556.2(FLNA):c.116C>G (p.Ala39Gly) rs137853313
NM_001110556.2(FLNA):c.122G>A (p.Trp41Ter)
NM_001110556.2(FLNA):c.123G>A (p.Trp41Ter)
NM_001110556.2(FLNA):c.138_139dup (p.Asn47fs) rs2067802877
NM_001110556.2(FLNA):c.1430-1G>T rs786205177
NM_001110556.2(FLNA):c.145_146del (p.Phe49fs)
NM_001110556.2(FLNA):c.1525_1528del (p.Gly509fs)
NM_001110556.2(FLNA):c.1759G>T (p.Glu587Ter) rs1447594194
NM_001110556.2(FLNA):c.1829-2A>G rs786205183
NM_001110556.2(FLNA):c.1907G>A (p.Trp636Ter) rs2148116288
NM_001110556.2(FLNA):c.1923C>T (p.Gly641=) rs80338841
NM_001110556.2(FLNA):c.1924G>T (p.Glu642Ter) rs782178831
NM_001110556.2(FLNA):c.1932_1938del (p.Val645fs) rs2067741257
NM_001110556.2(FLNA):c.2026_2029dup (p.Ala677fs)
NM_001110556.2(FLNA):c.2190_2193del (p.Tyr731fs) rs863223630
NM_001110556.2(FLNA):c.2191_2192insGT (p.Tyr731fs) rs2148115776
NM_001110556.2(FLNA):c.2280+389T>A rs1557178535
NM_001110556.2(FLNA):c.2283dup (p.Asn762fs) rs2067723474
NM_001110556.2(FLNA):c.2452del (p.Ala818fs) rs1603361851
NM_001110556.2(FLNA):c.245A>T (p.Glu82Val) rs28935169
NM_001110556.2(FLNA):c.2527dup (p.Ala843fs) rs782312089
NM_001110556.2(FLNA):c.2565+1G>A rs786205186
NM_001110556.2(FLNA):c.2565+1G>C rs786205186
NM_001110556.2(FLNA):c.259_260insG (p.Lys87fs)
NM_001110556.2(FLNA):c.2751_2752dup (p.Asp918fs) rs2148114051
NM_001110556.2(FLNA):c.2752dup (p.Asp918fs)
NM_001110556.2(FLNA):c.2761C>T (p.Arg921Ter) rs398123614
NM_001110556.2(FLNA):c.2762del (p.Arg921fs) rs1569551736
NM_001110556.2(FLNA):c.287_291del (p.Arg96fs) rs863223297
NM_001110556.2(FLNA):c.2941G>T (p.Glu981Ter)
NM_001110556.2(FLNA):c.2947dup (p.Val983fs) rs2148113628
NM_001110556.2(FLNA):c.2963_2964del (p.Asp988fs) rs2148113604
NM_001110556.2(FLNA):c.2965C>T (p.Gln989Ter) rs1557178045
NM_001110556.2(FLNA):c.3296_3304delinsTCGG (p.Gly1099fs) rs1603361195
NM_001110556.2(FLNA):c.334_335insGAGAACGTGTCGG (p.Glu112fs) rs2148121859
NM_001110556.2(FLNA):c.3529G>T (p.Glu1177Ter) rs1557177738
NM_001110556.2(FLNA):c.3596C>T (p.Ser1199Leu) rs28935473
NM_001110556.2(FLNA):c.3668C>T (p.Pro1223Leu) rs1060500716
NM_001110556.2(FLNA):c.373+1G>A rs863223296
NM_001110556.2(FLNA):c.3742C>T (p.Gln1248Ter) rs2067693064
NM_001110556.2(FLNA):c.3775C>T (p.Gln1259Ter) rs1557177663
NM_001110556.2(FLNA):c.3814del (p.Arg1272fs) rs1557177636
NM_001110556.2(FLNA):c.383C>T (p.Ala128Val) rs137853315
NM_001110556.2(FLNA):c.3865G>T (p.Gly1289Ter) rs1557177623
NM_001110556.2(FLNA):c.4138dup (p.Thr1380fs) rs2148111417
NM_001110556.2(FLNA):c.4147del (p.Ala1383fs) rs863223299
NM_001110556.2(FLNA):c.4281del (p.Tyr1428fs) rs2148111202
NM_001110556.2(FLNA):c.4446_4447dup (p.Leu1483fs) rs398123620
NM_001110556.2(FLNA):c.4450C>T (p.Gln1484Ter) rs1057516198
NM_001110556.2(FLNA):c.4543C>T (p.Arg1515Ter) rs186214592
NM_001110556.2(FLNA):c.4824C>A (p.Tyr1608Ter) rs781789823
NM_001110556.2(FLNA):c.4840_4852del (p.Gly1614fs) rs1557177086
NM_001110556.2(FLNA):c.5084_5085del (p.Glu1695fs)
NM_001110556.2(FLNA):c.5146del (p.Gln1716fs) rs1557176615
NM_001110556.2(FLNA):c.5160C>G (p.Tyr1720Ter)
NM_001110556.2(FLNA):c.5217G>A (p.Thr1739=) rs387907371
NM_001110556.2(FLNA):c.5363_5369del (p.Leu1788fs)
NM_001110556.2(FLNA):c.544C>T (p.Gln182Ter) rs137853310
NM_001110556.2(FLNA):c.5643del (p.Asn1881fs) rs1569551502
NM_001110556.2(FLNA):c.5760C>A (p.Cys1920Ter) rs1359141531
NM_001110556.2(FLNA):c.577C>T (p.Gln193Ter) rs2148119354
NM_001110556.2(FLNA):c.5796del (p.Asp1931_Tyr1932insTer) rs2067639563
NM_001110556.2(FLNA):c.586C>T (p.Arg196Trp) rs137853317
NM_001110556.2(FLNA):c.5879dup (p.Met1960fs) rs1603359464
NM_001110556.2(FLNA):c.5988_5989del (p.Cys1997fs) rs1060500718
NM_001110556.2(FLNA):c.620C>T (p.Pro207Leu) rs28935469
NM_001110556.2(FLNA):c.623-3C>G rs398123622
NM_001110556.2(FLNA):c.6318C>G (p.Tyr2106Ter) rs2148104651
NM_001110556.2(FLNA):c.6329_6330del (p.Glu2110fs) rs2148104615
NM_001110556.2(FLNA):c.6355_6356del (p.Lys2119fs) rs786205201
NM_001110556.2(FLNA):c.6395_6396del (p.Val2132fs)
NM_001110556.2(FLNA):c.6496del (p.Ile2166fs)
NM_001110556.2(FLNA):c.656del (p.Ser219fs) rs2148119182
NM_001110556.2(FLNA):c.6586del (p.His2196fs) rs2067626336
NM_001110556.2(FLNA):c.6635_6638del (p.Val2212fs) rs786205178
NM_001110556.2(FLNA):c.6677dup (p.Gln2227fs) rs2148103917
NM_001110556.2(FLNA):c.6724C>T (p.Arg2242Ter) rs1060500717
NM_001110556.2(FLNA):c.676C>T (p.Arg226Ter) rs1569551861
NM_001110556.2(FLNA):c.6770_6774del (p.Ala2257fs)
NM_001110556.2(FLNA):c.6898C>T (p.Gln2300Ter) rs2148103458
NM_001110556.2(FLNA):c.6915C>G (p.Tyr2305Ter) rs781910090
NM_001110556.2(FLNA):c.7005_7008del (p.Thr2336fs) rs2148103004
NM_001110556.2(FLNA):c.7021C>T (p.Gln2341Ter) rs1603358919
NM_001110556.2(FLNA):c.720+2T>C rs863223295
NM_001110556.2(FLNA):c.7202del (p.Leu2401fs)
NM_001110556.2(FLNA):c.7255C>T (p.Arg2419Ter) rs782308324
NM_001110556.2(FLNA):c.7285_7286dup (p.Gly2430fs) rs2148101228
NM_001110556.2(FLNA):c.7363_7364insCGTGAACACCA (p.Ser2455delinsThrTer)
NM_001110556.2(FLNA):c.7545dup (p.Val2516fs)
NM_001110556.2(FLNA):c.760G>A (p.Glu254Lys) rs28935470
NM_001110556.2(FLNA):c.812del (p.Pro271fs) rs2148118964
NM_001110556.2(FLNA):c.829_835del (p.Arg276_Pro277insTer) rs2148118942
NM_001110556.2(FLNA):c.82A>G (p.Met28Val) rs1557180226
NM_001110556.2(FLNA):c.853C>T (p.Arg285Cys) rs1557179536
NM_001110556.2(FLNA):c.917_918del (p.Val306fs)
NM_001110556.2(FLNA):c.999_1008dup (p.Asp337delinsArgGlnTer) rs1557179357

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