ClinVar Miner

List of variants in gene FLNA reported by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 120
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HGVS dbSNP gnomAD frequency
NM_001110556.2(FLNA):c.1029C>T (p.Ser343=) rs199853721 0.00118
NM_001110556.2(FLNA):c.4451A>G (p.Gln1484Arg) rs200130356 0.00081
NM_001110556.2(FLNA):c.1191C>T (p.Ile397=) rs200048692 0.00071
NM_001110556.2(FLNA):c.5251C>T (p.Pro1751Ser) rs56102764 0.00069
NM_001110556.2(FLNA):c.753C>T (p.Asn251=) rs377507152 0.00069
NM_001110556.2(FLNA):c.651C>T (p.Asp217=) rs34644500 0.00062
NM_001110556.2(FLNA):c.3876C>T (p.His1292=) rs199917719 0.00060
NM_001110556.2(FLNA):c.3915G>A (p.Thr1305=) rs201488545 0.00056
NM_001110556.2(FLNA):c.1579C>T (p.Arg527Cys) rs202029322 0.00046
NM_001110556.2(FLNA):c.1716C>T (p.Thr572=) rs201550267 0.00032
NM_001110556.2(FLNA):c.2449C>T (p.Pro817Ser) rs200053635 0.00029
NM_001110556.2(FLNA):c.5193G>A (p.Val1731=) rs201458268 0.00029
NM_001110556.2(FLNA):c.2178C>T (p.Asn726=) rs371501734 0.00028
NM_001110556.2(FLNA):c.5313+4C>T rs377330443 0.00028
NM_001110556.2(FLNA):c.3421G>A (p.Ala1141Thr) rs201908251 0.00025
NM_001110556.2(FLNA):c.3872C>T (p.Pro1291Leu) rs137853319 0.00023
NM_001110556.2(FLNA):c.6412G>T (p.Gly2138Cys) rs200524526 0.00023
NM_001110556.2(FLNA):c.732C>T (p.Pro244=) rs371092631 0.00020
NM_001110556.2(FLNA):c.2103C>T (p.His701=) rs200227077 0.00018
NM_001110556.2(FLNA):c.3995A>G (p.Asp1332Gly) rs200615848 0.00018
NM_001110556.2(FLNA):c.958G>A (p.Val320Met) rs781889196 0.00018
NM_001110556.2(FLNA):c.1812C>T (p.Asp604=) rs370735674 0.00015
NM_001110556.2(FLNA):c.3045G>A (p.Ala1015=) rs370868704 0.00014
NM_001110556.2(FLNA):c.2725G>A (p.Val909Ile) rs199911951 0.00013
NM_001110556.2(FLNA):c.6350A>G (p.Asn2117Ser) rs375205247 0.00013
NM_001110556.2(FLNA):c.1310G>A (p.Arg437Gln) rs782320818 0.00011
NM_001110556.2(FLNA):c.4824C>T (p.Tyr1608=) rs781789823 0.00010
NM_001110556.2(FLNA):c.2571G>A (p.Thr857=) rs1208353421 0.00008
NM_001110556.2(FLNA):c.901C>T (p.Arg301Trp) rs192609440 0.00007
NM_001110556.2(FLNA):c.5710G>A (p.Gly1904Ser) rs782549964 0.00006
NM_001110556.2(FLNA):c.6303G>A (p.Thr2101=) rs372978023 0.00006
NM_001110556.2(FLNA):c.4551G>C (p.Gly1517=) rs370476531 0.00005
NM_001110556.2(FLNA):c.500C>A (p.Thr167Asn) rs863223641 0.00005
NM_001110556.2(FLNA):c.6048G>A (p.Thr2016=) rs782745205 0.00005
NM_001110556.2(FLNA):c.7067G>A (p.Ser2356Asn) rs782739586 0.00005
NM_001110556.2(FLNA):c.968C>T (p.Pro323Leu) rs371830740 0.00005
NM_001110556.2(FLNA):c.1248C>T (p.Val416=) rs781947994 0.00004
NM_001110556.2(FLNA):c.1665G>A (p.Thr555=) rs782376419 0.00004
NM_001110556.2(FLNA):c.1964G>A (p.Arg655His) rs782563602 0.00004
NM_001110556.2(FLNA):c.5151G>A (p.Pro1717=) rs782646183 0.00004
NM_001110556.2(FLNA):c.5218-4G>A rs370196495 0.00004
NM_001110556.2(FLNA):c.6273C>T (p.Asp2091=) rs781913265 0.00004
NM_001110556.2(FLNA):c.1242C>T (p.Gly414=) rs782598234 0.00003
NM_001110556.2(FLNA):c.1365C>T (p.Thr455=) rs782726997 0.00003
NM_001110556.2(FLNA):c.3523G>A (p.Ala1175Thr) rs370202395 0.00003
NM_001110556.2(FLNA):c.5951C>T (p.Thr1984Met) rs782639698 0.00003
NM_001110556.2(FLNA):c.7353C>T (p.Val2451=) rs1057521797 0.00003
NM_001110556.2(FLNA):c.759C>T (p.Asp253=) rs782701643 0.00003
NM_001110556.2(FLNA):c.1000G>A (p.Ala334Thr) rs886044859 0.00002
NM_001110556.2(FLNA):c.2724C>T (p.Asp908=) rs1557178153 0.00002
NM_001110556.2(FLNA):c.4917C>T (p.Thr1639=) rs370608721 0.00002
NM_001110556.2(FLNA):c.5481C>T (p.Thr1827=) rs782576165 0.00002
NM_001110556.2(FLNA):c.5763C>T (p.Ser1921=) rs781929535 0.00002
NM_001110556.2(FLNA):c.6002G>A (p.Arg2001Gln) rs1483960506 0.00002
NM_001110556.2(FLNA):c.6507T>C (p.Ile2169=) rs1247682661 0.00002
NM_001110556.2(FLNA):c.915T>C (p.Thr305=) rs782439408 0.00002
NM_001110556.2(FLNA):c.936C>A (p.Gly312=) rs782475689 0.00002
NM_001110556.2(FLNA):c.1794G>A (p.Val598=) rs368304859 0.00001
NM_001110556.2(FLNA):c.1851G>A (p.Ser617=) rs782587128 0.00001
NM_001110556.2(FLNA):c.1963C>T (p.Arg655Cys) rs376867823 0.00001
NM_001110556.2(FLNA):c.1995C>T (p.Asp665=) rs368889011 0.00001
NM_001110556.2(FLNA):c.2047G>C (p.Glu683Gln) rs1294632938 0.00001
NM_001110556.2(FLNA):c.3006C>A (p.Gly1002=) rs782396211 0.00001
NM_001110556.2(FLNA):c.3095G>A (p.Arg1032His) rs781782783 0.00001
NM_001110556.2(FLNA):c.3282C>T (p.Gly1094=) rs369583365 0.00001
NM_001110556.2(FLNA):c.3573G>A (p.Ala1191=) rs782300292 0.00001
NM_001110556.2(FLNA):c.5255T>C (p.Leu1752Pro) rs1363194253 0.00001
NM_001110556.2(FLNA):c.546G>C (p.Gln182His) rs1557179648 0.00001
NM_001110556.2(FLNA):c.5826C>T (p.His1942=) rs377667830 0.00001
NM_001110556.2(FLNA):c.6601C>T (p.Arg2201Cys) rs782621818 0.00001
NM_001110556.2(FLNA):c.7183C>T (p.Arg2395Trp) rs368038166 0.00001
NM_001110556.2(FLNA):c.7401C>T (p.Asp2467=) rs886039087 0.00001
NM_001110556.2(FLNA):c.122G>T (p.Trp41Leu)
NM_001110556.2(FLNA):c.132C>G (p.Ile44Met) rs2067802950
NM_001110556.2(FLNA):c.1332C>T (p.Cys444=)
NM_001110556.2(FLNA):c.1486C>T (p.Arg496Trp) rs868994092
NM_001110556.2(FLNA):c.1923C>T (p.Gly641=) rs80338841
NM_001110556.2(FLNA):c.1997C>T (p.Ala666Val) rs374295965
NM_001110556.2(FLNA):c.2220_2223dup (p.Lys742fs)
NM_001110556.2(FLNA):c.2260A>G (p.Ile754Val) rs1569551769
NM_001110556.2(FLNA):c.2391C>G (p.Ala797=)
NM_001110556.2(FLNA):c.2391C>T (p.Ala797=) rs918799305
NM_001110556.2(FLNA):c.3255C>G (p.Pro1085=) rs782231907
NM_001110556.2(FLNA):c.3350A>G (p.Asn1117Ser) rs1209865046
NM_001110556.2(FLNA):c.3561C>T (p.Ser1187=) rs1396701849
NM_001110556.2(FLNA):c.3562G>A (p.Ala1188Thr) rs28935472
NM_001110556.2(FLNA):c.3607C>A (p.Leu1203Ile)
NM_001110556.2(FLNA):c.373+6G>T
NM_001110556.2(FLNA):c.4050C>T (p.Thr1350=) rs1603360933
NM_001110556.2(FLNA):c.4207A>T (p.Met1403Leu) rs781976719
NM_001110556.2(FLNA):c.4265A>G (p.Tyr1422Cys) rs2067685860
NM_001110556.2(FLNA):c.4292A>G (p.His1431Arg) rs1557177448
NM_001110556.2(FLNA):c.4514G>A (p.Gly1505Asp)
NM_001110556.2(FLNA):c.4589T>C (p.Val1530Ala) rs1603360612
NM_001110556.2(FLNA):c.468C>T (p.Asp156=)
NM_001110556.2(FLNA):c.4737G>C (p.Leu1579=) rs201904661
NM_001110556.2(FLNA):c.4750_4755+18del rs2067676994
NM_001110556.2(FLNA):c.5010G>A (p.Thr1670=) rs1449966344
NM_001110556.2(FLNA):c.5217G>A (p.Thr1739=) rs387907371
NM_001110556.2(FLNA):c.5218-6C>T
NM_001110556.2(FLNA):c.5242G>A (p.Val1748Met) rs1020587429
NM_001110556.2(FLNA):c.5505C>T (p.Ser1835=)
NM_001110556.2(FLNA):c.5592C>T (p.Asn1864=) rs782315233
NM_001110556.2(FLNA):c.5873T>G (p.Met1958Arg) rs587780336
NM_001110556.2(FLNA):c.6052G>A (p.Glu2018Lys) rs1603359376
NM_001110556.2(FLNA):c.6163C>T (p.Gln2055Ter) rs2148104977
NM_001110556.2(FLNA):c.6193C>T (p.Pro2065Ser) rs1603359334
NM_001110556.2(FLNA):c.62_64dup (p.Val21dup) rs782721874
NM_001110556.2(FLNA):c.6372C>T (p.His2124=)
NM_001110556.2(FLNA):c.6445C>T (p.Arg2149Trp) rs1603359214
NM_001110556.2(FLNA):c.6503-1G>A
NM_001110556.2(FLNA):c.6541C>A (p.Pro2181Thr) rs1569551460
NM_001110556.2(FLNA):c.6635_6638del (p.Val2212fs) rs786205178
NM_001110556.2(FLNA):c.6805G>A (p.Gly2269Arg) rs2067623386
NM_001110556.2(FLNA):c.690G>A (p.Gln230=) rs1557179590
NM_001110556.2(FLNA):c.7013C>T (p.Ser2338Phe) rs781878646
NM_001110556.2(FLNA):c.705G>A (p.Trp235Ter) rs2067772652
NM_001110556.2(FLNA):c.7500G>A (p.Lys2500=)
NM_001110556.2(FLNA):c.797A>C (p.Lys266Thr)
NM_001110556.2(FLNA):c.853C>T (p.Arg285Cys) rs1557179536

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