ClinVar Miner

List of variants in gene FLNA reported as likely benign for X-linked syndromic intellectual disability

Included ClinVar conditions (212):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 114
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HGVS dbSNP
NM_001110556.2(FLNA):c.1038C>T (p.Tyr346=) rs1057522072
NM_001110556.2(FLNA):c.108G>A (p.Ala36=) rs782572024
NM_001110556.2(FLNA):c.1120G>A (p.Val374Met) rs201681328
NM_001110556.2(FLNA):c.1170C>A (p.Gly390=) rs1603362865
NM_001110556.2(FLNA):c.1229-8C>T rs376190976
NM_001110556.2(FLNA):c.1260C>T (p.Ile420=) rs1351119633
NM_001110556.2(FLNA):c.141C>T (p.Asn47=) rs1603363922
NM_001110556.2(FLNA):c.1429+9G>A rs782226711
NM_001110556.2(FLNA):c.1665G>A (p.Thr555=) rs782376419
NM_001110556.2(FLNA):c.1771G>A (p.Val591Ile) rs200673062
NM_001110556.2(FLNA):c.1813G>A (p.Asp605Asn) rs201093148
NM_001110556.2(FLNA):c.1815C>T (p.Asp605=) rs781821848
NM_001110556.2(FLNA):c.1902C>T (p.Arg634=) rs782136908
NM_001110556.2(FLNA):c.1932C>T (p.Ala644=) rs1221420896
NM_001110556.2(FLNA):c.1997C>T (p.Ala666Val) rs374295965
NM_001110556.2(FLNA):c.2001C>T (p.Pro667=) rs782344845
NM_001110556.2(FLNA):c.2019C>T (p.Asp673=) rs1557178734
NM_001110556.2(FLNA):c.2023-5G>A rs782694533
NM_001110556.2(FLNA):c.2027A>G (p.Lys676Arg) rs781798819
NM_001110556.2(FLNA):c.2178C>T (p.Asn726=) rs371501734
NM_001110556.2(FLNA):c.2205C>T (p.Tyr735=) rs782551055
NM_001110556.2(FLNA):c.2280+9A>G rs1603362191
NM_001110556.2(FLNA):c.2309A>G (p.Asn770Ser) rs1557178374
NM_001110556.2(FLNA):c.2310C>T (p.Asn770=) rs202109957
NM_001110556.2(FLNA):c.237G>T (p.Ala79=) rs200626788
NM_001110556.2(FLNA):c.2389G>A (p.Ala797Thr) rs201073998
NM_001110556.2(FLNA):c.2405-4G>A rs368187218
NM_001110556.2(FLNA):c.2454C>T (p.Ala818=) rs374672498
NM_001110556.2(FLNA):c.2472C>T (p.Phe824=) rs782669943
NM_001110556.2(FLNA):c.2505G>A (p.Thr835=) rs782013801
NM_001110556.2(FLNA):c.2706T>C (p.Ala902=) rs781842762
NM_001110556.2(FLNA):c.2838C>T (p.Gly946=) rs782612987
NM_001110556.2(FLNA):c.3147C>T (p.Gly1049=) rs398123615
NM_001110556.2(FLNA):c.3225G>A (p.Pro1075=) rs782292169
NM_001110556.2(FLNA):c.3255C>T (p.Pro1085=) rs782231907
NM_001110556.2(FLNA):c.3306G>T (p.Leu1102=) rs782062750
NM_001110556.2(FLNA):c.333C>T (p.Leu111=) rs782684723
NM_001110556.2(FLNA):c.3378C>T (p.Tyr1126=) rs782643175
NM_001110556.2(FLNA):c.3429C>A (p.Thr1143=) rs183899917
NM_001110556.2(FLNA):c.3573G>A (p.Ala1191=) rs782300292
NM_001110556.2(FLNA):c.3612G>A (p.Pro1204=) rs782273962
NM_001110556.2(FLNA):c.3695C>T (p.Thr1232Ile) rs782495669
NM_001110556.2(FLNA):c.373+10G>A rs368292402
NM_001110556.2(FLNA):c.3768C>T (p.Ser1256=) rs782528841
NM_001110556.2(FLNA):c.3805+10C>T rs1603361041
NM_001110556.2(FLNA):c.3843C>T (p.Asp1281=) rs367931067
NM_001110556.2(FLNA):c.3864C>T (p.Thr1288=) rs374068639
NM_001110556.2(FLNA):c.3915G>A (p.Thr1305=) rs201488545
NM_001110556.2(FLNA):c.3939C>T (p.Gly1313=) rs374178910
NM_001110556.2(FLNA):c.3996C>T (p.Asp1332=) rs782414490
NM_001110556.2(FLNA):c.4017C>T (p.Pro1339=) rs781934382
NM_001110556.2(FLNA):c.4023C>T (p.Pro1341=) rs1375431086
NM_001110556.2(FLNA):c.4106C>T (p.Thr1369Ile) rs376774130
NM_001110556.2(FLNA):c.4155G>T (p.Thr1385=) rs782110572
NM_001110556.2(FLNA):c.4179G>A (p.Glu1393=) rs182074603
NM_001110556.2(FLNA):c.4236C>T (p.Val1412=) rs782589572
NM_001110556.2(FLNA):c.4263C>T (p.Thr1421=) rs398123618
NM_001110556.2(FLNA):c.4344G>A (p.Ala1448=) rs782529594
NM_001110556.2(FLNA):c.4368C>T (p.Pro1456=) rs782080545
NM_001110556.2(FLNA):c.441C>T (p.His147=) rs781951563
NM_001110556.2(FLNA):c.444C>T (p.Tyr148=) rs935727195
NM_001110556.2(FLNA):c.4594C>T (p.Arg1532Trp) rs782563345
NM_001110556.2(FLNA):c.4755+5G>A rs199803218
NM_001110556.2(FLNA):c.4824C>T (p.Tyr1608=) rs781789823
NM_001110556.2(FLNA):c.4899C>T (p.Arg1633=) rs781846478
NM_001110556.2(FLNA):c.4945+3G>A rs372673802
NM_001110556.2(FLNA):c.5138C>T (p.Thr1713Met) rs782555986
NM_001110556.2(FLNA):c.5151G>A (p.Pro1717=) rs782646183
NM_001110556.2(FLNA):c.5251C>T (p.Pro1751Ser) rs56102764
NM_001110556.2(FLNA):c.5271G>A (p.Leu1757=) rs782031542
NM_001110556.2(FLNA):c.5283C>T (p.Tyr1761=) rs782313331
NM_001110556.2(FLNA):c.5292C>T (p.Ala1764=) rs1027131950
NM_001110556.2(FLNA):c.5313+4C>T rs377330443
NM_001110556.2(FLNA):c.5342A>G (p.Asn1781Ser) rs373089783
NM_001110556.2(FLNA):c.543G>C (p.Pro181=) rs201486643
NM_001110556.2(FLNA):c.5559A>C (p.Gly1853=) rs372028899
NM_001110556.2(FLNA):c.5610C>T (p.Ala1870=) rs782040591
NM_001110556.2(FLNA):c.5861-9C>T rs782153045
NM_001110556.2(FLNA):c.5911A>T (p.Ile1971Phe) rs190712778
NM_001110556.2(FLNA):c.5952G>A (p.Thr1984=) rs782618234
NM_001110556.2(FLNA):c.5973G>A (p.Ser1991=) rs375252292
NM_001110556.2(FLNA):c.5978G>A (p.Arg1993Gln) rs782401919
NM_001110556.2(FLNA):c.60C>T (p.Gly20=) rs1557180245
NM_001110556.2(FLNA):c.6217C>T (p.Arg2073Cys) rs782069230
NM_001110556.2(FLNA):c.6219C>T (p.Arg2073=) rs782365685
NM_001110556.2(FLNA):c.622+10C>T rs781889769
NM_001110556.2(FLNA):c.6238C>T (p.Leu2080Phe) rs782157246
NM_001110556.2(FLNA):c.6273C>T (p.Asp2091=) rs781913265
NM_001110556.2(FLNA):c.6289C>T (p.Leu2097=) rs782255283
NM_001110556.2(FLNA):c.6350A>G (p.Asn2117Ser) rs375205247
NM_001110556.2(FLNA):c.6376C>T (p.Pro2126Ser) rs782400832
NM_001110556.2(FLNA):c.6412G>T (p.Gly2138Cys) rs200524526
NM_001110556.2(FLNA):c.6540C>T (p.Ser2180=) rs781992483
NM_001110556.2(FLNA):c.6564C>G (p.Ala2188=) rs782053327
NM_001110556.2(FLNA):c.6612C>T (p.Pro2204=) rs375499070
NM_001110556.2(FLNA):c.6657G>A (p.Gln2219=) rs1210861581
NM_001110556.2(FLNA):c.6804T>C (p.Ala2268=) rs376461465
NM_001110556.2(FLNA):c.6891T>C (p.Tyr2297=) rs1557175875
NM_001110556.2(FLNA):c.6951C>T (p.Pro2317=) rs782356784
NM_001110556.2(FLNA):c.6984G>A (p.Pro2328=) rs374786760
NM_001110556.2(FLNA):c.6993C>T (p.Asp2331=) rs201153928
NM_001110556.2(FLNA):c.7089G>A (p.Ala2363=) rs781843787
NM_001110556.2(FLNA):c.7152C>T (p.Asp2384=) rs1603358785
NM_001110556.2(FLNA):c.7164T>C (p.Tyr2388=) rs1557175472
NM_001110556.2(FLNA):c.720+8C>T rs371927910
NM_001110556.2(FLNA):c.7275T>C (p.His2425=) rs781857682
NM_001110556.2(FLNA):c.7305C>T (p.Tyr2435=) rs782750091
NM_001110556.2(FLNA):c.7326T>C (p.Gly2442=) rs1026564714
NM_001110556.2(FLNA):c.7365C>G (p.Ser2455Arg) rs199677057
NM_001110556.2(FLNA):c.7410C>A (p.Ser2470=) rs368746337
NM_001110556.2(FLNA):c.93C>T (p.Thr31=) rs1436289913
NM_001110556.2(FLNA):c.957C>T (p.Tyr319=) rs373561030
NM_001110556.2(FLNA):c.988-10C>T rs1603362942
NM_001110556.2(FLNA):c.999C>T (p.Thr333=) rs1167180795

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