List of variants in gene FLNA reported as uncertain significance for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 73

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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.3717C>T (p.Pro1239=)	rs372265042	0.00046
NM_001110556.2(FLNA):c.2813C>T (p.Thr938Met)	rs782180774	0.00014
NM_001110556.2(FLNA):c.1238C>T (p.Thr413Met)	rs782549299	0.00011
NM_001110556.2(FLNA):c.5764G>A (p.Val1922Met)	rs371366175	0.00011
NM_001110556.2(FLNA):c.6307A>G (p.Arg2103Gly)	rs370277156	0.00010
NM_001110556.2(FLNA):c.7135T>C (p.Tyr2379His)	rs781881872	0.00010
NM_001110556.2(FLNA):c.2123G>A (p.Arg708Gln)	rs371707134	0.00009
NM_001110556.2(FLNA):c.7066A>C (p.Ser2356Arg)	rs781823700	0.00009
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.66C>T (p.Asp22=)	rs782358007	0.00006
NM_001110556.2(FLNA):c.6394G>A (p.Val2132Met)	rs201396725	0.00005
NM_001110556.2(FLNA):c.1964G>A (p.Arg655His)	rs782563602	0.00004
NM_001110556.2(FLNA):c.4232C>T (p.Ser1411Leu)	rs782426283	0.00004
NM_001110556.2(FLNA):c.6175G>A (p.Glu2059Lys)	rs782779958	0.00004
NM_001110556.2(FLNA):c.1291G>C (p.Glu431Gln)	rs781915319	0.00003
NM_001110556.2(FLNA):c.2538C>T (p.Tyr846=)	rs782571710	0.00003
NM_001110556.2(FLNA):c.2613C>T (p.Asp871=)	rs188212919	0.00003
NM_001110556.2(FLNA):c.3224C>T (p.Pro1075Leu)	rs782406278	0.00003
NM_001110556.2(FLNA):c.3368C>G (p.Ser1123Cys)	rs782361719	0.00003
NM_001110556.2(FLNA):c.3523G>A (p.Ala1175Thr)	rs370202395	0.00003
NM_001110556.2(FLNA):c.3695C>T (p.Thr1232Ile)	rs782495669	0.00003
NM_001110556.2(FLNA):c.4517C>T (p.Thr1506Ile)	rs797045579	0.00003
NM_001110556.2(FLNA):c.4625C>T (p.Thr1542Ile)	rs782281134	0.00003
NM_001110556.2(FLNA):c.6846G>A (p.Glu2282=)	rs781972193	0.00003
NM_001110556.2(FLNA):c.6863G>A (p.Arg2288His)	rs782275601	0.00003
NM_001110556.2(FLNA):c.806T>A (p.Leu269Gln)	rs782157170	0.00003
NM_001110556.2(FLNA):c.1000G>A (p.Ala334Thr)	rs886044859	0.00002
NM_001110556.2(FLNA):c.1580G>A (p.Arg527His)	rs782450368	0.00002
NM_001110556.2(FLNA):c.3934C>T (p.Arg1312Cys)	rs781928289	0.00002
NM_001110556.2(FLNA):c.4420G>A (p.Asp1474Asn)	rs782129236	0.00002
NM_001110556.2(FLNA):c.461T>C (p.Met154Thr)	rs782240483	0.00002
NM_001110556.2(FLNA):c.4899C>T (p.Arg1633=)	rs781846478	0.00002
NM_001110556.2(FLNA):c.5447C>T (p.Ala1816Val)	rs12395634	0.00002
NM_001110556.2(FLNA):c.5451G>A (p.Gln1817=)	rs782390251	0.00002
NM_001110556.2(FLNA):c.6728C>G (p.Ala2243Gly)	rs953454766	0.00002
NM_001110556.2(FLNA):c.7259T>C (p.Val2420Ala)	rs782289803	0.00002
NM_001110556.2(FLNA):c.7389G>A (p.Ser2463=)	rs373103712	0.00002
NM_001110556.2(FLNA):c.841C>G (p.Pro281Ala)	rs2067770833	0.00002
NM_001110556.2(FLNA):c.1372G>A (p.Val458Ile)	rs782791907	0.00001
NM_001110556.2(FLNA):c.1765G>A (p.Gly589Ser)	rs782371876	0.00001
NM_001110556.2(FLNA):c.2521C>T (p.Arg841Trp)	rs782772998	0.00001
NM_001110556.2(FLNA):c.2671A>G (p.Lys891Glu)	rs1459255199	0.00001
NM_001110556.2(FLNA):c.3323G>A (p.Cys1108Tyr)	rs371677498	0.00001
NM_001110556.2(FLNA):c.4069C>T (p.Arg1357Trp)	rs373073505	0.00001
NM_001110556.2(FLNA):c.4222G>A (p.Gly1408Ser)	rs797045578	0.00001
NM_001110556.2(FLNA):c.5515C>G (p.Leu1839Val)	rs1479378222	0.00001
NM_001110556.2(FLNA):c.6338A>G (p.Asn2113Ser)	rs1057518479	0.00001
NM_001110556.2(FLNA):c.6415C>T (p.Arg2139Trp)	rs782761341	0.00001
NM_001110556.2(FLNA):c.6719A>G (p.Lys2240Arg)	rs797045581	0.00001
NM_001110556.2(FLNA):c.6725G>A (p.Arg2242Gln)	rs781984274	0.00001
NM_001110556.2(FLNA):c.6983C>T (p.Pro2328Leu)	rs782310851	0.00001
NM_001110556.2(FLNA):c.7051G>A (p.Ala2351Thr)	rs1557175653	0.00001
NM_001110556.2(FLNA):c.1117T>A (p.Tyr373Asn)	rs2148118056
NM_001110556.2(FLNA):c.1628A>G (p.Tyr543Cys)	rs41304984
NM_001110556.2(FLNA):c.217G>C (p.Asp73His)	rs1557180192
NM_001110556.2(FLNA):c.2254_2268delinsCACCCTGAAGGG (p.Val752_Asn756delinsHisProGluGly)	rs863223631
NM_001110556.2(FLNA):c.2405-8_2405-5dup	rs782040815
NM_001110556.2(FLNA):c.25G>T (p.Gly9Cys)	rs782292045
NM_001110556.2(FLNA):c.2788G>A (p.Asp930Asn)
NM_001110556.2(FLNA):c.2826+20C>T
NM_001110556.2(FLNA):c.3487G>C (p.Val1163Leu)	rs2148112185
NM_001110556.2(FLNA):c.393C>A (p.Asp131Glu)
NM_001110556.2(FLNA):c.4083C>A (p.His1361Gln)	rs201475771
NM_001110556.2(FLNA):c.4113C>T (p.Asn1371=)	rs1557177508
NM_001110556.2(FLNA):c.4142+17G>A
NM_001110556.2(FLNA):c.4818G>A (p.Val1606=)	rs2148109762
NM_001110556.2(FLNA):c.4A>T (p.Ser2Cys)
NM_001110556.2(FLNA):c.521G>A (p.Gly174Asp)	rs1557179659
NM_001110556.2(FLNA):c.6263G>A (p.Ser2088Asn)	rs797045580
NM_001110556.2(FLNA):c.6372C>G (p.His2124Gln)	rs781999359
NM_001110556.2(FLNA):c.6875C>T (p.Ser2292Phe)	rs1557175878

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