ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 47
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001110556.2(FLNA):c.5251C>T (p.Pro1751Ser) rs56102764 0.00069
NM_001110556.2(FLNA):c.2449C>T (p.Pro817Ser) rs200053635 0.00029
NM_001110556.2(FLNA):c.6412G>T (p.Gly2138Cys) rs200524526 0.00023
NM_001110556.2(FLNA):c.3045G>A (p.Ala1015=) rs370868704 0.00014
NM_001110556.2(FLNA):c.5710G>A (p.Gly1904Ser) rs782549964 0.00006
NM_001110556.2(FLNA):c.500C>A (p.Thr167Asn) rs863223641 0.00005
NM_001110556.2(FLNA):c.968C>T (p.Pro323Leu) rs371830740 0.00005
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.1000G>A (p.Ala334Thr) rs886044859 0.00002
NM_001110556.2(FLNA):c.6002G>A (p.Arg2001Gln) rs1483960506 0.00002
NM_001110556.2(FLNA):c.1963C>T (p.Arg655Cys) rs376867823 0.00001
NM_001110556.2(FLNA):c.2047G>C (p.Glu683Gln) rs1294632938 0.00001
NM_001110556.2(FLNA):c.3095G>A (p.Arg1032His) rs781782783 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.6601C>T (p.Arg2201Cys) rs782621818 0.00001
NM_001110556.2(FLNA):c.7183C>T (p.Arg2395Trp) rs368038166 0.00001
NM_001110556.2(FLNA):c.7324G>A (p.Gly2442Ser) rs782189345 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.1486C>T (p.Arg496Trp) rs868994092
NM_001110556.2(FLNA):c.1864G>A (p.Glu622Lys) rs1131691935
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.2260A>G (p.Ile754Val) rs1569551769
NM_001110556.2(FLNA):c.3021G>C (p.Lys1007Asn)
NM_001110556.2(FLNA):c.3607C>A (p.Leu1203Ile)
NM_001110556.2(FLNA):c.373+6G>T
NM_001110556.2(FLNA):c.3856A>T (p.Thr1286Ser) rs2067691272
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.5242G>A (p.Val1748Met) rs1020587429
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.6193C>T (p.Pro2065Ser) rs1603359334
NM_001110556.2(FLNA):c.6445C>T (p.Arg2149Trp) rs1603359214
NM_001110556.2(FLNA):c.6541C>A (p.Pro2181Thr) rs1569551460
NM_001110556.2(FLNA):c.6805G>A (p.Gly2269Arg) rs2067623386
NM_001110556.2(FLNA):c.7013C>T (p.Ser2338Phe) rs781878646
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
NM_001110556.2(FLNA):c.995T>C (p.Val332Ala)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.