ClinVar Miner

List of variants in gene FLNC reported as uncertain significance by EGL Genetic Diagnostics,Eurofins Clinical Diagnostics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 44
Download table as spreadsheet
HGVS dbSNP
NM_001458.4(FLNC):c.1197C>T (p.Asp399=) rs756546984
NM_001458.4(FLNC):c.1502C>T (p.Thr501Ile) rs794727967
NM_001458.4(FLNC):c.1505A>T (p.Lys502Met)
NM_001458.4(FLNC):c.1519G>A (p.Gly507Arg) rs189525930
NM_001458.4(FLNC):c.1600G>A (p.Glu534Lys) rs201905890
NM_001458.4(FLNC):c.1698C>T (p.Ser566=) rs112194548
NM_001458.4(FLNC):c.1813+11G>T rs138716837
NM_001458.4(FLNC):c.2008-7C>T rs767576240
NM_001458.4(FLNC):c.2040C>T (p.Thr680=) rs368121231
NM_001458.4(FLNC):c.2130C>T (p.Asp710=) rs778781499
NM_001458.4(FLNC):c.2244C>A (p.Asn748Lys) rs752145129
NM_001458.4(FLNC):c.2390-8C>G rs146063718
NM_001458.4(FLNC):c.2459A>T (p.Asp820Val) rs886044638
NM_001458.4(FLNC):c.272A>C (p.Asn91Thr) rs886042565
NM_001458.4(FLNC):c.2733G>A (p.Lys911=)
NM_001458.4(FLNC):c.3054C>T (p.Gly1018=) rs769624093
NM_001458.4(FLNC):c.3243G>A (p.Ala1081=) rs534482249
NM_001458.4(FLNC):c.3489G>C (p.Pro1163=) rs369853278
NM_001458.4(FLNC):c.3949A>G (p.Thr1317Ala)
NM_001458.4(FLNC):c.3966C>T (p.Gly1322=) rs200237564
NM_001458.4(FLNC):c.4009A>C (p.Lys1337Gln) rs1554399580
NM_001458.4(FLNC):c.4022G>A (p.Arg1341Gln) rs149641783
NM_001458.4(FLNC):c.4133C>T (p.Ala1378Val) rs748008658
NM_001458.4(FLNC):c.4301G>A (p.Arg1434His) rs143623535
NM_001458.4(FLNC):c.4488T>C (p.Asn1496=) rs377258966
NM_001458.4(FLNC):c.4553A>G (p.Lys1518Arg) rs201635205
NM_001458.4(FLNC):c.4576C>T (p.Arg1526Cys) rs746275035
NM_001458.4(FLNC):c.4880G>A (p.Arg1627His) rs751592993
NM_001458.4(FLNC):c.4952G>A (p.Gly1651Asp) rs762493974
NM_001458.4(FLNC):c.5375C>T (p.Ala1792Val) rs200233856
NM_001458.4(FLNC):c.5418G>A (p.Ser1806=) rs376078394
NM_001458.4(FLNC):c.5644A>G (p.Ile1882Val) rs184018403
NM_001458.4(FLNC):c.6405G>A (p.Lys2135=) rs886043826
NM_001458.4(FLNC):c.6441C>T (p.Ile2147=) rs762017885
NM_001458.4(FLNC):c.6485-8C>T rs369347947
NM_001458.4(FLNC):c.6714C>T (p.Thr2238=) rs10268251
NM_001458.4(FLNC):c.6808G>A (p.Glu2270Lys) rs202223616
NM_001458.4(FLNC):c.6998-5C>T rs139030003
NM_001458.4(FLNC):c.7289C>T (p.Ala2430Val) rs200516164
NM_001458.4(FLNC):c.7291G>A (p.Val2431Met) rs572952653
NM_001458.4(FLNC):c.7382G>A (p.Ser2461Asn) rs550547714
NM_001458.4(FLNC):c.7862G>A (p.Arg2621Gln) rs201636548
NM_001458.4(FLNC):c.8003T>C (p.Met2668Thr) rs200502811
NM_001458.4(FLNC):c.8070G>T (p.Arg2690=) rs373087529

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.