ClinVar Miner

List of variants in gene FLNC reported as uncertain significance for Myofibrillar myopathy, filamin C-related; Myopathy, distal, 4; Cardiomyopathy, familial hypertrophic, 26

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
Download table as spreadsheet
HGVS dbSNP
NM_001458.4(FLNC):c.1081C>T (p.Arg361Cys) rs200206944
NM_001458.4(FLNC):c.5020G>A (p.Gly1674Ser) rs374124083
NM_001458.4(FLNC):c.5128G>A (p.Glu1710Lys)
NM_001458.4(FLNC):c.5272C>T (p.Arg1758Trp)
NM_001458.4(FLNC):c.5792G>A (p.Arg1931His) rs780685346
NM_001458.4(FLNC):c.643G>A (p.Val215Met) rs754309921
NM_001458.4(FLNC):c.7289C>T (p.Ala2430Val) rs200516164
NM_001458.4(FLNC):c.925G>A (p.Glu309Lys)

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.