ClinVar Miner

List of variants in gene FLNC studied for Cardiomyopathy, familial hypertrophic, 26

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
Download table as spreadsheet
HGVS dbSNP
NM_001458.4(FLNC):c.3547_3548delinsCT (p.Ala1183Leu) rs1131692185
NM_001458.4(FLNC):c.3557C>T (p.Ala1186Val) rs1114167361
NM_001458.4(FLNC):c.368T>C (p.Val123Ala) rs1562991002
NM_001458.4(FLNC):c.4566G>T (p.Gln1522His) rs559667295
NM_001458.4(FLNC):c.4615G>A (p.Ala1539Thr) rs1562999443
NM_001458.4(FLNC):c.6175G>A (p.Val2059Met) rs201333104
NM_001458.4(FLNC):c.6943C>A (p.His2315Asn) rs1563003848
NM_001458.4(FLNC):c.7087G>A (p.Asp2363Asn) rs1554401490
NM_001458.4(FLNC):c.7511A>G (p.Asp2504Gly)
NM_001458.4(FLNC):c.7947C>T (p.Phe2649=) rs368849358

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.