ClinVar Miner

List of variants in gene TNNT2 reported as benign for Cardiomyopathy

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
Download table as spreadsheet
NM_000364.4(TNNT2):c.200-11A>G rs368658464
NM_000364.4(TNNT2):c.237G>A (p.Ser79=) rs3729845
NM_000364.4(TNNT2):c.348C>T (p.Ile116=) rs3729547
NM_000364.4(TNNT2):c.412-6_412-4del rs397516462
NM_000364.4(TNNT2):c.474G>C (p.Arg158=) rs35914325
NM_000364.4(TNNT2):c.522C>T (p.Asn174=) rs483352833
NM_000364.4(TNNT2):c.53-11_53-7del rs45533739
NM_000364.4(TNNT2):c.53-12del rs730881094
NM_000364.4(TNNT2):c.601-90G>A rs11810834
NM_000364.4(TNNT2):c.63T>G (p.Val21=) rs397516477
NM_000364.4(TNNT2):c.68-8A>G rs115805892
NM_000364.4(TNNT2):c.779A>G (p.Lys260Arg) rs3730238

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.