ClinVar Miner

Submissions for variant NM_000363.5(TNNI3):c.184G>T (p.Glu62Ter)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
MVZ Medizinische Genetik Mainz RCV004545966 SCV005040945 uncertain significance Dilated cardiomyopathy 1FF 2023-04-13 criteria provided, single submitter clinical testing ACMG Criteria: PM2_SUP,PP3
Institute of Immunology and Genetics Kaiserslautern RCV004587646 SCV005077725 likely pathogenic Dilated cardiomyopathy 2A; Dilated cardiomyopathy 1FF 2024-06-14 criteria provided, single submitter clinical testing ACMG Criteria: PVS1, PM2; Variant was found in heterozygous state.

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.