ClinVar Miner

Submissions for variant NM_000094.4(COL7A1):c.1191C>G (p.Thr397=)

gnomAD frequency: 0.00096  dbSNP: rs143270071
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000899902 SCV001044192 benign not provided 2024-11-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000899902 SCV005305470 benign not provided criteria provided, single submitter not provided
Natera, Inc. RCV001830962 SCV002079306 likely benign Epidermolysis bullosa dystrophica 2019-10-24 no assertion criteria provided clinical testing
PreventionGenetics, part of Exact Sciences RCV003950542 SCV004759157 likely benign COL7A1-related disorder 2019-11-06 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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.