ClinVar Miner

Submissions for variant NM_003722.5(TP63):c.1827A>G (p.Glu609=)

gnomAD frequency: 0.00031  dbSNP: rs147538847
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000316384 SCV000337785 uncertain significance not provided 2015-11-25 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002059164 SCV002442122 benign TP63-Related Spectrum Disorders 2023-08-29 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003957437 SCV004769089 likely benign TP63-related disorder 2023-10-17 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.