ClinVar Miner

Submissions for variant NM_000546.6(TP53):c.460_463del (p.Gly154fs)

dbSNP: rs1567553658
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
German Consortium for Hereditary Breast and Ovarian Cancer, University Hospital Cologne RCV000785249 SCV000923817 pathogenic Ovarian neoplasm 2018-12-01 no assertion criteria provided research
Salgia Laboratory, City of Hope RCV003322617 SCV003804203 pathogenic Lung sarcomatoid carcinoma no assertion criteria provided clinical testing

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.