ClinVar Miner

Submissions for variant NM_004448.4(ERBB2):c.2570A>G (p.Asn857Ser)

gnomAD frequency: 0.00001  dbSNP: rs28933370
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
OMIM RCV000014894 SCV000035149 pathogenic Ovarian neoplasm 2004-09-30 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000427276 SCV000510502 likely pathogenic Ovarian adenocarcinoma 2016-05-13 no assertion criteria provided literature only

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.