ClinVar Miner

Submissions for variant NM_000141.5(FGFR2):c.1647T>A (p.Asn549Lys)

dbSNP: rs121913476
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 5
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000441770 SCV000505185 likely pathogenic Breast neoplasm 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000424055 SCV000505186 likely pathogenic Lung adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000433483 SCV000505187 likely pathogenic Endometrial Endometrioid Adenocarcinoma, Variant with Squamous Differentiation 2014-12-26 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000443743 SCV000505188 likely pathogenic Malignant neoplasm of body of uterus 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000426965 SCV000505189 likely pathogenic Nasopharyngeal neoplasm 2016-05-31 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.