ClinVar Miner

List of variants studied for epithelial neoplasm by Genetics, Bhagwan Mahavir Medical Research Centre

Included ClinVar conditions (286):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 6
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_005228.5(EGFR):c.2327G>A (p.Arg776His) rs483352806 0.00001
NM_005228.5(EGFR):c.2155G>C (p.Gly719Arg) rs28929495
NM_005228.5(EGFR):c.2176G>A (p.Val726Met) rs483352805
NM_005228.5(EGFR):c.2188C>G (p.Leu730Val) rs121913434
NM_005228.5(EGFR):c.2393T>A (p.Leu798His) rs483352807
NM_005228.5(EGFR):c.2471G>A (p.Gly824Asp) rs483352808

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.