ClinVar Miner

List of variants reported as likely pathogenic for Endometrial Endometrioid Adenocarcinoma, Variant with Squamous Differentiation

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 18
Download table as spreadsheet
NM_000141.5(FGFR2):c.1605G>A (p.Met535Ile) rs1057519800
NM_000141.5(FGFR2):c.1605G>C (p.Met535Ile) rs1057519800
NM_000141.5(FGFR2):c.1605G>T (p.Met535Ile) rs1057519800
NM_000141.5(FGFR2):c.1611G>A (p.Met537Ile) rs1057519799
NM_000141.5(FGFR2):c.1611G>C (p.Met537Ile) rs1057519799
NM_000141.5(FGFR2):c.1611G>T (p.Met537Ile) rs1057519799
NM_000141.5(FGFR2):c.1639A>G (p.Ile547Val) rs1057519798
NM_000141.5(FGFR2):c.1645A>C (p.Asn549His) rs1057519045
NM_000141.5(FGFR2):c.1647T>A (p.Asn549Lys) rs121913476
NM_000141.5(FGFR2):c.1647T>G (p.Asn549Lys) rs121913476
NM_000141.5(FGFR2):c.1690G>A (p.Val564Ile) rs1057519797
NM_000141.5(FGFR2):c.1694A>G (p.Glu565Gly) rs121918506
NM_000141.5(FGFR2):c.1849T>A (p.Leu617Met) rs1057519796
NM_000141.5(FGFR2):c.1975A>G (p.Lys659Glu) rs1057519795
NM_000141.5(FGFR2):c.755C>G (p.Ser252Trp) rs79184941
NM_005027.4(PIK3R2):c.1681A>G (p.Asn561Asp) rs1057519801
NM_005163.2(AKT1):c.49G>A (p.Glu17Lys) rs121434592
NM_005228.5(EGFR):c.2068G>A (p.Glu690Lys) rs1057519794

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.