ClinVar Miner

List of variants reported as likely benign for Renal cell carcinoma, papillary, 1 by Mendelics

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 18
Download table as spreadsheet
HGVS dbSNP
NM_001127500.3(MET):c.1306G>A (p.Glu436Lys) rs200740468
NM_001127500.3(MET):c.1393-2A>T
NM_001127500.3(MET):c.1715G>A (p.Ser572Asn) rs199771406
NM_001127500.3(MET):c.1973T>C (p.Val658Ala)
NM_001127500.3(MET):c.2103-1G>T rs1336351205
NM_001127500.3(MET):c.2103-2A>T
NM_001127500.3(MET):c.2419-21G>C
NM_001127500.3(MET):c.252C>T (p.Tyr84=)
NM_001127500.3(MET):c.2638-1G>T
NM_001127500.3(MET):c.2638-3C>T rs1337305891
NM_001127500.3(MET):c.2769C>T (p.Ser923=) rs45572835
NM_001127500.3(MET):c.2962C>T (p.Arg988Cys) rs34589476
NM_001127500.3(MET):c.3686+42C>G
NM_001127500.3(MET):c.4141G>A (p.Ala1381Thr) rs45578433
NM_001127500.3(MET):c.504G>T (p.Glu168Asp) rs55985569
NM_001127500.3(MET):c.71G>A (p.Gly24Glu) rs180985111
NM_001127500.3(MET):c.850A>G (p.Ile284Val) rs776014448
NM_004958.4(MTOR):c.889G>A (p.Asp297Asn)

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.