ClinVar Miner

List of variants reported as likely benign for Renal cell carcinoma, papillary, 1 by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 41
Download table as spreadsheet
HGVS dbSNP
NM_001127500.3(MET):c.*1010G>T rs150534017
NM_001127500.3(MET):c.*1220G>A rs139535303
NM_001127500.3(MET):c.*1224C>T rs149713628
NM_001127500.3(MET):c.*1636C>T rs186175651
NM_001127500.3(MET):c.*1784T>A rs554029534
NM_001127500.3(MET):c.*1886T>A rs536185931
NM_001127500.3(MET):c.*1987C>T rs76322625
NM_001127500.3(MET):c.*2134T>A rs144156652
NM_001127500.3(MET):c.*2202G>A rs14456
NM_001127500.3(MET):c.*231T>G rs59399612
NM_001127500.3(MET):c.*385G>A rs181068390
NM_001127500.3(MET):c.*602C>T rs147343288
NM_001127500.3(MET):c.*655C>T rs563978117
NM_001127500.3(MET):c.*656G>A rs531456758
NM_001127500.3(MET):c.*76C>T rs527496385
NM_001127500.3(MET):c.*787G>A rs143472935
NM_001127500.3(MET):c.*87G>A rs41281081
NM_001127500.3(MET):c.*944A>G rs565768785
NM_001127500.3(MET):c.*984C>T rs573510587
NM_001127500.3(MET):c.-14-4G>A rs144126521
NM_001127500.3(MET):c.1039G>A (p.Ala347Thr) rs200074800
NM_001127500.3(MET):c.1076G>A (p.Arg359Gln) rs201274041
NM_001127500.3(MET):c.1085T>C (p.Met362Thr) rs77523018
NM_001127500.3(MET):c.144G>A (p.Ala48=) rs11762213
NM_001127500.3(MET):c.1715G>A (p.Ser572Asn) rs199771406
NM_001127500.3(MET):c.1965+14T>C rs543293293
NM_001127500.3(MET):c.1992G>A (p.Pro664=) rs373842614
NM_001127500.3(MET):c.2638-7del rs587780736
NM_001127500.3(MET):c.2962C>T (p.Arg988Cys) rs34589476
NM_001127500.3(MET):c.3029C>T (p.Thr1010Ile) rs56391007
NM_001127500.3(MET):c.3576+12G>T rs200624981
NM_001127500.3(MET):c.3577-12C>G rs186524917
NM_001127500.3(MET):c.36C>T (p.Leu12=) rs188625702
NM_001127500.3(MET):c.3864C>T (p.Gly1288=) rs200865810
NM_001127500.3(MET):c.390C>T (p.Leu130=) rs150588908
NM_001127500.3(MET):c.4141G>A (p.Ala1381Thr) rs45578433
NM_001127500.3(MET):c.467C>T (p.Ser156Leu) rs56311081
NM_001127500.3(MET):c.504G>T (p.Glu168Asp) rs55985569
NM_001127500.3(MET):c.632T>G (p.Leu211Trp) rs45483396
NM_001127500.3(MET):c.948A>G (p.Ile316Met) rs35225896
NM_001127500.3(MET):c.959C>T (p.Ala320Val) rs35776110

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.