ClinVar Miner

List of variants reported as uncertain significance for colonic neoplasm by Centre for Mendelian Genomics,University Medical Centre Ljubljana

Included ClinVar conditions (19):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
Download table as spreadsheet
NM_000546.5(TP53):c.1060C>A (p.Gln354Lys) rs755394212
NM_001128425.1(MUTYH):c.933+3A>C rs587780751
NM_004360.5(CDH1):c.892G>A (p.Ala298Thr) rs142822590

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.