ClinVar Miner

Submissions for variant NM_001128425.1(MUTYH):c.1491T>G (p.Tyr497Ter) (rs1064793198)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000485940 SCV000565257 likely pathogenic not provided 2014-12-22 criteria provided, single submitter clinical testing This pathogenic variant is denoted MUTYH c.1491T>G at the cDNA level and p.Tyr497Ter (Y497X) at the protein level. The substitution creates a nonsense variant, which changes a Tyrosine to a premature stop codon (TAT>TAG), and is predicted to cause loss of normal protein function through protein truncation. Although this variant has not, to our knowledge, been reported in the literature, it is considered likely pathogenic.

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.