ClinVar Miner

Submissions for variant NM_005896.4(IDH1):c.274T>G (p.Trp92Gly)

dbSNP: rs1048933669
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
Ambry Genetics RCV004064108 SCV002752120 uncertain significance not specified 2024-02-09 criteria provided, single submitter clinical testing The p.W92G variant (also known as c.274T>G), located in coding exon 2 of the IDH1 gene, results from a T to G substitution at nucleotide position 274. The tryptophan at codon 92 is replaced by glycine, an amino acid with highly dissimilar properties. This amino acid position is conserved. In addition, this alteration is predicted to be deleterious by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

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.