ClinVar Miner

Submissions for variant NM_005476.7(GNE):c.1234G>A (p.Val412Ile) (rs369714039)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000366622 SCV000344729 uncertain significance not provided 2016-08-08 criteria provided, single submitter clinical testing
Invitae RCV000688282 SCV000815887 uncertain significance GNE myopathy; Sialuria 2018-02-06 criteria provided, single submitter clinical testing This sequence change replaces valine with isoleucine at codon 443 of the GNE protein (p.Val443Ile). The valine residue is highly conserved and there is a small physicochemical difference between valine and isoleucine. This variant is present in population databases (rs369714039, ExAC 0.006%). This variant has not been reported in the literature in individuals with GNE-related disease. ClinVar contains an entry for this variant (Variation ID: 290219). Algorithms developed to predict the effect of missense changes on protein structure and function do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Benign"; Align-GVGD: "Class C25"). In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

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.