ClinVar Miner

Submissions for variant NM_015087.5(SPART):c.752T>G (p.Val251Gly)

gnomAD frequency: 0.00003  dbSNP: rs766063946
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
Labcorp Genetics (formerly Invitae), Labcorp RCV001972155 SCV002207539 uncertain significance not provided 2021-07-17 criteria provided, single submitter clinical testing 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. Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be disruptive. This variant has not been reported in the literature in individuals affected with SPART-related conditions. This variant is present in population databases (rs766063946, ExAC 0.03%). This sequence change replaces valine with glycine at codon 251 of the SPART protein (p.Val251Gly). The valine residue is highly conserved and there is a moderate physicochemical difference between valine and glycine.

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.