ClinVar Miner

Submissions for variant NM_007074.4(CORO1A):c.286G>A (p.Val96Ile)

gnomAD frequency: 0.00001  dbSNP: rs756845489
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 RCV001239820 SCV001412721 uncertain significance Severe combined immunodeficiency due to CORO1A deficiency 2021-09-01 criteria provided, single submitter clinical testing This sequence change replaces valine with isoleucine at codon 96 of the CORO1A protein (p.Val96Ile). The valine residue is moderately conserved and there is a small physicochemical difference between valine and isoleucine. This variant is present in population databases (rs756845489, ExAC 0.002%). This variant has not been reported in the literature in individuals affected with CORO1A-related conditions. 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 tolerated. 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.