ClinVar Miner

Submissions for variant NM_000023.4(SGCA):c.229dup (p.Arg77fs)

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
Labcorp Genetics (formerly Invitae), Labcorp RCV003020880 SCV003301740 pathogenic Autosomal recessive limb-girdle muscular dystrophy type 2D 2023-09-21 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Arg77Profs*28) in the SGCA gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in SGCA are known to be pathogenic (PMID: 9192266). For these reasons, this variant has been classified as Pathogenic. ClinVar contains an entry for this variant (Variation ID: 2090379). This variant has not been reported in the literature in individuals affected with SGCA-related conditions. This variant is not present in population databases (gnomAD no frequency).
Baylor Genetics RCV003020880 SCV004208728 likely pathogenic Autosomal recessive limb-girdle muscular dystrophy type 2D 2022-03-23 criteria provided, single submitter clinical testing

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.