ClinVar Miner

Submissions for variant NM_001130987.2(DYSF):c.5831G>A (p.Arg1944Gln)

gnomAD frequency: 0.00001  dbSNP: rs886043057
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
Eurofins Ntd Llc (ga) RCV000346517 SCV000338205 uncertain significance not provided 2015-12-07 criteria provided, single submitter clinical testing
Invitae RCV001343503 SCV001537491 uncertain significance Qualitative or quantitative defects of dysferlin 2021-09-01 criteria provided, single submitter clinical testing This sequence change replaces arginine with glutamine at codon 1905 of the DYSF protein (p.Arg1905Gln). The arginine residue is moderately conserved and there is a small physicochemical difference between arginine and glutamine. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals affected with DYSF-related conditions. ClinVar contains an entry for this variant (Variation ID: 285259). Algorithms developed to predict the effect of missense changes on protein structure and function output the following: SIFT: "Tolerated"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0". The glutamine amino acid residue is found in multiple mammalian species, which suggests that this missense change does not adversely affect protein function. 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.