ClinVar Miner

Submissions for variant NM_001849.3(COL6A2):c.902G>T (p.Gly301Val) (rs1555872965)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory,University of Chicago RCV000499945 SCV000594199 uncertain significance not specified 2015-09-19 criteria provided, single submitter clinical testing
Invitae RCV001063163 SCV001227998 pathogenic Bethlem myopathy 1 2019-04-15 criteria provided, single submitter clinical testing This sequence change replaces glycine with valine at codon 301 of the COL6A2 protein (p.Gly301Val). The glycine residue is highly conserved and there is a moderate physicochemical difference between glycine and valine. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with autosomal dominant COL6A2-related conditions. ClinVar contains an entry for this variant (Variation ID: 434815). Glycine residues within the Gly-Xaa-Yaa repeats of the triple helix domain are required for the structure and stability of fibrillar collagens (PMID: 7695699, 8218237, 19344236). In COL6A2, missense variants at these glycine residues are significantly enriched in individuals with disease (PMID: 15689448, 24038877) compared to the general population (ExAC). Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may create or strengthen a splice site, but this prediction has not been confirmed by published transcriptional studies. This variant disrupts the p.Gly301 amino acid residue in COL6A2. Other variant(s) that disrupt this residue (p.Gly301Asp, p.Gly301Cys, p.Gly301Ser) have been determined to be pathogenic in individuals affected with autosomal dominant type VI collagenopathy (PMID: 7785673, 24271325). This suggests that this residue is clinically significant, and that variants that disrupt this residue are likely to be disease-causing. For these reasons, this variant has been classified as Pathogenic.

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