ClinVar Miner

Submissions for variant NM_000090.4(COL3A1):c.944G>C (p.Gly315Ala)

dbSNP: rs587779487
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000087420 SCV002266669 likely pathogenic Ehlers-Danlos syndrome, type 4 2022-02-17 criteria provided, single submitter clinical testing Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is expected to disrupt COL3A1 protein function. This variant disrupts the triple helix domain of COL3A1. 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 COL3A1, variants that affect these glycine residues are significantly enriched in individuals with disease (PMID: 24922459, 25758994) compared to the general population (ExAC). In summary, the currently available evidence indicates that the variant is pathogenic, but additional data are needed to prove that conclusively. Therefore, this variant has been classified as Likely Pathogenic. ClinVar contains an entry for this variant (Variation ID: 101183). This sequence change replaces glycine, which is neutral and non-polar, with alanine, which is neutral and non-polar, at codon 315 of the COL3A1 protein (p.Gly315Ala). This variant is not present in population databases (gnomAD no frequency). This missense change has been observed in individual(s) with clinical features of Ehlers-Danlos syndrome (PMID: 24922459).
All of Us Research Program, National Institutes of Health RCV000087420 SCV005427273 uncertain significance Ehlers-Danlos syndrome, type 4 2023-03-28 criteria provided, single submitter clinical testing
Collagen Diagnostic Laboratory, University of Washington RCV000087420 SCV000120304 pathogenic Ehlers-Danlos syndrome, type 4 no assertion criteria provided clinical testing

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