ClinVar Miner

Submissions for variant NM_000090.4(COL3A1):c.3204CCCTGCTGG[1] (p.1069PAG[1])

dbSNP: rs771791598
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001377514 SCV001574865 pathogenic Ehlers-Danlos syndrome, type 4 2023-10-03 criteria provided, single submitter clinical testing This variant, c.3213_3221del, results in the deletion of 3 amino acid(s) of the COL3A1 protein (p.Pro1072_Gly1074del), but otherwise preserves the integrity of the reading frame. This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with COL3A1-related conditions. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site. 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). This variant disrupts a region of the COL3A1 protein in which other variant(s) (p.Gly1074Asp) have been determined to be pathogenic (Invitae). This suggests that this is a clinically significant region of the protein, and that variants that disrupt it are likely to be disease-causing. For these reasons, this variant has been classified as Pathogenic.

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