ClinVar Miner

Submissions for variant NM_000093.5(COL5A1):c.2482C>T (p.Arg828Trp)

gnomAD frequency: 0.00005  dbSNP: rs185912761
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000470723 SCV000725554 likely benign not provided 2020-10-06 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002230680 SCV001667814 likely benign Ehlers-Danlos syndrome, classic type, 1 2024-12-24 criteria provided, single submitter clinical testing
Ambry Genetics RCV002431360 SCV002740416 likely benign Familial thoracic aortic aneurysm and aortic dissection 2018-07-03 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
PreventionGenetics, part of Exact Sciences RCV003960087 SCV004775502 likely benign COL5A1-related disorder 2022-05-25 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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