ClinVar Miner

Submissions for variant NM_000093.5(COL5A1):c.2493C>T (p.Ile831=)

gnomAD frequency: 0.00011  dbSNP: rs199630108
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000245129 SCV000302165 likely benign not specified criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000327066 SCV000478544 uncertain significance Ehlers-Danlos syndrome type 7A 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV000866278 SCV000512701 likely benign not provided 2019-12-04 criteria provided, single submitter clinical testing
Ambry Genetics RCV002313969 SCV000738628 likely benign Familial thoracic aortic aneurysm and aortic dissection 2016-07-28 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.
Illumina Laboratory Services, Illumina RCV001165823 SCV001328067 likely benign Ehlers-Danlos syndrome, classic type 2018-01-13 criteria provided, single submitter clinical testing This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score and internal cut-off values, a variant classified as likely benign is not then subjected to further curation. The score for this variant resulted in a classification of likely benign for this disease.
Labcorp Genetics (formerly Invitae), Labcorp RCV001521595 SCV001730960 benign Ehlers-Danlos syndrome, classic type, 1 2024-01-04 criteria provided, single submitter clinical testing

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