ClinVar Miner

Submissions for variant NM_000093.5(COL5A1):c.4984T>C (p.Cys1662Arg)

dbSNP: rs2132887638
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV002251640 SCV002522045 uncertain significance not provided 2021-11-24 criteria provided, single submitter clinical testing Has not been previously published as pathogenic or benign to our knowledge; Not observed at significant frequency in large population cohorts (gnomAD); In silico analysis supports that this missense variant has a deleterious effect on protein structure/function; Not located in the triple helical region, where the majority of pathogenic missense variants occur (Symoens et al., 2012; HGMD)

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