ClinVar Miner

Submissions for variant NM_000348.4(SRD5A2):c.544C>T (p.Gln182Ter)

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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 RCV003607695 SCV004386215 pathogenic 3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency 2023-12-20 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Gln182*) in the SRD5A2 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in SRD5A2 are known to be pathogenic (PMID: 1406794, 1944596). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with SRD5A2-related conditions. For these reasons, this variant has been classified as Pathogenic.

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