ClinVar Miner

Submissions for variant NM_000322.5(PRPH2):c.774C>G (p.Tyr258Ter)

dbSNP: rs121918564
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002568181 SCV003460764 pathogenic PRPH2-related disorder 2023-11-27 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Tyr258*) in the PRPH2 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in PRPH2 are known to be pathogenic (PMID: 8111389, 8485575, 8485576, 8675410, 16916875, 17504850, 22863181, 25675413, 26061163, 27365499, 29555955, 33546218). This variant is not present in population databases (gnomAD no frequency). This premature translational stop signal has been observed in individual(s) with inherited retinal dystrophy (PMID: 29555955). ClinVar contains an entry for this variant (Variation ID: 1175302). For these reasons, this variant has been classified as Pathogenic.
Leiden Open Variation Database RCV001530381 SCV001745190 pathogenic not provided 2021-04-06 no assertion criteria provided curation Curator: Global Variome, with Curator vacancy. Submitters to LOVD: LOVD, Manon Peeters.

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