ClinVar Miner

Submissions for variant NM_000322.5(PRPH2):c.68del (p.Met23fs)

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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 RCV003757555 SCV004429355 pathogenic PRPH2-related disorder 2023-01-06 criteria provided, single submitter clinical testing This variant is not present in population databases (gnomAD no frequency). This sequence change creates a premature translational stop signal (p.Met23Argfs*15) 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 has not been reported in the literature in individuals affected with PRPH2-related conditions. For these reasons, this variant has been classified as Pathogenic.
CeGaT Center for Human Genetics Tuebingen RCV004723413 SCV005330605 pathogenic not provided 2024-08-01 criteria provided, single submitter clinical testing PRPH2: PVS1, PM2, PS4:Supporting

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