ClinVar Miner

Submissions for variant NM_000322.5(PRPH2):c.259_266del (p.Asp87fs)

dbSNP: rs1554270834
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
NEI Ophthalmic Genomics Laboratory, National Institutes of Health RCV001250294 SCV001424607 pathogenic Stargardt disease 2020-01-07 criteria provided, single submitter clinical testing The variant NM_000322.4:c.259_266delGACCCAGC in the PRPH2 gene has been previously studied (PMIDs 24608669, 28041643). We found this variant in 2 patient(s) in a PRPH2 cohort study (Reeves et al. 2020). This variant is listed in dbSNP and/or HGMD (CD143729). It is absent in gnomAD browser. It is enriched in the PRPH2 disease cohort. We invoked ACMG criteria [PVS1, PS4, PM2, PP5] and classified NM_000322.4:c.259_266delGACCCAGC in the PRPH2 gene as a Pathogenic mutation.
Labcorp Genetics (formerly Invitae), Labcorp RCV001857204 SCV002227706 pathogenic PRPH2-related disorder 2023-07-31 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. ClinVar contains an entry for this variant (Variation ID: 437964). This premature translational stop signal has been observed in individual(s) with autosomal dominant PRPH2-related conditions (PMID: 24608669, 28041643, 32531846, 32581362). This variant is not present in population databases (gnomAD no frequency). This sequence change creates a premature translational stop signal (p.Asp87Glnfs*87) 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).
NIHR Bioresource Rare Diseases, University of Cambridge RCV000504674 SCV000598700 pathogenic Retinal dystrophy 2015-01-01 no assertion criteria provided research
Leiden Open Variation Database RCV001530215 SCV001744936 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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