ClinVar Miner

Submissions for variant NM_000322.5(PRPH2):c.52del (p.Gln18fs)

dbSNP: rs2152011142
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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 RCV001387459 SCV001588076 pathogenic PRPH2-related disorder 2020-10-19 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. This variant has not been reported in the literature in individuals with PRPH2-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change creates a premature translational stop signal (p.Gln18Lysfs*6) 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, 8485576, 8675410, 16916875, 17504850, 25675413, 26061163, 27365499, 29555955).

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