ClinVar Miner

Submissions for variant NM_001171613.2(PREPL):c.634del (p.Tyr212fs)

dbSNP: rs2103925424
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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 RCV002037702 SCV002233617 pathogenic Myasthenic syndrome, congenital, 22 2022-02-03 criteria provided, single submitter clinical testing This variant has not been reported in the literature in individuals affected with PREPL-related conditions. For these reasons, this variant has been classified as Pathogenic. This variant is not present in population databases (gnomAD no frequency). This sequence change creates a premature translational stop signal (p.Tyr301Thrfs*24) in the PREPL gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in PREPL are known to be pathogenic (PMID: 24610330, 28726805, 29913539).

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