ClinVar Miner

Submissions for variant NM_001005373.4(LRSAM1):c.1546C>T (p.Gln516Ter)

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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 RCV003643362 SCV004548027 pathogenic Charcot-Marie-Tooth disease axonal type 2P 2023-03-01 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.Gln516*) in the LRSAM1 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in LRSAM1 are known to be pathogenic (PMID: 20865121, 33414056). This variant has not been reported in the literature in individuals affected with LRSAM1-related conditions. For these reasons, this variant has been classified as Pathogenic.

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