ClinVar Miner

Submissions for variant NM_020631.6(PLEKHG5):c.2902del (p.Val968fs)

dbSNP: rs773188120
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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 RCV002587493 SCV002948138 pathogenic Neuronopathy, distal hereditary motor, autosomal recessive 4; Charcot-Marie-Tooth disease recessive intermediate C 2022-07-19 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 affected with PLEKHG5-related conditions. This variant is present in population databases (rs773188120, gnomAD 0.007%). This sequence change creates a premature translational stop signal (p.Val968Serfs*16) in the PLEKHG5 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in PLEKHG5 are known to be pathogenic (PMID: 17564964, 23777631).
Fulgent Genetics, Fulgent Genetics RCV002587493 SCV005659015 likely pathogenic Neuronopathy, distal hereditary motor, autosomal recessive 4; Charcot-Marie-Tooth disease recessive intermediate C 2024-03-28 criteria provided, single submitter clinical testing

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