ClinVar Miner

Submissions for variant NM_015164.4(PLEKHM2):c.2963del (p.Lys988fs)

dbSNP: rs753628124
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001049231 SCV001213272 uncertain significance Dilated Cardiomyopathy, Recessive 2020-01-30 criteria provided, single submitter clinical testing In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Experimental studies and prediction algorithms are not available for this variant, and the functional significance of the affected amino acid(s) is currently unknown. This variant has not been reported in the literature in individuals with PLEKHM2-related conditions. This variant is present in population databases (rs753628124, ExAC 0.002%). This sequence change results in a premature translational stop signal in the PLEKHM2 gene (p.Lys988Argfs*8). While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 32 amino acids of the PLEKHM2 protein.

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