ClinVar Miner

Submissions for variant NM_005373.3(MPL):c.1678del (p.Cys560fs)

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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 RCV002781329 SCV003034548 pathogenic Congenital amegakaryocytic thrombocytopenia; Essential thrombocythemia 2022-10-28 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. This variant disrupts a region of the MPL protein in which other variant(s) (p.Pro635Leu) have been determined to be pathogenic (PMID: 10971406, 11071383, 18422784). This suggests that this is a clinically significant region of the protein, and that variants that disrupt it are likely to be disease-causing. This variant has not been reported in the literature in individuals affected with MPL-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change creates a premature translational stop signal (p.Cys560Valfs*70) in the MPL gene. While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 76 amino acid(s) of the MPL protein.

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