ClinVar Miner

Submissions for variant NM_005373.3(MPL):c.230del (p.Cys77fs)

gnomAD frequency: 0.00003  dbSNP: rs1291157023
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001381839 SCV001580374 pathogenic Congenital amegakaryocytic thrombocytopenia; Essential thrombocythemia 2023-12-02 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Cys77Serfs*3) in the MPL gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in MPL are known to be pathogenic (PMID: 8073287, 11133753). This variant is present in population databases (no rsID available, gnomAD 0.002%). This variant has not been reported in the literature in individuals affected with MPL-related conditions. ClinVar contains an entry for this variant (Variation ID: 1069872). For these reasons, this variant has been classified as Pathogenic.

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