ClinVar Miner

Submissions for variant NM_001754.5(RUNX1):c.764_765del (p.His255fs)

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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 RCV005203948 SCV005841245 pathogenic Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 2024-11-13 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.His255Leufs*5) in the RUNX1 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in RUNX1 are known to be pathogenic (PMID: 18723428, 24100448). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with RUNX1-related conditions. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site. For these reasons, this variant has been classified as Pathogenic.

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