ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.1390A>G (p.Lys464Glu)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV003321355 SCV004025721 uncertain significance not provided 2023-02-10 criteria provided, single submitter clinical testing Not observed at significant frequency in large population cohorts (gnomAD); In silico analysis supports that this missense variant has a deleterious effect on protein structure/function; Has not been previously published as pathogenic or benign to our knowledge; This variant is associated with the following publications: (PMID: 29294058, 31125631)

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