ClinVar Miner

Submissions for variant NM_000435.3(NOTCH3):c.5243G>A (p.Arg1748His)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV005234725 SCV005876229 uncertain significance not provided 2024-01-24 criteria provided, single submitter clinical testing The NOTCH3 c.5243G>A; p.Arg1748His variant (rs769483312), to our knowledge, is not reported in the medical literature or gene-specific databases. This variant is observed in the general population with an overall allele frequency of 0.002% (5/280496 alleles) in the Genome Aggregation Database (v2.1.1). Computational analyses predict that this variant is deleterious (REVEL: 0.806). Most pathogenic NOTCH3 variants occur in exons 2-24 and either create or destroy a cysteine residue within an EGF-like domain (Rutten 2014). However, there are several amino acid substitutions not involving cysteine that may be disease-associated (Muino 2017). Although the p.Arg1748His variant does not occur within this critical region or involve a cysteine residue, due to its low population frequency, its clinical significance is uncertain. References: Muino E et al. Systematic Review of Cysteine-Sparing NOTCH3 Missense Mutations in Patients with Clinical Suspicion of CADASIL. Int J Mol Sci. 2017 Sep 13;18(9). pii: E1964. PMID: 28902129. Rutten JW et al. Interpretation of NOTCH3 mutations in the diagnosis of CADASIL. Expert Rev Mol Diagn. 2014 Jun;14(5):593-603. PMID: 24844136.

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