ClinVar Miner

Submissions for variant NM_000435.3(NOTCH3):c.224G>C (p.Arg75Pro) (rs145069047)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000779253 SCV000915820 pathogenic Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy 2017-05-10 criteria provided, single submitter clinical testing Across a selection of available literature, the NOTCH3 c.224G>C (p.Arg75Pro) variant has been reported in a heterozygous state in at least 32 patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) from more than 10 independent families (Kim et al. 2006; Wang et al. 2011; Kim et al. 2012; Kim et al. 2014; Park et al. 2014; Yoon et al. 2015; Mizuno et al. 2016). These patients were of Korean, Japanese, or Chinese descent. Ueda et al. (2015) suggest that the p.Arg75Pro variant may be associated with a later age of onset and milder phenotype compared to other NOTCH3 variants seen in patients with CADASIL. The p.Arg75Pro variant was absent from 900 control alleles (Kim et al. 2006; Wang et al. 2011; Mizuno et al. 2016) and is not found in the 1000 Genomes Project, the Exome Sequencing Project, the Exome Aggregation Consortium, or the Genome Aggregation Database. Based on the evidence, the p.Arg75Pro variant is classified as pathogenic for cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. This variant was observed by ICSL as part of a predisposition screen in an ostensibly healthy population.

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