ClinVar Miner

Submissions for variant NM_006267.5(RANBP2):c.1843A>T (p.Ile615Leu)

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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 RCV003032113 SCV003329037 uncertain significance Familial acute necrotizing encephalopathy 2022-08-31 criteria provided, single submitter clinical testing In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be tolerated. This variant has not been reported in the literature in individuals affected with RANBP2-related conditions. This variant is present in population databases (rs769717484, gnomAD 0.007%). This sequence change replaces isoleucine, which is neutral and non-polar, with leucine, which is neutral and non-polar, at codon 615 of the RANBP2 protein (p.Ile615Leu).

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