ClinVar Miner

Submissions for variant NM_006267.5(RANBP2):c.1964C>G (p.Ala655Gly)

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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 RCV003620847 SCV004491270 uncertain significance Familial acute necrotizing encephalopathy 2022-12-24 criteria provided, single submitter clinical testing This variant has not been reported in the literature in individuals affected with RANBP2-related conditions. 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 are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Benign"; Align-GVGD: "Class C55"). This variant is not present in population databases (gnomAD no frequency). This sequence change replaces alanine, which is neutral and non-polar, with glycine, which is neutral and non-polar, at codon 655 of the RANBP2 protein (p.Ala655Gly).

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