ClinVar Miner

Submissions for variant NM_006267.5(RANBP2):c.7760A>G (p.Gln2587Arg)

dbSNP: rs1553498323
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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 RCV000530705 SCV000646846 uncertain significance Familial acute necrotizing encephalopathy 2017-04-10 criteria provided, single submitter clinical testing This sequence change replaces glutamine with arginine at codon 2587 of the RANBP2 protein (p.Gln2587Arg). The glutamine residue is highly conserved and there is a small physicochemical difference between glutamine and arginine. This variant is not present in population databases (ExAC no frequency) and has not been reported in the literature in individuals with a RANBP2-related disease. 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, but these predictions have not been confirmed by published functional studies. In summary, this variant is a novel missense change that is not predicted to affect protein function. There is no indication that it causes disease, but the available evidence is currently insufficient to prove that conclusively. Therefore, it has been classified as a Variant of Uncertain Significance.

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