ClinVar Miner

Submissions for variant NM_006267.5(RANBP2):c.7892A>T (p.Asp2631Val)

dbSNP: rs1677511241
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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 RCV001061303 SCV001226041 uncertain significance Familial acute necrotizing encephalopathy 2022-06-04 criteria provided, single submitter clinical testing This variant is not present in population databases (gnomAD no frequency). 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 disruptive. ClinVar contains an entry for this variant (Variation ID: 855945). This variant has not been reported in the literature in individuals affected with RANBP2-related conditions. This sequence change replaces aspartic acid, which is acidic and polar, with valine, which is neutral and non-polar, at codon 2631 of the RANBP2 protein (p.Asp2631Val).

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