ClinVar Miner

Submissions for variant NM_002617.4(PEX10):c.772C>G (p.Arg258Gly)

dbSNP: rs760632208
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001235815 SCV001408520 uncertain significance Peroxisome biogenesis disorder, complementation group 7 2022-08-02 criteria provided, single submitter clinical testing This sequence change replaces arginine, which is basic and polar, with glycine, which is neutral and non-polar, at codon 278 of the PEX10 protein (p.Arg278Gly). This variant is present in population databases (rs760632208, gnomAD 0.03%). This variant has not been reported in the literature in individuals affected with PEX10-related conditions. ClinVar contains an entry for this variant (Variation ID: 962031). 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. 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.

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