ClinVar Miner

Submissions for variant NM_020964.3(EPG5):c.4790C>T (p.Ala1597Val)

dbSNP: rs2145575510
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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 RCV001998682 SCV002275847 uncertain significance Vici syndrome 2020-11-11 criteria provided, single submitter clinical testing This sequence change replaces alanine with valine at codon 1597 of the EPG5 protein (p.Ala1597Val). The alanine residue is moderately conserved and there is a small physicochemical difference between alanine and valine. This variant is not present in population databases (ExAC 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, but these predictions have not been confirmed by published functional studies and their clinical significance is uncertain. This variant has not been reported in the literature in individuals with EPG5-related conditions.

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