ClinVar Miner

Submissions for variant NM_020964.3(EPG5):c.6964A>G (p.Met2322Val)

gnomAD frequency: 0.00001  dbSNP: rs1257071280
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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 RCV002041043 SCV002314725 uncertain significance Vici syndrome 2021-08-31 criteria provided, single submitter clinical testing This sequence change replaces methionine with valine at codon 2322 of the EPG5 protein (p.Met2322Val). The methionine residue is highly conserved and there is a small physicochemical difference between methionine and valine. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals affected with EPG5-related conditions. 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: "Possibly Damaging"; Align-GVGD: "Class C0"). 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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