ClinVar Miner

Submissions for variant NM_014324.6(AMACR):c.670A>G (p.Arg224Gly)

gnomAD frequency: 0.00001  dbSNP: rs1348790589
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001919021 SCV002185380 uncertain significance Alpha-methylacyl-CoA racemase deficiency 2021-09-24 criteria provided, single submitter clinical testing This sequence change replaces arginine with glycine at codon 224 of the AMACR protein (p.Arg224Gly). The arginine residue is weakly conserved and there is a moderate physicochemical difference between arginine and glycine. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with AMACR-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: "Tolerated"; 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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