ClinVar Miner

Submissions for variant NM_000666.3(ACY1):c.977C>G (p.Ala326Gly)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Neuberg Centre For Genomic Medicine, NCGM RCV004555808 SCV005044817 uncertain significance Aminoacylase 1 deficiency criteria provided, single submitter clinical testing The missense c.977C>G p.Ala326Gly variant in ACY1 gene has not been reported previously as a pathogenic variant nor as a benign variant, to our knowledge. The p.Ala326Gly variant is novel not in any individuals in gnomAD Exomes and 1000 Genomes. This variant has not been reported to the ClinVar database. The amino acid change p.Ala326Gly in ACY1 is predicted as conserved by GERP++ and PhyloP across 100 vertebrates. The amino acid Ala at position 326 is changed to a Gly changing protein sequence and it might alter its composition and physico-chemical properties. For these reasons, this variant has been classified as Variant of Uncertain Significance VUS.

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