The c.562G>A variant in ACADVL is a missense variant predicted to cause substitution of glycine by serine at amino acid 188 (p.Gly188Ser). Information provided to the ACADVL VCEP provided by an external clinical laboratory shows increased C14:1 level in a pattern consistent with very long chain acyl-CoA dehydrogenase (VLCAD) deficiency in one patient (PP4_moderate) who was homozygous for the variant (PM3_supporting). One publication describes this variant in an affected individual, but this individual does not meet our PP4 guidelines and was not counted (Nikolayeva, E.A. et al., Symptomatic epilepsy as a manifestation of very long chain acyl-CoA dehydrogenase deficiency. 2008. Rossiiskii Vestnik Perinatologii i Pediatrii 53(3): 87-91 (in Russian)). This variant is absent from gnomAD v2.1.1. The computational predictor REVEL gives a score of 0.882, which is above the threshold of 0.75, evidence that correlates with impact to ACADVL function. In summary, this variant meets the criteria to be classified as a variant of uncertain significance for autosomal recessive (VLCAD) deficiency based on the ACMG/AMP criteria applied, as specified by the ClinGen ACADVL Variant Curation Expert Panel: PM2_supporting, PM3_supporting, PP3, PP4_moderate (ACADVL VCEP specifications version 1; approved November 9, 2021). This variant was originally curated April 12, 2022 and the recurated classification was approved by the expert panel on April 11, 2023.