The NM_000156.6:c.317A>C variant in GAMT is a missense variant that is predicted to result in the substitution of glutamine by proline at amino acid 106 (p.Gln106Pro). The highest population minor allele frequency in gnomAD v2.1.1 is 0.000156 (3/19226 alleles) in the African/African American population, which is lower than the ClinGen CCDS VCEP’s threshold for PM2_Supporting (<0.0004), meeting this criterion (PM2_Supporting). In HeLa cells, expression of the variant resulted in <15% of wild-type GAMT enzyme activity (PMID: 26003046) (PS3_Supporting). The computational predictor REVEL gives a score of 0.75 which meets the threshold of 0.75, evidence that correlates with impact to GAMT function (PP3). To our knowledge, this variant has not been reported in an individual with GAMT deficiency in the published literature. There is a ClinVar entry for this variant (Variation ID: 449690). In summary, this variant meets the criteria to be classified as a variant of uncertain significance for GAMT deficiency. GAMT-specific ACMG/AMP criteria applied, as specified by the ClinGen Cerebral Creatine Deficiency Syndromes Variant Curation Expert Panel (Specifications Version 1.1.0): PP3, PS3_Supporting, PM2_Supporting. (Classification approved by the ClinGen Cerebral Creatine Deficiency Syndromes Variant Curation Expert Panel on May 11, 2023)