The NM_000156.6:c.152A>C variant in GAMT is a missense variant that is predicted to result in the substitution of histidine by proline at amino acid 51 (p.His51Pro). One proband has been reported with mild developmental delay, anti-epileptic drug responsive seizures, and autistic features, with a normal brain MRI. This individual had elevated guanidinoacetate in urine and, on MRS, creatine peak was partially absent and guanidinoacetate peak was absent (PMID: 15108290, 24415674) (PP4_Strong). This individual is compound heterozygous for the variant and another variant in GAMT that has been classified as pathogenic by the ClinGen CCDS VCEP, c.526dupG. The variants were confirmed to be in trans by parental testing (PM3). The variant is absent in gnomAD v4.1.0. (PM2_Supporting). When the variant was expressed in a primary GAMT-deficient human fibroblast cell line, no detectable expression could be seen on Western blot and the GAMT activity was very low (<4%) (PMID 24415674) (PS3_Supporting). The computational predictor REVEL gives a score of 0.814 which is in the range of 0.773-0.932, evidence that correlates with impact to GAMT function at the moderate level (PMID: 36413997) (PP3_Moderate). There is a ClinVar entry for this variant (Variation ID: 2138184). In summary, this variant meets the criteria to be classified as pathogenic for GAMT deficiency. GAMT-specific ACMG/AMP criteria met, based on the specifications of the ClinGen Cerebral Creatine Deficiencies Variant Curation Expert Panel (Specifications Version 2.0.0): PP4_Strong, PM3, PP3_Moderate, PS3_Supporting, PM2_Supporting. (Classification approved by the ClinGen Cerebral Creatine Deficiency Syndromes Variant Curation Expert Panel on December 10, 2025)