The NM_000156.6:c.438A>G (p.Thr146=) variant in GAMT is a synonymous (silent) variant that is not predicted by SpliceAI to impact splicing. In addition, it occurs at a nucleotide that is not conserved as shown by phyloP (score -4.7) (BP4, BP7). This variant has been previously reported in an individual with GAMT deficiency who had significantly decreased creatine peak on MRS (PMID: 7808840) and GAMT activity <0.1% versus normal in fibroblasts (PMID: 11978605). Familial analysis showed that this individual harbored the variant in cis with NM_000156.6:c.299_311dup, (ClinVar Variation ID: 8302; pathogenic based on classification by the ClinGen CCDS VCEP) and had co-inherited these variants from his unaffected mother (BP2); he harbored these variants in trans with the pathogenic variant c.327G>A (ClinVar ID: 21065), inherited from his father. Of note, his unaffected brother was heterozygous for the two maternally co-inherited (c.438A>G and c.299_311dup) variants. The highest population minor allele frequency in gnomAD v4.1.0. is 0.00003333 (2/60006 alleles) in the Admixed American, which is lower than the ClinGen CCDS VCEP’s threshold for PM2_Supporting (<0.0004), meeting this criterion (PM2_Supporting). There is a ClinVar entry for this variant (Variation ID: 21066). In summary, this variant meets the criteria to be classified as a variant of uncertain significance for GAMT deficiency. Although the evidence is tending likely benign, the lack of data regarding the impact of this variant on it's own, in the ansence of the other two variants, led to a VUS classification based on the GAMT-specific ACMG/AMP criteria applied, as specified by the ClinGen Cerebral Creatine Deficiency Syndromes Variant Curation Expert Panel (Specifications Version 2.0.0): PM2_Supporting, BP2, BP4, BP7. (Classification approved by the ClinGen Cerebral Creatine Deficiency Syndromes Variant Curation Expert Panel on March 13, 2025)