The NM_001482.3: c.778C>T (p.Arg260Ter) variant in GATM is a nonsense variant predicted to cause a premature stop codon in biologically-relevant-exon 5 out of a total of 9 exons, leading to nonsense mediated decay in a gene in which loss-of-function is an established disease mechanism (PVS1). The highest population minor allele frequency in gnomAD v4.1.0. is 8.474e-7 (1/1180024 alleles) in the European non-Finnish population, which is lower than the ClinGen CCDS VCEP’s threshold for PM2_Supporting (<0.000055), meeting this criterion (PM2_Supporting). To our knowledge, this variant has not been reported in the published literature. However, there is a ClinVar entry for this variant (Variation ID: 205617). The variant has been observed in a child with seizures referred for an epilepsy panel (GeneDx); no second variant in GATM was identified (insufficient evidence for PP4 or PM3). The classification of this variant has been upgraded from Variant of Uncertain Significance to Likely Pathogenic based on the recommendations of the ClinGen Sequence Variant Interpretation Working Group, that a variant meeting PVS1 and PM2_Supporting is classified as Likely Pathogenic (https://clinicalgenome.org/site/assets/files/5182/pm2_-_svi_recommendation_-_approved_sept2020.pdf ). GATM-specific ACMG/AMP codes met, as specified by the ClinGen Cerebral Creatine Deficiency Syndromes VCEP (Specifications Version 2.0.0): PVS1, PM2_Supporting. (Classification approved by the ClinGen CCDS VCEP on May 22, 2025).