NM_005214.5(CTLA4):c.75del (p.Leu28PhefsTer?) is a frameshift variant that introduces a premature stop codon into exon 1 of 4 and is predicted to trigger nonsense-mediated decay in CTLA4, in which loss-of-function is an established mechanism of disease (PVS1). This variant is present in gnomAD v4.1.0 at an allele frequency of 0.0000006195, with 1 allele / 1,614,092 total alleles across all populations of gnomAD, which is higher than the ClinGen Antibody Deficiencies VCEP PM2_Supporting threshold of <0.000000143, so PM2_Supporting is not met. This variant is present in gnomAD v4.1.0 at a GrpMax allele frequency of 0.000000847, with 1 allele / 1,179,912 total alleles in the European (non-Finnish) population, which is lower than the BS1 threshold of >0.00000111, so BS1 is not met. The variant has been observed in at least 1 patient with a phenotype that includes hepatosplenomegaly (2 pts), autoimmune hemolytic anemia and thrombocytopenia (2 pts), pulmonary nodules (4 pts), infiltrative lesions (2 pts) in the cerebrum (1 pt), and activated T cells showing a partial decrease in expression of CTLA-4 by flow cytometry, with genotyping by exome sequencing identifying no alternative basis for disease in other loci, which together are highly specific for CTLA4 insufficiency (11 total pts, PMID: 25213377, PP4_Moderate). In summary, this variant meets the criteria to be classified as pathogenic for autosomal dominant autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency based on the ACMG/AMP criteria applied, as specified by the ClinGen Antibody Deficiencies VCEP: PVS1 and PP4_Moderate. (VCEP specifications version 1.0.0; date of approval 09/18/2025).