The c.349C>T (NM_000215.4) variant in JAK3 is a missense variant predicted to cause the substitution of Arginine by Cysteine at amino acid 117 (p.Arg117Cys). The highest population minor allele frequency in gnomAD v2.1.1 is 0.0001755 (1/5698 alleles) in the "Other" population; this frequency will not be considered here as the "Other" population is characterized on gnomAD as a bottleneck population. The second highest MAF is 0.00003543 (1/28224 alleles) in the South Asia population, which is lower than the ClinGen SCID VCEP threshold (<0.000115) for PM2_Supporting, meeting this criterion (PM2_Supporting). No homozygotes have been observed in gnomAD (BS2 is not met). This variant has been described in at least two patients in the literature (PMIDs: 32215810 and 23069490). At least one patient with this variant displayed: *Diagnostic criteria for Leaky SCID 0.5 pts + *Reduced or constitutive cytokine-induced JAK3 tyrosine phosphorylation in patient cells 1 pt + *T-B+NK- lymphocyte subset profile not applied because only IL7R was sequenced, so we can not rule out alternative cause. Total is 1.5 points, PP4_Supporting (PMID: 23069490). The patient is homozygous for this variant (0.5 pts, PM3_Supporting, PMID: 23069490) In summary, this variant meets the criteria to be classified as a variant of uncertain significance for autosomal recessive T-B+ severe combined immunodeficiency due to JAK3 deficiency based on the ACMG/AMP criteria applied, as specified by the ClinGen SCID VCEP. Criteria applied: PM2_Supporting, PM3_Supporting, and PP4_Supporting (VCEP specifications version 1.0).