N33S (p.Asn33Ser) variant of IL2RG (P31785)
N33S (p.Asn33Ser) in IL2RG (P31785) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The record also includes structural context.
N33S (p.Asn33Ser) variant details
- p.Asn33Ser
- rs2519648645
- ClinGen CA413497603
- ClinVar RCV003131264
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available