W116Y (p.Trp116Tyr) variant of IL2RB (P14784)
W116Y (p.Trp116Tyr) in IL2RB (P14784) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as likely benign in the context of not provided.
W116Y (p.Trp116Tyr) variant details
- p.Trp116Tyr
- rs2146239158
- ClinGen CA2573158131
- ClinVar RCV002103994
- Ensembl rs2146239158
- Likely benign
- not provided
- Missense
- ClinVar: Likely benign (not provided)
- EBI: Likely benign
- UniProt: Likely benign