E109Q (p.Glu109Gln) variant of IL2RG (P31785)
E109Q (p.Glu109Gln) in IL2RG (P31785) is a missense change. Clinical records from EBI and UniProt describe it as benign. The record also includes structural context.
E109Q (p.Glu109Gln) variant details
- p.Glu109Gln
- 1000Genomes rs17875899
- ESP rs17875899
- ExAC rs17875899
- TOPMed rs17875899
- Benign
- Missense
- EBI: Benign (in dbSNP:rs17875899)
- UniProt: Benign (in dbSNP:rs17875899)
- Structural context available