H33Q (p.His33Gln) variant of IL2RA (P01589)
H33Q (p.His33Gln) in IL2RA (P01589) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
H33Q (p.His33Gln) variant details
- p.His33Gln
- NCI-TCGA Cosmic COSV5691
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available