A86P (p.Ala86Pro) variant of IL2RA (P01589)
A86P (p.Ala86Pro) 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.
A86P (p.Ala86Pro) variant details
- p.Ala86Pro
- NCI-TCGA Cosmic COSV5692
- cosmic curated COSV56920
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available