T56P (p.Thr56Pro) variant of IL7R (P16871)
T56P (p.Thr56Pro) in IL7R (P16871) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
T56P (p.Thr56Pro) variant details
- p.Thr56Pro
- NCI-TCGA Cosmic COSV1002
- cosmic curated COSV10028
- NCI-TCGA Cosmic COSV5740
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available