P78T (p.Pro78Thr) variant of STAT2 (P52630)
P78T (p.Pro78Thr) in STAT2 (P52630) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
P78T (p.Pro78Thr) variant details
- p.Pro78Thr
- NCI-TCGA Cosmic COSV1000
- cosmic curated COSV10002
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available