P137H (p.Pro137His) variant of STAT2 (P52630)
P137H (p.Pro137His) 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.
P137H (p.Pro137His) variant details
- p.Pro137His
- NCI-TCGA Cosmic COSV5847
- cosmic curated COSV58474
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available