S132G (p.Ser132Gly) variant of STAT5B (P51692)
S132G (p.Ser132Gly) in STAT5B (P51692) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S132G (p.Ser132Gly) variant details
- p.Ser132Gly
- NCI-TCGA Cosmic COSV9951
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available