E13D (p.Glu13Asp) variant of STAT5B (P51692)
E13D (p.Glu13Asp) 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.
E13D (p.Glu13Asp) variant details
- p.Glu13Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available