D79N (p.Asp79Asn) variant of STAT5B (P51692)
D79N (p.Asp79Asn) 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.
D79N (p.Asp79Asn) variant details
- p.Asp79Asn
- NCI-TCGA Cosmic COSV5318
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available