Y69N (p.Tyr69Asn) variant of STAT2 (P52630)
Y69N (p.Tyr69Asn) 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.
Y69N (p.Tyr69Asn) variant details
- p.Tyr69Asn
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available