H149Y (p.His149Tyr) variant of ATP13A2 (Q9NQ11)
H149Y (p.His149Tyr) in ATP13A2 (Q9NQ11) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
H149Y (p.His149Tyr) variant details
- p.His149Tyr
- NCI-TCGA Cosmic COSV5870
- cosmic curated COSV58703
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available