Q147L (p.Gln147Leu) variant of ATP13A2 (Q9NQ11)
Q147L (p.Gln147Leu) 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.
Q147L (p.Gln147Leu) variant details
- p.Gln147Leu
- NCI-TCGA Cosmic COSV1004
- cosmic curated COSV10045
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available