P7S (p.Pro7Ser) variant of ATP13A2 (Q9NQ11)
P7S (p.Pro7Ser) 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.
P7S (p.Pro7Ser) variant details
- p.Pro7Ser
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available