P78A (p.Pro78Ala) variant of PPP2R5D (Q14738)
P78A (p.Pro78Ala) in PPP2R5D (Q14738) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes variant effect predictions and structural context.
P78A (p.Pro78Ala) variant details
- p.Pro78Ala
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- SIFT 0.02
- UniProt: Variant assessed as somatic; high impact.
- Structural context available