R7V (p.Arg7Val) variant of ATP1A1 (P05023)
R7V (p.Arg7Val) in ATP1A1 (P05023) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
R7V (p.Arg7Val) variant details
- p.Arg7Val
- NCI-TCGA Cosmic COSV5518
- NCI-TCGA Cosmic COSV5519
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available