A48D (p.Ala48Asp) variant of PRKAR1A (P10644)
A48D (p.Ala48Asp) in PRKAR1A (P10644) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
A48D (p.Ala48Asp) variant details
- p.Ala48Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available