A78G (p.Ala78Gly) variant of IRAK1 (P51617)
A78G (p.Ala78Gly) in IRAK1 (P51617) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A78G (p.Ala78Gly) variant details
- p.Ala78Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available