A19G (p.Ala19Gly) variant of ITPR2 (Q14571)
A19G (p.Ala19Gly) in ITPR2 (Q14571) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A19G (p.Ala19Gly) variant details
- p.Ala19Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available