A110T (p.Ala110Thr) variant of IDH2 (P48735)
A110T (p.Ala110Thr) in IDH2 (P48735) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A110T (p.Ala110Thr) variant details
- p.Ala110Thr
- NCI-TCGA TCGA novel
- ESP rs368655225
- ExAC rs368655225
- TOPMed rs368655225
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available