A110G (p.Ala110Gly) variant of ETFA (P13804)
A110G (p.Ala110Gly) in ETFA (P13804) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A110G (p.Ala110Gly) variant details
- p.Ala110Gly
- NCI-TCGA Cosmic COSV9914
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available