G181T (p.Gly181Thr) variant of ETFA (P13804)
G181T (p.Gly181Thr) 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.
G181T (p.Gly181Thr) variant details
- p.Gly181Thr
- NCI-TCGA Cosmic COSV5121
- cosmic curated COSV51211
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available