R26W (p.Arg26Trp) variant of ETFB (P38117)
R26W (p.Arg26Trp) in ETFB (P38117) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
R26W (p.Arg26Trp) variant details
- p.Arg26Trp
- NCI-TCGA Cosmic COSV1004
- cosmic curated COSV10049
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available