R26T (p.Arg26Thr) variant of ABCG8 (Q9H221)
R26T (p.Arg26Thr) in ABCG8 (Q9H221) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
R26T (p.Arg26Thr) variant details
- p.Arg26Thr
- NCI-TCGA Cosmic COSV5539
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available