G26R (p.Gly26Arg) variant of LAG3 (P18627)
G26R (p.Gly26Arg) in LAG3 (P18627) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G26R (p.Gly26Arg) variant details
- p.Gly26Arg
- NCI-TCGA Cosmic COSV9918
- cosmic curated COSV99180
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available