F11C (p.Phe11Cys) variant of LAG3 (P18627)
F11C (p.Phe11Cys) 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.
F11C (p.Phe11Cys) variant details
- p.Phe11Cys
- NCI-TCGA Cosmic COSV9917
- cosmic curated COSV99179
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available