F11L (p.Phe11Leu) variant of LAG3 (P18627)
F11L (p.Phe11Leu) 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.
F11L (p.Phe11Leu) variant details
- p.Phe11Leu
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available