L11R (p.Leu11Arg) variant of GRM5 (P41594)
L11R (p.Leu11Arg) in GRM5 (P41594) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
L11R (p.Leu11Arg) variant details
- p.Leu11Arg
- NCI-TCGA Cosmic COSV5962
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.