S109R (p.Ser109Arg) variant of GRM5 (P41594)
S109R (p.Ser109Arg) in GRM5 (P41594) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
S109R (p.Ser109Arg) variant details
- p.Ser109Arg
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.