R61S (p.Arg61Ser) variant of GRM5 (P41594)
R61S (p.Arg61Ser) in GRM5 (P41594) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
R61S (p.Arg61Ser) variant details
- p.Arg61Ser
- NCI-TCGA Cosmic COSV1005
- cosmic curated COSV10055
- NCI-TCGA Cosmic COSV5963
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.