G92C (p.Gly92Cys) variant of GRM5 (P41594)
G92C (p.Gly92Cys) in GRM5 (P41594) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
G92C (p.Gly92Cys) variant details
- p.Gly92Cys
- NCI-TCGA Cosmic COSV5959
- NCI-TCGA Cosmic COSV5961
- cosmic curated COSV59614
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.