G92D (p.Gly92Asp) variant of GRM5 (P41594)
G92D (p.Gly92Asp) in GRM5 (P41594) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
G92D (p.Gly92Asp) variant details
- p.Gly92Asp
- NCI-TCGA Cosmic COSV5959
- cosmic curated COSV59595
- NCI-TCGA Cosmic COSV5960
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.