D82G (p.Asp82Gly) variant of GRM5 (P41594)
D82G (p.Asp82Gly) in GRM5 (P41594) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
D82G (p.Asp82Gly) variant details
- p.Asp82Gly
- NCI-TCGA Cosmic COSV5960
- cosmic curated COSV59604
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.