E111V (p.Glu111Val) variant of GRM5 (P41594)
E111V (p.Glu111Val) in GRM5 (P41594) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
E111V (p.Glu111Val) variant details
- p.Glu111Val
- NCI-TCGA Cosmic COSV5960
- NCI-TCGA Cosmic COSV5962
- cosmic curated COSV59625
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.