E111A (p.Glu111Ala) variant of GRM5 (P41594)
E111A (p.Glu111Ala) in GRM5 (P41594) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
E111A (p.Glu111Ala) variant details
- p.Glu111Ala
- NCI-TCGA Cosmic COSV5960
- cosmic curated COSV59603
- NCI-TCGA Cosmic COSV5962
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.