E77K (p.Glu77Lys) variant of GRM5 (P41594)
E77K (p.Glu77Lys) in GRM5 (P41594) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
E77K (p.Glu77Lys) variant details
- p.Glu77Lys
- NCI-TCGA Cosmic COSV5959
- cosmic curated COSV59599
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.