I66F (p.Ile66Phe) variant of GRM5 (P41594)
I66F (p.Ile66Phe) in GRM5 (P41594) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
I66F (p.Ile66Phe) variant details
- p.Ile66Phe
- NCI-TCGA Cosmic COSV1005
- cosmic curated COSV10055
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.