S151P (p.Ser151Pro) variant of GRM5 (P41594)
S151P (p.Ser151Pro) in GRM5 (P41594) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
S151P (p.Ser151Pro) variant details
- p.Ser151Pro
- NCI-TCGA Cosmic COSV5961
- cosmic curated COSV59613
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.