S8P (p.Ser8Pro) variant of GRM5 (P41594)
S8P (p.Ser8Pro) in GRM5 (P41594) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
S8P (p.Ser8Pro) variant details
- p.Ser8Pro
- NCI-TCGA Cosmic COSV5963
- cosmic curated COSV59630
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.