S109I (p.Ser109Ile) variant of GRM5 (P41594)
S109I (p.Ser109Ile) in GRM5 (P41594) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
S109I (p.Ser109Ile) variant details
- p.Ser109Ile
- NCI-TCGA Cosmic COSV1005
- cosmic curated COSV10055
- NCI-TCGA Cosmic COSV5959
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.