S136F (p.Ser136Phe) variant of GRM5 (P41594)
S136F (p.Ser136Phe) in GRM5 (P41594) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
S136F (p.Ser136Phe) variant details
- p.Ser136Phe
- NCI-TCGA Cosmic COSV5960
- cosmic curated COSV59601
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.