T75N (p.Thr75Asn) variant of GRM5 (P41594)
T75N (p.Thr75Asn) in GRM5 (P41594) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
T75N (p.Thr75Asn) variant details
- p.Thr75Asn
- NCI-TCGA Cosmic COSV1005
- cosmic curated COSV10055
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.