A155S (p.Ala155Ser) variant of GRM5 (P41594)
A155S (p.Ala155Ser) in GRM5 (P41594) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
A155S (p.Ala155Ser) variant details
- p.Ala155Ser
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.