V16A (p.Val16Ala) variant of GRM5 (P41594)
V16A (p.Val16Ala) in GRM5 (P41594) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
V16A (p.Val16Ala) variant details
- p.Val16Ala
- NCI-TCGA Cosmic COSV5959
- cosmic curated COSV59597
- NCI-TCGA Cosmic COSV5960
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.