F112L (p.Phe112Leu) variant of GRM5 (P41594)
F112L (p.Phe112Leu) in GRM5 (P41594) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
F112L (p.Phe112Leu) variant details
- p.Phe112Leu
- NCI-TCGA Cosmic COSV1005
- cosmic curated COSV10055
- NCI-TCGA Cosmic COSV5958
- cosmic curated COSV59587
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.