W100L (p.Trp100Leu) variant of GRM5 (P41594)
W100L (p.Trp100Leu) in GRM5 (P41594) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
W100L (p.Trp100Leu) variant details
- p.Trp100Leu
- NCI-TCGA Cosmic COSV5963
- cosmic curated COSV59634
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.