V25G (p.Val25Gly) variant of GABRG2 (P18507)
V25G (p.Val25Gly) in GABRG2 (P18507) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
V25G (p.Val25Gly) variant details
- p.Val25Gly
- NCI-TCGA Cosmic COSV1007
- cosmic curated COSV10072
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available