S12L (p.Ser12Leu) variant of GABRG2 (P18507)
S12L (p.Ser12Leu) 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.
S12L (p.Ser12Leu) variant details
- p.Ser12Leu
- NCI-TCGA Cosmic COSV6271
- cosmic curated COSV62717
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available