P119S (p.Pro119Ser) variant of GABRB3 (P28472)
P119S (p.Pro119Ser) in GABRB3 (P28472) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
P119S (p.Pro119Ser) variant details
- p.Pro119Ser
- NCI-TCGA Cosmic COSV5465
- cosmic curated COSV54652
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available