S129V (p.Ser129Val) variant of GABRB3 (P28472)
S129V (p.Ser129Val) in GABRB3 (P28472) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
S129V (p.Ser129Val) variant details
- p.Ser129Val
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available