W26* (p.Trp26Ter) variant of GABRG2 (P18507)
W26* (p.Trp26Ter) in GABRG2 (P18507) is a protein-truncating change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
W26* (p.Trp26Ter) variant details
- p.Trp26Ter
- 1000Genomes rs564088820
- gnomAD rs564088820
- NCI-TCGA Cosmic COSV1007
- cosmic curated COSV10072
- Variant assessed as somatic; high impact.
- Stop Gained
- UniProt: Variant assessed as somatic; high impact.
- Structural context available