M1? variant of GABRG2 (P18507)
M1? in GABRG2 (P18507) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
M1? variant details
- NCI-TCGA Cosmic COSV6272
- cosmic curated COSV62722
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available