M1? variant of SMAD4 (SMAD family member 4)
M1? in SMAD4 (SMAD family member 4) 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 COSV1007
- cosmic curated COSV10074
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available