M1? variant of CHEK1 (O14757)
M1? in CHEK1 (O14757) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes population frequency data and structural context.
M1? variant details
- NCI-TCGA Cosmic COSV5402
- cosmic curated COSV54024
- TOPMed rs1940631418
- cosmic curated COSV10459
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Population evidence available
- Structural context available