M1? variant of SLCO1B1 (Q9Y6L6)
M1? in SLCO1B1 (Q9Y6L6) 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 COSV9991
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available