C108G (p.Cys108Gly) variant of CYP27B1 (O15528)
C108G (p.Cys108Gly) in CYP27B1 (O15528) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
C108G (p.Cys108Gly) variant details
- p.Cys108Gly
- NCI-TCGA Cosmic COSV9914
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available