R57M (p.Arg57Met) variant of CYP11B1 (P15538)
R57M (p.Arg57Met) in CYP11B1 (P15538) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
R57M (p.Arg57Met) variant details
- p.Arg57Met
- NCI-TCGA Cosmic COSV9945
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available