V68A (p.Val68Ala) variant of CYP11B1 (P15538)
V68A (p.Val68Ala) 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.
V68A (p.Val68Ala) variant details
- p.Val68Ala
- NCI-TCGA Cosmic COSV5282
- cosmic curated COSV52828
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available