A40D (p.Ala40Asp) variant of CYP11B1 (P15538)
A40D (p.Ala40Asp) 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.
A40D (p.Ala40Asp) variant details
- p.Ala40Asp
- NCI-TCGA Cosmic COSV5282
- NCI-TCGA Cosmic COSV9945
- cosmic curated COSV99455
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available