P14R (p.Pro14Arg) variant of CYP11B1 (P15538)
P14R (p.Pro14Arg) 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.
P14R (p.Pro14Arg) variant details
- p.Pro14Arg
- NCI-TCGA Cosmic COSV5282
- cosmic curated COSV52825
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available