I55N (p.Ile55Asn) variant of CYP11B1 (P15538)
I55N (p.Ile55Asn) 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.
I55N (p.Ile55Asn) variant details
- p.Ile55Asn
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available