N51D (p.Asn51Asp) variant of CYP17A1 (P05093)
N51D (p.Asn51Asp) in CYP17A1 (P05093) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
N51D (p.Asn51Asp) variant details
- p.Asn51Asp
- NCI-TCGA Cosmic COSV6400
- cosmic curated COSV64005
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available