D86N (p.Asp86Asn) variant of DCX (O43602)
D86N (p.Asp86Asn) in DCX (O43602) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact in the context of in SBHX. The record also includes structural context.
D86N (p.Asp86Asn) variant details
- p.Asp86Asn
- NCI-TCGA Cosmic COSV5756
- cosmic curated COSV57566
- Variant assessed as somatic; moderate impact.
- in SBHX
- Missense
- UniProt: Variant assessed as somatic; moderate impact. (in SBHX)
- Structural context available