A71D (p.Ala71Asp) variant of DCX (O43602)
A71D (p.Ala71Asp) 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 LISX1. The record also includes structural context.
A71D (p.Ala71Asp) variant details
- p.Ala71Asp
- NCI-TCGA Cosmic COSV1005
- cosmic curated COSV10057
- NCI-TCGA Cosmic COSV5757
- Ensembl rs2147276379
- Variant assessed as somatic; moderate impact.
- in LISX1
- Missense
- UniProt: Variant assessed as somatic; moderate impact. (in LISX1)
- Structural context available