D11N (p.Asp11Asn) variant of CDC42 (P60953)
D11N (p.Asp11Asn) in CDC42 (P60953) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and structural context.
D11N (p.Asp11Asn) variant details
- p.Asp11Asn
- NCI-TCGA Cosmic COSV1002
- cosmic curated COSV10021
- NCI-TCGA Cosmic COSV5966
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.76
- MetaSVM 0.79
- SIFT 0.03
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available