D38N (p.Asp38Asn) variant of CDC42 (P60953)
D38N (p.Asp38Asn) 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.
D38N (p.Asp38Asn) variant details
- p.Asp38Asn
- NCI-TCGA Cosmic COSV1002
- cosmic curated COSV10021
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.61
- MetaSVM 0.41
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available