L3F (p.Leu3Phe) variant of DCX (O43602)
L3F (p.Leu3Phe) in DCX (O43602) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.70 / 1. The record also includes population frequency data and structural context.
L3F (p.Leu3Phe) variant details
- p.Leu3Phe
- NCI-TCGA Cosmic COSV5757
- cosmic curated COSV57571
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.699
- CADD 25.20
- PolyPhen-2 0.64
- SIFT 0.01
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)
- Structural context available