R39Q (p.Arg39Gln) variant of DCX (O43602)
R39Q (p.Arg39Gln) 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 0.40 / 1. The record also includes structural context.
R39Q (p.Arg39Gln) variant details
- p.Arg39Gln
- rs892512121
- NCI-TCGA Cosmic COSV5756
- cosmic curated COSV57566
- Ensembl rs892512121
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.405
- AlphaMissense 0.99
- MetaLR 0.24
- MetaSVM -0.66
- SIFT 0.00
- EVE 0.59
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available