R238W (p.Arg238Trp) variant of CRMP1 (Q14194)
R238W (p.Arg238Trp) in CRMP1 (Q14194) 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 0.98 / 1. The record also includes structural context.
R238W (p.Arg238Trp) variant details
- p.Arg238Trp
- NCI-TCGA Cosmic COSV6147
- cosmic curated COSV61478
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.975
- ESM-1b 1.00
- AlphaMissense 0.95
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available