A299T (p.Ala299Thr) variant of CRMP1 (Q14194)
A299T (p.Ala299Thr) 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 0.91 / 1. The record also includes structural context.
A299T (p.Ala299Thr) variant details
- p.Ala299Thr
- NCI-TCGA Cosmic COSV1002
- cosmic curated COSV10027
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.913
- ESM-1b 1.00
- AlphaMissense 0.81
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available