T218A (p.Thr218Ala) variant of CRMP1 (Q14194)
T218A (p.Thr218Ala) 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 0.60 / 1. The record also includes structural context.
T218A (p.Thr218Ala) variant details
- p.Thr218Ala
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.6
- ESM-1b 1.00
- AlphaMissense 0.12
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available