G99S (p.Gly99Ser) variant of CRMP1 (Q14194)
G99S (p.Gly99Ser) 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 0.86 / 1. The record also includes structural context.
G99S (p.Gly99Ser) variant details
- p.Gly99Ser
- cosmic curated COSV10462
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.865
- ESM-1b 1.00
- AlphaMissense 0.70
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available