S292G (p.Ser292Gly) variant of CRMP1 (Q14194)
S292G (p.Ser292Gly) 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 0.63 / 1. The record also includes structural context.
S292G (p.Ser292Gly) variant details
- p.Ser292Gly
- NCI-TCGA Cosmic COSV1002
- cosmic curated COSV10027
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.626
- ESM-1b 1.00
- AlphaMissense 0.18
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available