V302M (p.Val302Met) variant of CRMP1 (Q14194)
V302M (p.Val302Met) 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 0.87 / 1. The record also includes population frequency data and structural context.
V302M (p.Val302Met) variant details
- p.Val302Met
- rs371645916
- cosmic curated COSV61478
- ESP rs371645916
- ExAC rs371645916
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.871
- ESM-1b 1.00
- AlphaMissense 0.73
- MetaLR 0.81
- MetaSVM 0.79
- PolyPhen-2 1.00
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available