Q29H (p.Gln29His) variant of CRMP1 (Q14194)
Q29H (p.Gln29His) 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 0.54 / 1. The record also includes population frequency data and structural context.
Q29H (p.Gln29His) variant details
- p.Gln29His
- rs777215799
- NCI-TCGA Cosmic COSV1002
- cosmic curated COSV10027
- 1000Genomes rs777215799
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.539
- ESM-1b 0.88
- AlphaMissense 0.17
- MetaLR 0.46
- MetaSVM -0.51
- PolyPhen-2 0.00
- SIFT 0.24
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available