R22H (p.Arg22His) variant of BCR (P11274)
R22H (p.Arg22His) in BCR (P11274) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and structural context.
R22H (p.Arg22His) variant details
- p.Arg22His
- 1000Genomes rs376532812
- ESP rs376532812
- ExAC rs376532812
- TOPMed rs376532812
- Missense
- Variant Prioritization Score for Impact Estimate 0.287
- REVEL 0.09
- CADD 22.60
- PolyPhen-2 0.00
- SIFT 0.03
- Most common in the REMAINING population (allele frequency 0.00048)
- Structural context available