R26H (p.Arg26His) variant of BCR (P11274)
R26H (p.Arg26His) in BCR (P11274) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data, published literature, and structural context.
R26H (p.Arg26His) variant details
- p.Arg26His
- gnomAD 22-23181037-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.266
- REVEL 0.11
- CADD 17.80
- PolyPhen-2 0.44
- SIFT 0.09
- Most common in the REMAINING population (allele frequency 0.00048)
- Structural context available
- Literature evidence available