R26L (p.Arg26Leu) variant of BCR (P11274)
R26L (p.Arg26Leu) in BCR (P11274) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data, published literature, and structural context.
R26L (p.Arg26Leu) variant details
- p.Arg26Leu
- gnomAD 22-23181037-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.259
- REVEL 0.09
- CADD 20.90
- PolyPhen-2 0.23
- SIFT 0.01
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)
- Structural context available
- Literature evidence available