R26C (p.Arg26Cys) variant of BCR (P11274)
R26C (p.Arg26Cys) in BCR (P11274) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes population frequency data and structural context.
R26C (p.Arg26Cys) variant details
- p.Arg26Cys
- ExAC rs753721385
- TOPMed rs753721385
- gnomAD rs753721385
- Missense
- Variant Prioritization Score for Impact Estimate 0.347
- REVEL 0.16
- CADD 23.70
- PolyPhen-2 0.68
- SIFT 0.01
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available