R26S (p.Arg26Ser) variant of BCR (P11274)
R26S (p.Arg26Ser) 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 and structural context.
R26S (p.Arg26Ser) variant details
- p.Arg26Ser
- ExAC rs753721385
- TOPMed rs753721385
- gnomAD rs753721385
- Missense
- Variant Prioritization Score for Impact Estimate 0.264
- REVEL 0.07
- CADD 16.40
- PolyPhen-2 0.12
- SIFT 0.14
- Most common in the 1KG:CLM population (allele frequency 0.0053)
- Structural context available