P16R (p.Pro16Arg) variant of BCR (P11274)
P16R (p.Pro16Arg) in BCR (P11274) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.46 / 1. The record also includes population frequency data and structural context.
P16R (p.Pro16Arg) variant details
- p.Pro16Arg
- ExAC rs765207801
- TOPMed rs765207801
- gnomAD rs765207801
- Missense
- Variant Prioritization Score for Impact Estimate 0.463
- REVEL 0.28
- CADD 25.10
- PolyPhen-2 0.84
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available