P16L (p.Pro16Leu) variant of BCR (P11274)
P16L (p.Pro16Leu) in BCR (P11274) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.43 / 1. The record also includes population frequency data and structural context.
P16L (p.Pro16Leu) variant details
- p.Pro16Leu
- ExAC rs765207801
- TOPMed rs765207801
- gnomAD rs765207801
- Missense
- Variant Prioritization Score for Impact Estimate 0.428
- REVEL 0.23
- CADD 25.10
- PolyPhen-2 0.52
- SIFT 0.00
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)
- Structural context available