D17Y (p.Asp17Tyr) variant of BCR (P11274)
D17Y (p.Asp17Tyr) in BCR (P11274) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.38 / 1. The record also includes population frequency data, published literature, and structural context.
D17Y (p.Asp17Tyr) variant details
- p.Asp17Tyr
- gnomAD 22-23181009-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.385
- REVEL 0.22
- CADD 25.70
- PolyPhen-2 0.77
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)
- Structural context available
- Literature evidence available