D17G (p.Asp17Gly) variant of BCR (P11274)
D17G (p.Asp17Gly) in BCR (P11274) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data, published literature, and structural context.
D17G (p.Asp17Gly) variant details
- p.Asp17Gly
- gnomAD 22-23181010-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.209
- REVEL 0.09
- CADD 22.60
- PolyPhen-2 0.24
- SIFT 0.21
- Population evidence available
- Structural context available
- Literature evidence available