V28G (p.Val28Gly) variant of BCR (P11274)
V28G (p.Val28Gly) in BCR (P11274) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data, published literature, and structural context.
V28G (p.Val28Gly) variant details
- p.Val28Gly
- gnomAD 22-23181043-T-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.338
- REVEL 0.32
- CADD 24.80
- PolyPhen-2 0.80
- SIFT 0.00
- Most common in the 1KG:CLM population (allele frequency 0.0053)
- Structural context available
- Literature evidence available