V2L (p.Val2Leu) variant of BCR (P11274)
V2L (p.Val2Leu) in BCR (P11274) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data, published literature, and structural context.
V2L (p.Val2Leu) variant details
- p.Val2Leu
- gnomAD 22-23180964-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.332
- REVEL 0.09
- CADD 23.10
- PolyPhen-2 0.21
- SIFT 0.01
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available
- Literature evidence available