V2A (p.Val2Ala) variant of BCR (P11274)
V2A (p.Val2Ala) in BCR (P11274) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data and structural context.
V2A (p.Val2Ala) variant details
- p.Val2Ala
- gnomAD rs1457503277
- Missense
- Variant Prioritization Score for Impact Estimate 0.257
- REVEL 0.13
- CADD 26.00
- PolyPhen-2 0.51
- SIFT 0.05
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)
- Structural context available