V28M (p.Val28Met) variant of BCR (P11274)
V28M (p.Val28Met) in BCR (P11274) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data and structural context.
V28M (p.Val28Met) variant details
- p.Val28Met
- gnomAD rs1397011387
- Missense
- Variant Prioritization Score for Impact Estimate 0.249
- REVEL 0.05
- CADD 16.60
- PolyPhen-2 0.13
- SIFT 0.10
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)
- Structural context available