F7F (p.Phe7Phe) variant of BCR (P11274)
F7F (p.Phe7Phe) in BCR (P11274) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.51 / 1. The record also includes population frequency data, published literature, and structural context.
F7F (p.Phe7Phe) variant details
- p.Phe7Phe
- gnomAD 22-23180981-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.514
- CADD 14.80
- Most common in the Middle Eastern population (allele frequency 0.0007)
- Structural context available
- Literature evidence available