D17D (p.Asp17Asp) variant of BCR (P11274)
D17D (p.Asp17Asp) in BCR (P11274) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data, published literature, and structural context.
D17D (p.Asp17Asp) variant details
- p.Asp17Asp
- rs758542346
- gnomAD 22-23181011-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.317
- CADD 11.40
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)
- Structural context available
- Literature evidence available