E32D (p.Glu32Asp) variant of BCR (P11274)
E32D (p.Glu32Asp) in BCR (P11274) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data and structural context.
E32D (p.Glu32Asp) variant details
- p.Glu32Asp
- 1000Genomes rs144606065
- ESP rs144606065
- ExAC rs144606065
- TOPMed rs144606065
- Missense
- Variant Prioritization Score for Impact Estimate 0.23
- REVEL 0.08
- CADD 23.90
- PolyPhen-2 0.45
- SIFT 0.00
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available