E37D (p.Glu37Asp) variant of BCL11B (B-cell lymphoma/leukemia 11B)
E37D (p.Glu37Asp) in BCL11B (B-cell lymphoma/leukemia 11B) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data and structural context.
E37D (p.Glu37Asp) variant details
- p.Glu37Asp
- TOPMed rs1299952326
- gnomAD rs1299952326
- Missense
- Variant Prioritization Score for Impact Estimate 0.164
- REVEL 0.06
- CADD 15.60
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)
- Structural context available