G68R (p.Gly68Arg) variant of BCL11B (B-cell lymphoma/leukemia 11B)
G68R (p.Gly68Arg) in BCL11B (B-cell lymphoma/leukemia 11B) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.43 / 1. The record also includes population frequency data and structural context.
G68R (p.Gly68Arg) variant details
- p.Gly68Arg
- gnomAD rs1300560260
- Missense
- Variant Prioritization Score for Impact Estimate 0.428
- REVEL 0.20
- CADD 23.70
- PolyPhen-2 0.14
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.4e-05)
- Structural context available