P66L (p.Pro66Leu) variant of BCL11B (B-cell lymphoma/leukemia 11B)
P66L (p.Pro66Leu) in BCL11B (B-cell lymphoma/leukemia 11B) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.58 / 1. The record also includes population frequency data and structural context.
P66L (p.Pro66Leu) variant details
- p.Pro66Leu
- NCI-TCGA Cosmic COSV1005
- cosmic curated COSV10059
- NCI-TCGA Cosmic COSV6173
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.58
- REVEL 0.43
- CADD 27.20
- PolyPhen-2 0.82
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available