E139D (p.Glu139Asp) variant of BCL11B (B-cell lymphoma/leukemia 11B)
E139D (p.Glu139Asp) 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 record also includes structural context.
E139D (p.Glu139Asp) variant details
- p.Glu139Asp
- NCI-TCGA Cosmic COSV6173
- cosmic curated COSV61732
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available