D41L (p.Asp41Leu) variant of ERBB4 (Q15303)
D41L (p.Asp41Leu) in ERBB4 (Q15303) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
D41L (p.Asp41Leu) variant details
- p.Asp41Leu
- NCI-TCGA Cosmic COSV5358
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available