E56D (p.Glu56Asp) variant of CUL3 (Cullin-3)
E56D (p.Glu56Asp) in CUL3 (Cullin-3) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
E56D (p.Glu56Asp) variant details
- p.Glu56Asp
- cosmic curated COSV52370
- 1000Genomes rs558688318
- ExAC rs558688318
- gnomAD rs558688318
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available