R47G (p.Arg47Gly) variant of ERBB4 (Q15303)
R47G (p.Arg47Gly) in ERBB4 (Q15303) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
R47G (p.Arg47Gly) variant details
- p.Arg47Gly
- cosmic curated COSV53497
- ExAC rs772401914
- TOPMed rs772401914
- gnomAD rs772401914
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available