G28C (p.Gly28Cys) variant of RET (P07949)
G28C (p.Gly28Cys) in RET (P07949) is a missense change. Clinical records from EBI and UniProt describe it as benign. The record also includes structural context.
G28C (p.Gly28Cys) variant details
- p.Gly28Cys
- ExAC rs779905135
- TOPMed rs779905135
- gnomAD rs779905135
- Benign
- Missense
- EBI: Benign
- UniProt: Benign
- Structural context available