H38Q (p.His38Gln) variant of CDKN1B (P46527)
H38Q (p.His38Gln) in CDKN1B (P46527) is a missense change. Clinical records from EBI and UniProt describe it as benign. The record also includes population frequency data and structural context.
H38Q (p.His38Gln) variant details
- p.His38Gln
- 1000Genomes rs141178987
- ESP rs141178987
- ExAC rs141178987
- TOPMed rs141178987
- Benign
- Missense
- EBI: Benign
- UniProt: Benign
- Population evidence available
- Structural context available