Q28K (p.Gln28Lys) variant of CCND2 (G1/S-specific cyclin-D2)
Q28K (p.Gln28Lys) in CCND2 (G1/S-specific cyclin-D2) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Inborn genetic diseases. The record also includes structural context.
Q28K (p.Gln28Lys) variant details
- p.Gln28Lys
- Ensembl rs1418862467
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- UniProt: Uncertain significance
- Structural context available