| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.44147807C>T | CA152959 | GCK | c.*704G>A (n.*704G>A) c.706G>A (p.Glu236Lys) c.709G>A (p.Glu237Lys) c.703G>A (p.Glu235Lys) c.655G>A (p.Glu219Lys) n.82+59C>T | ClinVar dbSNP |
| 7 | g.44147807C= | CA1703634951 | GCK | c.*704G= (n.*704G=) c.706G= (p.Glu236=) c.709G= (p.Glu237=) c.703G= (p.Glu235=) c.655G= (p.Glu219=) n.82+59C= | dbSNP |