| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.44149823T>G | CA152955 | GCK | c.*614A>C (n.*614A>C) c.616A>C (p.Thr206Pro) n.1102A>C c.619A>C (p.Thr207Pro) c.613A>C (p.Thr205Pro) c.565A>C (p.Thr189Pro) | ClinVar dbSNP |
| 7 | g.44149823T= | CA1703635880 | GCK | c.*614A= (n.*614A=) c.616A= (p.Thr206=) n.1102A= c.619A= (p.Thr207=) c.613A= (p.Thr205=) c.565A= (p.Thr189=) | dbSNP |