| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.44153387A>G | CA16609270 | GCK | c.*120T>C (n.*120T>C) c.122T>C (p.Met41Thr) n.608T>C c.125T>C (p.Met42Thr) c.119T>C (p.Met40Thr) | ClinVar dbSNP |
| 7 | g.44153387A= | CA1703637554 | GCK | c.*120T= (n.*120T=) c.122T= (p.Met41=) n.608T= c.125T= (p.Met42=) c.119T= (p.Met40=) | dbSNP |
| 7 | g.44153387A>C | CA367403469 | GCK | c.*120T>G (n.*120T>G) c.122T>G (p.Met41Arg) n.608T>G c.125T>G (p.Met42Arg) c.119T>G (p.Met40Arg) | ClinVar dbSNP |