| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.44153325C>T | CA16618472 | GCK | c.*182G>A (n.*182G>A) c.184G>A (p.Val62Met) n.670G>A c.187G>A (p.Val63Met) c.181G>A (p.Val61Met) | ClinVar dbSNP gnomAD v4 |
| 7 | g.44153325C= | CA1703637521 | GCK | c.*182G= (n.*182G=) c.184G= (p.Val62=) n.670G= c.187G= (p.Val63=) c.181G= (p.Val61=) | dbSNP |