| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.44153338C>T | CA16618473 | GCK | c.*169G>A (n.*169G>A) c.171G>A (p.Met57Ile) n.657G>A c.174G>A (p.Met58Ile) c.168G>A (p.Met56Ile) | ClinVar dbSNP |
| 7 | g.44153338C>A | CA16603236 | GCK | c.*169G>T (n.*169G>T) c.171G>T (p.Met57Ile) n.657G>T c.174G>T (p.Met58Ile) c.168G>T (p.Met56Ile) | ClinVar dbSNP |