| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.25209896A>T | CA273160 | KRAS | c.127T>A (p.Phe43Ile) c.466T>A (p.Phe156Ile) c.*437T>A (n.*437T>A) c.*164T>A (n.*164T>A) n.940T>A c.269T>A c.*427T>A (n.*427T>A) c.268T>A (p.Phe90Ile) c.391T>A (p.Phe131Ile) c.*20T>A (n.*20T>A) | ClinVar dbSNP |
| 12 | g.25209896A>C | CA261709 | KRAS | c.127T>G (p.Phe43Val) c.466T>G (p.Phe156Val) c.*437T>G (n.*437T>G) c.*164T>G (n.*164T>G) n.940T>G c.269T>G c.*427T>G (n.*427T>G) c.268T>G (p.Phe90Val) c.391T>G (p.Phe131Val) c.*20T>G (n.*20T>G) | ClinVar dbSNP |