| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.25209904T>A | CA256478 | KRAS | c.119A>T (p.Asp40Val) c.458A>T (p.Asp153Val) c.*429A>T (n.*429A>T) c.*156A>T (n.*156A>T) n.932A>T c.261A>T c.*419A>T (n.*419A>T) c.260A>T (p.Asp87Val) c.383A>T (p.Asp128Val) c.*12A>T (n.*12A>T) | ClinVar dbSNP COSMIC |
| 12 | g.25209904T>C | CA261707 | KRAS | c.119A>G (p.Asp40Gly) c.458A>G (p.Asp153Gly) c.*429A>G (n.*429A>G) c.*156A>G (n.*156A>G) n.932A>G c.261A>G c.*419A>G (n.*419A>G) c.260A>G (p.Asp87Gly) c.383A>G (p.Asp128Gly) c.*12A>G (n.*12A>G) | ClinVar dbSNP gnomAD v4 |