| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.25209908C>A | CA261705 | KRAS | c.115G>T (p.Val39Phe) c.454G>T (p.Val152Phe) c.*425G>T (n.*425G>T) c.*152G>T (n.*152G>T) n.928G>T c.257G>T c.*415G>T (n.*415G>T) c.256G>T (p.Val86Phe) c.379G>T (p.Val127Phe) c.*8G>T (n.*8G>T) | ClinVar dbSNP |
| 12 | g.25209908C= | CA2022884741 | KRAS | c.115G= (p.Val39=) c.454G= (p.Val152=) c.*425G= (n.*425G=) c.*152G= (n.*152G=) n.928G= c.257G= c.*415G= (n.*415G=) c.256G= (p.Val86=) c.379G= (p.Val127=) c.*8G= (n.*8G=) | dbSNP |