| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.25209907A>G | CA384148531 | KRAS | c.116T>C (p.Val39Ala) c.455T>C (p.Val152Ala) c.*426T>C (n.*426T>C) c.*153T>C (n.*153T>C) n.929T>C c.258T>C c.*416T>C (n.*416T>C) c.257T>C (p.Val86Ala) c.380T>C (p.Val127Ala) c.*9T>C (n.*9T>C) | dbSNP gnomAD v3 gnomAD v4 |
| 12 | g.25209907A>C | CA256482 | KRAS | c.116T>G (p.Val39Gly) c.455T>G (p.Val152Gly) c.*426T>G (n.*426T>G) c.*153T>G (n.*153T>G) n.929T>G c.258T>G c.*416T>G (n.*416T>G) c.257T>G (p.Val86Gly) c.380T>G (p.Val127Gly) c.*9T>G (n.*9T>G) | ClinVar dbSNP |
| 12 | g.25209907A= | CA2022884736 | KRAS | c.116T= (p.Val39=) c.455T= (p.Val152=) c.*426T= (n.*426T=) c.*153T= (n.*153T=) n.929T= c.258T= c.*416T= (n.*416T=) c.257T= (p.Val86=) c.380T= (p.Val127=) c.*9T= (n.*9T=) | dbSNP |