| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55174762T>C | CA16602541 | EGFR | c.2066T>C (p.Val689Ala) c.574T>C c.2225T>C (p.Val742Ala) c.*28+1834T>C (n.*28+1834T>C) c.2090T>C (p.Val697Ala) c.1424T>C (p.Val475Ala) | ClinVar dbSNP COSMIC |
| 7 | g.55174762T>A | CA367584110 | EGFR | c.2066T>A (p.Val689Asp) c.574T>A c.2225T>A (p.Val742Asp) c.*28+1834T>A (n.*28+1834T>A) c.2090T>A (p.Val697Asp) c.1424T>A (p.Val475Asp) | dbSNP |
| 7 | g.55174762T>G | CA367584112 | EGFR | c.2066T>G (p.Val689Gly) c.574T>G c.2225T>G (p.Val742Gly) c.*28+1834T>G (n.*28+1834T>G) c.2090T>G (p.Val697Gly) c.1424T>G (p.Val475Gly) | dbSNP |
| 7 | g.55174762T= | CA1708918299 | EGFR | c.2066T= (p.Val689=) c.574T= c.2225T= (p.Val742=) c.*28+1834T= (n.*28+1834T=) c.2090T= (p.Val697=) c.1424T= (p.Val475=) | dbSNP |