| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.29209798C>G | CA346469570 | ALK | c.3824G>C (p.Arg1275Pro) c.1051G>C n.701G>C c.620G>C (p.Arg207Pro) c.704G>C (p.Arg235Pro) c.2693G>C (p.Arg898Pro) c.977G>C (p.Arg326Pro) | dbSNP |
| 2 | g.29209798C>A | CA16602804 | ALK | c.3824G>T (p.Arg1275Leu) c.1051G>T n.701G>T c.620G>T (p.Arg207Leu) c.704G>T (p.Arg235Leu) c.2693G>T (p.Arg898Leu) c.977G>T (p.Arg326Leu) | ClinVar dbSNP COSMIC |
| 2 | g.29209798C>T | CA341482 | ALK | c.3824G>A (p.Arg1275Gln) c.1051G>A n.701G>A c.620G>A (p.Arg207Gln) c.704G>A (p.Arg235Gln) c.2693G>A (p.Arg898Gln) c.977G>A (p.Arg326Gln) | ClinVar dbSNP COSMIC |