| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.29220747C>A | CA346473026 | ALK | c.3604G>T (p.Gly1202Ter) c.831G>T n.481G>T c.400G>T (p.Gly134Ter) c.484G>T (p.Gly162Ter) c.2473G>T (p.Gly825Ter) c.757G>T (p.Gly253Ter) | dbSNP |
| 2 | g.29220747C>G | CA346473027 | ALK | c.3604G>C (p.Gly1202Arg) c.831G>C n.481G>C c.400G>C (p.Gly134Arg) c.484G>C (p.Gly162Arg) c.2473G>C (p.Gly825Arg) c.757G>C (p.Gly253Arg) | dbSNP |
| 2 | g.29220747C>T | CA16602592 | ALK | c.3604G>A (p.Gly1202Arg) c.831G>A n.481G>A c.400G>A (p.Gly134Arg) c.484G>A (p.Gly162Arg) c.2473G>A (p.Gly825Arg) c.757G>A (p.Gly253Arg) | ClinVar dbSNP gnomAD v4 COSMIC |