| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.29222584C>G | CA341484 | ALK | c.3383G>C (p.Gly1128Ala) c.610G>C n.260G>C c.179G>C (p.Gly60Ala) c.263G>C (p.Gly88Ala) c.77G>C (p.Gly26Ala) c.2252G>C (p.Gly751Ala) c.536G>C (p.Gly179Ala) | ClinVar dbSNP COSMIC |
| 2 | g.29222584C>T | CA346464122 | ALK | c.3383G>A (p.Gly1128Glu) c.610G>A n.260G>A c.179G>A (p.Gly60Glu) c.263G>A (p.Gly88Glu) c.77G>A (p.Gly26Glu) c.2252G>A (p.Gly751Glu) c.536G>A (p.Gly179Glu) | ClinVar dbSNP |
| 2 | g.29222584C= | CA1241090644 | ALK | c.3383G= (p.Gly1128=) c.610G= n.260G= c.179G= (p.Gly60=) c.263G= (p.Gly88=) c.77G= (p.Gly26=) c.2252G= (p.Gly751=) c.536G= (p.Gly179=) | dbSNP |