| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.84955510A>G | CA120116 | NTRK2 | c.2081A>G (p.Tyr694Cys) n.2651A>G n.2782A>G c.2117A>G (p.Tyr706Cys) c.2165A>G (p.Tyr722Cys) n.3195A>G n.430A>G n.3050A>G n.836A>G c.1649A>G (p.Tyr550Cys) c.1697A>G (p.Tyr566Cys) | ClinVar dbSNP |
| 9 | g.84955510A>T | CA374010396 | NTRK2 | c.2081A>T (p.Tyr694Phe) n.2651A>T n.2782A>T c.2117A>T (p.Tyr706Phe) c.2165A>T (p.Tyr722Phe) n.3195A>T n.430A>T n.3050A>T n.836A>T c.1649A>T (p.Tyr550Phe) c.1697A>T (p.Tyr566Phe) | dbSNP |
| 9 | g.84955510A= | CA1860774570 | NTRK2 | c.2081A= (p.Tyr694=) n.2651A= n.2782A= c.2117A= (p.Tyr706=) c.2165A= (p.Tyr722=) n.3195A= n.430A= n.3050A= n.836A= c.1649A= (p.Tyr550=) c.1697A= (p.Tyr566=) | dbSNP |