| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.156868562T>A | CA16617006 | NTRK1 | c.470T>A (p.Val157Glu) c.632T>A (p.Val211Glu) c.542T>A (p.Val181Glu) n.313-5071T>A n.690T>A | ClinVar dbSNP |
| 1 | g.156868562T= | CA1200782255 | NTRK1 | c.470T= (p.Val157=) c.632T= (p.Val211=) c.542T= (p.Val181=) n.313-5071T= n.690T= | dbSNP |