Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.156876526A>T | CA342938642 | NTRK1 | c.1579A>T (p.Met527Leu) c.*351A>T (n.*351A>T) c.1759A>T (p.Met587Leu) c.1750A>T (p.Met584Leu) c.1741A>T (p.Met581Leu) c.1651A>T (p.Met551Leu) n.2212A>T | dbSNP |
1 | g.156876526A>G | CA256300 | NTRK1 | c.1579A>G (p.Met527Val) c.*351A>G (n.*351A>G) c.1759A>G (p.Met587Val) c.1750A>G (p.Met584Val) c.1741A>G (p.Met581Val) c.1651A>G (p.Met551Val) n.2212A>G | ClinVar dbSNP |