| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.81143914A>G | CA118194 | TSHR | c.1856A>G (p.Asp619Gly) c.759A>G c.1577A>G (p.Asp526Gly) n.2086+21279T>C n.853+21279T>C n.854+21279T>C n.865+21279T>C n.861+21279T>C n.855+21279T>C n.2753+21279T>C n.929+21279T>C | ClinVar dbSNP COSMIC |
| 14 | g.81143914A= | CA2150076059 | TSHR | c.1856A= (p.Asp619=) c.759A= c.1577A= (p.Asp526=) n.2086+21279T= n.853+21279T= n.854+21279T= n.865+21279T= n.861+21279T= n.855+21279T= n.2753+21279T= n.929+21279T= | dbSNP |