| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.89008492A>G | CA226554991 | GRM5 | c.661+38720T>C (n.661+38720T>C) c.725+543T>C (n.725+543T>C) c.223+543T>C | dbSNP |
| 11 | g.89008492A= | CA1989836332 | GRM5 | c.661+38720T= (n.661+38720T=) c.725+543T= (n.725+543T=) c.223+543T= | dbSNP |