| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.149978353T>C | CA16040989 | SLC26A2 | n.933T>C c.699+2T>C (n.699+2T>C) c.372+2T>C (n.372+2T>C) | ClinVar dbSNP |
| 5 | g.149978353T= | CA1590737508 | SLC26A2 | n.933T= c.699+2T= (n.699+2T=) c.372+2T= (n.372+2T=) | dbSNP |