| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.119833296T>G | CA2067156531 | CIT | c.660-432A>C (n.660-432A>C) c.267+16878A>C (n.267+16878A>C) | dbSNP |
| 12 | g.119833296T>A | CA15730772 | CIT | c.660-432A>T (n.660-432A>T) c.267+16878A>T (n.267+16878A>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |