| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.70537556C>A | CA11252080 | TGFA | c.40+16172G>T (n.40+16172G>T) c.58+15628G>T (n.58+15628G>T) n.99+16172G>T n.93+16545G>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.70537556C>G | CA1259617242 | TGFA | c.40+16172G>C (n.40+16172G>C) c.58+15628G>C (n.58+15628G>C) n.99+16172G>C n.93+16545G>C | dbSNP |