| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.155461298G>C | CA1754593998 | EN2 | c.686-1073G>C (n.686-1073G>C) | dbSNP |
| 7 | g.155461298G>T | CA1109065256 | EN2 | c.686-1073G>T (n.686-1073G>T) | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.155461298G>A | CA126741 | EN2 | c.686-1073G>A (n.686-1073G>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |