| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.25551359C>T | CA13047143 | n.50-787G>A n.674-787G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 | |
| 9 | g.25551359C>A | CA1841175530 | n.50-787G>T n.674-787G>T | dbSNP | |
| 9 | g.25551359C= | CA1841175529 | n.50-787G= n.674-787G= | dbSNP |