| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 6 | g.109287294C>A | CA2712341674 | CCDC162P | n.3773+776C>A n.349+776C>A n.3744+776C>A | dbSNP |
| 6 | g.109287294C>G | CA2712341673 | CCDC162P | n.3773+776C>G n.349+776C>G n.3744+776C>G | dbSNP |
| 6 | g.109287294C>T | CA15451735 | CCDC162P | n.3773+776C>T n.349+776C>T n.3744+776C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |