| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.81645798C>A | CA51761763 | n.563+66189C>A n.485+97051C>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 | |
| 2 | g.81645798C>T | CA1264999445 | n.563+66189C>T n.485+97051C>T | dbSNP | |
| 2 | g.81645798C= | CA1264999444 | n.563+66189C= n.485+97051C= | dbSNP |