| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.146425696T>C | CA168600549 | CNTNAP2 | c.97+308723T>C (n.97+308723T>C) n.26+308723T>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.146425696T>G | CA578575599 | CNTNAP2 | c.97+308723T>G (n.97+308723T>G) n.26+308723T>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.146425696T>A | CA1750256474 | CNTNAP2 | c.97+308723T>A (n.97+308723T>A) n.26+308723T>A | dbSNP |