| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.146262151T>G | CA16318150 | CNTNAP2 | c.97+145178T>G (n.97+145178T>G) n.26+145178T>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.146262151T= | CA1750181811 | CNTNAP2 | c.97+145178T= (n.97+145178T=) n.26+145178T= | dbSNP |