| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.97784318C>A | CA1866686862 | PTCSC2 | n.363+25577G>T n.777+19933G>T | dbSNP |
| 9 | g.97784318C>G | CA1866686863 | PTCSC2 | n.363+25577G>C n.777+19933G>C | dbSNP gnomAD v3 gnomAD v4 |
| 9 | g.97784318C>T | CA13034677 | PTCSC2 | n.363+25577G>A n.777+19933G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |