| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.97786731A>G | CA13119615 | PTCSC2 | n.363+23164T>C n.66A>G n.777+17520T>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.97786731A>T | CA1866687909 | PTCSC2 | n.363+23164T>A n.66A>T n.777+17520T>A | dbSNP |
| 9 | g.97786731A= | CA1866687908 | PTCSC2 | n.363+23164T= n.66A= n.777+17520T= | dbSNP |