| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.49717706A>G | CA2090581606 | KPNA3 | c.771+2069T>C (n.771+2069T>C) c.699+2069T>C (n.699+2069T>C) | dbSNP |
| 13 | g.49717706A>C | CA13859468 | KPNA3 | c.771+2069T>G (n.771+2069T>G) c.699+2069T>G (n.699+2069T>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |