| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.40439840T>G | CA2086427258 | LINC00598 | n.663+20442A>C n.803+11224A>C | dbSNP |
| 13 | g.40439840T>A | CA2086427257 | LINC00598 | n.663+20442A>T n.803+11224A>T | dbSNP gnomAD v4 |
| 13 | g.40439840T>C | CA15772325 | LINC00598 | n.663+20442A>G n.803+11224A>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |