| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.52316377G>A | CA260912324 | PTGER2 | c.843+986G>A (n.843+986G>A) c.78+986G>A (n.78+986G>A) | dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.52316377G>T | CA13977496 | PTGER2 | c.843+986G>T (n.843+986G>T) c.78+986G>T (n.78+986G>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |