| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.36663564G>A | CA7159029 | PAX9 | c.631+41G>A (n.631+41G>A) c.70+41G>A (n.70+41G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.36663564G>C | CA705377830 | PAX9 | c.631+41G>C (n.631+41G>C) c.70+41G>C (n.70+41G>C) | dbSNP |
| 14 | g.36663564G= | CA2129503172 | PAX9 | c.631+41G= (n.631+41G=) c.70+41G= (n.70+41G=) | dbSNP dbSNP |