| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.202467690G>T | CA350399890 | BMPR2 | c.418+1G>T (n.418+1G>T) c.349+1G>T (n.349+1G>T) n.325+1G>T | ClinVar dbSNP |
| 2 | g.202467690G>C | CA350399889 | BMPR2 | c.418+1G>C (n.418+1G>C) c.349+1G>C (n.349+1G>C) n.325+1G>C | ClinVar dbSNP |