| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.202565733T>G | CA10613660 | BMPR2 | c.*5787T>G (n.*5787T>G) c.*6031T>G (n.*6031T>G) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.202565733T>A | CA64005826 | BMPR2 | c.*5787T>A (n.*5787T>A) c.*6031T>A (n.*6031T>A) | dbSNP |