Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.202377501G>T | CA350396611 | BMPR2 | c.27G>T (p.Trp9Cys) | dbSNP |
2 | g.202377501G>A | CA350396608 | BMPR2 | c.27G>A (p.Trp9Ter) | ClinVar dbSNP COSMIC |
2 | g.202377501G= | CA1321474679 | BMPR2 | c.27G= (p.Trp9=) | dbSNP |