Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.202532613A>T | CA350341741 | BMPR2 | c.1157A>T (p.Glu386Val) c.1088A>T (p.Glu363Val) | ClinVar dbSNP |
2 | g.202532613A>G | CA350341740 | BMPR2 | c.1157A>G (p.Glu386Gly) c.1088A>G (p.Glu363Gly) | ClinVar dbSNP COSMIC |
2 | g.202532613A>C | CA350341739 | BMPR2 | c.1157A>C (p.Glu386Ala) c.1088A>C (p.Glu363Ala) | ClinVar dbSNP |