Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.202377552T>C | CA350396817 | BMPR2 | c.76+2T>C (n.76+2T>C) | ClinVar dbSNP |
2 | g.202377552T>G | CA350396819 | BMPR2 | c.76+2T>G (n.76+2T>G) | ClinVar dbSNP |
2 | g.202377552T= | CA1321474709 | BMPR2 | c.76+2T= (n.76+2T=) | dbSNP |
2 | g.202377552T>A | CA350396815 | BMPR2 | c.76+2T>A (n.76+2T>A) | ClinVar dbSNP |