Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.202377551G>T | CA350396811 | BMPR2 | c.76+1G>T (n.76+1G>T) | ClinVar dbSNP |
2 | g.202377551G>A | CA350396807 | BMPR2 | c.76+1G>A (n.76+1G>A) | ClinVar dbSNP |
2 | g.202377551G= | CA1321474708 | BMPR2 | c.76+1G= (n.76+1G=) | dbSNP |