| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.119672657G>A | CA352059 | BAG3 | c.909+1G>A (n.909+1G>A) c.735+1G>A (n.735+1G>A) | ClinVar dbSNP |
| 10 | g.119672657G>C | CA378296184 | BAG3 | c.909+1G>C (n.909+1G>C) c.735+1G>C (n.735+1G>C) | ClinVar dbSNP |
| 10 | g.119672657G= | CA1940193583 | BAG3 | c.909+1G= (n.909+1G=) c.735+1G= (n.735+1G=) | dbSNP |