| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.47302841G>C | CA143711 | ITGB3 | c.2134+1G>C (n.2134+1G>C) c.2099+1G>C | ClinVar dbSNP |
| 17 | g.47302841G= | CA2262612896 | ITGB3 | c.2134+1G= (n.2134+1G=) c.2099+1G= | dbSNP |
| 17 | g.47302841G>T | CA400033345 | ITGB3 | c.2134+1G>T (n.2134+1G>T) c.2099+1G>T | ClinVar dbSNP |