| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.47284514G>T | CA123226 | ITGB3 | c.433G>T (p.Asp145Tyr) c.398G>T | ClinVar dbSNP |
| 17 | g.47284514G>A | CA400021939 | ITGB3 | c.433G>A (p.Asp145Asn) c.398G>A | ClinVar dbSNP |
| 17 | g.47284514G= | CA2262605303 | ITGB3 | c.433G= (p.Asp145=) c.398G= | dbSNP |