| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.47291027G>A | CA123244 | ITGB3 | c.1199G>A (p.Cys400Tyr) c.1164G>A | ClinVar dbSNP |
| 17 | g.47291027G= | CA2262608036 | ITGB3 | c.1199G= (p.Cys400=) c.1164G= | dbSNP |
| 17 | g.47291027G>T | CA400027853 | ITGB3 | c.1199G>T (p.Cys400Phe) c.1164G>T | dbSNP gnomAD v4 |