Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.47286394A>G | CA16043530 | ITGB3 | c.749A>G (p.Asp250Gly) c.714A>G | ClinVar dbSNP |
17 | g.47286394A>T | CA400023649 | ITGB3 | c.749A>T (p.Asp250Val) c.714A>T | dbSNP |
17 | g.47286394A= | CA2262606021 | ITGB3 | c.749A= (p.Asp250=) c.714A= | dbSNP |