Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.97515795del | CA16040803 | DPYD | c.1671del (p.Ser558GlnfsTer2) c.1524+33765del (n.1524+33765del) c.1560del (p.Ser521GlnfsTer2) c.1176del (p.Ser393GlnfsTer2) | ClinVar dbSNP |
1 | g.97515795T= | CA1182902277 | DPYD | c.1671A= (p.Thr557=) c.1524+33765A= (n.1524+33765A=) c.1560A= (p.Thr520=) c.1176A= (p.Thr392=) | dbSNP dbSNP |