| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.97450133C>A | CA16040801 | DPYD | c.1831G>T (p.Glu611Ter) c.1615G>T (p.Glu539Ter) c.1720G>T (p.Glu574Ter) c.1336G>T (p.Glu446Ter) | ClinVar dbSNP gnomAD v4 |
| 1 | g.97450133C>G | CA341376064 | DPYD | c.1831G>C (p.Glu611Gln) c.1615G>C (p.Glu539Gln) c.1720G>C (p.Glu574Gln) c.1336G>C (p.Glu446Gln) | dbSNP |
| 1 | g.97450133C= | CA1182873453 | DPYD | c.1831G= (p.Glu611=) c.1615G= (p.Glu539=) c.1720G= (p.Glu574=) c.1336G= (p.Glu446=) | dbSNP |