| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.97450190G>A | CA963238 | DPYD | c.1774C>T (p.Arg592Trp) c.1558C>T (p.Arg520Trp) c.1663C>T (p.Arg555Trp) c.1279C>T (p.Arg427Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.97450190G= | CA1140682889 | DPYD | c.1774C= (p.Arg592=) c.1558C= (p.Arg520=) c.1663C= (p.Arg555=) c.1279C= (p.Arg427=) | dbSNP |