Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.97450189C>T | CA963237 | DPYD | c.1775G>A (p.Arg592Gln) c.1559G>A (p.Arg520Gln) c.1664G>A (p.Arg555Gln) c.1280G>A (p.Arg427Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.97450189C= | CA1141628630 | DPYD | c.1775G= (p.Arg592=) c.1559G= (p.Arg520=) c.1664G= (p.Arg555=) c.1280G= (p.Arg427=) | dbSNP |