Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.97699474T>A | CA341379824 | DPYD | c.557A>T (p.Tyr186Phe) n.321A>T c.446A>T (p.Tyr149Phe) c.62A>T (p.Tyr21Phe) | dbSNP |
1 | g.97699474T>C | CA228159 | DPYD | c.557A>G (p.Tyr186Cys) n.321A>G c.446A>G (p.Tyr149Cys) c.62A>G (p.Tyr21Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |