Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.97699430T>C | CA341379738 | DPYD | c.601A>G (p.Ser201Gly) n.365A>G c.490A>G (p.Ser164Gly) c.106A>G (p.Ser36Gly) | dbSNP |
1 | g.97699430T>G | CA963612 | DPYD | c.601A>C (p.Ser201Arg) n.365A>C c.490A>C (p.Ser164Arg) c.106A>C (p.Ser36Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.97699430T>A | CA341379737 | DPYD | c.601A>T (p.Ser201Cys) n.365A>T c.490A>T (p.Ser164Cys) c.106A>T (p.Ser36Cys) | dbSNP |