Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.97450187C>T | CA963236 | DPYD | c.1777G>A (p.Gly593Arg) c.1561G>A (p.Gly521Arg) c.1666G>A (p.Gly556Arg) c.1282G>A (p.Gly428Arg) | dbSNP ExAC gnomAD v2 |
1 | g.97450187C= | CA1142074294 | DPYD | c.1777G= (p.Gly593=) c.1561G= (p.Gly521=) c.1666G= (p.Gly556=) c.1282G= (p.Gly428=) | dbSNP |