Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.97098598C>T | CA114282 | DPYD,DPYD-AS1 | c.2657G>A (p.Arg886His) n.64+2612C>T c.2441G>A (p.Arg814His) c.2546G>A (p.Arg849His) c.2162G>A (p.Arg721His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.97098598C= | CA1139894829 | DPYD,DPYD-AS1 | c.2657G= (p.Arg886=) n.64+2612C= c.2441G= (p.Arg814=) c.2546G= (p.Arg849=) c.2162G= (p.Arg721=) | dbSNP |
1 | g.97098598C>G | CA341374922 | DPYD,DPYD-AS1 | c.2657G>C (p.Arg886Pro) n.64+2612C>G c.2441G>C (p.Arg814Pro) c.2546G>C (p.Arg849Pro) c.2162G>C (p.Arg721Pro) | dbSNP |
1 | g.97098598C>A | CA341374923 | DPYD,DPYD-AS1 | c.2657G>T (p.Arg886Leu) n.64+2612C>A c.2441G>T (p.Arg814Leu) c.2546G>T (p.Arg849Leu) c.2162G>T (p.Arg721Leu) | dbSNP gnomAD v4 |