Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
20 | g.44406196G>A | CA16043128 | HNF4A | c.188G>A (p.Arg63Gln) c.254G>A (p.Arg85Gln) c.228G>A c.230G>A (p.Arg77Gln) c.207G>A n.230G>A c.211G>A (p.Gly71Arg) c.*21G>A (n.*21G>A) c.179G>A (p.Arg60Gln) c.233G>A (p.Arg78Gln) c.371G>A (p.Arg124Gln) c.302G>A (p.Arg101Gln) | ClinVar dbSNP COSMIC COSMIC COSMIC |
20 | g.44406196G= | CA2365758039 | HNF4A | c.188G= (p.Arg63=) c.254G= (p.Arg85=) c.228G= c.230G= (p.Arg77=) c.207G= n.230G= c.211G= (p.Gly71=) c.*21G= (n.*21G=) c.179G= (p.Arg60=) c.233G= (p.Arg78=) c.371G= (p.Arg124=) c.302G= (p.Arg101=) | dbSNP |