Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.95637169C>T | CA16042724 | ALDH18A1 | c.482G>A (p.Cys161Tyr) n.674G>A c.149G>A (p.Cys50Tyr) c.453+118G>A (n.453+118G>A) c.-78-3520G>A (n.-78-3520G>A) | ClinVar dbSNP |
10 | g.95637169C= | CA1929619771 | ALDH18A1 | c.482G= (p.Cys161=) n.674G= c.149G= (p.Cys50=) c.453+118G= (n.453+118G=) c.-78-3520G= (n.-78-3520G=) | dbSNP |