| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.64807662C>T | CA16605982 | MEN1 | c.688G>A (p.Gly230Arg) c.659G>A (p.Arg220Lys) c.673G>A (p.Gly225Arg) c.420G>A c.24G>A n.705G>A n.635G>A n.333G>A n.713G>A n.950G>A c.399G>A c.568G>A (p.Gly190Arg) | ClinVar dbSNP |
| 11 | g.64807662C= | CA1978892152 | MEN1 | c.688G= (p.Gly230=) c.659G= (p.Arg220=) c.673G= (p.Gly225=) c.420G= c.24G= n.705G= n.635G= n.333G= n.713G= n.950G= c.399G= c.568G= (p.Gly190=) | dbSNP |