| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.133536201C>T | CA256006 | GPC3 | c.855G>A n.697G>A c.1618G>A (p.Gly540Arg) n.610G>A c.953G>A c.1666G>A (p.Gly556Arg) c.1735G>A (p.Gly579Arg) n.544G>A n.953G>A n.733G>A n.732G>A c.1504G>A (p.Gly502Arg) | ClinVar dbSNP |
| X | g.133536201C>G | CA414702626 | GPC3 | c.855G>C n.697G>C c.1618G>C (p.Gly540Arg) n.610G>C c.953G>C c.1666G>C (p.Gly556Arg) c.1735G>C (p.Gly579Arg) n.544G>C n.953G>C n.733G>C n.732G>C c.1504G>C (p.Gly502Arg) | ClinVar dbSNP |