| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.57273122G>A | CA185937 | TCF12 | c.1838G>A (p.Arg613His) c.1766G>A (p.Arg589His) c.1256G>A (p.Arg419His) c.1058G>A (p.Arg353His) c.1328G>A (p.Arg443His) c.1826G>A (p.Arg609His) c.737G>A (p.Arg246His) c.668G>A (p.Arg223His) n.495G>A n.761G>A n.872G>A c.1664G>A (p.Arg555His) c.1874G>A (p.Arg625His) c.1871G>A (p.Arg624His) c.1802G>A (p.Arg601His) c.1799G>A (p.Arg600His) c.1190G>A (p.Arg397His) c.1130G>A (p.Arg377His) c.1118G>A (p.Arg373His) c.1253G>A (p.Arg418His) c.1835G>A (p.Arg612His) c.1181G>A (p.Arg394His) c.1592G>A (p.Arg531His) c.1763G>A (p.Arg588His) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
| 15 | g.57273122G>T | CA392592633 | TCF12 | c.1838G>T (p.Arg613Leu) c.1766G>T (p.Arg589Leu) c.1256G>T (p.Arg419Leu) c.1058G>T (p.Arg353Leu) c.1328G>T (p.Arg443Leu) c.1826G>T (p.Arg609Leu) c.737G>T (p.Arg246Leu) c.668G>T (p.Arg223Leu) n.495G>T n.761G>T n.872G>T c.1664G>T (p.Arg555Leu) c.1874G>T (p.Arg625Leu) c.1871G>T (p.Arg624Leu) c.1802G>T (p.Arg601Leu) c.1799G>T (p.Arg600Leu) c.1190G>T (p.Arg397Leu) c.1130G>T (p.Arg377Leu) c.1118G>T (p.Arg373Leu) c.1253G>T (p.Arg418Leu) c.1835G>T (p.Arg612Leu) c.1181G>T (p.Arg394Leu) c.1592G>T (p.Arg531Leu) c.1763G>T (p.Arg588Leu) | ClinVar dbSNP |
| 15 | g.57273122G= | CA2179732871 | TCF12 | c.1838G= (p.Arg613=) c.1766G= (p.Arg589=) c.1256G= (p.Arg419=) c.1058G= (p.Arg353=) c.1328G= (p.Arg443=) c.1826G= (p.Arg609=) c.737G= (p.Arg246=) c.668G= (p.Arg223=) n.495G= n.761G= n.872G= c.1664G= (p.Arg555=) c.1874G= (p.Arg625=) c.1871G= (p.Arg624=) c.1802G= (p.Arg601=) c.1799G= (p.Arg600=) c.1190G= (p.Arg397=) c.1130G= (p.Arg377=) c.1118G= (p.Arg373=) c.1253G= (p.Arg418=) c.1835G= (p.Arg612=) c.1181G= (p.Arg394=) c.1592G= (p.Arg531=) c.1763G= (p.Arg588=) | dbSNP |