| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.43114501_43114502delinsTG | CA008334 | RET | c.1505_1506delinsTG (p.Cys502Leu) n.1475_1476delinsTG n.1466_1467delinsTG c.1901_1902delinsTG (p.Cys634Leu) c.*495_*496delinsTG (n.*495_*496delinsTG) c.452_453delinsTG (p.Cys151Leu) c.1289+3269_1289+3270delinsTG (n.1289+3269_1289+3270delinsTG) c.1139_1140delinsTG (p.Cys380Leu) | dbSNP |
| 10 | g.43114501_43114502delinsTT | CA2580081463 | RET | c.1505_1506delinsTT (p.Cys502Phe) n.1475_1476delinsTT n.1466_1467delinsTT c.1901_1902delinsTT (p.Cys634Phe) c.*495_*496delinsTT (n.*495_*496delinsTT) c.452_453delinsTT (p.Cys151Phe) c.1289+3269_1289+3270delinsTT (n.1289+3269_1289+3270delinsTT) c.1139_1140delinsTT (p.Cys380Phe) | ClinVar dbSNP |