Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.43113628_43113629delinsTT | CA007910 | RET | c.1436_1437delinsTT (p.Cys479Phe) n.1406_1407delinsTT n.593_594delinsTT c.1832_1833delinsTT (p.Cys611Phe) c.*426_*427delinsTT (n.*426_*427delinsTT) c.383_384delinsTT (p.Cys128Phe) c.1289+2396_1289+2397delinsTT (n.1289+2396_1289+2397delinsTT) c.1070_1071delinsTT (p.Cys357Phe) | dbSNP |
10 | g.43113628_43113629delinsCT | CA007903 | RET | c.1436_1437delinsCT (p.Cys479Ser) n.1406_1407delinsCT n.593_594delinsCT c.1832_1833delinsCT (p.Cys611Ser) c.*426_*427delinsCT (n.*426_*427delinsCT) c.383_384delinsCT (p.Cys128Ser) c.1289+2396_1289+2397delinsCT (n.1289+2396_1289+2397delinsCT) c.1070_1071delinsCT (p.Cys357Ser) | dbSNP |
10 | g.43113628_43113629delinsAT | CA007894 | RET | c.1436_1437delinsAT (p.Cys479Tyr) n.1406_1407delinsAT n.593_594delinsAT c.1832_1833delinsAT (p.Cys611Tyr) c.*426_*427delinsAT (n.*426_*427delinsAT) c.383_384delinsAT (p.Cys128Tyr) c.1289+2396_1289+2397delinsAT (n.1289+2396_1289+2397delinsAT) c.1070_1071delinsAT (p.Cys357Tyr) | ClinVar dbSNP |