| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.140781602_140781603delinsGA | CA16602534 | BRAF | c.1405_1406delinsTC (p.Gly469Ser) c.1525_1526delinsTC (p.Gly509Ser) c.75_76delinsTC c.*855_*856delinsTC (n.*855_*856delinsTC) c.*483_*484delinsTC (n.*483_*484delinsTC) n.847_848delinsTC n.1795_1796delinsTC c.501_502delinsTC n.1494_1495delinsTC n.535_536delinsTC c.448_449delinsTC (p.Gly150Ser) c.228_229delinsTC c.1440_1441delinsTC (n.1440_1441delinsTC) n.1413_1414delinsTC n.1710_1711delinsTC n.1533_1534delinsTC c.1414_1415delinsTC (p.Gly472Ser) c.1339_1340delinsTC (p.Gly447Ser) c.1303_1304delinsTC (p.Gly435Ser) c.1294_1295delinsTC (p.Gly432Ser) c.1249_1250delinsTC (p.Gly417Ser) c.1141_1142delinsTC (p.Gly381Ser) | ClinVar dbSNP COSMIC |
| 7 | g.140781602_140781603delinsAA | CA16602429 | BRAF | c.1405_1406delinsTT (p.Gly469Leu) c.1525_1526delinsTT (p.Gly509Leu) c.75_76delinsTT c.*855_*856delinsTT (n.*855_*856delinsTT) c.*483_*484delinsTT (n.*483_*484delinsTT) n.847_848delinsTT n.1795_1796delinsTT c.501_502delinsTT n.1494_1495delinsTT n.535_536delinsTT c.448_449delinsTT (p.Gly150Leu) c.228_229delinsTT c.1440_1441delinsTT (n.1440_1441delinsTT) n.1413_1414delinsTT n.1710_1711delinsTT n.1533_1534delinsTT c.1414_1415delinsTT (p.Gly472Leu) c.1339_1340delinsTT (p.Gly447Leu) c.1303_1304delinsTT (p.Gly435Leu) c.1294_1295delinsTT (p.Gly432Leu) c.1249_1250delinsTT (p.Gly417Leu) c.1141_1142delinsTT (p.Gly381Leu) | ClinVar dbSNP COSMIC |