Mutation | AA change | Consequence type | BoostDM score | IntOGen frequency |
---|---|---|---|---|
12:112450406:A | E76K | missense_variant | 1.00 | 6 |
12:112450407:G | E76G | missense_variant | 1.00 | 4 |
12:112450361:T | D61Y | missense_variant | 0.99 | 3 |
12:112450385:A | E69K | missense_variant | 1.00 | 2 |
12:112489084:T | G507V | missense_variant | 1.00 | 2 |
12:112450407:C | E76A | missense_variant | 1.00 | 2 |
12:112450395:A | A72D | missense_variant | 0.99 | 2 |
12:112450394:C | A72P | missense_variant | 1.00 | 1 |
12:112450394:A | A72T | missense_variant | 1.00 | 1 |
12:112450358:C | G60R | missense_variant | 0.99 | 1 |
12:112489080:G | S506A | missense_variant | 0.93 | 1 |
12:112450394:T | A72S | missense_variant | 1.00 | 0 |
12:112450406:C | E76Q | missense_variant | 1.00 | 0 |
12:112450385:C | E69Q | missense_variant | 1.00 | 0 |
12:112450406:T | E76* | stop_gained | 1.00 | 0 |
12:112450385:T | E69* | stop_gained | 1.00 | 0 |
12:112489084:A | G507E | missense_variant | 1.00 | 0 |
12:112489084:C | G507A | missense_variant | 1.00 | 0 |
12:112489083:C | G507R | missense_variant | 1.00 | 0 |
12:112489083:A | G507R | missense_variant | 1.00 | 0 |
12:112489083:T | G507W | missense_variant | 1.00 | 0 |
12:112450386:C | E69A | missense_variant | 1.00 | 0 |
12:112450407:T | E76V | missense_variant | 1.00 | 0 |
12:112450386:T | E69V | missense_variant | 1.00 | 0 |
12:112450386:G | E69G | missense_variant | 1.00 | 0 |
12:112450361:C | D61H | missense_variant | 0.99 | 0 |
12:112450358:T | G60C | missense_variant | 0.99 | 0 |
12:112450359:A | G60D | missense_variant | 0.99 | 0 |
12:112450359:C | G60A | missense_variant | 0.99 | 0 |
12:112450359:T | G60V | missense_variant | 0.99 | 0 |
12:112450361:A | D61N | missense_variant | 0.99 | 0 |
12:112450358:A | G60S | missense_variant | 0.99 | 0 |
12:112450395:G | A72G | missense_variant | 0.99 | 0 |
12:112450395:T | A72V | missense_variant | 0.99 | 0 |
12:112450362:C | D61A | missense_variant | 0.99 | 0 |
12:112450362:T | D61V | missense_variant | 0.99 | 0 |
12:112450362:G | D61G | missense_variant | 0.99 | 0 |
12:112489081:T | S506L | missense_variant | 0.98 | 0 |
12:112489081:A | S506* | stop_gained | 0.98 | 0 |
12:112489081:G | S506* | stop_gained | 0.98 | 0 |
12:112450387:T | E69D | missense_variant | 0.97 | 0 |
12:112450387:C | E69D | missense_variant | 0.97 | 0 |
12:112489080:A | S506T | missense_variant | 0.93 | 0 |
12:112489080:C | S506P | missense_variant | 0.93 | 0 |
12:112450408:C | E76D | missense_variant | 0.78 | 0 |
12:112450408:T | E76D | missense_variant | 0.78 | 0 |
12:112450363:A | D61E | missense_variant | 0.78 | 0 |
12:112450363:G | D61E | missense_variant | 0.78 | 0 |
12:112450403:A | A75T | missense_variant | 0.67 | 0 |
12:112450403:T | A75S | missense_variant | 0.67 | 0 |
12:112450403:C | A75P | missense_variant | 0.67 | 0 |
12:112450388:G | K70E | missense_variant | 0.52 | 0 |
12:112450389:C | K70T | missense_variant | 0.52 | 0 |
12:112450389:G | K70R | missense_variant | 0.52 | 0 |
12:112450389:T | K70I | missense_variant | 0.52 | 0 |
12:112450397:G | T73A | missense_variant | 0.52 | 0 |
12:112450397:C | T73P | missense_variant | 0.52 | 0 |
12:112450397:T | T73S | missense_variant | 0.52 | 0 |
12:112450388:C | K70Q | missense_variant | 0.52 | 0 |
Cancer type | Selected cancer type | Mutational discovery Index | Feature Complexity |
---|---|---|---|
(MM) Multiple myeloma | MM | 0.83 | 0.12 |