Mutation | AA change | Consequence type | BoostDM score | IntOGen frequency |
---|---|---|---|---|
12:25245350:T | G12D | missense_variant | 1.00 | 132 |
12:25245350:A | G12V | missense_variant | 1.00 | 117 |
12:25245347:T | G13D | missense_variant | 1.00 | 75 |
12:25245351:A | G12C | missense_variant | 1.00 | 51 |
12:25245350:G | G12A | missense_variant | 1.00 | 29 |
12:25245351:T | G12S | missense_variant | 1.00 | 27 |
12:25225628:T | A146T | missense_variant | 1.00 | 24 |
12:25227341:G | Q61H | missense_variant | 1.00 | 9 |
12:25225713:A | K117N | missense_variant | 1.00 | 6 |
12:25225627:A | A146V | missense_variant | 0.97 | 6 |
12:25245348:A | G13C | missense_variant | 1.00 | 5 |
12:25227341:A | Q61H | missense_variant | 1.00 | 4 |
12:25227342:C | Q61R | missense_variant | 1.00 | 4 |
12:25227342:A | Q61L | missense_variant | 1.00 | 4 |
12:25245351:G | G12R | missense_variant | 1.00 | 3 |
12:25245328:A | L19F | missense_variant | 0.81 | 2 |
12:25245345:T | V14I | missense_variant | 1.00 | 1 |
12:25227342:G | Q61P | missense_variant | 1.00 | 1 |
12:25227345:T | G60D | missense_variant | 1.00 | 1 |
12:25227343:C | Q61E | missense_variant | 0.99 | 1 |
12:25227348:T | A59E | missense_variant | 0.99 | 1 |
12:25227343:T | Q61K | missense_variant | 0.99 | 1 |
12:25245284:A | P34L | missense_variant | 0.93 | 1 |
12:25245284:C | P34R | missense_variant | 0.93 | 1 |
12:25245328:G | L19F | missense_variant | 0.81 | 1 |
12:25245348:G | G13R | missense_variant | 1.00 | 0 |
12:25245345:A | V14L | missense_variant | 1.00 | 0 |
12:25245345:G | V14L | missense_variant | 1.00 | 0 |
12:25245347:G | G13A | missense_variant | 1.00 | 0 |
12:25245347:A | G13V | missense_variant | 1.00 | 0 |
12:25245348:T | G13S | missense_variant | 1.00 | 0 |
12:25225628:G | A146P | missense_variant | 1.00 | 0 |
12:25225628:A | A146S | missense_variant | 1.00 | 0 |
12:25225713:G | K117N | missense_variant | 1.00 | 0 |
12:25227345:G | G60A | missense_variant | 1.00 | 0 |
12:25227345:A | G60V | missense_variant | 1.00 | 0 |
12:25227346:A | G60C | missense_variant | 1.00 | 0 |
12:25227346:G | G60R | missense_variant | 1.00 | 0 |
12:25227346:T | G60S | missense_variant | 1.00 | 0 |
12:25227349:A | A59S | missense_variant | 1.00 | 0 |
12:25227349:G | A59P | missense_variant | 1.00 | 0 |
12:25227349:T | A59T | missense_variant | 1.00 | 0 |
12:25227348:A | A59V | missense_variant | 0.99 | 0 |
12:25227348:C | A59G | missense_variant | 0.99 | 0 |
12:25245344:C | V14G | missense_variant | 0.99 | 0 |
12:25245344:T | V14E | missense_variant | 0.99 | 0 |
12:25245344:G | V14A | missense_variant | 0.99 | 0 |
12:25225627:C | A146G | missense_variant | 0.97 | 0 |
12:25227351:T | T58K | missense_variant | 0.97 | 0 |
12:25227351:C | T58R | missense_variant | 0.97 | 0 |
12:25227351:A | T58I | missense_variant | 0.97 | 0 |
12:25225627:T | A146E | missense_variant | 0.97 | 0 |
12:25227352:C | T58A | missense_variant | 0.95 | 0 |
12:25227352:A | T58S | missense_variant | 0.95 | 0 |
12:25227352:G | T58P | missense_variant | 0.95 | 0 |
12:25227333:G | Y64S | missense_variant | 0.95 | 0 |
12:25227333:A | Y64F | missense_variant | 0.95 | 0 |
12:25227333:C | Y64C | missense_variant | 0.95 | 0 |
12:25245285:C | P34A | missense_variant | 0.93 | 0 |
12:25245285:A | P34S | missense_variant | 0.93 | 0 |
12:25245284:T | P34Q | missense_variant | 0.93 | 0 |
12:25245285:T | P34T | missense_variant | 0.93 | 0 |
12:25225714:G | K117T | missense_variant | 0.90 | 0 |
12:25225715:G | K117Q | missense_variant | 0.90 | 0 |
12:25225714:A | K117I | missense_variant | 0.90 | 0 |
12:25225714:C | K117R | missense_variant | 0.90 | 0 |
12:25225715:C | K117E | missense_variant | 0.90 | 0 |
Cancer type | Selected cancer type | Mutational discovery Index | Feature Complexity |
---|---|---|---|
(COREAD) Colorectal adenocarcinoma | COREAD | 0.94 | 0.15 |