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Note: You're navigating the results of models obtained with the previous release of IntOGen (2020). A new boostDM version corresponding to the current IntOGen release will be available soon.
KRAS COREAD ×
Select a mutation to see further information
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
In silico saturation mutagenesis
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Cancer type Selected cancer type Mutational discovery Index Feature Complexity
(COREAD) Colorectal adenocarcinoma COREAD 0.94 0.15