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Note: You're navigating the results of models obtained with IntOGen (2020). A new boostDM version is available here.
AR PRAD ×
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Mutation AA change Consequence type BoostDM score IntOGen frequency
X:67711621:A L702H missense_variant 1.00 45
X:67723710:G T878A missense_variant 1.00 36
X:67723701:T H875Y missense_variant 1.00 30
X:67717530:C W742C missense_variant 1.00 9
X:67717529:T W742L missense_variant 1.00 7
X:67717530:T W742C missense_variant 1.00 7
X:67723711:G T878S missense_variant 1.00 4
X:67723755:T P893S missense_variant 1.00 4
X:67723707:C F877L missense_variant 1.00 2
X:67723709:A F877L missense_variant 1.00 2
X:67723743:G S889G missense_variant 1.00 2
X:67723787:C Q903H missense_variant 1.00 2
X:67723710:T T878S missense_variant 1.00 1
X:67723709:G F877L missense_variant 1.00 1
X:67711662:C V716L missense_variant 1.00 1
X:67711662:A V716M missense_variant 1.00 1
X:67723749:C D891H missense_variant 1.00 1
X:67717530:A W742* stop_gained 0.99 1
X:67723701:G H875D missense_variant 1.00 0
X:67723701:A H875N missense_variant 1.00 0
X:67711621:C L702P missense_variant 1.00 0
X:67711621:G L702R missense_variant 1.00 0
X:67723707:A F877I missense_variant 1.00 0
X:67723707:G F877V missense_variant 1.00 0
X:67723710:C T878P missense_variant 1.00 0
X:67723708:G F877C missense_variant 1.00 0
X:67723708:A F877Y missense_variant 1.00 0
X:67723708:C F877S missense_variant 1.00 0
X:67723702:T H875L missense_variant 1.00 0
X:67723702:G H875R missense_variant 1.00 0
X:67723702:C H875P missense_variant 1.00 0
X:67723711:T T878I missense_variant 1.00 0
X:67723711:A T878N missense_variant 1.00 0
X:67723703:G H875Q missense_variant 1.00 0
X:67723703:A H875Q missense_variant 1.00 0
X:67723755:A P893T missense_variant 1.00 0
X:67723756:A P893Q missense_variant 1.00 0
X:67723756:G P893R missense_variant 1.00 0
X:67723756:T P893L missense_variant 1.00 0
X:67723785:A Q903K missense_variant 1.00 0
X:67723785:G Q903E missense_variant 1.00 0
X:67723755:G P893A missense_variant 1.00 0
X:67711662:T V716L missense_variant 1.00 0
X:67717528:C W742R missense_variant 1.00 0
X:67717528:G W742G missense_variant 1.00 0
X:67717528:A W742R missense_variant 1.00 0
X:67717529:C W742S missense_variant 1.00 0
X:67723750:C D891A missense_variant 1.00 0
X:67723750:G D891G missense_variant 1.00 0
X:67723750:T D891V missense_variant 1.00 0
X:67723749:T D891Y missense_variant 1.00 0
X:67723749:A D891N missense_variant 1.00 0
X:67723743:C S889R missense_variant 1.00 0
X:67723743:T S889C missense_variant 1.00 0
X:67723787:T Q903H missense_variant 1.00 0
X:67723786:T Q903L missense_variant 1.00 0
X:67723786:G Q903R missense_variant 1.00 0
X:67723786:C Q903P missense_variant 1.00 0
X:67723744:C S889T missense_variant 1.00 0
X:67723744:A S889N missense_variant 1.00 0
X:67723744:T S889I missense_variant 1.00 0
X:67723745:A S889R missense_variant 1.00 0
X:67723745:G S889R missense_variant 1.00 0
X:67711663:C V716A missense_variant 1.00 0
X:67711663:A V716E missense_variant 1.00 0
X:67711663:G V716G missense_variant 1.00 0
X:67711620:G L702V missense_variant 1.00 0
X:67711620:T L702F missense_variant 1.00 0
X:67711620:A L702I missense_variant 1.00 0
X:67723751:G D891E missense_variant 1.00 0
X:67723751:A D891E missense_variant 1.00 0
X:67723785:T Q903* stop_gained 1.00 0
X:67717529:A W742* stop_gained 0.99 0
In silico saturation mutagenesis
Alt text Show figure caption
Cancer type Selected cancer type Mutational discovery Index Feature Complexity
(PRAD) Prostate adenocarcinoma PRAD 0.82 0.11