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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.
NRAS AML ×
Select a mutation to see further information
Mutation AA change Consequence type BoostDM score IntOGen frequency
1:114716126:T G12D missense_variant 1.00 12
1:114716123:T G13D missense_variant 1.00 12
1:114713909:T Q61K missense_variant 1.00 6
1:114716127:T G12S missense_variant 1.00 4
1:114713908:C Q61R missense_variant 1.00 4
1:114716124:G G13R missense_variant 1.00 3
1:114713907:A Q61H missense_variant 1.00 2
1:114716124:A G13C missense_variant 1.00 1
1:114716126:G G12A missense_variant 1.00 1
1:114716127:G G12R missense_variant 1.00 1
1:114713908:G Q61P missense_variant 1.00 1
1:114713907:G Q61H missense_variant 1.00 1
1:114716124:T G13S missense_variant 1.00 0
1:114716123:A G13V missense_variant 1.00 0
1:114716127:A G12C missense_variant 1.00 0
1:114716126:A G12V missense_variant 1.00 0
1:114716123:G G13A missense_variant 1.00 0
1:114713908:A Q61L missense_variant 1.00 0
1:114713909:C Q61E missense_variant 1.00 0
1:114713909:A Q61* stop_gained 1.00 0
1:114713902:A E63V missense_variant 0.99 0
1:114713902:C E63G missense_variant 0.99 0
1:114713902:G E63A missense_variant 0.99 0
1:114713905:C E62G missense_variant 0.99 0
1:114713905:A E62V missense_variant 0.99 0
1:114713905:G E62A missense_variant 0.99 0
1:114713914:T A59D missense_variant 0.99 0
1:114713914:A A59V missense_variant 0.99 0
1:114713914:C A59G missense_variant 0.99 0
1:114713900:C Y64D missense_variant 0.99 0
1:114713900:G Y64H missense_variant 0.99 0
1:114713900:T Y64N missense_variant 0.99 0
1:114713903:G E63Q missense_variant 0.99 0
1:114713903:T E63K missense_variant 0.99 0
1:114713901:A E63D missense_variant 0.99 0
1:114713901:G E63D missense_variant 0.99 0
1:114713911:A G60V missense_variant 0.99 0
1:114713906:T E62K missense_variant 0.99 0
1:114713906:G E62Q missense_variant 0.99 0
1:114713912:T G60R missense_variant 0.99 0
1:114713912:G G60R missense_variant 0.99 0
1:114713911:T G60E missense_variant 0.99 0
1:114713911:G G60A missense_variant 0.99 0
1:114713904:A E62D missense_variant 0.99 0
1:114713904:G E62D missense_variant 0.99 0
1:114713903:A E63* stop_gained 0.99 0
1:114713906:A E62* stop_gained 0.98 0
1:114713912:A G60* stop_gained 0.98 0
In silico saturation mutagenesis
Alt text Show figure caption
Cancer type Selected cancer type Mutational discovery Index Feature Complexity
(AML) Acute myeloid leukemia AML 0.94 0.07