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 |
Cancer type | Selected cancer type | Mutational discovery Index | Feature Complexity |
---|---|---|---|
(AML) Acute myeloid leukemia | AML | 0.94 | 0.07 |