ALK | ACGTQRTAP | LUNG | 1501 | p.S1495fs | c.4485_4485delC | Frame_Shift_Del | 5 | 0.11 | NCIH1836 | N | 0 | 0 | 0 | N |
ALK | APGLQRNPP | LUNG | 1508 | p.S1495fs | c.4485_4485delC | Frame_Shift_Del | 5 | 0.11 | NCIH1836 | N | 1 | 0 | 0 | N |
ALK | CGTQRTAPG | LUNG | 1502 | p.S1495fs | c.4485_4485delC | Frame_Shift_Del | 5 | 0.11 | NCIH1836 | N | 0 | 0 | 0 | N |
ALK | ELHKVHGSE | LUNG | 1488 | p.S1495fs | c.4485_4485delC | Frame_Shift_Del | 1 | 0.11 | NCIH1836 | N | 0 | 0 | 0 | N |
ALK | ETSPPACGT | LUNG | 1496 | p.S1495fs | c.4485_4485delC | Frame_Shift_Del | 5 | 0.11 | NCIH1836 | N | 1 | 0 | 0 | N |
ALK | GLQRNPPKR | LUNG | 1510 | p.S1495fs | c.4485_4485delC | Frame_Shift_Del | 5 | 0.11 | NCIH1836 | N | 6 | 0 | 0 | N |
ALK | GSETSPPAC | LUNG | 1494 | p.S1495fs | c.4485_4485delC | Frame_Shift_Del | 4 | 0.11 | NCIH1836 | N | 2 | 0 | 0 | N |
ALK | GTQRTAPGL | LUNG | 1503 | p.S1495fs | c.4485_4485delC | Frame_Shift_Del | 5 | 0.11 | NCIH1836 | N | 6 | 0 | 0 | Y |
ALK | HGSETSPPA | LUNG | 1493 | p.S1495fs | c.4485_4485delC | Frame_Shift_Del | 4 | 0.11 | NCIH1836 | N | 2 | 0 | 0 | N |
ALK | HKVHGSETS | LUNG | 1490 | p.S1495fs | c.4485_4485delC | Frame_Shift_Del | 3 | 0.11 | NCIH1836 | N | 1 | 0 | 0 | N |
ALK | KVHGSETSP | LUNG | 1491 | p.S1495fs | c.4485_4485delC | Frame_Shift_Del | 3 | 0.11 | NCIH1836 | N | 0 | 0 | 0 | N |
ALK | LHKVHGSET | LUNG | 1489 | p.S1495fs | c.4485_4485delC | Frame_Shift_Del | 2 | 0.11 | NCIH1836 | N | 0 | 0 | 0 | N |
ALK | LQRNPPKRI | LUNG | 1511 | p.S1495fs | c.4485_4485delC | Frame_Shift_Del | 5 | 0.11 | NCIH1836 | N | 6 | 0 | 10 | N |
ALK | PACGTQRTA | LUNG | 1500 | p.S1495fs | c.4485_4485delC | Frame_Shift_Del | 4 | 0.11 | NCIH1836 | N | 0 | 0 | 0 | N |
ALK | PGLQRNPPK | LUNG | 1509 | p.S1495fs | c.4485_4485delC | Frame_Shift_Del | 5 | 0.11 | NCIH1836 | N | 0 | 0 | 0 | N |
ALK | PPACGTQRT | LUNG | 1499 | p.S1495fs | c.4485_4485delC | Frame_Shift_Del | 5 | 0.11 | NCIH1836 | N | 0 | 0 | 0 | N |
ALK | QRNPPKRII | LUNG | 1512 | p.S1495fs | c.4485_4485delC | Frame_Shift_Del | 5 | 0.11 | NCIH1836 | Y | 3 | 10 | 0 | N |
ALK | QRTAPGLQR | LUNG | 1505 | p.S1495fs | c.4485_4485delC | Frame_Shift_Del | 5 | 0.11 | NCIH1836 | N | 3 | 0 | 0 | Y |
ALK | RNPPKRIIL | LUNG | 1513 | p.S1495fs | c.4485_4485delC | Frame_Shift_Del | 5 | 0.11 | NCIH1836 | Y | 11 | 16 | 0 | N |
ALK | RTAPGLQRN | LUNG | 1506 | p.S1495fs | c.4485_4485delC | Frame_Shift_Del | 5 | 0.11 | NCIH1836 | N | 1 | 0 | 0 | Y |
ALK | SETSPPACG | LUNG | 1495 | p.S1495fs | c.4485_4485delC | Frame_Shift_Del | 5 | 0.11 | NCIH1836 | N | 0 | 0 | 0 | N |
ALK | SPPACGTQR | LUNG | 1498 | p.S1495fs | c.4485_4485delC | Frame_Shift_Del | 5 | 0.11 | NCIH1836 | N | 3 | 0 | 0 | N |
ALK | TAPGLQRNP | LUNG | 1507 | p.S1495fs | c.4485_4485delC | Frame_Shift_Del | 5 | 0.11 | NCIH1836 | N | 0 | 0 | 0 | N |
ALK | TQRTAPGLQ | LUNG | 1504 | p.S1495fs | c.4485_4485delC | Frame_Shift_Del | 5 | 0.11 | NCIH1836 | N | 0 | 0 | 0 | Y |
ALK | TSPPACGTQ | LUNG | 1497 | p.S1495fs | c.4485_4485delC | Frame_Shift_Del | 5 | 0.11 | NCIH1836 | N | 0 | 0 | 0 | N |
ALK | VHGSETSPP | LUNG | 1492 | p.S1495fs | c.4485_4485delC | Frame_Shift_Del | 4 | 0.11 | NCIH1836 | N | 0 | 0 | 0 | N |
ALK | AAPVQSQRA | OVARY | 165 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | N | 4 | 0 | 0 | N |
ALK | APPSLPDLR | OVARY | 213 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 4 | 0.11 | OC316 | N | 3 | 0 | 0 | Y |
ALK | APVQSQRAV | OVARY | 166 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | Y | 12 | 9 | 0 | N |
ALK | AREEGVGSG | OVARY | 191 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | N | 1 | 0 | 0 | N |
ALK | ATEDPPDAR | OVARY | 184 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | N | 5 | 0 | 0 | N |
ALK | AVQLVDSPR | OVARY | 173 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | N | 6 | 0 | 0 | N |
ALK | AVRGNSRLP | OVARY | 204 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | N | 0 | 0 | 0 | N |
ALK | CGAAPVQSQ | OVARY | 163 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | N | 0 | 0 | 0 | N |
ALK | CVGPPRGGG | OVARY | 154 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 4 | 0.11 | OC316 | N | 0 | 0 | 0 | Y |
ALK | DAREEGVGS | OVARY | 190 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | N | 3 | 0 | 0 | N |
ALK | DPPDAREEG | OVARY | 187 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 4 | 0.11 | OC316 | N | 0 | 0 | 0 | N |
ALK | DSPRRRATE | OVARY | 178 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 4 | 0.11 | OC316 | N | 0 | 0 | 0 | N |
ALK | EDPPDAREE | OVARY | 186 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | N | 0 | 0 | 0 | N |
ALK | EEGVGSGQR | OVARY | 193 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 4 | 0.11 | OC316 | N | 1 | 0 | 0 | N |
ALK | EGCVGPPRG | OVARY | 152 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 2 | 0.11 | OC316 | N | 0 | 0 | 0 | N |
ALK | EGVGSGQRG | OVARY | 194 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 4 | 0.11 | OC316 | N | 0 | 0 | 0 | N |
ALK | GAAPVQSQR | OVARY | 164 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | Y | 3 | 10 | 0 | N |
ALK | GCGAAPVQS | OVARY | 162 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | N | 0 | 0 | 0 | N |
ALK | GCVGPPRGG | OVARY | 153 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 3 | 0.11 | OC316 | N | 0 | 0 | 0 | N |
ALK | GGCGAAPVQ | OVARY | 161 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 4 | 0.11 | OC316 | N | 0 | 0 | 0 | N |
ALK | GGGCGAAPV | OVARY | 160 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 3 | 0.11 | OC316 | N | 7 | 0 | 0 | N |
ALK | GKAVRGNSR | OVARY | 202 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | N | 1 | 0 | 0 | N |
ALK | GNSRLPAPP | OVARY | 207 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | N | 0 | 0 | 0 | N |
ALK | GPPRGGGCG | OVARY | 156 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 4 | 0.11 | OC316 | N | 0 | 0 | 0 | N |
ALK | GQRGKAVRG | OVARY | 199 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 4 | 0.11 | OC316 | N | 0 | 0 | 0 | N |
ALK | GSGQRGKAV | OVARY | 197 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | N | 4 | 0 | 0 | N |
ALK | GVGSGQRGK | OVARY | 195 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 4 | 0.11 | OC316 | N | 3 | 0 | 0 | N |
ALK | KAVRGNSRL | OVARY | 203 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | N | 16 | 0 | 0 | N |
ALK | LEGCVGPPR | OVARY | 151 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 1 | 0.11 | OC316 | N | 0 | 0 | 0 | N |
ALK | LPAPPSLPD | OVARY | 211 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 4 | 0.11 | OC316 | N | 2 | 0 | 0 | N |
ALK | LVDSPRRRA | OVARY | 176 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | Y | 2 | 11 | 5 | N |
ALK | NSRLPAPPS | OVARY | 208 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | N | 0 | 0 | 0 | N |
ALK | PAPPSLPDL | OVARY | 212 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 4 | 0.11 | OC316 | N | 1 | 0 | 0 | N |
ALK | PDAREEGVG | OVARY | 189 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | N | 0 | 0 | 0 | N |
ALK | PPDAREEGV | OVARY | 188 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 4 | 0.11 | OC316 | N | 5 | 0 | 0 | N |
ALK | PPRGGGCGA | OVARY | 157 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 4 | 0.11 | OC316 | N | 4 | 0 | 0 | N |
ALK | PPSLPDLRD | OVARY | 214 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 4 | 0.11 | OC316 | N | 0 | 0 | 0 | N |
ALK | PRGGGCGAA | OVARY | 158 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 4 | 0.11 | OC316 | N | 1 | 0 | 0 | N |
ALK | PRRRATEDP | OVARY | 180 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | N | 0 | 0 | 0 | N |
ALK | PSLPDLRDW | OVARY | 215 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 4 | 0.11 | OC316 | N | 1 | 0 | 0 | N |
ALK | PVQSQRAVQ | OVARY | 167 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | N | 0 | 0 | 0 | N |
ALK | QLVDSPRRR | OVARY | 175 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 6 | 0.11 | OC316 | N | 5 | 0 | 0 | N |
ALK | QRAVQLVDS | OVARY | 171 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 4 | 0.11 | OC316 | N | 2 | 0 | 0 | N |
ALK | QRGKAVRGN | OVARY | 200 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 4 | 0.11 | OC316 | N | 2 | 0 | 0 | N |
ALK | QSQRAVQLV | OVARY | 169 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 4 | 0.11 | OC316 | N | 2 | 0 | 0 | N |
ALK | RATEDPPDA | OVARY | 183 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | N | 3 | 0 | 0 | N |
ALK | RAVQLVDSP | OVARY | 172 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 4 | 0.11 | OC316 | N | 0 | 0 | 0 | N |
ALK | REEGVGSGQ | OVARY | 192 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | N | 0 | 0 | 0 | N |
ALK | RGGGCGAAP | OVARY | 159 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 4 | 0.11 | OC316 | N | 0 | 0 | 0 | N |
ALK | RGKAVRGNS | OVARY | 201 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 4 | 0.11 | OC316 | N | 0 | 0 | 0 | N |
ALK | RGNSRLPAP | OVARY | 206 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | N | 0 | 0 | 0 | N |
ALK | RLPAPPSLP | OVARY | 210 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 4 | 0.11 | OC316 | N | 0 | 0 | 0 | N |
ALK | RRATEDPPD | OVARY | 182 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 6 | 0.11 | OC316 | N | 2 | 0 | 0 | N |
ALK | RRRATEDPP | OVARY | 181 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 6 | 0.11 | OC316 | N | 3 | 0 | 0 | N |
ALK | SGQRGKAVR | OVARY | 198 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | N | 1 | 0 | 0 | N |
ALK | SLPDLRDWS | OVARY | 216 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 4 | 0.11 | OC316 | N | 0 | 0 | 0 | N |
ALK | SPRRRATED | OVARY | 179 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | N | 2 | 0 | 0 | N |
ALK | SQRAVQLVD | OVARY | 170 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 4 | 0.11 | OC316 | N | 1 | 0 | 0 | N |
ALK | SRLPAPPSL | OVARY | 209 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 4 | 0.11 | OC316 | Y | 7 | 10 | 0 | N |
ALK | TEDPPDARE | OVARY | 185 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 6 | 0.11 | OC316 | N | 0 | 0 | 0 | N |
ALK | VDSPRRRAT | OVARY | 177 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | N | 1 | 0 | 0 | N |
ALK | VGPPRGGGC | OVARY | 155 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | N | 1 | 0 | 0 | Y |
ALK | VGSGQRGKA | OVARY | 196 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | N | 2 | 0 | 1 | N |
ALK | VQLVDSPRR | OVARY | 174 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | N | 6 | 0 | 4 | N |
ALK | VQSQRAVQL | OVARY | 168 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | N | 13 | 0 | 2 | N |
ALK | VRGNSRLPA | OVARY | 205 | p.P158fs | c.474_475insC | Frame_Shift_Ins | 5 | 0.11 | OC316 | N | 6 | 0 | 37 | N |
ALK | ENNSVLGLN | STOMACH | 862 | p.865_866SS>S | c.2595_2597delCTC | In_Frame_Del | 2 | 0.11 | HUG1N | N | 0 | 0 | 0 | N |
ALK | ERLENNSVL | STOMACH | 859 | p.865_866SS>S | c.2595_2597delCTC | In_Frame_Del | 2 | 0.11 | HUG1N | N | 7 | 0 | 0 | N |
ALK | LENNSVLGL | STOMACH | 861 | p.865_866SS>S | c.2595_2597delCTC | In_Frame_Del | 3 | 0.11 | HUG1N | N | 10 | 0 | 9 | N |
ALK | NNSVLGLNG | STOMACH | 863 | p.865_866SS>S | c.2595_2597delCTC | In_Frame_Del | 1 | 0.11 | HUG1N | N | 0 | 0 | 0 | N |
ALK | NSVLGLNGN | STOMACH | 864 | p.865_866SS>S | c.2595_2597delCTC | In_Frame_Del | 1 | 0.11 | HUG1N | N | 0 | 0 | 0 | N |
ALK | PERLENNSV | STOMACH | 858 | p.865_866SS>S | c.2595_2597delCTC | In_Frame_Del | 1 | 0.11 | HUG1N | N | 2 | 0 | 0 | N |
ALK | RLENNSVLG | STOMACH | 860 | p.865_866SS>S | c.2595_2597delCTC | In_Frame_Del | 3 | 0.11 | HUG1N | N | 1 | 0 | 0 | N |
ALK | AKREERSPA | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1430 | p.E1435del | c.4303_4305delGAG | In_Frame_Del | 3 | 0.33 | HUT102 | N | 2 | 0 | 0 | N |
ALK | AKREERSPA | PANCREAS | 1430 | p.E1435del | c.4303_4305delGAG | In_Frame_Del | 3 | 0.33 | L33 | N | 2 | 0 | 0 | N |
ALK | AKREERSPA | LUNG | 1430 | p.E1435del | c.4303_4305delGAG | In_Frame_Del | 3 | 0.33 | NCIH1373 | N | 2 | 0 | 0 | N |
ALK | KREERSPAA | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1431 | p.E1435del | c.4303_4305delGAG | In_Frame_Del | 2 | 0.33 | HUT102 | N | 3 | 0 | 0 | N |
ALK | KREERSPAA | PANCREAS | 1431 | p.E1435del | c.4303_4305delGAG | In_Frame_Del | 2 | 0.33 | L33 | N | 3 | 0 | 0 | N |
ALK | KREERSPAA | LUNG | 1431 | p.E1435del | c.4303_4305delGAG | In_Frame_Del | 2 | 0.33 | NCIH1373 | N | 3 | 0 | 0 | N |
ALK | QAKREERSP | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1429 | p.E1435del | c.4303_4305delGAG | In_Frame_Del | 3 | 0.33 | HUT102 | N | 0 | 0 | 0 | N |
ALK | QAKREERSP | PANCREAS | 1429 | p.E1435del | c.4303_4305delGAG | In_Frame_Del | 3 | 0.33 | L33 | N | 0 | 0 | 0 | N |
ALK | QAKREERSP | LUNG | 1429 | p.E1435del | c.4303_4305delGAG | In_Frame_Del | 3 | 0.33 | NCIH1373 | N | 0 | 0 | 0 | N |
ALK | QQAKREERS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1428 | p.E1435del | c.4303_4305delGAG | In_Frame_Del | 2 | 0.33 | HUT102 | N | 0 | 0 | 0 | N |
ALK | QQAKREERS | PANCREAS | 1428 | p.E1435del | c.4303_4305delGAG | In_Frame_Del | 2 | 0.33 | L33 | N | 0 | 0 | 0 | N |
ALK | QQAKREERS | LUNG | 1428 | p.E1435del | c.4303_4305delGAG | In_Frame_Del | 2 | 0.33 | NCIH1373 | N | 0 | 0 | 0 | N |
ALK | REERSPAAP | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1432 | p.E1435del | c.4303_4305delGAG | In_Frame_Del | 1 | 0.33 | HUT102 | N | 0 | 0 | 0 | N |
ALK | REERSPAAP | PANCREAS | 1432 | p.E1435del | c.4303_4305delGAG | In_Frame_Del | 1 | 0.33 | L33 | N | 0 | 0 | 0 | N |
ALK | REERSPAAP | LUNG | 1432 | p.E1435del | c.4303_4305delGAG | In_Frame_Del | 1 | 0.33 | NCIH1373 | N | 0 | 0 | 0 | N |
ALK | SQQAKREER | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 1427 | p.E1435del | c.4303_4305delGAG | In_Frame_Del | 1 | 0.33 | HUT102 | N | 5 | 0 | 0 | N |
ALK | SQQAKREER | PANCREAS | 1427 | p.E1435del | c.4303_4305delGAG | In_Frame_Del | 1 | 0.33 | L33 | N | 5 | 0 | 0 | N |
ALK | SQQAKREER | LUNG | 1427 | p.E1435del | c.4303_4305delGAG | In_Frame_Del | 1 | 0.33 | NCIH1373 | N | 5 | 0 | 0 | N |
ALK | AAGGGGCWN | OVARY | 876 | p.G882C | c.2644G>T | Missense_Mutation | 1 | 0.11 | EFO27 | N | 1 | 0 | 0 | N |
ALK | AAGRKGGKN | LUNG | 741 | p.G744R | c.2230G>A | Missense_Mutation | 1 | 0.11 | NCIH1435 | N | 1 | 0 | 0 | N |
ALK | AAICASQPR | LUNG | 206 | p.R209C | c.625C>T | Missense_Mutation | 1 | 0.11 | DV90 | N | 4 | 0 | 0 | N |
ALK | AAIEILLMP | UPPER_AERODIGESTIVE_TRACT | 371 | p.R373I | c.1118G>T | Missense_Mutation | 1 | 0.11 | PECAPJ34CLONEC12 | N | 0 | 0 | 0 | N |
ALK | AALGLLQFN | OESOPHAGUS | 161 | p.V163L | c.487G>T | Missense_Mutation | 1 | 0.11 | KYSE520 | N | 2 | 0 | 0 | N |
ALK | AAREILLMS | SKIN | 371 | p.P379S | c.1135C>T | Missense_Mutation | 1 | 0.11 | SKMEL2 | N | 2 | 0 | 0 | N |
ALK | ACPSTTQLI | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 782 | p.N787T | c.2360A>C | Missense_Mutation | 1 | 0.11 | DND41 | Y | 5 | 10 | 0 | N |
ALK | AERSKEMPT | LUNG | 309 | p.R317T | c.950G>C | Missense_Mutation | 1 | 0.11 | CORL23 | N | 5 | 0 | 0 | N |
ALK | AGGGGCWND | OVARY | 877 | p.G882C | c.2644G>T | Missense_Mutation | 1 | 0.11 | EFO27 | N | 0 | 0 | 0 | N |
ALK | AGRKGGKNT | LUNG | 742 | p.G744R | c.2230G>A | Missense_Mutation | 1 | 0.11 | NCIH1435 | N | 1 | 0 | 0 | N |
ALK | AHLLPHNEA | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 363 | p.Q364H | c.1092G>C | Missense_Mutation | 1 | 0.11 | DAUDI | N | 1 | 0 | 0 | N |
ALK | AICASQPRL | LUNG | 207 | p.R209C | c.625C>T | Missense_Mutation | 1 | 0.11 | DV90 | N | 3 | 0 | 0 | N |
ALK | AIEILLMPT | UPPER_AERODIGESTIVE_TRACT | 372 | p.R373I | c.1118G>T | Missense_Mutation | 1 | 0.11 | PECAPJ34CLONEC12 | N | 1 | 0 | 0 | N |
ALK | AILEGCVGH | OESOPHAGUS | 149 | p.P157H | c.470C>A | Missense_Mutation | 1 | 0.11 | TE5 | N | 0 | 0 | 0 | N |
ALK | AKQLVRELG | LUNG | 138 | p.L143R | c.428T>G | Missense_Mutation | 1 | 0.11 | NCIH1651 | N | 0 | 0 | 0 | N |
ALK | ALGLLQFNL | OESOPHAGUS | 162 | p.V163L | c.487G>T | Missense_Mutation | 1 | 0.11 | KYSE520 | Y | 10 | 10 | 0 | N |
ALK | ALQRSFTCW | OVARY | 436 | p.S439R | c.1317C>G | Missense_Mutation | 1 | 0.11 | OV56 | N | 4 | 0 | 0 | N |
ALK | APLLRLLRP | LUNG | 96 | p.G103R | c.307G>C | Missense_Mutation | 1 | 0.11 | SW900 | N | 0 | 0 | 0 | Y |
ALK | AQLLPHKEA | LUNG | 363 | p.N369K | c.1107C>G | Missense_Mutation | 1 | 0.11 | NCIH1693 | N | 2 | 0 | 0 | N |
ALK | AQLLSHNEA | LARGE_INTESTINE | 363 | p.P367S | c.1099C>T | Missense_Mutation | 1 | 0.11 | SNU81 | N | 2 | 0 | 0 | N |
ALK | AREILLMST | SKIN | 372 | p.P379S | c.1135C>T | Missense_Mutation | 1 | 0.11 | SKMEL2 | N | 2 | 0 | 0 | N |
ALK | ARKSLQEGA | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 892 | p.G893R | c.2677G>A | Missense_Mutation | 1 | 0.11 | OCILY10 | Y | 2 | 10 | 0 | N |
ALK | ATDTYSILG | CENTRAL_NERVOUS_SYSTEM | 730 | p.S737L | c.2210C>T | Missense_Mutation | 1 | 0.11 | AM38 | N | 1 | 0 | 0 | N |
ALK | AVEGGHMNM | LARGE_INTESTINE | 1470 | p.V1476M | c.4426G>A | Missense_Mutation | 1 | 0.11 | LS513 | N | 2 | 0 | 0 | N |
ALK | AWLIRGVLR | LUNG | 553 | p.S553A | c.1657T>G | Missense_Mutation | 1 | 0.11 | NCIH2087 | N | 2 | 0 | 0 | N |
ALK | CAPLLRLLR | LUNG | 95 | p.G103R | c.307G>C | Missense_Mutation | 1 | 0.11 | SW900 | N | 4 | 0 | 0 | Y |
ALK | CASQPRLLF | LUNG | 209 | p.R209C | c.625C>T | Missense_Mutation | 1 | 0.11 | DV90 | N | 3 | 0 | 0 | N |
ALK | CCIGVSLQS | ENDOMETRIUM | 1181 | p.R1181C | c.3541C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 0 | 0 | 0 | N |
ALK | CELEYSPLL | SKIN | 272 | p.P279L | c.836C>T | Missense_Mutation | 1 | 0.11 | SKMEL30 | N | 12 | 0 | 0 | N |
ALK | CELRMAWLI | LUNG | 548 | p.S553A | c.1657T>G | Missense_Mutation | 1 | 0.11 | NCIH2087 | Y | 7 | 13 | 0 | N |
ALK | CPDNPFRVA | STOMACH | 395 | p.R395C | c.1183C>T | Missense_Mutation | 1 | 0.11 | SNU1 | N | 8 | 0 | 0 | N |
ALK | CPSTTQLIQ | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 783 | p.N787T | c.2360A>C | Missense_Mutation | 1 | 0.11 | DND41 | N | 0 | 0 | 0 | N |
ALK | CRASGPHGP | SKIN | 688 | p.G689R | c.2065G>A | Missense_Mutation | 1 | 0.11 | G361 | N | 1 | 0 | 0 | N |
ALK | CTVPSNVAT | LARGE_INTESTINE | 1539 | p.P1543S | c.4627C>T | Missense_Mutation | 1 | 0.11 | SW48 | N | 1 | 0 | 0 | N |
ALK | CVGHPGEAA | OESOPHAGUS | 154 | p.P157H | c.470C>A | Missense_Mutation | 1 | 0.11 | TE5 | N | 1 | 0 | 0 | N |
ALK | CWNDNTSLL | OVARY | 882 | p.G882C | c.2644G>T | Missense_Mutation | 1 | 0.11 | EFO27 | Y | 9 | 11 | 0 | N |
ALK | CYLTISRED | LARGE_INTESTINE | 634 | p.G640R | c.1918G>A | Missense_Mutation | 1 | 0.11 | SNUC5 | N | 0 | 0 | 0 | N |
ALK | DACPSTTQL | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 781 | p.N787T | c.2360A>C | Missense_Mutation | 1 | 0.11 | DND41 | N | 11 | 0 | 0 | N |
ALK | DCYLTISRE | LARGE_INTESTINE | 633 | p.G640R | c.1918G>A | Missense_Mutation | 1 | 0.11 | SNUC5 | N | 0 | 0 | 0 | N |
ALK | DLKEVPWKN | LARGE_INTESTINE | 1107 | p.R1113W | c.3337C>T | Missense_Mutation | 1 | 0.11 | SNU175 | N | 2 | 0 | 0 | N |
ALK | DNTSLLWAR | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 885 | p.G893R | c.2677G>A | Missense_Mutation | 1 | 0.11 | OCILY10 | N | 2 | 0 | 0 | N |
ALK | DPSPLQVVV | THYROID | 1141 | p.A1148V | c.3443C>T | Missense_Mutation | 1 | 0.11 | FTC133 | Y | 12 | 9 | 0 | N |
ALK | DTYSILGYG | CENTRAL_NERVOUS_SYSTEM | 732 | p.S737L | c.2210C>T | Missense_Mutation | 1 | 0.11 | AM38 | N | 0 | 0 | 0 | N |
ALK | EAAIEILLM | UPPER_AERODIGESTIVE_TRACT | 370 | p.R373I | c.1118G>T | Missense_Mutation | 1 | 0.11 | PECAPJ34CLONEC12 | Y | 4 | 9 | 0 | N |
ALK | EAALGLLQF | OESOPHAGUS | 160 | p.V163L | c.487G>T | Missense_Mutation | 1 | 0.11 | KYSE520 | Y | 6 | 9 | 0 | N |
ALK | EDACPSTTQ | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 780 | p.N787T | c.2360A>C | Missense_Mutation | 1 | 0.11 | DND41 | N | 0 | 0 | 0 | N |
ALK | EGCVGHPGE | OESOPHAGUS | 152 | p.P157H | c.470C>A | Missense_Mutation | 1 | 0.11 | TE5 | N | 0 | 0 | 0 | N |
ALK | EGGHMNMAF | LARGE_INTESTINE | 1472 | p.V1476M | c.4426G>A | Missense_Mutation | 1 | 0.11 | LS513 | N | 5 | 0 | 0 | N |
ALK | EGHGEVNVK | LARGE_INTESTINE | 974 | p.I981V | c.2941A>G | Missense_Mutation | 1 | 0.11 | MDST8 | N | 0 | 0 | 0 | N |
ALK | EGRLSAAIC | LUNG | 201 | p.R209C | c.625C>T | Missense_Mutation | 1 | 0.11 | DV90 | N | 0 | 0 | 0 | N |
ALK | EGSCTVPSN | LARGE_INTESTINE | 1536 | p.P1543S | c.4627C>T | Missense_Mutation | 1 | 0.11 | SW48 | N | 0 | 0 | 0 | N |
ALK | EILLMSTPG | SKIN | 374 | p.P379S | c.1135C>T | Missense_Mutation | 1 | 0.11 | SKMEL2 | N | 0 | 0 | 0 | N |
ALK | EKKVSEVGR | LARGE_INTESTINE | 192 | p.A195V | c.584C>T | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 1 | 0 | 0 | N |
ALK | ELEYSPLLH | SKIN | 273 | p.P279L | c.836C>T | Missense_Mutation | 1 | 0.11 | SKMEL30 | N | 1 | 0 | 0 | N |
ALK | ELRMAWLIR | LUNG | 549 | p.S553A | c.1657T>G | Missense_Mutation | 1 | 0.11 | NCIH2087 | N | 5 | 0 | 0 | N |
ALK | EMPTGSFLL | LUNG | 314 | p.R317T | c.950G>C | Missense_Mutation | 1 | 0.11 | CORL23 | N | 13 | 0 | 0 | N |
ALK | ENKTGNEQG | SKIN | 570 | p.K575N | c.1725G>C | Missense_Mutation | 1 | 0.11 | K029AX | N | 0 | 0 | 0 | N |
ALK | ERSKEMPTG | LUNG | 310 | p.R317T | c.950G>C | Missense_Mutation | 1 | 0.11 | CORL23 | N | 0 | 0 | 0 | N |
ALK | ESPTNMPSR | BREAST | 228 | p.P236R | c.707C>G | Missense_Mutation | 1 | 0.11 | MDAMB415 | N | 3 | 0 | 0 | N |
ALK | ESPTNVPSP | PANCREAS | 228 | p.M233V | c.697A>G | Missense_Mutation | 1 | 0.11 | SNU213 | N | 0 | 0 | 0 | N |
ALK | ETIGGFGGG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 916 | p.R918I | c.2753G>T | Missense_Mutation | 1 | 0.11 | TOLEDO | N | 0 | 0 | 0 | N |
ALK | ETRPRPSQS | LARGE_INTESTINE | 1210 | p.P1218S | c.3652C>T | Missense_Mutation | 1 | 0.11 | CW2 | N | 1 | 0 | 0 | N |
ALK | EVNVKHYLN | LARGE_INTESTINE | 978 | p.I981V | c.2941A>G | Missense_Mutation | 1 | 0.11 | MDST8 | N | 0 | 0 | 0 | Y |
ALK | EVPWKNITL | LARGE_INTESTINE | 1110 | p.R1113W | c.3337C>T | Missense_Mutation | 1 | 0.11 | SNU175 | Y | 8 | 10 | 0 | N |
ALK | EYSPLLHDL | SKIN | 275 | p.P279L | c.836C>T | Missense_Mutation | 1 | 0.11 | SKMEL30 | Y | 9 | 9 | 0 | N |
ALK | FGAAGGGGG | ENDOMETRIUM | 874 | p.S874F | c.2621C>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 2 | 0 | 0 | Y |
ALK | FGGGGGGYS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 921 | p.C928Y | c.2783G>A | Missense_Mutation | 1 | 0.11 | REH | N | 3 | 0 | 0 | Y |
ALK | FGGGRGGCS | OESOPHAGUS | 921 | p.G925R | c.2773G>A | Missense_Mutation | 1 | 0.11 | KYSE450 | N | 3 | 0 | 0 | N |
ALK | FNHQNIVCC | ENDOMETRIUM | 1174 | p.R1181C | c.3541C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 3 | 0 | 7 | N |
ALK | FNLNELFSW | LARGE_INTESTINE | 168 | p.S171N | c.512G>A | Missense_Mutation | 1 | 0.11 | SNU503 | N | 4 | 0 | 3 | N |
ALK | FTTCRASGP | SKIN | 685 | p.G689R | c.2065G>A | Missense_Mutation | 1 | 0.11 | G361 | N | 2 | 0 | 0 | Y |
ALK | GAAGGGGCW | OVARY | 875 | p.G882C | c.2644G>T | Missense_Mutation | 1 | 0.11 | EFO27 | N | 2 | 0 | 0 | N |
ALK | GAAGRKGGK | LUNG | 740 | p.G744R | c.2230G>A | Missense_Mutation | 1 | 0.11 | NCIH1435 | N | 2 | 0 | 0 | N |
ALK | GCPDNPFRV | STOMACH | 394 | p.R395C | c.1183C>T | Missense_Mutation | 1 | 0.11 | SNU1 | Y | 4 | 9 | 0 | N |
ALK | GCVGHPGEA | OESOPHAGUS | 153 | p.P157H | c.470C>A | Missense_Mutation | 1 | 0.11 | TE5 | N | 2 | 0 | 0 | N |
ALK | GCWNDNTSL | OVARY | 881 | p.G882C | c.2644G>T | Missense_Mutation | 1 | 0.11 | EFO27 | N | 6 | 0 | 0 | N |
ALK | GEAALGLLQ | OESOPHAGUS | 159 | p.V163L | c.487G>T | Missense_Mutation | 1 | 0.11 | KYSE520 | N | 1 | 0 | 0 | N |
ALK | GEDACPSTT | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 779 | p.N787T | c.2360A>C | Missense_Mutation | 1 | 0.11 | DND41 | N | 5 | 0 | 0 | N |
ALK | GEVNVKHYL | LARGE_INTESTINE | 977 | p.I981V | c.2941A>G | Missense_Mutation | 1 | 0.11 | MDST8 | Y | 8 | 10 | 0 | Y |
ALK | GFGGGGGGY | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 920 | p.C928Y | c.2783G>A | Missense_Mutation | 1 | 0.11 | REH | N | 2 | 0 | 0 | N |
ALK | GFGGGRGGC | OESOPHAGUS | 920 | p.G925R | c.2773G>A | Missense_Mutation | 1 | 0.11 | KYSE450 | N | 1 | 0 | 0 | N |
ALK | GGCWNDNTS | OVARY | 880 | p.G882C | c.2644G>T | Missense_Mutation | 1 | 0.11 | EFO27 | N | 0 | 0 | 0 | N |
ALK | GGFGGGRGG | OESOPHAGUS | 919 | p.G925R | c.2773G>A | Missense_Mutation | 1 | 0.11 | KYSE450 | N | 0 | 0 | 0 | N |
ALK | GGGCWNDNT | OVARY | 879 | p.G882C | c.2644G>T | Missense_Mutation | 1 | 0.11 | EFO27 | N | 1 | 0 | 0 | N |
ALK | GGGGCWNDN | OVARY | 878 | p.G882C | c.2644G>T | Missense_Mutation | 1 | 0.11 | EFO27 | N | 0 | 0 | 0 | N |
ALK | GGGGGGYSS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 922 | p.C928Y | c.2783G>A | Missense_Mutation | 1 | 0.11 | REH | N | 0 | 0 | 0 | N |
ALK | GGGGGYSSG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 923 | p.C928Y | c.2783G>A | Missense_Mutation | 1 | 0.11 | REH | N | 0 | 0 | 0 | N |
ALK | GGGGYSSGG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 924 | p.C928Y | c.2783G>A | Missense_Mutation | 1 | 0.11 | REH | N | 0 | 0 | 0 | N |
ALK | GGGRGGCSS | OESOPHAGUS | 922 | p.G925R | c.2773G>A | Missense_Mutation | 1 | 0.11 | KYSE450 | N | 0 | 0 | 0 | N |
ALK | GGGYSSGGG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 925 | p.C928Y | c.2783G>A | Missense_Mutation | 1 | 0.11 | REH | N | 0 | 0 | 0 | N |
ALK | GGHMNMAFS | LARGE_INTESTINE | 1473 | p.V1476M | c.4426G>A | Missense_Mutation | 1 | 0.11 | LS513 | N | 1 | 0 | 0 | N |
ALK | GGRGGCSSG | OESOPHAGUS | 923 | p.G925R | c.2773G>A | Missense_Mutation | 1 | 0.11 | KYSE450 | N | 0 | 0 | 0 | N |
ALK | GGSLRKLRR | LUNG | 129 | p.V132L | c.394G>C | Missense_Mutation | 1 | 0.11 | NCIH650 | N | 1 | 0 | 0 | Y |
ALK | GGSVHKLRR | LARGE_INTESTINE | 129 | p.R133H | c.398G>A | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 1 | 0 | 0 | N |
ALK | GGYSSGGGG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 926 | p.C928Y | c.2783G>A | Missense_Mutation | 1 | 0.11 | REH | N | 0 | 0 | 0 | N |
ALK | GHGEVNVKH | LARGE_INTESTINE | 975 | p.I981V | c.2941A>G | Missense_Mutation | 1 | 0.11 | MDST8 | N | 0 | 0 | 0 | N |
ALK | GHMNMAFSQ | LARGE_INTESTINE | 1474 | p.V1476M | c.4426G>A | Missense_Mutation | 1 | 0.11 | LS513 | N | 0 | 0 | 0 | N |
ALK | GHPGEAAVG | OESOPHAGUS | 156 | p.P157H | c.470C>A | Missense_Mutation | 1 | 0.11 | TE5 | N | 0 | 0 | 0 | N |
ALK | GKHSWTVLQ | SKIN | 382 | p.G385S | c.1153G>A | Missense_Mutation | 1 | 0.11 | G361 | N | 0 | 0 | 0 | N |
ALK | GLLQFNLNE | LARGE_INTESTINE | 164 | p.S171N | c.512G>A | Missense_Mutation | 1 | 0.11 | SNU503 | N | 2 | 0 | 0 | N |
ALK | GLNGNFGAA | ENDOMETRIUM | 869 | p.S874F | c.2621C>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 4 | 0 | 0 | N |
ALK | GLNSNSGAA | KIDNEY | 869 | p.G872S | c.2614G>A | Missense_Mutation | 1 | 0.11 | A498 | N | 3 | 0 | 0 | N |
ALK | GNEQGRMVW | SKIN | 574 | p.K575N | c.1725G>C | Missense_Mutation | 1 | 0.11 | K029AX | N | 2 | 0 | 0 | N |
ALK | GNFGAAGGG | ENDOMETRIUM | 872 | p.S874F | c.2621C>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | N |
ALK | GPAVEGGHM | LARGE_INTESTINE | 1468 | p.V1476M | c.4426G>A | Missense_Mutation | 1 | 0.11 | LS513 | N | 11 | 0 | 0 | N |
ALK | GPPGEAALG | OESOPHAGUS | 156 | p.V163L | c.487G>T | Missense_Mutation | 1 | 0.11 | KYSE520 | N | 0 | 0 | 0 | Y |
ALK | GRGGCSSGG | OESOPHAGUS | 924 | p.G925R | c.2773G>A | Missense_Mutation | 1 | 0.11 | KYSE450 | N | 1 | 0 | 0 | N |
ALK | GRIGCPDNP | STOMACH | 391 | p.R395C | c.1183C>T | Missense_Mutation | 1 | 0.11 | SNU1 | N | 1 | 0 | 0 | N |
ALK | GRKGGKNTM | LUNG | 743 | p.G744R | c.2230G>A | Missense_Mutation | 1 | 0.11 | NCIH1435 | Y | 4 | 9 | 0 | N |
ALK | GRLSAAICA | LUNG | 202 | p.R209C | c.625C>T | Missense_Mutation | 1 | 0.11 | DV90 | N | 3 | 0 | 0 | N |
ALK | GRYIAHLLP | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 359 | p.Q364H | c.1092G>C | Missense_Mutation | 1 | 0.11 | DAUDI | N | 2 | 0 | 0 | N |
ALK | GRYIAQLLS | LARGE_INTESTINE | 359 | p.P367S | c.1099C>T | Missense_Mutation | 1 | 0.11 | SNU81 | N | 3 | 0 | 0 | N |
ALK | GSCTVPSNV | LARGE_INTESTINE | 1537 | p.P1543S | c.4627C>T | Missense_Mutation | 1 | 0.11 | SW48 | N | 4 | 0 | 0 | N |
ALK | GSKMALQRS | OVARY | 432 | p.S439R | c.1317C>G | Missense_Mutation | 1 | 0.11 | OV56 | N | 0 | 0 | 0 | N |
ALK | GSLRKLRRA | LUNG | 130 | p.V132L | c.394G>C | Missense_Mutation | 1 | 0.11 | NCIH650 | Y | 3 | 11 | 0 | N |
ALK | GSVHKLRRA | LARGE_INTESTINE | 130 | p.R133H | c.398G>A | Missense_Mutation | 1 | 0.11 | SNU1040 | Y | 3 | 9 | 0 | N |
ALK | GSYIAQLLP | LUNG | 359 | p.R360S | c.1080G>T | Missense_Mutation | 1 | 0.11 | DV90 | N | 0 | 0 | 0 | N |
ALK | GVSLQSLPQ | SOFT_TISSUE | 1184 | p.R1192Q | c.3575G>A | Missense_Mutation | 1 | 0.11 | SKUT1 | N | 0 | 0 | 0 | N |
ALK | GVSLQSLPW | ENDOMETRIUM | 1184 | p.R1192W | c.3574C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 1 | 0 | 0 | N |
ALK | GWETIGGFG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 914 | p.R918I | c.2753G>T | Missense_Mutation | 1 | 0.11 | TOLEDO | N | 0 | 0 | 0 | N |
ALK | GYGAAGRKG | LUNG | 738 | p.G744R | c.2230G>A | Missense_Mutation | 1 | 0.11 | NCIH1435 | N | 0 | 0 | 0 | N |
ALK | GYSSGGGGG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 927 | p.C928Y | c.2783G>A | Missense_Mutation | 1 | 0.11 | REH | N | 0 | 0 | 0 | N |
ALK | HGEVNVKHY | LARGE_INTESTINE | 976 | p.I981V | c.2941A>G | Missense_Mutation | 1 | 0.11 | MDST8 | N | 4 | 0 | 0 | N |
ALK | HKEAAREIL | LUNG | 368 | p.N369K | c.1107C>G | Missense_Mutation | 1 | 0.11 | NCIH1693 | N | 3 | 0 | 0 | N |
ALK | HKLRRAKQL | LARGE_INTESTINE | 133 | p.R133H | c.398G>A | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 6 | 0 | 0 | N |
ALK | HLLPHNEAA | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 364 | p.Q364H | c.1092G>C | Missense_Mutation | 1 | 0.11 | DAUDI | N | 3 | 0 | 0 | N |
ALK | HLQPSGSYI | LUNG | 354 | p.R360S | c.1080G>T | Missense_Mutation | 1 | 0.11 | DV90 | Y | 5 | 15 | 0 | N |
ALK | HMNMAFSQS | LARGE_INTESTINE | 1475 | p.V1476M | c.4426G>A | Missense_Mutation | 1 | 0.11 | LS513 | N | 0 | 0 | 0 | N |
ALK | HNEAAIEIL | UPPER_AERODIGESTIVE_TRACT | 368 | p.R373I | c.1118G>T | Missense_Mutation | 1 | 0.11 | PECAPJ34CLONEC12 | N | 5 | 0 | 0 | N |
ALK | HPGEAAVGL | OESOPHAGUS | 157 | p.P157H | c.470C>A | Missense_Mutation | 1 | 0.11 | TE5 | N | 16 | 0 | 0 | N |
ALK | HQNIVCCIG | ENDOMETRIUM | 1176 | p.R1181C | c.3541C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 0 | 0 | 0 | N |
ALK | HRHLQPSGS | LUNG | 352 | p.R360S | c.1080G>T | Missense_Mutation | 1 | 0.11 | DV90 | N | 2 | 0 | 0 | N |
ALK | HSWTVLQGR | SKIN | 384 | p.G385S | c.1153G>A | Missense_Mutation | 1 | 0.11 | G361 | N | 4 | 0 | 0 | N |
ALK | HWLFTTCRA | SKIN | 682 | p.G689R | c.2065G>A | Missense_Mutation | 1 | 0.11 | G361 | N | 1 | 0 | 0 | N |
ALK | IAHLLPHNE | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 362 | p.Q364H | c.1092G>C | Missense_Mutation | 1 | 0.11 | DAUDI | N | 0 | 0 | 1 | N |
ALK | IAQLLPHKE | LUNG | 362 | p.N369K | c.1107C>G | Missense_Mutation | 1 | 0.11 | NCIH1693 | N | 0 | 0 | 0 | N |
ALK | IAQLLSHNE | LARGE_INTESTINE | 362 | p.P367S | c.1099C>T | Missense_Mutation | 1 | 0.11 | SNU81 | N | 0 | 0 | 1 | N |
ALK | ICASQPRLL | LUNG | 208 | p.R209C | c.625C>T | Missense_Mutation | 1 | 0.11 | DV90 | N | 7 | 0 | 2 | N |
ALK | IDYNPNYCF | SKIN | 1090 | p.T1090I | c.3269C>T | Missense_Mutation | 1 | 0.11 | WM88 | N | 7 | 0 | 0 | N |
ALK | IEILLMPTP | UPPER_AERODIGESTIVE_TRACT | 373 | p.R373I | c.1118G>T | Missense_Mutation | 1 | 0.11 | PECAPJ34CLONEC12 | N | 2 | 0 | 0 | N |
ALK | IGCPDNPFR | STOMACH | 393 | p.R395C | c.1183C>T | Missense_Mutation | 1 | 0.11 | SNU1 | N | 1 | 0 | 0 | N |
ALK | IGGFGGGGG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 918 | p.R918I | c.2753G>T | Missense_Mutation | 1 | 0.11 | TOLEDO | N | 0 | 0 | 0 | N |
ALK | ILEGCVGHP | OESOPHAGUS | 150 | p.P157H | c.470C>A | Missense_Mutation | 1 | 0.11 | TE5 | N | 0 | 0 | 0 | N |
ALK | ILGYGAAGG | CENTRAL_NERVOUS_SYSTEM | 736 | p.S737L | c.2210C>T | Missense_Mutation | 1 | 0.11 | AM38 | N | 0 | 0 | 4 | N |
ALK | ILLMSTPGK | SKIN | 375 | p.P379S | c.1135C>T | Missense_Mutation | 1 | 0.11 | SKMEL2 | N | 6 | 0 | 32 | N |
ALK | IMIDYNPNY | SKIN | 1088 | p.T1090I | c.3269C>T | Missense_Mutation | 1 | 0.11 | WM88 | N | 10 | 0 | 11 | N |
ALK | IRLMPEKKV | LARGE_INTESTINE | 187 | p.A195V | c.584C>T | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 4 | 0 | 12 | N |
ALK | ISDLKEVPW | LARGE_INTESTINE | 1105 | p.R1113W | c.3337C>T | Missense_Mutation | 1 | 0.11 | SNU175 | N | 4 | 0 | 0 | Y |
ALK | ISGYGAAGR | LUNG | 736 | p.G744R | c.2230G>A | Missense_Mutation | 1 | 0.11 | NCIH1435 | N | 3 | 0 | 0 | N |
ALK | ISREDKILQ | LARGE_INTESTINE | 638 | p.G640R | c.1918G>A | Missense_Mutation | 1 | 0.11 | SNUC5 | N | 0 | 0 | 0 | N |
ALK | IVCCIGVSL | ENDOMETRIUM | 1179 | p.R1181C | c.3541C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 10 | 0 | 6 | N |
ALK | KEAAREILL | LUNG | 369 | p.N369K | c.1107C>G | Missense_Mutation | 1 | 0.11 | NCIH1693 | Y | 12 | 13 | 0 | N |
ALK | KEMPTGSFL | LUNG | 313 | p.R317T | c.950G>C | Missense_Mutation | 1 | 0.11 | CORL23 | N | 12 | 0 | 0 | N |
ALK | KEVPWKNIT | LARGE_INTESTINE | 1109 | p.R1113W | c.3337C>T | Missense_Mutation | 1 | 0.11 | SNU175 | N | 5 | 0 | 0 | N |
ALK | KFNHQNIVC | ENDOMETRIUM | 1173 | p.R1181C | c.3541C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 1 | 0 | 0 | N |
ALK | KGGSLRKLR | LUNG | 128 | p.V132L | c.394G>C | Missense_Mutation | 1 | 0.11 | NCIH650 | N | 0 | 0 | 0 | N |
ALK | KGGSVHKLR | LARGE_INTESTINE | 128 | p.R133H | c.398G>A | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 0 | 0 | 0 | N |
ALK | KHSWTVLQG | SKIN | 383 | p.G385S | c.1153G>A | Missense_Mutation | 1 | 0.11 | G361 | N | 0 | 0 | 0 | N |
ALK | KKVSEVGRE | LARGE_INTESTINE | 193 | p.A195V | c.584C>T | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 0 | 0 | 0 | N |
ALK | KKWGWETIG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 911 | p.R918I | c.2753G>T | Missense_Mutation | 1 | 0.11 | TOLEDO | N | 1 | 0 | 0 | N |
ALK | KLRTSTIMI | SKIN | 1082 | p.T1090I | c.3269C>T | Missense_Mutation | 1 | 0.11 | WM88 | N | 9 | 0 | 0 | N |
ALK | KMALQRSFT | OVARY | 434 | p.S439R | c.1317C>G | Missense_Mutation | 1 | 0.11 | OV56 | N | 3 | 0 | 0 | N |
ALK | KQLVRELGE | LUNG | 139 | p.L143R | c.428T>G | Missense_Mutation | 1 | 0.11 | NCIH1651 | N | 0 | 0 | 0 | N |
ALK | KTGNEQGRM | SKIN | 572 | p.K575N | c.1725G>C | Missense_Mutation | 1 | 0.11 | K029AX | N | 2 | 0 | 0 | N |
ALK | KVGSVRKLR | OVARY | 128 | p.G129V | c.386G>T | Missense_Mutation | 1 | 0.11 | OVTOKO | Y | 6 | 9 | 0 | N |
ALK | KVSEVGREG | LARGE_INTESTINE | 194 | p.A195V | c.584C>T | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 0 | 0 | 0 | N |
ALK | KWGWETIGG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 912 | p.R918I | c.2753G>T | Missense_Mutation | 1 | 0.11 | TOLEDO | N | 0 | 0 | 0 | N |
ALK | LDCYLTISR | LARGE_INTESTINE | 632 | p.G640R | c.1918G>A | Missense_Mutation | 1 | 0.11 | SNUC5 | N | 0 | 0 | 0 | N |
ALK | LEGCVGHPG | OESOPHAGUS | 151 | p.P157H | c.470C>A | Missense_Mutation | 1 | 0.11 | TE5 | N | 0 | 0 | 0 | N |
ALK | LEGSCTVPS | LARGE_INTESTINE | 1535 | p.P1543S | c.4627C>T | Missense_Mutation | 1 | 0.11 | SW48 | N | 3 | 0 | 13 | N |
ALK | LESPTNVPS | PANCREAS | 227 | p.M233V | c.697A>G | Missense_Mutation | 1 | 0.11 | SNU213 | N | 3 | 0 | 0 | N |
ALK | LEYSPLLHD | SKIN | 274 | p.P279L | c.836C>T | Missense_Mutation | 1 | 0.11 | SKMEL30 | N | 1 | 0 | 0 | N |
ALK | LFTTCRASG | SKIN | 684 | p.G689R | c.2065G>A | Missense_Mutation | 1 | 0.11 | G361 | N | 0 | 0 | 0 | N |
ALK | LGLLQFNLS | OESOPHAGUS | 163 | p.V163L | c.487G>T | Missense_Mutation | 1 | 0.11 | KYSE520 | N | 1 | 0 | 5 | N |
ALK | LGLNGNFGA | ENDOMETRIUM | 868 | p.S874F | c.2621C>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 3 | 0 | 8 | N |
ALK | LGLNSNSGA | KIDNEY | 868 | p.G872S | c.2614G>A | Missense_Mutation | 1 | 0.11 | A498 | N | 3 | 0 | 8 | N |
ALK | LGYGAAGGK | CENTRAL_NERVOUS_SYSTEM | 737 | p.S737L | c.2210C>T | Missense_Mutation | 1 | 0.11 | AM38 | N | 1 | 0 | 0 | N |
ALK | LKEVPWKNI | LARGE_INTESTINE | 1108 | p.R1113W | c.3337C>T | Missense_Mutation | 1 | 0.11 | SNU175 | N | 2 | 0 | 0 | N |
ALK | LKGGSLRKL | LUNG | 127 | p.V132L | c.394G>C | Missense_Mutation | 1 | 0.11 | NCIH650 | N | 4 | 0 | 0 | N |
ALK | LKGGSVHKL | LARGE_INTESTINE | 127 | p.R133H | c.398G>A | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 4 | 0 | 0 | N |
ALK | LKVGSVRKL | OVARY | 127 | p.G129V | c.386G>T | Missense_Mutation | 1 | 0.11 | OVTOKO | N | 7 | 0 | 1 | N |
ALK | LLHDLRNQS | SKIN | 279 | p.P279L | c.836C>T | Missense_Mutation | 1 | 0.11 | SKMEL30 | N | 0 | 0 | 8 | N |
ALK | LLMSTPGKH | SKIN | 376 | p.P379S | c.1135C>T | Missense_Mutation | 1 | 0.11 | SKMEL2 | N | 0 | 0 | 11 | N |
ALK | LLPHKEAAR | LUNG | 365 | p.N369K | c.1107C>G | Missense_Mutation | 1 | 0.11 | NCIH1693 | N | 5 | 0 | 0 | N |
ALK | LLPHNEAAI | UPPER_AERODIGESTIVE_TRACT | 365 | p.R373I | c.1118G>T | Missense_Mutation | 1 | 0.11 | PECAPJ34CLONEC12 | Y | 10 | 15 | 0 | N |
ALK | LLQFNLNEL | LARGE_INTESTINE | 165 | p.S171N | c.512G>A | Missense_Mutation | 1 | 0.11 | SNU503 | Y | 15 | 12 | 5 | N |
ALK | LLRLLRPAP | LUNG | 98 | p.G103R | c.307G>C | Missense_Mutation | 1 | 0.11 | SW900 | N | 0 | 0 | 8 | N |
ALK | LLRPAPGVS | LUNG | 101 | p.G103R | c.307G>C | Missense_Mutation | 1 | 0.11 | SW900 | N | 0 | 0 | 0 | N |
ALK | LLSHNEAAR | LARGE_INTESTINE | 365 | p.P367S | c.1099C>T | Missense_Mutation | 1 | 0.11 | SNU81 | Y | 5 | 10 | 0 | N |
ALK | LLWARKSLQ | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 889 | p.G893R | c.2677G>A | Missense_Mutation | 1 | 0.11 | OCILY10 | N | 0 | 0 | 11 | N |
ALK | LMPEKKVSE | LARGE_INTESTINE | 189 | p.A195V | c.584C>T | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 0 | 0 | 1 | N |
ALK | LMPTPGKHS | SKIN | 377 | p.G385S | c.1153G>A | Missense_Mutation | 1 | 0.11 | G361 | N | 0 | 0 | 0 | N |
ALK | LMSTPGKHG | SKIN | 377 | p.P379S | c.1135C>T | Missense_Mutation | 1 | 0.11 | SKMEL2 | N | 1 | 0 | 0 | N |
ALK | LNELFSWWI | LARGE_INTESTINE | 170 | p.S171N | c.512G>A | Missense_Mutation | 1 | 0.11 | SNU503 | N | 4 | 0 | 0 | N |
ALK | LNGNFGAAG | ENDOMETRIUM | 870 | p.S874F | c.2621C>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | N |
ALK | LNSNSGAAG | KIDNEY | 870 | p.G872S | c.2614G>A | Missense_Mutation | 1 | 0.11 | A498 | N | 0 | 0 | 0 | N |
ALK | LPHKEAARE | LUNG | 366 | p.N369K | c.1107C>G | Missense_Mutation | 1 | 0.11 | NCIH1693 | N | 1 | 0 | 2 | N |
ALK | LPHNEAAIE | UPPER_AERODIGESTIVE_TRACT | 366 | p.R373I | c.1118G>T | Missense_Mutation | 1 | 0.11 | PECAPJ34CLONEC12 | N | 1 | 0 | 0 | N |
ALK | LPQFILLEL | SOFT_TISSUE | 1190 | p.R1192Q | c.3575G>A | Missense_Mutation | 1 | 0.11 | SKUT1 | Y | 21 | 10 | 3 | N |
ALK | LPWFILLEL | ENDOMETRIUM | 1190 | p.R1192W | c.3574C>T | Missense_Mutation | 1 | 0.11 | HEC59 | Y | 26 | 10 | 3 | N |
ALK | LQFNLNELF | LARGE_INTESTINE | 166 | p.S171N | c.512G>A | Missense_Mutation | 1 | 0.11 | SNU503 | N | 9 | 0 | 3 | N |
ALK | LQGRIGCPD | STOMACH | 389 | p.R395C | c.1183C>T | Missense_Mutation | 1 | 0.11 | SNU1 | N | 0 | 0 | 3 | N |
ALK | LQPSGSYIA | LUNG | 355 | p.R360S | c.1080G>T | Missense_Mutation | 1 | 0.11 | DV90 | N | 5 | 0 | 4 | N |
ALK | LQRSFTCWN | OVARY | 437 | p.S439R | c.1317C>G | Missense_Mutation | 1 | 0.11 | OV56 | N | 1 | 0 | 7 | N |
ALK | LQSLPQFIL | SOFT_TISSUE | 1187 | p.R1192Q | c.3575G>A | Missense_Mutation | 1 | 0.11 | SKUT1 | N | 13 | 0 | 5 | N |
ALK | LQSLPWFIL | ENDOMETRIUM | 1187 | p.R1192W | c.3574C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 13 | 0 | 5 | N |
ALK | LQVVVKTLP | THYROID | 1145 | p.A1148V | c.3443C>T | Missense_Mutation | 1 | 0.11 | FTC133 | N | 0 | 0 | 0 | N |
ALK | LRKLRRAKQ | LUNG | 132 | p.V132L | c.394G>C | Missense_Mutation | 1 | 0.11 | NCIH650 | N | 2 | 0 | 32 | N |
ALK | LRLLRPAPG | LUNG | 99 | p.G103R | c.307G>C | Missense_Mutation | 1 | 0.11 | SW900 | N | 2 | 0 | 45 | Y |
ALK | LRMAWLIRG | LUNG | 550 | p.S553A | c.1657T>G | Missense_Mutation | 1 | 0.11 | NCIH2087 | N | 1 | 0 | 41 | Y |
ALK | LRPAPGVSW | LUNG | 102 | p.G103R | c.307G>C | Missense_Mutation | 1 | 0.11 | SW900 | N | 4 | 0 | 2 | N |
ALK | LRRAKQLVR | LUNG | 135 | p.L143R | c.428T>G | Missense_Mutation | 1 | 0.11 | NCIH1651 | N | 3 | 0 | 21 | N |
ALK | LRTSTIMID | SKIN | 1083 | p.T1090I | c.3269C>T | Missense_Mutation | 1 | 0.11 | WM88 | N | 1 | 0 | 14 | N |
ALK | LSAAICASQ | LUNG | 204 | p.R209C | c.625C>T | Missense_Mutation | 1 | 0.11 | DV90 | N | 0 | 0 | 0 | N |
ALK | LSHNEAARE | LARGE_INTESTINE | 366 | p.P367S | c.1099C>T | Missense_Mutation | 1 | 0.11 | SNU81 | N | 0 | 0 | 0 | N |
ALK | LSRVLKVGS | OVARY | 123 | p.G129V | c.386G>T | Missense_Mutation | 1 | 0.11 | OVTOKO | N | 0 | 0 | 12 | N |
ALK | LTISREDKI | LARGE_INTESTINE | 636 | p.G640R | c.1918G>A | Missense_Mutation | 1 | 0.11 | SNUC5 | N | 7 | 0 | 0 | N |
ALK | LVENKTGNE | SKIN | 568 | p.K575N | c.1725G>C | Missense_Mutation | 1 | 0.11 | K029AX | N | 0 | 0 | 1 | N |
ALK | LVRELGEEA | LUNG | 141 | p.L143R | c.428T>G | Missense_Mutation | 1 | 0.11 | NCIH1651 | N | 2 | 0 | 4 | N |
ALK | LWARKSLQE | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 890 | p.G893R | c.2677G>A | Missense_Mutation | 1 | 0.11 | OCILY10 | N | 0 | 0 | 3 | N |
ALK | MALQRSFTC | OVARY | 435 | p.S439R | c.1317C>G | Missense_Mutation | 1 | 0.11 | OV56 | N | 5 | 0 | 7 | N |
ALK | MAWLIRGVL | LUNG | 552 | p.S553A | c.1657T>G | Missense_Mutation | 1 | 0.11 | NCIH2087 | N | 20 | 0 | 0 | N |
ALK | MEGHGEVNV | LARGE_INTESTINE | 973 | p.I981V | c.2941A>G | Missense_Mutation | 1 | 0.11 | MDST8 | Y | 8 | 13 | 0 | N |
ALK | MIDYNPNYC | SKIN | 1089 | p.T1090I | c.3269C>T | Missense_Mutation | 1 | 0.11 | WM88 | N | 0 | 0 | 1 | N |
ALK | MKKWGWETI | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 910 | p.R918I | c.2753G>T | Missense_Mutation | 1 | 0.11 | TOLEDO | N | 3 | 0 | 0 | N |
ALK | MNMAFSQSN | LARGE_INTESTINE | 1476 | p.V1476M | c.4426G>A | Missense_Mutation | 1 | 0.11 | LS513 | N | 0 | 0 | 3 | N |
ALK | MPEKKVSEV | LARGE_INTESTINE | 190 | p.A195V | c.584C>T | Missense_Mutation | 1 | 0.11 | SNU1040 | Y | 11 | 9 | 0 | N |
ALK | MPSRSPDYF | BREAST | 233 | p.P236R | c.707C>G | Missense_Mutation | 1 | 0.11 | MDAMB415 | Y | 10 | 9 | 0 | N |
ALK | MPTGSFLLL | LUNG | 315 | p.R317T | c.950G>C | Missense_Mutation | 1 | 0.11 | CORL23 | Y | 18 | 11 | 0 | N |
ALK | MPTPGKHSW | SKIN | 378 | p.G385S | c.1153G>A | Missense_Mutation | 1 | 0.11 | G361 | Y | 7 | 10 | 0 | N |
ALK | MSTPGKHGW | SKIN | 378 | p.P379S | c.1135C>T | Missense_Mutation | 1 | 0.11 | SKMEL2 | N | 4 | 0 | 0 | N |
ALK | NDPSPLQVV | THYROID | 1140 | p.A1148V | c.3443C>T | Missense_Mutation | 1 | 0.11 | FTC133 | N | 5 | 0 | 0 | N |
ALK | NEAAIEILL | UPPER_AERODIGESTIVE_TRACT | 369 | p.R373I | c.1118G>T | Missense_Mutation | 1 | 0.11 | PECAPJ34CLONEC12 | Y | 8 | 11 | 0 | N |
ALK | NELFSWWIR | LARGE_INTESTINE | 171 | p.S171N | c.512G>A | Missense_Mutation | 1 | 0.11 | SNU503 | Y | 0 | 9 | 0 | N |
ALK | NEQGRMVWH | SKIN | 575 | p.K575N | c.1725G>C | Missense_Mutation | 1 | 0.11 | K029AX | N | 0 | 0 | 0 | N |
ALK | NFGAAGGGG | ENDOMETRIUM | 873 | p.S874F | c.2621C>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | N |
ALK | NGNFGAAGG | ENDOMETRIUM | 871 | p.S874F | c.2621C>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 0 | N |
ALK | NHQNIVCCI | ENDOMETRIUM | 1175 | p.R1181C | c.3541C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 5 | 0 | 0 | N |
ALK | NIVCCIGVS | ENDOMETRIUM | 1178 | p.R1181C | c.3541C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 0 | 0 | 0 | N |
ALK | NKTGNEQGR | SKIN | 571 | p.K575N | c.1725G>C | Missense_Mutation | 1 | 0.11 | K029AX | N | 1 | 0 | 0 | N |
ALK | NLNELFSWW | LARGE_INTESTINE | 169 | p.S171N | c.512G>A | Missense_Mutation | 1 | 0.11 | SNU503 | N | 5 | 0 | 0 | N |
ALK | NMPSRSPDY | BREAST | 232 | p.P236R | c.707C>G | Missense_Mutation | 1 | 0.11 | MDAMB415 | N | 6 | 0 | 0 | N |
ALK | NSNSGAAGG | KIDNEY | 871 | p.G872S | c.2614G>A | Missense_Mutation | 1 | 0.11 | A498 | N | 0 | 0 | 0 | N |
ALK | NSSVLGLNS | KIDNEY | 864 | p.G872S | c.2614G>A | Missense_Mutation | 1 | 0.11 | A498 | N | 0 | 0 | 0 | N |
ALK | NTSLLWARK | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 886 | p.G893R | c.2677G>A | Missense_Mutation | 1 | 0.11 | OCILY10 | Y | 1 | 11 | 0 | Y |
ALK | NVKHYLNCS | LARGE_INTESTINE | 980 | p.I981V | c.2941A>G | Missense_Mutation | 1 | 0.11 | MDST8 | N | 0 | 0 | 0 | N |
ALK | NVPSPSPDY | PANCREAS | 232 | p.M233V | c.697A>G | Missense_Mutation | 1 | 0.11 | SNU213 | N | 4 | 0 | 0 | N |
ALK | PATDTYSIL | CENTRAL_NERVOUS_SYSTEM | 729 | p.S737L | c.2210C>T | Missense_Mutation | 1 | 0.11 | AM38 | N | 2 | 0 | 0 | N |
ALK | PAVEGGHMN | LARGE_INTESTINE | 1469 | p.V1476M | c.4426G>A | Missense_Mutation | 1 | 0.11 | LS513 | N | 0 | 0 | 0 | N |
ALK | PCELEYSPL | SKIN | 271 | p.P279L | c.836C>T | Missense_Mutation | 1 | 0.11 | SKMEL30 | N | 0 | 0 | 0 | N |
ALK | PCELRMAWL | LUNG | 547 | p.S553A | c.1657T>G | Missense_Mutation | 1 | 0.11 | NCIH2087 | N | 0 | 0 | 0 | N |
ALK | PEKKVSEVG | LARGE_INTESTINE | 191 | p.A195V | c.584C>T | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 0 | 0 | 0 | N |
ALK | PGEAALGLL | OESOPHAGUS | 158 | p.V163L | c.487G>T | Missense_Mutation | 1 | 0.11 | KYSE520 | N | 0 | 0 | 0 | N |
ALK | PGKHSWTVL | SKIN | 381 | p.G385S | c.1153G>A | Missense_Mutation | 1 | 0.11 | G361 | N | 0 | 0 | 0 | N |
ALK | PGSKMALQR | OVARY | 431 | p.S439R | c.1317C>G | Missense_Mutation | 1 | 0.11 | OV56 | N | 0 | 0 | 0 | N |
ALK | PHKEAAREI | LUNG | 367 | p.N369K | c.1107C>G | Missense_Mutation | 1 | 0.11 | NCIH1693 | N | 0 | 0 | 0 | N |
ALK | PHNEAAIEI | UPPER_AERODIGESTIVE_TRACT | 367 | p.R373I | c.1118G>T | Missense_Mutation | 1 | 0.11 | PECAPJ34CLONEC12 | N | 1 | 0 | 0 | N |
ALK | PLLHDLRNQ | SKIN | 278 | p.P279L | c.836C>T | Missense_Mutation | 1 | 0.11 | SKMEL30 | N | 0 | 0 | 0 | N |
ALK | PLLRLLRPA | LUNG | 97 | p.G103R | c.307G>C | Missense_Mutation | 1 | 0.11 | SW900 | N | 2 | 0 | 0 | Y |
ALK | PLQVVVKTL | THYROID | 1144 | p.A1148V | c.3443C>T | Missense_Mutation | 1 | 0.11 | FTC133 | N | 2 | 0 | 0 | N |
ALK | PPGEAALGL | OESOPHAGUS | 157 | p.V163L | c.487G>T | Missense_Mutation | 1 | 0.11 | KYSE520 | N | 9 | 0 | 0 | N |
ALK | PQFILLELM | SOFT_TISSUE | 1191 | p.R1192Q | c.3575G>A | Missense_Mutation | 1 | 0.11 | SKUT1 | N | 2 | 0 | 0 | N |
ALK | PRPSQSSSL | LARGE_INTESTINE | 1213 | p.P1218S | c.3652C>T | Missense_Mutation | 1 | 0.11 | CW2 | N | 3 | 0 | 0 | N |
ALK | PSGRYIAHL | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 357 | p.Q364H | c.1092G>C | Missense_Mutation | 1 | 0.11 | DAUDI | N | 1 | 0 | 0 | N |
ALK | PSGSYIAQL | LUNG | 357 | p.R360S | c.1080G>T | Missense_Mutation | 1 | 0.11 | DV90 | N | 1 | 0 | 0 | N |
ALK | PSNVATGRL | LARGE_INTESTINE | 1542 | p.P1543S | c.4627C>T | Missense_Mutation | 1 | 0.11 | SW48 | N | 0 | 0 | 0 | N |
ALK | PSPLQVVVK | THYROID | 1142 | p.A1148V | c.3443C>T | Missense_Mutation | 1 | 0.11 | FTC133 | N | 0 | 0 | 0 | N |
ALK | PSQSSSLAM | LARGE_INTESTINE | 1215 | p.P1218S | c.3652C>T | Missense_Mutation | 1 | 0.11 | CW2 | N | 0 | 0 | 0 | N |
ALK | PSRSPDYFT | BREAST | 234 | p.P236R | c.707C>G | Missense_Mutation | 1 | 0.11 | MDAMB415 | N | 0 | 0 | 0 | N |
ALK | PSTTQLIQK | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 784 | p.N787T | c.2360A>C | Missense_Mutation | 1 | 0.11 | DND41 | N | 0 | 0 | 0 | N |
ALK | PTGSFLLLN | LUNG | 316 | p.R317T | c.950G>C | Missense_Mutation | 1 | 0.11 | CORL23 | N | 0 | 0 | 0 | N |
ALK | PTNMPSRSP | BREAST | 230 | p.P236R | c.707C>G | Missense_Mutation | 1 | 0.11 | MDAMB415 | N | 0 | 0 | 0 | N |
ALK | PTNVPSPSP | PANCREAS | 230 | p.M233V | c.697A>G | Missense_Mutation | 1 | 0.11 | SNU213 | N | 0 | 0 | 0 | N |
ALK | PTPGKHSWT | SKIN | 379 | p.G385S | c.1153G>A | Missense_Mutation | 1 | 0.11 | G361 | N | 0 | 0 | 0 | N |
ALK | PWFILLELM | ENDOMETRIUM | 1191 | p.R1192W | c.3574C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 1 | 0 | 0 | N |
ALK | PWKNITLIR | LARGE_INTESTINE | 1112 | p.R1113W | c.3337C>T | Missense_Mutation | 1 | 0.11 | SNU175 | N | 0 | 0 | 0 | N |
ALK | QFILLELMA | SOFT_TISSUE | 1192 | p.R1192Q | c.3575G>A | Missense_Mutation | 1 | 0.11 | SKUT1 | N | 1 | 0 | 0 | N |
ALK | QFNLNELFS | LARGE_INTESTINE | 167 | p.S171N | c.512G>A | Missense_Mutation | 1 | 0.11 | SNU503 | N | 0 | 0 | 0 | N |
ALK | QGRIGCPDN | STOMACH | 390 | p.R395C | c.1183C>T | Missense_Mutation | 1 | 0.11 | SNU1 | N | 0 | 0 | 0 | N |
ALK | QLLPHKEAA | LUNG | 364 | p.N369K | c.1107C>G | Missense_Mutation | 1 | 0.11 | NCIH1693 | N | 3 | 0 | 0 | N |
ALK | QLLSHNEAA | LARGE_INTESTINE | 364 | p.P367S | c.1099C>T | Missense_Mutation | 1 | 0.11 | SNU81 | N | 3 | 0 | 0 | N |
ALK | QLVRELGEE | LUNG | 140 | p.L143R | c.428T>G | Missense_Mutation | 1 | 0.11 | NCIH1651 | N | 0 | 0 | 0 | N |
ALK | QNIVCCIGV | ENDOMETRIUM | 1177 | p.R1181C | c.3541C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 1 | 0 | 0 | N |
ALK | QPSGRYIAH | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 356 | p.Q364H | c.1092G>C | Missense_Mutation | 1 | 0.11 | DAUDI | Y | 0 | 11 | 0 | N |
ALK | QPSGSYIAQ | LUNG | 356 | p.R360S | c.1080G>T | Missense_Mutation | 1 | 0.11 | DV90 | N | 0 | 0 | 0 | N |
ALK | QRSFTCWNG | OVARY | 438 | p.S439R | c.1317C>G | Missense_Mutation | 1 | 0.11 | OV56 | N | 1 | 0 | 0 | N |
ALK | QSLPQFILL | SOFT_TISSUE | 1188 | p.R1192Q | c.3575G>A | Missense_Mutation | 1 | 0.11 | SKUT1 | Y | 17 | 10 | 0 | N |
ALK | QSLPWFILL | ENDOMETRIUM | 1188 | p.R1192W | c.3574C>T | Missense_Mutation | 1 | 0.11 | HEC59 | Y | 17 | 10 | 0 | N |
ALK | QSSSLAMLD | LARGE_INTESTINE | 1217 | p.P1218S | c.3652C>T | Missense_Mutation | 1 | 0.11 | CW2 | N | 0 | 0 | 0 | N |
ALK | QVVVKTLPE | THYROID | 1146 | p.A1148V | c.3443C>T | Missense_Mutation | 1 | 0.11 | FTC133 | N | 0 | 0 | 0 | N |
ALK | RAKQLVREL | LUNG | 137 | p.L143R | c.428T>G | Missense_Mutation | 1 | 0.11 | NCIH1651 | Y | 13 | 9 | 0 | N |
ALK | RASGPHGPT | SKIN | 689 | p.G689R | c.2065G>A | Missense_Mutation | 1 | 0.11 | G361 | N | 3 | 0 | 0 | N |
ALK | REDKILQNT | LARGE_INTESTINE | 640 | p.G640R | c.1918G>A | Missense_Mutation | 1 | 0.11 | SNUC5 | N | 6 | 0 | 0 | N |
ALK | REILLMSTP | SKIN | 373 | p.P379S | c.1135C>T | Missense_Mutation | 1 | 0.11 | SKMEL2 | N | 2 | 0 | 0 | N |
ALK | RELGEEAIL | LUNG | 143 | p.L143R | c.428T>G | Missense_Mutation | 1 | 0.11 | NCIH1651 | Y | 12 | 12 | 0 | N |
ALK | RGGCSSGGG | OESOPHAGUS | 925 | p.G925R | c.2773G>A | Missense_Mutation | 1 | 0.11 | KYSE450 | N | 0 | 0 | 0 | N |
ALK | RGGFGGGRG | OESOPHAGUS | 918 | p.G925R | c.2773G>A | Missense_Mutation | 1 | 0.11 | KYSE450 | N | 0 | 0 | 0 | N |
ALK | RHLQPSGSY | LUNG | 353 | p.R360S | c.1080G>T | Missense_Mutation | 1 | 0.11 | DV90 | N | 3 | 0 | 0 | N |
ALK | RIGCPDNPF | STOMACH | 392 | p.R395C | c.1183C>T | Missense_Mutation | 1 | 0.11 | SNU1 | N | 6 | 0 | 0 | N |
ALK | RKGGKNTMM | LUNG | 744 | p.G744R | c.2230G>A | Missense_Mutation | 1 | 0.11 | NCIH1435 | N | 3 | 0 | 0 | N |
ALK | RKSLQEGAT | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 893 | p.G893R | c.2677G>A | Missense_Mutation | 1 | 0.11 | OCILY10 | N | 1 | 0 | 0 | N |
ALK | RLLRPAPGV | LUNG | 100 | p.G103R | c.307G>C | Missense_Mutation | 1 | 0.11 | SW900 | Y | 9 | 12 | 0 | N |
ALK | RLMPEKKVS | LARGE_INTESTINE | 188 | p.A195V | c.584C>T | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 0 | 0 | 0 | N |
ALK | RLSAAICAS | LUNG | 203 | p.R209C | c.625C>T | Missense_Mutation | 1 | 0.11 | DV90 | N | 0 | 0 | 0 | N |
ALK | RMAWLIRGV | LUNG | 551 | p.S553A | c.1657T>G | Missense_Mutation | 1 | 0.11 | NCIH2087 | Y | 5 | 12 | 0 | N |
ALK | RPAPGVSWT | LUNG | 103 | p.G103R | c.307G>C | Missense_Mutation | 1 | 0.11 | SW900 | Y | 5 | 13 | 0 | N |
ALK | RPRPSQSSS | LARGE_INTESTINE | 1212 | p.P1218S | c.3652C>T | Missense_Mutation | 1 | 0.11 | CW2 | N | 4 | 0 | 0 | N |
ALK | RPSQSSSLA | LARGE_INTESTINE | 1214 | p.P1218S | c.3652C>T | Missense_Mutation | 1 | 0.11 | CW2 | N | 8 | 0 | 0 | N |
ALK | RRAKQLVRE | LUNG | 136 | p.L143R | c.428T>G | Missense_Mutation | 1 | 0.11 | NCIH1651 | N | 2 | 0 | 0 | N |
ALK | RSFTCWNGT | OVARY | 439 | p.S439R | c.1317C>G | Missense_Mutation | 1 | 0.11 | OV56 | N | 2 | 0 | 0 | N |
ALK | RSKEMPTGS | LUNG | 311 | p.R317T | c.950G>C | Missense_Mutation | 1 | 0.11 | CORL23 | N | 2 | 0 | 0 | N |
ALK | RSPDYFTWN | BREAST | 236 | p.P236R | c.707C>G | Missense_Mutation | 1 | 0.11 | MDAMB415 | N | 3 | 0 | 0 | N |
ALK | RTLSRVLKV | OVARY | 121 | p.G129V | c.386G>T | Missense_Mutation | 1 | 0.11 | OVTOKO | Y | 10 | 12 | 0 | N |
ALK | RTSTIMIDY | SKIN | 1084 | p.T1090I | c.3269C>T | Missense_Mutation | 1 | 0.11 | WM88 | Y | 9 | 10 | 0 | N |
ALK | RVLKGGSLR | LUNG | 125 | p.V132L | c.394G>C | Missense_Mutation | 1 | 0.11 | NCIH650 | N | 6 | 0 | 0 | N |
ALK | RVLKGGSVH | LARGE_INTESTINE | 125 | p.R133H | c.398G>A | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 1 | 0 | 0 | N |
ALK | RVLKVGSVR | OVARY | 125 | p.G129V | c.386G>T | Missense_Mutation | 1 | 0.11 | OVTOKO | N | 6 | 0 | 0 | N |
ALK | RYIAHLLPH | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 360 | p.Q364H | c.1092G>C | Missense_Mutation | 1 | 0.11 | DAUDI | N | 1 | 0 | 0 | N |
ALK | RYIAQLLSH | LARGE_INTESTINE | 360 | p.P367S | c.1099C>T | Missense_Mutation | 1 | 0.11 | SNU81 | N | 0 | 0 | 0 | N |
ALK | SAAICASQP | LUNG | 205 | p.R209C | c.625C>T | Missense_Mutation | 1 | 0.11 | DV90 | N | 0 | 0 | 0 | N |
ALK | SCTVPSNVA | LARGE_INTESTINE | 1538 | p.P1543S | c.4627C>T | Missense_Mutation | 1 | 0.11 | SW48 | N | 0 | 0 | 0 | N |
ALK | SDLKEVPWK | LARGE_INTESTINE | 1106 | p.R1113W | c.3337C>T | Missense_Mutation | 1 | 0.11 | SNU175 | N | 0 | 0 | 0 | Y |
ALK | SGAAGGGGC | OVARY | 874 | p.G882C | c.2644G>T | Missense_Mutation | 1 | 0.11 | EFO27 | N | 1 | 0 | 0 | Y |
ALK | SGRYIAHLL | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 358 | p.Q364H | c.1092G>C | Missense_Mutation | 1 | 0.11 | DAUDI | N | 11 | 0 | 0 | N |
ALK | SGSYIAQLL | LUNG | 358 | p.R360S | c.1080G>T | Missense_Mutation | 1 | 0.11 | DV90 | N | 12 | 0 | 0 | N |
ALK | SGYGAAGRK | LUNG | 737 | p.G744R | c.2230G>A | Missense_Mutation | 1 | 0.11 | NCIH1435 | N | 1 | 0 | 0 | N |
ALK | SHNEAAREI | LARGE_INTESTINE | 367 | p.P367S | c.1099C>T | Missense_Mutation | 1 | 0.11 | SNU81 | N | 3 | 0 | 0 | N |
ALK | SILGYGAAG | CENTRAL_NERVOUS_SYSTEM | 735 | p.S737L | c.2210C>T | Missense_Mutation | 1 | 0.11 | AM38 | N | 0 | 0 | 0 | N |
ALK | SKEMPTGSF | LUNG | 312 | p.R317T | c.950G>C | Missense_Mutation | 1 | 0.11 | CORL23 | N | 2 | 0 | 0 | N |
ALK | SKMALQRSF | OVARY | 433 | p.S439R | c.1317C>G | Missense_Mutation | 1 | 0.11 | OV56 | N | 2 | 0 | 0 | N |
ALK | SLESPTNVP | PANCREAS | 226 | p.M233V | c.697A>G | Missense_Mutation | 1 | 0.11 | SNU213 | N | 0 | 0 | 0 | N |
ALK | SLLWARKSL | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 888 | p.G893R | c.2677G>A | Missense_Mutation | 1 | 0.11 | OCILY10 | Y | 12 | 11 | 0 | N |
ALK | SLPQFILLE | SOFT_TISSUE | 1189 | p.R1192Q | c.3575G>A | Missense_Mutation | 1 | 0.11 | SKUT1 | N | 1 | 0 | 0 | N |
ALK | SLPWFILLE | ENDOMETRIUM | 1189 | p.R1192W | c.3574C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 1 | 0 | 0 | N |
ALK | SLQSLPQFI | SOFT_TISSUE | 1186 | p.R1192Q | c.3575G>A | Missense_Mutation | 1 | 0.11 | SKUT1 | N | 7 | 0 | 0 | N |
ALK | SLQSLPWFI | ENDOMETRIUM | 1186 | p.R1192W | c.3574C>T | Missense_Mutation | 1 | 0.11 | HEC59 | Y | 8 | 11 | 0 | N |
ALK | SLRKLRRAK | LUNG | 131 | p.V132L | c.394G>C | Missense_Mutation | 1 | 0.11 | NCIH650 | Y | 2 | 16 | 0 | N |
ALK | SNSGAAGGG | KIDNEY | 872 | p.G872S | c.2614G>A | Missense_Mutation | 1 | 0.11 | A498 | N | 0 | 0 | 0 | N |
ALK | SNVATGRLP | LARGE_INTESTINE | 1543 | p.P1543S | c.4627C>T | Missense_Mutation | 1 | 0.11 | SW48 | N | 0 | 0 | 0 | N |
ALK | SPCELRMAW | LUNG | 546 | p.S553A | c.1657T>G | Missense_Mutation | 1 | 0.11 | NCIH2087 | N | 7 | 0 | 0 | N |
ALK | SPLLHDLRN | SKIN | 277 | p.P279L | c.836C>T | Missense_Mutation | 1 | 0.11 | SKMEL30 | N | 3 | 0 | 0 | Y |
ALK | SPLQVVVKT | THYROID | 1143 | p.A1148V | c.3443C>T | Missense_Mutation | 1 | 0.11 | FTC133 | N | 6 | 0 | 0 | N |
ALK | SPTNMPSRS | BREAST | 229 | p.P236R | c.707C>G | Missense_Mutation | 1 | 0.11 | MDAMB415 | N | 3 | 0 | 0 | N |
ALK | SPTNVPSPS | PANCREAS | 229 | p.M233V | c.697A>G | Missense_Mutation | 1 | 0.11 | SNU213 | N | 3 | 0 | 0 | N |
ALK | SQSSSLAML | LARGE_INTESTINE | 1216 | p.P1218S | c.3652C>T | Missense_Mutation | 1 | 0.11 | CW2 | N | 12 | 0 | 0 | N |
ALK | SREDKILQN | LARGE_INTESTINE | 639 | p.G640R | c.1918G>A | Missense_Mutation | 1 | 0.11 | SNUC5 | N | 2 | 0 | 0 | N |
ALK | SRSPDYFTW | BREAST | 235 | p.P236R | c.707C>G | Missense_Mutation | 1 | 0.11 | MDAMB415 | Y | 3 | 9 | 0 | N |
ALK | SRVLKGGSL | LUNG | 124 | p.V132L | c.394G>C | Missense_Mutation | 1 | 0.11 | NCIH650 | N | 7 | 0 | 0 | N |
ALK | SRVLKVGSV | OVARY | 124 | p.G129V | c.386G>T | Missense_Mutation | 1 | 0.11 | OVTOKO | Y | 4 | 11 | 0 | N |
ALK | SSLESPTNV | PANCREAS | 225 | p.M233V | c.697A>G | Missense_Mutation | 1 | 0.11 | SNU213 | N | 7 | 0 | 0 | N |
ALK | SSPCELRMA | LUNG | 545 | p.S553A | c.1657T>G | Missense_Mutation | 1 | 0.11 | NCIH2087 | N | 2 | 0 | 0 | N |
ALK | SSSLAMLDL | LARGE_INTESTINE | 1218 | p.P1218S | c.3652C>T | Missense_Mutation | 1 | 0.11 | CW2 | Y | 8 | 9 | 0 | N |
ALK | SSVLGLNSN | KIDNEY | 865 | p.G872S | c.2614G>A | Missense_Mutation | 1 | 0.11 | A498 | N | 0 | 0 | 0 | N |
ALK | STIMIDYNP | SKIN | 1086 | p.T1090I | c.3269C>T | Missense_Mutation | 1 | 0.11 | WM88 | N | 0 | 0 | 0 | N |
ALK | STPGKHGWT | SKIN | 379 | p.P379S | c.1135C>T | Missense_Mutation | 1 | 0.11 | SKMEL2 | N | 2 | 0 | 0 | N |
ALK | STTQLIQKV | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 785 | p.N787T | c.2360A>C | Missense_Mutation | 1 | 0.11 | DND41 | N | 3 | 0 | 0 | N |
ALK | SVHKLRRAK | LARGE_INTESTINE | 131 | p.R133H | c.398G>A | Missense_Mutation | 1 | 0.11 | SNU1040 | Y | 2 | 14 | 0 | N |
ALK | SVLGLNGNF | ENDOMETRIUM | 866 | p.S874F | c.2621C>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 3 | 0 | 0 | N |
ALK | SVLGLNSNS | KIDNEY | 866 | p.G872S | c.2614G>A | Missense_Mutation | 1 | 0.11 | A498 | N | 0 | 0 | 0 | N |
ALK | SWTVLQGRI | SKIN | 385 | p.G385S | c.1153G>A | Missense_Mutation | 1 | 0.11 | G361 | N | 4 | 0 | 0 | N |
ALK | SYIAQLLPH | LUNG | 360 | p.R360S | c.1080G>T | Missense_Mutation | 1 | 0.11 | DV90 | N | 0 | 0 | 0 | N |
ALK | TCRASGPHG | SKIN | 687 | p.G689R | c.2065G>A | Missense_Mutation | 1 | 0.11 | G361 | N | 0 | 0 | 0 | N |
ALK | TDTYSILGY | CENTRAL_NERVOUS_SYSTEM | 731 | p.S737L | c.2210C>T | Missense_Mutation | 1 | 0.11 | AM38 | N | 3 | 0 | 0 | N |
ALK | TGNEQGRMV | SKIN | 573 | p.K575N | c.1725G>C | Missense_Mutation | 1 | 0.11 | K029AX | N | 5 | 0 | 0 | N |
ALK | TGSFLLLNT | LUNG | 317 | p.R317T | c.950G>C | Missense_Mutation | 1 | 0.11 | CORL23 | N | 1 | 0 | 0 | N |
ALK | TIGGFGGGG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 917 | p.R918I | c.2753G>T | Missense_Mutation | 1 | 0.11 | TOLEDO | N | 0 | 0 | 0 | N |
ALK | TIMIDYNPN | SKIN | 1087 | p.T1090I | c.3269C>T | Missense_Mutation | 1 | 0.11 | WM88 | N | 0 | 0 | 0 | N |
ALK | TISREDKIL | LARGE_INTESTINE | 637 | p.G640R | c.1918G>A | Missense_Mutation | 1 | 0.11 | SNUC5 | N | 3 | 0 | 0 | N |
ALK | TLSRVLKVG | OVARY | 122 | p.G129V | c.386G>T | Missense_Mutation | 1 | 0.11 | OVTOKO | N | 0 | 0 | 0 | N |
ALK | TNMPSRSPD | BREAST | 231 | p.P236R | c.707C>G | Missense_Mutation | 1 | 0.11 | MDAMB415 | N | 0 | 0 | 0 | N |
ALK | TNVPSPSPD | PANCREAS | 231 | p.M233V | c.697A>G | Missense_Mutation | 1 | 0.11 | SNU213 | N | 0 | 0 | 0 | N |
ALK | TPGKHSWTV | SKIN | 380 | p.G385S | c.1153G>A | Missense_Mutation | 1 | 0.11 | G361 | N | 12 | 0 | 0 | N |
ALK | TQLIQKVCI | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 787 | p.N787T | c.2360A>C | Missense_Mutation | 1 | 0.11 | DND41 | N | 12 | 0 | 0 | N |
ALK | TRGGFGGGR | OESOPHAGUS | 917 | p.G925R | c.2773G>A | Missense_Mutation | 1 | 0.11 | KYSE450 | N | 3 | 0 | 0 | N |
ALK | TRPRPSQSS | LARGE_INTESTINE | 1211 | p.P1218S | c.3652C>T | Missense_Mutation | 1 | 0.11 | CW2 | N | 2 | 0 | 0 | N |
ALK | TSLLWARKS | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 887 | p.G893R | c.2677G>A | Missense_Mutation | 1 | 0.11 | OCILY10 | N | 0 | 0 | 0 | Y |
ALK | TSTIMIDYN | SKIN | 1085 | p.T1090I | c.3269C>T | Missense_Mutation | 1 | 0.11 | WM88 | N | 0 | 0 | 0 | N |
ALK | TTCRASGPH | SKIN | 686 | p.G689R | c.2065G>A | Missense_Mutation | 1 | 0.11 | G361 | N | 0 | 0 | 0 | N |
ALK | TTQLIQKVC | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 786 | p.N787T | c.2360A>C | Missense_Mutation | 1 | 0.11 | DND41 | N | 1 | 0 | 0 | N |
ALK | TVLQGRIGC | STOMACH | 387 | p.R395C | c.1183C>T | Missense_Mutation | 1 | 0.11 | SNU1 | N | 2 | 0 | 0 | N |
ALK | TVPSNVATG | LARGE_INTESTINE | 1540 | p.P1543S | c.4627C>T | Missense_Mutation | 1 | 0.11 | SW48 | Y | 1 | 9 | 0 | N |
ALK | TYSILGYGA | CENTRAL_NERVOUS_SYSTEM | 733 | p.S737L | c.2210C>T | Missense_Mutation | 1 | 0.11 | AM38 | Y | 1 | 9 | 0 | N |
ALK | VCCIGVSLQ | ENDOMETRIUM | 1180 | p.R1181C | c.3541C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 0 | 0 | 6 | N |
ALK | VEGGHMNMA | LARGE_INTESTINE | 1471 | p.V1476M | c.4426G>A | Missense_Mutation | 1 | 0.11 | LS513 | N | 7 | 0 | 0 | N |
ALK | VENKTGNEQ | SKIN | 569 | p.K575N | c.1725G>C | Missense_Mutation | 1 | 0.11 | K029AX | N | 0 | 0 | 1 | N |
ALK | VGHPGEAAV | OESOPHAGUS | 155 | p.P157H | c.470C>A | Missense_Mutation | 1 | 0.11 | TE5 | Y | 7 | 12 | 0 | N |
ALK | VGLLQFNLN | LARGE_INTESTINE | 163 | p.S171N | c.512G>A | Missense_Mutation | 1 | 0.11 | SNU503 | N | 0 | 0 | 1 | N |
ALK | VGPPGEAAL | OESOPHAGUS | 155 | p.V163L | c.487G>T | Missense_Mutation | 1 | 0.11 | KYSE520 | Y | 12 | 12 | 0 | N |
ALK | VGSVRKLRR | OVARY | 129 | p.G129V | c.386G>T | Missense_Mutation | 1 | 0.11 | OVTOKO | N | 1 | 0 | 8 | N |
ALK | VHKLRRAKQ | LARGE_INTESTINE | 132 | p.R133H | c.398G>A | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 0 | 0 | 23 | N |
ALK | VHWLFTTCR | SKIN | 681 | p.G689R | c.2065G>A | Missense_Mutation | 1 | 0.11 | G361 | N | 1 | 0 | 8 | N |
ALK | VKHYLNCSH | LARGE_INTESTINE | 981 | p.I981V | c.2941A>G | Missense_Mutation | 1 | 0.11 | MDST8 | N | 1 | 0 | 14 | N |
ALK | VLGLNGNFG | ENDOMETRIUM | 867 | p.S874F | c.2621C>T | Missense_Mutation | 1 | 0.11 | HEC251 | N | 0 | 0 | 1 | N |
ALK | VLGLNSNSG | KIDNEY | 867 | p.G872S | c.2614G>A | Missense_Mutation | 1 | 0.11 | A498 | N | 0 | 0 | 9 | N |
ALK | VLKGGSLRK | LUNG | 126 | p.V132L | c.394G>C | Missense_Mutation | 1 | 0.11 | NCIH650 | Y | 5 | 18 | 1 | N |
ALK | VLKGGSVHK | LARGE_INTESTINE | 126 | p.R133H | c.398G>A | Missense_Mutation | 1 | 0.11 | SNU1040 | Y | 4 | 17 | 0 | N |
ALK | VLKVGSVRK | OVARY | 126 | p.G129V | c.386G>T | Missense_Mutation | 1 | 0.11 | OVTOKO | Y | 4 | 17 | 4 | N |
ALK | VLQGRIGCP | STOMACH | 388 | p.R395C | c.1183C>T | Missense_Mutation | 1 | 0.11 | SNU1 | N | 0 | 0 | 0 | N |
ALK | VLVENKTGN | SKIN | 567 | p.K575N | c.1725G>C | Missense_Mutation | 1 | 0.11 | K029AX | N | 2 | 0 | 0 | N |
ALK | VNVKHYLNC | LARGE_INTESTINE | 979 | p.I981V | c.2941A>G | Missense_Mutation | 1 | 0.11 | MDST8 | N | 1 | 0 | 1 | N |
ALK | VPSNVATGR | LARGE_INTESTINE | 1541 | p.P1543S | c.4627C>T | Missense_Mutation | 1 | 0.11 | SW48 | N | 5 | 0 | 0 | N |
ALK | VPSPSPDYF | PANCREAS | 233 | p.M233V | c.697A>G | Missense_Mutation | 1 | 0.11 | SNU213 | N | 12 | 0 | 0 | N |
ALK | VPWKNITLI | LARGE_INTESTINE | 1111 | p.R1113W | c.3337C>T | Missense_Mutation | 1 | 0.11 | SNU175 | N | 18 | 0 | 0 | N |
ALK | VRELGEEAI | LUNG | 142 | p.L143R | c.428T>G | Missense_Mutation | 1 | 0.11 | NCIH1651 | N | 4 | 0 | 0 | N |
ALK | VSEVGREGR | LARGE_INTESTINE | 195 | p.A195V | c.584C>T | Missense_Mutation | 1 | 0.11 | SNU1040 | N | 4 | 0 | 0 | N |
ALK | VSLQSLPQF | SOFT_TISSUE | 1185 | p.R1192Q | c.3575G>A | Missense_Mutation | 1 | 0.11 | SKUT1 | N | 5 | 0 | 0 | N |
ALK | VSLQSLPWF | ENDOMETRIUM | 1185 | p.R1192W | c.3574C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 6 | 0 | 0 | N |
ALK | VVKTLPEVC | THYROID | 1148 | p.A1148V | c.3443C>T | Missense_Mutation | 1 | 0.11 | FTC133 | N | 0 | 0 | 2 | N |
ALK | VVVKTLPEV | THYROID | 1147 | p.A1148V | c.3443C>T | Missense_Mutation | 1 | 0.11 | FTC133 | N | 5 | 0 | 17 | N |
ALK | WARKSLQEG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 891 | p.G893R | c.2677G>A | Missense_Mutation | 1 | 0.11 | OCILY10 | N | 1 | 0 | 3 | N |
ALK | WETIGGFGG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 915 | p.R918I | c.2753G>T | Missense_Mutation | 1 | 0.11 | TOLEDO | N | 2 | 0 | 2 | N |
ALK | WFILLELMA | ENDOMETRIUM | 1192 | p.R1192W | c.3574C>T | Missense_Mutation | 1 | 0.11 | HEC59 | N | 4 | 0 | 16 | N |
ALK | WGWETIGGF | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 913 | p.R918I | c.2753G>T | Missense_Mutation | 1 | 0.11 | TOLEDO | N | 12 | 0 | 0 | N |
ALK | WKNITLIRG | LARGE_INTESTINE | 1113 | p.R1113W | c.3337C>T | Missense_Mutation | 1 | 0.11 | SNU175 | N | 2 | 0 | 10 | N |
ALK | WLFTTCRAS | SKIN | 683 | p.G689R | c.2065G>A | Missense_Mutation | 1 | 0.11 | G361 | N | 3 | 0 | 13 | N |
ALK | YGAAGRKGG | LUNG | 739 | p.G744R | c.2230G>A | Missense_Mutation | 1 | 0.11 | NCIH1435 | N | 1 | 0 | 0 | N |
ALK | YIAHLLPHN | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 361 | p.Q364H | c.1092G>C | Missense_Mutation | 1 | 0.11 | DAUDI | N | 1 | 0 | 0 | N |
ALK | YIAQLLPHK | LUNG | 361 | p.N369K | c.1107C>G | Missense_Mutation | 1 | 0.11 | NCIH1693 | N | 6 | 0 | 1 | N |
ALK | YIAQLLSHN | LARGE_INTESTINE | 361 | p.P367S | c.1099C>T | Missense_Mutation | 1 | 0.11 | SNU81 | N | 2 | 0 | 0 | N |
ALK | YLTISREDK | LARGE_INTESTINE | 635 | p.G640R | c.1918G>A | Missense_Mutation | 1 | 0.11 | SNUC5 | N | 5 | 0 | 4 | N |
ALK | YSILGYGAA | CENTRAL_NERVOUS_SYSTEM | 734 | p.S737L | c.2210C>T | Missense_Mutation | 1 | 0.11 | AM38 | N | 6 | 0 | 0 | N |
ALK | YSPLLHDLR | SKIN | 276 | p.P279L | c.836C>T | Missense_Mutation | 1 | 0.11 | SKMEL30 | N | 5 | 0 | 0 | Y |
ALK | YSSGGGGGG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 928 | p.C928Y | c.2783G>A | Missense_Mutation | 1 | 0.11 | REH | N | 1 | 0 | 0 | Y |
ALK | ALIISKLNH | AUTONOMIC_GANGLIA | 1168 | p.F1174L | c.3522C>A | Missense_Mutation | 1 | 0.22 | KELLY | N | 1 | 0 | 0 | N |
ALK | ALIISKLNH | AUTONOMIC_GANGLIA | 1168 | p.F1174L | c.3522C>A | Missense_Mutation | 1 | 0.22 | KPNRTBM1 | N | 1 | 0 | 0 | N |
ALK | EALIISKLN | AUTONOMIC_GANGLIA | 1167 | p.F1174L | c.3522C>A | Missense_Mutation | 1 | 0.22 | KELLY | N | 3 | 0 | 0 | N |
ALK | EALIISKLN | AUTONOMIC_GANGLIA | 1167 | p.F1174L | c.3522C>A | Missense_Mutation | 1 | 0.22 | KPNRTBM1 | N | 3 | 0 | 0 | N |
ALK | GTVLQLRQA | KIDNEY | 446 | p.G452R | c.1354G>A | Missense_Mutation | 1 | 0.22 | KMRC2 | N | 3 | 0 | 0 | N |
ALK | GTVLQLRQA | LUNG | 446 | p.G452R | c.1354G>A | Missense_Mutation | 1 | 0.22 | NCIH1651 | N | 3 | 0 | 0 | N |
ALK | IISKLNHQN | AUTONOMIC_GANGLIA | 1170 | p.F1174L | c.3522C>A | Missense_Mutation | 1 | 0.22 | KELLY | N | 0 | 0 | 2 | N |
ALK | IISKLNHQN | AUTONOMIC_GANGLIA | 1170 | p.F1174L | c.3522C>A | Missense_Mutation | 1 | 0.22 | KPNRTBM1 | N | 0 | 0 | 2 | N |
ALK | ISKLNHQNI | AUTONOMIC_GANGLIA | 1171 | p.F1174L | c.3522C>A | Missense_Mutation | 1 | 0.22 | KELLY | Y | 8 | 12 | 0 | N |
ALK | ISKLNHQNI | AUTONOMIC_GANGLIA | 1171 | p.F1174L | c.3522C>A | Missense_Mutation | 1 | 0.22 | KPNRTBM1 | Y | 8 | 12 | 0 | N |
ALK | KLNHQNIVR | AUTONOMIC_GANGLIA | 1173 | p.F1174L | c.3522C>A | Missense_Mutation | 1 | 0.22 | KELLY | Y | 7 | 9 | 0 | N |
ALK | KLNHQNIVR | AUTONOMIC_GANGLIA | 1173 | p.F1174L | c.3522C>A | Missense_Mutation | 1 | 0.22 | KPNRTBM1 | Y | 7 | 9 | 0 | N |
ALK | LIISKLNHQ | AUTONOMIC_GANGLIA | 1169 | p.F1174L | c.3522C>A | Missense_Mutation | 1 | 0.22 | KELLY | N | 0 | 0 | 19 | N |
ALK | LIISKLNHQ | AUTONOMIC_GANGLIA | 1169 | p.F1174L | c.3522C>A | Missense_Mutation | 1 | 0.22 | KPNRTBM1 | N | 0 | 0 | 19 | N |
ALK | LNHQNIVRC | AUTONOMIC_GANGLIA | 1174 | p.F1174L | c.3522C>A | Missense_Mutation | 1 | 0.22 | KELLY | N | 1 | 0 | 3 | N |
ALK | LNHQNIVRC | AUTONOMIC_GANGLIA | 1174 | p.F1174L | c.3522C>A | Missense_Mutation | 1 | 0.22 | KPNRTBM1 | N | 1 | 0 | 3 | N |
ALK | LQLRQACDF | KIDNEY | 449 | p.G452R | c.1354G>A | Missense_Mutation | 1 | 0.22 | KMRC2 | N | 8 | 0 | 12 | N |
ALK | LQLRQACDF | LUNG | 449 | p.G452R | c.1354G>A | Missense_Mutation | 1 | 0.22 | NCIH1651 | N | 8 | 0 | 12 | N |
ALK | LRQACDFHQ | KIDNEY | 451 | p.G452R | c.1354G>A | Missense_Mutation | 1 | 0.22 | KMRC2 | N | 1 | 0 | 1 | N |
ALK | LRQACDFHQ | LUNG | 451 | p.G452R | c.1354G>A | Missense_Mutation | 1 | 0.22 | NCIH1651 | N | 1 | 0 | 1 | N |
ALK | MEALIISKL | AUTONOMIC_GANGLIA | 1166 | p.F1174L | c.3522C>A | Missense_Mutation | 1 | 0.22 | KELLY | Y | 11 | 9 | 0 | N |
ALK | MEALIISKL | AUTONOMIC_GANGLIA | 1166 | p.F1174L | c.3522C>A | Missense_Mutation | 1 | 0.22 | KPNRTBM1 | Y | 11 | 9 | 0 | N |
ALK | NGTVLQLRQ | KIDNEY | 445 | p.G452R | c.1354G>A | Missense_Mutation | 1 | 0.22 | KMRC2 | N | 0 | 0 | 0 | N |
ALK | NGTVLQLRQ | LUNG | 445 | p.G452R | c.1354G>A | Missense_Mutation | 1 | 0.22 | NCIH1651 | N | 0 | 0 | 0 | N |
ALK | QLRQACDFH | KIDNEY | 450 | p.G452R | c.1354G>A | Missense_Mutation | 1 | 0.22 | KMRC2 | N | 0 | 0 | 0 | N |
ALK | QLRQACDFH | LUNG | 450 | p.G452R | c.1354G>A | Missense_Mutation | 1 | 0.22 | NCIH1651 | N | 0 | 0 | 0 | N |
ALK | RQACDFHQD | KIDNEY | 452 | p.G452R | c.1354G>A | Missense_Mutation | 1 | 0.22 | KMRC2 | N | 0 | 0 | 0 | N |
ALK | RQACDFHQD | LUNG | 452 | p.G452R | c.1354G>A | Missense_Mutation | 1 | 0.22 | NCIH1651 | N | 0 | 0 | 0 | N |
ALK | SKLNHQNIV | AUTONOMIC_GANGLIA | 1172 | p.F1174L | c.3522C>A | Missense_Mutation | 1 | 0.22 | KELLY | N | 3 | 0 | 0 | N |
ALK | SKLNHQNIV | AUTONOMIC_GANGLIA | 1172 | p.F1174L | c.3522C>A | Missense_Mutation | 1 | 0.22 | KPNRTBM1 | N | 3 | 0 | 0 | N |
ALK | TVLQLRQAC | KIDNEY | 447 | p.G452R | c.1354G>A | Missense_Mutation | 1 | 0.22 | KMRC2 | N | 2 | 0 | 0 | N |
ALK | TVLQLRQAC | LUNG | 447 | p.G452R | c.1354G>A | Missense_Mutation | 1 | 0.22 | NCIH1651 | N | 2 | 0 | 0 | N |
ALK | VLQLRQACD | KIDNEY | 448 | p.G452R | c.1354G>A | Missense_Mutation | 1 | 0.22 | KMRC2 | N | 0 | 0 | 1 | N |
ALK | VLQLRQACD | LUNG | 448 | p.G452R | c.1354G>A | Missense_Mutation | 1 | 0.22 | NCIH1651 | N | 0 | 0 | 1 | N |
ALK | WNGTVLQLR | KIDNEY | 444 | p.G452R | c.1354G>A | Missense_Mutation | 1 | 0.22 | KMRC2 | N | 4 | 0 | 2 | N |
ALK | WNGTVLQLR | LUNG | 444 | p.G452R | c.1354G>A | Missense_Mutation | 1 | 0.22 | NCIH1651 | N | 4 | 0 | 2 | N |
ALK | CVGPTGEAA | KIDNEY | 154 | p.P158T | c.472C>A | Missense_Mutation | 1 | 0.33 | KMRC2 | Y | 1 | 10 | 0 | N |
ALK | CVGPTGEAA | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 154 | p.P158T | c.472C>A | Missense_Mutation | 1 | 0.33 | SET2 | Y | 1 | 10 | 0 | N |
ALK | CVGPTGEAA | BILIARY_TRACT | 154 | p.P158T | c.472C>A | Missense_Mutation | 1 | 0.33 | SNU308 | Y | 1 | 10 | 0 | N |
ALK | EGCVGPTGE | KIDNEY | 152 | p.P158T | c.472C>A | Missense_Mutation | 1 | 0.33 | KMRC2 | N | 0 | 0 | 0 | N |
ALK | EGCVGPTGE | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 152 | p.P158T | c.472C>A | Missense_Mutation | 1 | 0.33 | SET2 | N | 0 | 0 | 0 | N |
ALK | EGCVGPTGE | BILIARY_TRACT | 152 | p.P158T | c.472C>A | Missense_Mutation | 1 | 0.33 | SNU308 | N | 0 | 0 | 0 | N |
ALK | GCVGPTGEA | KIDNEY | 153 | p.P158T | c.472C>A | Missense_Mutation | 1 | 0.33 | KMRC2 | N | 2 | 0 | 0 | N |
ALK | GCVGPTGEA | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 153 | p.P158T | c.472C>A | Missense_Mutation | 1 | 0.33 | SET2 | N | 2 | 0 | 0 | N |
ALK | GCVGPTGEA | BILIARY_TRACT | 153 | p.P158T | c.472C>A | Missense_Mutation | 1 | 0.33 | SNU308 | N | 2 | 0 | 0 | N |
ALK | GGKNTMMQS | LUNG | 746 | p.R753Q | c.2258G>A | Missense_Mutation | 1 | 0.33 | DV90 | N | 0 | 0 | 0 | N |
ALK | GGKNTMMQS | LUNG | 746 | p.R753Q | c.2258G>A | Missense_Mutation | 1 | 0.33 | HCC78 | N | 0 | 0 | 0 | N |
ALK | GGKNTMMQS | STOMACH | 746 | p.R753Q | c.2258G>A | Missense_Mutation | 1 | 0.33 | SNU520 | N | 0 | 0 | 0 | N |
ALK | GKNTMMQSH | LUNG | 747 | p.R753Q | c.2258G>A | Missense_Mutation | 1 | 0.33 | DV90 | N | 1 | 0 | 0 | N |
ALK | GKNTMMQSH | LUNG | 747 | p.R753Q | c.2258G>A | Missense_Mutation | 1 | 0.33 | HCC78 | N | 1 | 0 | 0 | N |
ALK | GKNTMMQSH | STOMACH | 747 | p.R753Q | c.2258G>A | Missense_Mutation | 1 | 0.33 | SNU520 | N | 1 | 0 | 0 | N |
ALK | GPTGEAAVG | KIDNEY | 156 | p.P158T | c.472C>A | Missense_Mutation | 1 | 0.33 | KMRC2 | N | 0 | 0 | 0 | N |
ALK | GPTGEAAVG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 156 | p.P158T | c.472C>A | Missense_Mutation | 1 | 0.33 | SET2 | N | 0 | 0 | 0 | N |
ALK | GPTGEAAVG | BILIARY_TRACT | 156 | p.P158T | c.472C>A | Missense_Mutation | 1 | 0.33 | SNU308 | N | 0 | 0 | 0 | N |
ALK | ILEGCVGPT | KIDNEY | 150 | p.P158T | c.472C>A | Missense_Mutation | 1 | 0.33 | KMRC2 | N | 1 | 0 | 0 | N |
ALK | ILEGCVGPT | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 150 | p.P158T | c.472C>A | Missense_Mutation | 1 | 0.33 | SET2 | N | 1 | 0 | 0 | N |
ALK | ILEGCVGPT | BILIARY_TRACT | 150 | p.P158T | c.472C>A | Missense_Mutation | 1 | 0.33 | SNU308 | N | 1 | 0 | 0 | N |
ALK | KGGKNTMMQ | LUNG | 745 | p.R753Q | c.2258G>A | Missense_Mutation | 1 | 0.33 | DV90 | N | 0 | 0 | 0 | N |
ALK | KGGKNTMMQ | LUNG | 745 | p.R753Q | c.2258G>A | Missense_Mutation | 1 | 0.33 | HCC78 | N | 0 | 0 | 0 | N |
ALK | KGGKNTMMQ | STOMACH | 745 | p.R753Q | c.2258G>A | Missense_Mutation | 1 | 0.33 | SNU520 | N | 0 | 0 | 0 | N |
ALK | KNTMMQSHG | LUNG | 748 | p.R753Q | c.2258G>A | Missense_Mutation | 1 | 0.33 | DV90 | N | 0 | 0 | 0 | N |
ALK | KNTMMQSHG | LUNG | 748 | p.R753Q | c.2258G>A | Missense_Mutation | 1 | 0.33 | HCC78 | N | 0 | 0 | 0 | N |
ALK | KNTMMQSHG | STOMACH | 748 | p.R753Q | c.2258G>A | Missense_Mutation | 1 | 0.33 | SNU520 | N | 0 | 0 | 0 | N |
ALK | LEGCVGPTG | KIDNEY | 151 | p.P158T | c.472C>A | Missense_Mutation | 1 | 0.33 | KMRC2 | N | 0 | 0 | 0 | N |
ALK | LEGCVGPTG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 151 | p.P158T | c.472C>A | Missense_Mutation | 1 | 0.33 | SET2 | N | 0 | 0 | 0 | N |
ALK | LEGCVGPTG | BILIARY_TRACT | 151 | p.P158T | c.472C>A | Missense_Mutation | 1 | 0.33 | SNU308 | N | 0 | 0 | 0 | N |
ALK | MMQSHGVSV | LUNG | 751 | p.R753Q | c.2258G>A | Missense_Mutation | 1 | 0.33 | DV90 | N | 6 | 0 | 3 | N |
ALK | MMQSHGVSV | LUNG | 751 | p.R753Q | c.2258G>A | Missense_Mutation | 1 | 0.33 | HCC78 | N | 6 | 0 | 3 | N |
ALK | MMQSHGVSV | STOMACH | 751 | p.R753Q | c.2258G>A | Missense_Mutation | 1 | 0.33 | SNU520 | N | 6 | 0 | 3 | N |
ALK | MQSHGVSVL | LUNG | 752 | p.R753Q | c.2258G>A | Missense_Mutation | 1 | 0.33 | DV90 | Y | 12 | 11 | 12 | N |
ALK | MQSHGVSVL | LUNG | 752 | p.R753Q | c.2258G>A | Missense_Mutation | 1 | 0.33 | HCC78 | Y | 12 | 11 | 12 | N |
ALK | MQSHGVSVL | STOMACH | 752 | p.R753Q | c.2258G>A | Missense_Mutation | 1 | 0.33 | SNU520 | Y | 12 | 11 | 12 | N |
ALK | NTMMQSHGV | LUNG | 749 | p.R753Q | c.2258G>A | Missense_Mutation | 1 | 0.33 | DV90 | N | 3 | 0 | 0 | N |
ALK | NTMMQSHGV | LUNG | 749 | p.R753Q | c.2258G>A | Missense_Mutation | 1 | 0.33 | HCC78 | N | 3 | 0 | 0 | N |
ALK | NTMMQSHGV | STOMACH | 749 | p.R753Q | c.2258G>A | Missense_Mutation | 1 | 0.33 | SNU520 | N | 3 | 0 | 0 | N |
ALK | PTGEAAVGL | KIDNEY | 157 | p.P158T | c.472C>A | Missense_Mutation | 1 | 0.33 | KMRC2 | N | 0 | 0 | 0 | N |
ALK | PTGEAAVGL | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 157 | p.P158T | c.472C>A | Missense_Mutation | 1 | 0.33 | SET2 | N | 0 | 0 | 0 | N |
ALK | PTGEAAVGL | BILIARY_TRACT | 157 | p.P158T | c.472C>A | Missense_Mutation | 1 | 0.33 | SNU308 | N | 0 | 0 | 0 | N |
ALK | QSHGVSVLG | LUNG | 753 | p.R753Q | c.2258G>A | Missense_Mutation | 1 | 0.33 | DV90 | N | 0 | 0 | 0 | N |
ALK | QSHGVSVLG | LUNG | 753 | p.R753Q | c.2258G>A | Missense_Mutation | 1 | 0.33 | HCC78 | N | 0 | 0 | 0 | N |
ALK | QSHGVSVLG | STOMACH | 753 | p.R753Q | c.2258G>A | Missense_Mutation | 1 | 0.33 | SNU520 | N | 0 | 0 | 0 | N |
ALK | TGEAAVGLL | KIDNEY | 158 | p.P158T | c.472C>A | Missense_Mutation | 1 | 0.33 | KMRC2 | N | 10 | 0 | 0 | N |
ALK | TGEAAVGLL | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 158 | p.P158T | c.472C>A | Missense_Mutation | 1 | 0.33 | SET2 | N | 10 | 0 | 0 | N |
ALK | TGEAAVGLL | BILIARY_TRACT | 158 | p.P158T | c.472C>A | Missense_Mutation | 1 | 0.33 | SNU308 | N | 10 | 0 | 0 | N |
ALK | TMMQSHGVS | LUNG | 750 | p.R753Q | c.2258G>A | Missense_Mutation | 1 | 0.33 | DV90 | N | 0 | 0 | 0 | N |
ALK | TMMQSHGVS | LUNG | 750 | p.R753Q | c.2258G>A | Missense_Mutation | 1 | 0.33 | HCC78 | N | 0 | 0 | 0 | N |
ALK | TMMQSHGVS | STOMACH | 750 | p.R753Q | c.2258G>A | Missense_Mutation | 1 | 0.33 | SNU520 | N | 0 | 0 | 0 | N |
ALK | VGPTGEAAV | KIDNEY | 155 | p.P158T | c.472C>A | Missense_Mutation | 1 | 0.33 | KMRC2 | N | 8 | 0 | 0 | N |
ALK | VGPTGEAAV | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 155 | p.P158T | c.472C>A | Missense_Mutation | 1 | 0.33 | SET2 | N | 8 | 0 | 0 | N |
ALK | VGPTGEAAV | BILIARY_TRACT | 155 | p.P158T | c.472C>A | Missense_Mutation | 1 | 0.33 | SNU308 | N | 8 | 0 | 0 | N |
ALK | AVEGGHVNT | KIDNEY | 1470 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KMRC3 | N | 1 | 0 | 0 | N |
ALK | AVEGGHVNT | CENTRAL_NERVOUS_SYSTEM | 1470 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KNS60 | N | 1 | 0 | 0 | N |
ALK | AVEGGHVNT | PANCREAS | 1470 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KP2 | N | 1 | 0 | 0 | N |
ALK | AVEGGHVNT | PANCREAS | 1470 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KP3 | N | 1 | 0 | 0 | N |
ALK | AVEGGHVNT | OVARY | 1470 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | TYKNU | N | 1 | 0 | 0 | N |
ALK | EGGHVNTAF | KIDNEY | 1472 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KMRC3 | N | 6 | 0 | 0 | N |
ALK | EGGHVNTAF | CENTRAL_NERVOUS_SYSTEM | 1472 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KNS60 | N | 6 | 0 | 0 | N |
ALK | EGGHVNTAF | PANCREAS | 1472 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KP2 | N | 6 | 0 | 0 | N |
ALK | EGGHVNTAF | PANCREAS | 1472 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KP3 | N | 6 | 0 | 0 | N |
ALK | EGGHVNTAF | OVARY | 1472 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | TYKNU | N | 6 | 0 | 0 | N |
ALK | GGHVNTAFS | KIDNEY | 1473 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KMRC3 | N | 1 | 0 | 0 | N |
ALK | GGHVNTAFS | CENTRAL_NERVOUS_SYSTEM | 1473 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KNS60 | N | 1 | 0 | 0 | N |
ALK | GGHVNTAFS | PANCREAS | 1473 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KP2 | N | 1 | 0 | 0 | N |
ALK | GGHVNTAFS | PANCREAS | 1473 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KP3 | N | 1 | 0 | 0 | N |
ALK | GGHVNTAFS | OVARY | 1473 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | TYKNU | N | 1 | 0 | 0 | N |
ALK | GHVNTAFSQ | KIDNEY | 1474 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KMRC3 | N | 0 | 0 | 0 | N |
ALK | GHVNTAFSQ | CENTRAL_NERVOUS_SYSTEM | 1474 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KNS60 | N | 0 | 0 | 0 | N |
ALK | GHVNTAFSQ | PANCREAS | 1474 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KP2 | N | 0 | 0 | 0 | N |
ALK | GHVNTAFSQ | PANCREAS | 1474 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KP3 | N | 0 | 0 | 0 | N |
ALK | GHVNTAFSQ | OVARY | 1474 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | TYKNU | N | 0 | 0 | 0 | N |
ALK | HVNTAFSQS | KIDNEY | 1475 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KMRC3 | N | 0 | 0 | 0 | N |
ALK | HVNTAFSQS | CENTRAL_NERVOUS_SYSTEM | 1475 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KNS60 | N | 0 | 0 | 0 | N |
ALK | HVNTAFSQS | PANCREAS | 1475 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KP2 | N | 0 | 0 | 0 | N |
ALK | HVNTAFSQS | PANCREAS | 1475 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KP3 | N | 0 | 0 | 0 | N |
ALK | HVNTAFSQS | OVARY | 1475 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | TYKNU | N | 0 | 0 | 0 | N |
ALK | NTAFSQSNP | KIDNEY | 1477 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KMRC3 | N | 0 | 0 | 0 | N |
ALK | NTAFSQSNP | CENTRAL_NERVOUS_SYSTEM | 1477 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KNS60 | N | 0 | 0 | 0 | N |
ALK | NTAFSQSNP | PANCREAS | 1477 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KP2 | N | 0 | 0 | 0 | N |
ALK | NTAFSQSNP | PANCREAS | 1477 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KP3 | N | 0 | 0 | 0 | N |
ALK | NTAFSQSNP | OVARY | 1477 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | TYKNU | N | 0 | 0 | 0 | N |
ALK | TAFSQSNPP | KIDNEY | 1478 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KMRC3 | N | 0 | 0 | 0 | N |
ALK | TAFSQSNPP | CENTRAL_NERVOUS_SYSTEM | 1478 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KNS60 | N | 0 | 0 | 0 | N |
ALK | TAFSQSNPP | PANCREAS | 1478 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KP2 | N | 0 | 0 | 0 | N |
ALK | TAFSQSNPP | PANCREAS | 1478 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KP3 | N | 0 | 0 | 0 | N |
ALK | TAFSQSNPP | OVARY | 1478 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | TYKNU | N | 0 | 0 | 0 | N |
ALK | VEGGHVNTA | KIDNEY | 1471 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KMRC3 | Y | 6 | 9 | 4 | N |
ALK | VEGGHVNTA | CENTRAL_NERVOUS_SYSTEM | 1471 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KNS60 | Y | 6 | 9 | 4 | N |
ALK | VEGGHVNTA | PANCREAS | 1471 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KP2 | Y | 6 | 9 | 4 | N |
ALK | VEGGHVNTA | PANCREAS | 1471 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KP3 | Y | 6 | 9 | 4 | N |
ALK | VEGGHVNTA | OVARY | 1471 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | TYKNU | Y | 6 | 9 | 4 | N |
ALK | VNTAFSQSN | KIDNEY | 1476 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KMRC3 | N | 0 | 0 | 0 | N |
ALK | VNTAFSQSN | CENTRAL_NERVOUS_SYSTEM | 1476 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KNS60 | N | 0 | 0 | 0 | N |
ALK | VNTAFSQSN | PANCREAS | 1476 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KP2 | N | 0 | 0 | 0 | N |
ALK | VNTAFSQSN | PANCREAS | 1476 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | KP3 | N | 0 | 0 | 0 | N |
ALK | VNTAFSQSN | OVARY | 1476 | p.M1478T | c.4433T>C | Missense_Mutation | 1 | 0.55 | TYKNU | N | 0 | 0 | 0 | N |