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The result page of search shows exclusive peptide/epitopes generated due to mutation [Neoepitope], the tissue of origin [Tissue], position of peptide in protein [Position], number of mismatches counted by aligning mutated and normal protein sequence [Num Mismatch, percentage of cell lines with this peptide over total number of cell lines [Promiscuity %]. The immune information include CTL epitopes (Yes/No), MHC I binders, MHC II binders (both given as number of alleles) and B cell epitopes (Yes/No). For more information, please click |
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Protein | Neoepitopes | Tissue | Position | Prot Mutation | cDNA Mutation | Mutation Type | Num Mismatch | Promiscuity (%) | Cell Line | CTL | MHC I | NHLApred | MHC II | Bcell | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
FLT3 | DLGLLSAGS | LARGE_INTESTINE | 980 | p.S985fs | c.2955_2956delTC | Frame_Shift_Del | 3 | 0.33 | GP2D | N | 0 | 0 | 0 | N | ||||||||||||
FLT3 | DLGLLSAGS | LARGE_INTESTINE | 980 | p.S985fs | c.2955_2956delTC | Frame_Shift_Del | 3 | 0.33 | HCT116 | N | 0 | 0 | 0 | N | ||||||||||||
FLT3 | DLGLLSAGS | LARGE_INTESTINE | 980 | p.S985fs | c.2955_2956delTC | Frame_Shift_Del | 3 | 0.33 | LS411N | N | 0 | 0 | 0 | N | ||||||||||||
FLT3 | EMDLGLLSA | LARGE_INTESTINE | 978 | p.S985fs | c.2955_2956delTC | Frame_Shift_Del | 1 | 0.33 | GP2D | N | 2 | 0 | 0 | N | ||||||||||||
FLT3 | EMDLGLLSA | LARGE_INTESTINE | 978 | p.S985fs | c.2955_2956delTC | Frame_Shift_Del | 1 | 0.33 | HCT116 | N | 2 | 0 | 0 | N | ||||||||||||
FLT3 | EMDLGLLSA | LARGE_INTESTINE | 978 | p.S985fs | c.2955_2956delTC | Frame_Shift_Del | 1 | 0.33 | LS411N | N | 2 | 0 | 0 | N | ||||||||||||
FLT3 | GLLSAGSGR | LARGE_INTESTINE | 982 | p.S985fs | c.2955_2956delTC | Frame_Shift_Del | 5 | 0.33 | GP2D | N | 6 | 0 | 0 | N | ||||||||||||
FLT3 | GLLSAGSGR | LARGE_INTESTINE | 982 | p.S985fs | c.2955_2956delTC | Frame_Shift_Del | 5 | 0.33 | HCT116 | N | 6 | 0 | 0 | N | ||||||||||||
FLT3 | GLLSAGSGR | LARGE_INTESTINE | 982 | p.S985fs | c.2955_2956delTC | Frame_Shift_Del | 5 | 0.33 | LS411N | N | 6 | 0 | 0 | N | ||||||||||||
FLT3 | LGLLSAGSG | LARGE_INTESTINE | 981 | p.S985fs | c.2955_2956delTC | Frame_Shift_Del | 4 | 0.33 | GP2D | N | 0 | 0 | 0 | N | ||||||||||||
FLT3 | LGLLSAGSG | LARGE_INTESTINE | 981 | p.S985fs | c.2955_2956delTC | Frame_Shift_Del | 4 | 0.33 | HCT116 | N | 0 | 0 | 0 | N | ||||||||||||
FLT3 | LGLLSAGSG | LARGE_INTESTINE | 981 | p.S985fs | c.2955_2956delTC | Frame_Shift_Del | 4 | 0.33 | LS411N | N | 0 | 0 | 0 | N | ||||||||||||
FLT3 | LLSAGSGRR | LARGE_INTESTINE | 983 | p.S985fs | c.2955_2956delTC | Frame_Shift_Del | 6 | 0.33 | GP2D | N | 5 | 0 | 2 | N | ||||||||||||
FLT3 | LLSAGSGRR | LARGE_INTESTINE | 983 | p.S985fs | c.2955_2956delTC | Frame_Shift_Del | 6 | 0.33 | HCT116 | N | 5 | 0 | 2 | N | ||||||||||||
FLT3 | LLSAGSGRR | LARGE_INTESTINE | 983 | p.S985fs | c.2955_2956delTC | Frame_Shift_Del | 6 | 0.33 | LS411N | N | 5 | 0 | 2 | N | ||||||||||||
FLT3 | LSAGSGRRF | LARGE_INTESTINE | 984 | p.S985fs | c.2955_2956delTC | Frame_Shift_Del | 6 | 0.33 | GP2D | N | 6 | 0 | 0 | N | ||||||||||||
FLT3 | LSAGSGRRF | LARGE_INTESTINE | 984 | p.S985fs | c.2955_2956delTC | Frame_Shift_Del | 6 | 0.33 | HCT116 | N | 6 | 0 | 0 | N | ||||||||||||
FLT3 | LSAGSGRRF | LARGE_INTESTINE | 984 | p.S985fs | c.2955_2956delTC | Frame_Shift_Del | 6 | 0.33 | LS411N | N | 6 | 0 | 0 | N | ||||||||||||
FLT3 | MDLGLLSAG | LARGE_INTESTINE | 979 | p.S985fs | c.2955_2956delTC | Frame_Shift_Del | 2 | 0.33 | GP2D | N | 0 | 0 | 0 | N | ||||||||||||
FLT3 | MDLGLLSAG | LARGE_INTESTINE | 979 | p.S985fs | c.2955_2956delTC | Frame_Shift_Del | 2 | 0.33 | HCT116 | N | 0 | 0 | 0 | N | ||||||||||||
FLT3 | MDLGLLSAG | LARGE_INTESTINE | 979 | p.S985fs | c.2955_2956delTC | Frame_Shift_Del | 2 | 0.33 | LS411N | N | 0 | 0 | 0 | N | ||||||||||||
FLT3 | SAGSGRRFV | LARGE_INTESTINE | 985 | p.S985fs | c.2955_2956delTC | Frame_Shift_Del | 5 | 0.33 | GP2D | Y | 3 | 9 | 0 | N | ||||||||||||
FLT3 | SAGSGRRFV | LARGE_INTESTINE | 985 | p.S985fs | c.2955_2956delTC | Frame_Shift_Del | 5 | 0.33 | HCT116 | Y | 3 | 9 | 0 | N | ||||||||||||
FLT3 | SAGSGRRFV | LARGE_INTESTINE | 985 | p.S985fs | c.2955_2956delTC | Frame_Shift_Del | 5 | 0.33 | LS411N | Y | 3 | 9 | 0 | N | ||||||||||||
FLT3 | AARNVLATH | ENDOMETRIUM | 813 | p.V819A | c.2456T>C | Missense_Mutation | 1 | 0.11 | HEC108 | Y | 0 | 11 | 0 | N | ||||||||||||
FLT3 | AARNVLVNH | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 813 | p.T820N | c.2459C>A | Missense_Mutation | 1 | 0.11 | ME1 | Y | 0 | 15 | 0 | N | ||||||||||||
FLT3 | AAVEVDVSP | LUNG | 79 | p.A87P | c.259G>C | Missense_Mutation | 1 | 0.11 | HCC1171 | N | 0 | 0 | 0 | N | ||||||||||||
FLT3 | ACLPVKWMA | ENDOMETRIUM | 848 | p.R849C | c.2545C>T | Missense_Mutation | 1 | 0.11 | HEC6 | N | 1 | 0 | 0 | N | ||||||||||||
FLT3 | ACPQIRCTW | PROSTATE | 375 | p.Y376C | c.1127A>G | Missense_Mutation | 1 | 0.11 | 22RV1 | N | 1 | 0 | 0 | N | ||||||||||||
FLT3 | ACQASCFSD | LUNG | 447 | p.S448C | c.1342A>T | Missense_Mutation | 1 | 0.11 | NCIH1568 | N | 0 | 0 | 0 | N | ||||||||||||
FLT3 | ADAEEVMYQ | ENDOMETRIUM | 948 | p.A953V | c.2858C>T | Missense_Mutation | 1 | 0.11 | HEC151 | N | 0 | 0 | 0 | N | ||||||||||||
FLT3 | AEASACQAS | LUNG | 443 | p.S448C | c.1342A>T | Missense_Mutation | 1 | 0.11 | NCIH1568 | N | 4 | 0 | 0 | N | ||||||||||||
FLT3 | AEEVMYQNV | ENDOMETRIUM | 950 | p.A953V | c.2858C>T | Missense_Mutation | 1 | 0.11 | HEC151 | N | 6 | 0 | 0 | N | ||||||||||||
FLT3 | AFVSSVARK | LUNG | 315 | p.N323K | c.969C>A | Missense_Mutation | 1 | 0.11 | A549 | Y | 2 | 13 | 0 | N | ||||||||||||
FLT3 | ALMSVLKMM | LUNG | 657 | p.E661V | c.1982A>T | Missense_Mutation | 1 | 0.11 | ABC1 | Y | 8 | 10 | 0 | N | ||||||||||||
FLT3 | ALRPQCSGT | LUNG | 66 | p.S71C | c.211A>T | Missense_Mutation | 1 | 0.11 | HCC1438 | N | 1 | 0 | 0 | N | ||||||||||||
FLT3 | AMYQNVDGS | LUNG | 953 | p.R961S | c.2881C>A | Missense_Mutation | 1 | 0.11 | HCC1359 | N | 4 | 0 | 0 | N | ||||||||||||
FLT3 | ARKDTGYYT | LUNG | 321 | p.N323K | c.969C>A | Missense_Mutation | 1 | 0.11 | A549 | Y | 2 | 10 | 0 | N | ||||||||||||
FLT3 | ARNVLATHG | ENDOMETRIUM | 814 | p.V819A | c.2456T>C | Missense_Mutation | 1 | 0.11 | HEC108 | N | 1 | 0 | 0 | N | ||||||||||||
FLT3 | ARNVLVNHG | HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 814 | p.T820N | c.2459C>A | Missense_Mutation | 1 | 0.11 | ME1 | Y | 1 | 9 | 0 | N | ||||||||||||
FLT3 | ASACQASCF | LUNG | 445 | p.S448C | c.1342A>T | Missense_Mutation | 1 | 0.11 | NCIH1568 | Y | 4 | 10 | 0 | N | ||||||||||||
FLT3 | ATAYGISNT | SKIN | 627 | p.K634N | c.1902A>T | Missense_Mutation | 1 | 0.11 | IPC298 | N | 1 | 0 | 0 | N | ||||||||||||
FLT3 | ATHGKVVKI | ENDOMETRIUM | 819 | p.V819A | c.2456T>C | Missense_Mutation | 1 | 0.11 | HEC108 | Y | 6 | 17 | 0 | N | ||||||||||||
FLT3 | AVEVDVSPS | LUNG | 80 | p.A87P | c.259G>C | Missense_Mutation | 1 | 0.11 | HCC1171 | N | 1 | 0 | 0 | N | ||||||||||||
FLT3 | AYGISNTGV | SKIN | 629 | p.K634N | c.1902A>T | Missense_Mutation | 1 | 0.11 | IPC298 | Y | 2 | 11 | 0 | N | ||||||||||||
FLT3 | CALRPQCSG | LUNG | 65 | p.S71C | c.211A>T | Missense_Mutation | 1 | 0.11 | HCC1438 | N | 0 | 0 | 0 | N | ||||||||||||
FLT3 | CFSVRFKAC | PROSTATE | 368 | p.Y376C | c.1127A>G | Missense_Mutation | 1 | 0.11 | 22RV1 | N | 1 | 0 | 0 | N | ||||||||||||
FLT3 | CLPVKWMAP | ENDOMETRIUM | 849 | p.R849C | c.2545C>T | Missense_Mutation | 1 | 0.11 | HEC6 | N | 0 | 0 | 0 | N | ||||||||||||
FLT3 | CPQIRCTWT | PROSTATE | 376 | p.Y376C | c.1127A>G | Missense_Mutation | 1 | 0.11 | 22RV1 | N | 5 | 0 | 0 | N | ||||||||||||
FLT3 | CQASCFSDG | LUNG | 448 | p.S448C | c.1342A>T | Missense_Mutation | 1 | 0.11 | NCIH1568 | N | 0 | 0 | 0 | N | ||||||||||||
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