Cancertope: In silico Platform for designing genome-based Personalized immunotherapy or Vaccine against Cancer

Cancertope

In silico Platform for designing genome-based
Personalized immunotherapy or Vaccine against Cancer

Browse Results ...

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 HERE

Protein	Neoepitopes	Tissue	Position	Prot Mutation	cDNA Mutation	Mutation Type	Num Mismatch	Promiscuity (%)	Cell Line	CTL	MHC I	NHLApred	MHC II	Bcell
Result		Search:
FGFR2	PHINGSVKH	ENDOMETRIUM	814	p.T822fs	c.2464_2464delA	Frame_Shift_Del	1	0.11	ISHIKAWAHERAKLIO02ER	N	0	0	0	N
FGFR2	ADTPHAGRG	LARGE_INTESTINE	456	p.P459fs	c.1377_1378insC	Frame_Shift_Ins	5	0.11	SNUC4	N	0	0	0	N
FGFR2	DTPHAGRGL	LARGE_INTESTINE	457	p.P459fs	c.1377_1378insC	Frame_Shift_Ins	6	0.11	SNUC4	N	6	0	0	N
FGFR2	LSSTADTPH	LARGE_INTESTINE	452	p.P459fs	c.1377_1378insC	Frame_Shift_Ins	1	0.11	SNUC4	N	0	0	0	N
FGFR2	PHAGRGLRV	LARGE_INTESTINE	459	p.P459fs	c.1377_1378insC	Frame_Shift_Ins	6	0.11	SNUC4	N	0	0	0	N
FGFR2	SSTADTPHA	LARGE_INTESTINE	453	p.P459fs	c.1377_1378insC	Frame_Shift_Ins	2	0.11	SNUC4	N	1	0	0	Y
FGFR2	STADTPHAG	LARGE_INTESTINE	454	p.P459fs	c.1377_1378insC	Frame_Shift_Ins	3	0.11	SNUC4	N	0	0	0	N
FGFR2	TADTPHAGR	LARGE_INTESTINE	455	p.P459fs	c.1377_1378insC	Frame_Shift_Ins	4	0.11	SNUC4	N	4	0	0	N
FGFR2	TPHAGRGLR	LARGE_INTESTINE	458	p.P459fs	c.1377_1378insC	Frame_Shift_Ins	6	0.11	SNUC4	N	4	0	0	N
FGFR2	AARNVLVTK	SKIN	629	p.E637K	c.1909G>A	Missense_Mutation	1	0.11	A375	Y	2	14	0	Y
FGFR2	ACTASSTVD	UPPER_AERODIGESTIVE_TRACT	106	p.R111S	c.333G>C	Missense_Mutation	1	0.11	SNU899	N	0	0	0	N
FGFR2	ACTQNGPLY	SKIN	554	p.D558N	c.1672G>A	Missense_Mutation	1	0.11	COLO679	N	4	0	0	N
FGFR2	ADAGEYICN	ENDOMETRIUM	333	p.K341N	c.1023G>T	Missense_Mutation	1	0.11	HEC251	N	1	0	0	N
FGFR2	AEVFVSENS	LARGE_INTESTINE	140	p.D142V	c.425A>T	Missense_Mutation	1	0.11	SNU283	N	5	0	0	N
FGFR2	AGEYICNVS	ENDOMETRIUM	335	p.K341N	c.1023G>T	Missense_Mutation	1	0.11	HEC251	N	0	0	0	N
FGFR2	AGGNPMSTM	LARGE_INTESTINE	181	p.P187S	c.559C>T	Missense_Mutation	1	0.11	SNU1040	N	5	0	0	N
FGFR2	AIYRIGVFL	ENDOMETRIUM	380	p.C383R	c.1147T>C	Missense_Mutation	1	0.11	JHUEM2	N	15	0	0	N
FGFR2	APGRKKEIT	LUNG	363	p.E367K	c.1099G>A	Missense_Mutation	1	0.11	SBC5	N	6	0	0	N
FGFR2	ARNVLVTKN	SKIN	630	p.E637K	c.1909G>A	Missense_Mutation	1	0.11	A375	N	2	0	0	N
FGFR2	ARRPLGMEY	LARGE_INTESTINE	579	p.P583L	c.1748C>T	Missense_Mutation	1	0.11	HCT116	Y	3	10	0	N
FGFR2	ARRPPGMEH	ENDOMETRIUM	579	p.Y587H	c.1759T>C	Missense_Mutation	1	0.11	EN	Y	2	11	0	Y
FGFR2	ASSTVDSET	UPPER_AERODIGESTIVE_TRACT	109	p.R111S	c.333G>C	Missense_Mutation	1	0.11	SNU899	N	1	0	0	N
FGFR2	ATGMEYLAS	LUNG	612	p.R613T	c.1838G>C	Missense_Mutation	1	0.11	NCIH2009	N	1	0	0	N
FGFR2	AVHKLTKRM	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	415	p.I423M	c.1269C>G	Missense_Mutation	1	0.11	OCIM1	N	3	0	0	N
FGFR2	AVHKLTKRV	LARGE_INTESTINE	415	p.I423V	c.1267A>G	Missense_Mutation	1	0.11	GP2D	N	2	0	0	N
FGFR2	AVTVVVKML	ENDOMETRIUM	512	p.A516V	c.1547C>T	Missense_Mutation	1	0.11	HEC59	Y	7	10	0	N
FGFR2	AYTPMLAGV	LARGE_INTESTINE	456	p.D457Y	c.1369G>T	Missense_Mutation	1	0.11	SNU175	N	3	0	0	N
FGFR2	CIGGYKVRN	BREAST	203	p.R203C	c.607C>T	Missense_Mutation	1	0.11	HCC1143	N	0	0	0	N
FGFR2	CLPQYTHIN	PANCREAS	809	p.P814T	c.2440C>A	Missense_Mutation	1	0.11	PSN1	N	2	0	0	N
FGFR2	CNVSNYIGQ	ENDOMETRIUM	340	p.K341N	c.1023G>T	Missense_Mutation	1	0.11	HEC251	N	0	0	0	Y
FGFR2	CPAGGNPMS	LARGE_INTESTINE	179	p.P187S	c.559C>T	Missense_Mutation	1	0.11	SNU1040	N	3	0	0	N
FGFR2	CQMKNTTKK	STOMACH	399	p.R400Q	c.1199G>A	Missense_Mutation	1	0.11	MKN74	N	6	0	0	N
FGFR2	CRMKNMTKK	PLEURA	399	p.T404M	c.1211C>T	Missense_Mutation	1	0.11	MSTO211H	N	2	0	0	N
FGFR2	CTASSTVDS	UPPER_AERODIGESTIVE_TRACT	107	p.R111S	c.333G>C	Missense_Mutation	1	0.11	SNU899	N	0	0	0	N
FGFR2	CTQNGPLYV	SKIN	555	p.D558N	c.1672G>A	Missense_Mutation	1	0.11	COLO679	Y	2	12	0	N
FGFR2	CTYQLATGM	LUNG	607	p.R613T	c.1838G>C	Missense_Mutation	1	0.11	NCIH2009	N	5	0	0	N
FGFR2	DAGEYICNV	ENDOMETRIUM	334	p.K341N	c.1023G>T	Missense_Mutation	1	0.11	HEC251	Y	4	9	0	N
FGFR2	DDTDGAEVF	LARGE_INTESTINE	135	p.D142V	c.425A>T	Missense_Mutation	1	0.11	SNU283	N	5	0	0	N
FGFR2	DGAEVFVSE	LARGE_INTESTINE	138	p.D142V	c.425A>T	Missense_Mutation	1	0.11	SNU283	N	0	0	0	Y
FGFR2	DGLPYLRVL	ENDOMETRIUM	304	p.K310R	c.929A>G	Missense_Mutation	1	0.11	AN3CA	N	17	0	0	N
FGFR2	DGPLYVVVE	BILIARY_TRACT	558	p.I564V	c.1690A>G	Missense_Mutation	1	0.11	SNU245	N	1	0	0	N
FGFR2	DKDKPKETV	LARGE_INTESTINE	505	p.A512T	c.1534G>A	Missense_Mutation	1	0.11	SNU503	N	1	0	0	N
FGFR2	DKPKETVTV	LARGE_INTESTINE	507	p.A512T	c.1534G>A	Missense_Mutation	1	0.11	SNU503	N	2	0	0	N
FGFR2	DPMPYEPYL	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	802	p.C809Y	c.2426G>A	Missense_Mutation	1	0.11	RCHACV	Y	19	10	0	N
FGFR2	DTDGAEVFV	LARGE_INTESTINE	136	p.D142V	c.425A>T	Missense_Mutation	1	0.11	SNU283	Y	3	11	0	N
FGFR2	DYLEIAIYR	ENDOMETRIUM	375	p.C383R	c.1147T>C	Missense_Mutation	1	0.11	JHUEM2	Y	2	9	0	N
FGFR2	EAVTVVVKM	ENDOMETRIUM	511	p.A516V	c.1547C>T	Missense_Mutation	1	0.11	HEC59	N	8	0	0	N
FGFR2	EDDTDGAEV	LARGE_INTESTINE	134	p.D142V	c.425A>T	Missense_Mutation	1	0.11	SNU283	N	3	0	0	N
FGFR2	EFKQEHCIG	BREAST	197	p.R203C	c.607C>T	Missense_Mutation	1	0.11	HCC1143	N	0	0	0	N
FGFR2	EHCIGGYKV	BREAST	201	p.R203C	c.607C>T	Missense_Mutation	1	0.11	HCC1143	N	2	0	0	N
FGFR2	EHSYDINRV	ENDOMETRIUM	586	p.Y587H	c.1759T>C	Missense_Mutation	1	0.11	EN	N	2	0	0	N
FGFR2	EIAIYRIGV	ENDOMETRIUM	378	p.C383R	c.1147T>C	Missense_Mutation	1	0.11	JHUEM2	N	1	0	0	N
FGFR2	EIFTLGGLP	ENDOMETRIUM	696	p.S703L	c.2108C>T	Missense_Mutation	1	0.11	HEC151	N	0	0	0	N
FGFR2	ENNVMKTAD	KIDNEY	637	p.I643T	c.1928T>C	Missense_Mutation	1	0.11	A498	N	0	0	0	N
FGFR2	EPCLPQYTH	PANCREAS	807	p.P814T	c.2440C>A	Missense_Mutation	1	0.11	PSN1	N	0	0	0	N
FGFR2	EPYLPQYPH	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	807	p.C809Y	c.2426G>A	Missense_Mutation	1	0.11	RCHACV	N	1	0	0	N
FGFR2	ETVTVAVKM	LARGE_INTESTINE	511	p.A512T	c.1534G>A	Missense_Mutation	1	0.11	SNU503	N	4	0	0	N
FGFR2	EVFVSENSN	LARGE_INTESTINE	141	p.D142V	c.425A>T	Missense_Mutation	1	0.11	SNU283	N	0	0	0	N
FGFR2	EYICNVSNY	ENDOMETRIUM	337	p.K341N	c.1023G>T	Missense_Mutation	1	0.11	HEC251	Y	5	14	0	N
FGFR2	EYLRARRPL	LARGE_INTESTINE	575	p.P583L	c.1748C>T	Missense_Mutation	1	0.11	HCT116	Y	9	10	0	N
FGFR2	FISLVVVTM	KIDNEY	7	p.C9S	c.25T>A	Missense_Mutation	1	0.11	A498	Y	6	9	29	N
FGFR2	FKQEHCIGG	BREAST	198	p.R203C	c.607C>T	Missense_Mutation	1	0.11	HCC1143	N	2	0	4	N
FGFR2	FTLGGLPYP	ENDOMETRIUM	698	p.S703L	c.2108C>T	Missense_Mutation	1	0.11	HEC151	N	2	0	0	N
FGFR2	GACTQNGPL	SKIN	553	p.D558N	c.1672G>A	Missense_Mutation	1	0.11	COLO679	N	9	0	0	N
FGFR2	GAEVFVSEN	LARGE_INTESTINE	139	p.D142V	c.425A>T	Missense_Mutation	1	0.11	SNU283	N	2	0	0	Y
FGFR2	GEYICNVSN	ENDOMETRIUM	336	p.K341N	c.1023G>T	Missense_Mutation	1	0.11	HEC251	N	4	0	0	N
FGFR2	GGLPYPGIP	ENDOMETRIUM	701	p.S703L	c.2108C>T	Missense_Mutation	1	0.11	HEC151	N	0	0	0	N
FGFR2	GGNPMSTMR	LARGE_INTESTINE	182	p.P187S	c.559C>T	Missense_Mutation	1	0.11	SNU1040	N	1	0	0	N
FGFR2	GKEFKQEHC	BREAST	195	p.R203C	c.607C>T	Missense_Mutation	1	0.11	HCC1143	N	1	0	0	N
FGFR2	GLPYLRVLK	ENDOMETRIUM	305	p.K310R	c.929A>G	Missense_Mutation	1	0.11	AN3CA	Y	4	14	0	N
FGFR2	GLPYPGIPV	ENDOMETRIUM	702	p.S703L	c.2108C>T	Missense_Mutation	1	0.11	HEC151	N	7	0	0	N
FGFR2	GLYACTASS	UPPER_AERODIGESTIVE_TRACT	103	p.R111S	c.333G>C	Missense_Mutation	1	0.11	SNU899	N	2	0	0	N
FGFR2	GMEHSYDIN	ENDOMETRIUM	584	p.Y587H	c.1759T>C	Missense_Mutation	1	0.11	EN	N	0	0	0	N
FGFR2	GNPMSTMRW	LARGE_INTESTINE	183	p.P187S	c.559C>T	Missense_Mutation	1	0.11	SNU1040	N	1	0	0	N
FGFR2	GPDGLPYLR	ENDOMETRIUM	302	p.K310R	c.929A>G	Missense_Mutation	1	0.11	AN3CA	N	6	0	0	N
FGFR2	GPLYVVVEY	BILIARY_TRACT	559	p.I564V	c.1690A>G	Missense_Mutation	1	0.11	SNU245	N	12	0	0	N
FGFR2	GRFISLVVV	KIDNEY	5	p.C9S	c.25T>A	Missense_Mutation	1	0.11	A498	N	7	0	0	N
FGFR2	GRKKEITAS	LUNG	365	p.E367K	c.1099G>A	Missense_Mutation	1	0.11	SBC5	N	2	0	0	N
FGFR2	HCIGGYKVR	BREAST	202	p.R203C	c.607C>T	Missense_Mutation	1	0.11	HCC1143	N	3	0	0	N
FGFR2	HKLTKRMPL	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	417	p.I423M	c.1269C>G	Missense_Mutation	1	0.11	OCIM1	N	5	0	0	N
FGFR2	HKLTKRVPL	LARGE_INTESTINE	417	p.I423V	c.1267A>G	Missense_Mutation	1	0.11	GP2D	N	5	0	0	N
FGFR2	HSYDINRVP	ENDOMETRIUM	587	p.Y587H	c.1759T>C	Missense_Mutation	1	0.11	EN	N	0	0	0	N
FGFR2	IAIYRIGVF	ENDOMETRIUM	379	p.C383R	c.1147T>C	Missense_Mutation	1	0.11	JHUEM2	N	10	0	7	N
FGFR2	ICNVSNYIG	ENDOMETRIUM	339	p.K341N	c.1023G>T	Missense_Mutation	1	0.11	HEC251	N	0	0	0	N
FGFR2	IDKDKPKET	LARGE_INTESTINE	504	p.A512T	c.1534G>A	Missense_Mutation	1	0.11	SNU503	N	2	0	0	N
FGFR2	IDYYKETTN	BREAST	655	p.K660E	c.1978A>G	Missense_Mutation	1	0.11	EFM19	N	1	0	0	N
FGFR2	IFTLGGLPY	ENDOMETRIUM	697	p.S703L	c.2108C>T	Missense_Mutation	1	0.11	HEC151	N	4	0	1	N
FGFR2	ILCQMKNTT	STOMACH	397	p.R400Q	c.1199G>A	Missense_Mutation	1	0.11	MKN74	N	2	0	4	N
FGFR2	ILCRMKNMT	PLEURA	397	p.T404M	c.1211C>T	Missense_Mutation	1	0.11	MSTO211H	N	2	0	5	N
FGFR2	INNIDYYKE	BREAST	652	p.K660E	c.1978A>G	Missense_Mutation	1	0.11	EFM19	N	0	0	0	N
FGFR2	ISLVVVTMA	KIDNEY	8	p.C9S	c.25T>A	Missense_Mutation	1	0.11	A498	N	3	0	3	N
FGFR2	ITTRLSLTA	LUNG	448	p.S454L	c.1361C>T	Missense_Mutation	1	0.11	NCIH647	N	3	0	2	N
FGFR2	IVEYLQIKG	LUNG	88	p.G89V	c.266G>T	Missense_Mutation	1	0.11	CAL12T	N	1	0	3	N
FGFR2	IYRIGVFLI	ENDOMETRIUM	381	p.C383R	c.1147T>C	Missense_Mutation	1	0.11	JHUEM2	Y	8	10	38	N
FGFR2	KDKPKETVT	LARGE_INTESTINE	506	p.A512T	c.1534G>A	Missense_Mutation	1	0.11	SNU503	N	2	0	0	N
FGFR2	KEAVTVVVK	ENDOMETRIUM	510	p.A516V	c.1547C>T	Missense_Mutation	1	0.11	HEC59	N	4	0	0	N
FGFR2	KEFKQEHCI	BREAST	196	p.R203C	c.607C>T	Missense_Mutation	1	0.11	HCC1143	Y	10	9	0	N
FGFR2	KETVTVAVK	LARGE_INTESTINE	510	p.A512T	c.1534G>A	Missense_Mutation	1	0.11	SNU503	N	3	0	0	N
FGFR2	KKEITASPD	LUNG	367	p.E367K	c.1099G>A	Missense_Mutation	1	0.11	SBC5	N	0	0	0	N
FGFR2	KLTKRMPLR	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	418	p.I423M	c.1269C>G	Missense_Mutation	1	0.11	OCIM1	Y	7	9	0	N
FGFR2	KLTKRVPLR	LARGE_INTESTINE	418	p.I423V	c.1267A>G	Missense_Mutation	1	0.11	GP2D	Y	7	10	0	N
FGFR2	KNMTKKPDF	PLEURA	402	p.T404M	c.1211C>T	Missense_Mutation	1	0.11	MSTO211H	N	7	0	0	N
FGFR2	KNNVMKIAD	SKIN	637	p.E637K	c.1909G>A	Missense_Mutation	1	0.11	A375	N	0	0	0	N
FGFR2	KPKEAVTVV	ENDOMETRIUM	508	p.A516V	c.1547C>T	Missense_Mutation	1	0.11	HEC59	Y	13	12	0	N
FGFR2	KPKETVTVA	LARGE_INTESTINE	508	p.A512T	c.1534G>A	Missense_Mutation	1	0.11	SNU503	N	10	0	0	N
FGFR2	KQEHCIGGY	BREAST	199	p.R203C	c.607C>T	Missense_Mutation	1	0.11	HCC1143	N	7	0	0	N
FGFR2	KQQAPGRKK	LUNG	360	p.E367K	c.1099G>A	Missense_Mutation	1	0.11	SBC5	N	2	0	0	N
FGFR2	KRMPLRRQV	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	421	p.I423M	c.1269C>G	Missense_Mutation	1	0.11	OCIM1	Y	4	12	0	N
FGFR2	KRVPLRRQV	LARGE_INTESTINE	421	p.I423V	c.1267A>G	Missense_Mutation	1	0.11	GP2D	Y	4	11	0	N
FGFR2	KTADFGLAR	KIDNEY	642	p.I643T	c.1928T>C	Missense_Mutation	1	0.11	A498	Y	7	12	0	Y
FGFR2	LATGMEYLA	LUNG	611	p.R613T	c.1838G>C	Missense_Mutation	1	0.11	NCIH2009	N	6	0	0	N
FGFR2	LCQMKNTTK	STOMACH	398	p.R400Q	c.1199G>A	Missense_Mutation	1	0.11	MKN74	N	1	0	5	N
FGFR2	LCRMKNMTK	PLEURA	398	p.T404M	c.1211C>T	Missense_Mutation	1	0.11	MSTO211H	N	2	0	15	N
FGFR2	LEIAIYRIG	ENDOMETRIUM	377	p.C383R	c.1147T>C	Missense_Mutation	1	0.11	JHUEM2	N	2	0	0	N
FGFR2	LGACTQNGP	SKIN	552	p.D558N	c.1672G>A	Missense_Mutation	1	0.11	COLO679	N	0	0	0	N
FGFR2	LGGLPYPGI	ENDOMETRIUM	700	p.S703L	c.2108C>T	Missense_Mutation	1	0.11	HEC151	N	8	0	0	N
FGFR2	LGMEYSYDI	LARGE_INTESTINE	583	p.P583L	c.1748C>T	Missense_Mutation	1	0.11	HCT116	N	10	0	9	Y
FGFR2	LIVEYLQIK	LUNG	87	p.G89V	c.266G>T	Missense_Mutation	1	0.11	CAL12T	N	4	0	0	N
FGFR2	LLGACTQNG	SKIN	551	p.D558N	c.1672G>A	Missense_Mutation	1	0.11	COLO679	N	0	0	6	N
FGFR2	LPQYTHING	PANCREAS	810	p.P814T	c.2440C>A	Missense_Mutation	1	0.11	PSN1	N	2	0	0	N
FGFR2	LPYLRVLKH	ENDOMETRIUM	306	p.K310R	c.929A>G	Missense_Mutation	1	0.11	AN3CA	N	4	0	29	N
FGFR2	LPYPGIPVE	ENDOMETRIUM	703	p.S703L	c.2108C>T	Missense_Mutation	1	0.11	HEC151	N	3	0	0	N
FGFR2	LRARRPLGM	LARGE_INTESTINE	577	p.P583L	c.1748C>T	Missense_Mutation	1	0.11	HCT116	Y	4	12	28	N
FGFR2	LRVLKHSGI	ENDOMETRIUM	309	p.K310R	c.929A>G	Missense_Mutation	1	0.11	AN3CA	N	7	0	27	N
FGFR2	LSLTADTPM	LUNG	452	p.S454L	c.1361C>T	Missense_Mutation	1	0.11	NCIH647	N	7	0	0	N
FGFR2	LSSTAYTPM	LARGE_INTESTINE	452	p.D457Y	c.1369G>T	Missense_Mutation	1	0.11	SNU175	N	8	0	0	N
FGFR2	LTADTPMLA	LUNG	454	p.S454L	c.1361C>T	Missense_Mutation	1	0.11	NCIH647	N	3	0	8	N
FGFR2	LTKRMPLRR	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	419	p.I423M	c.1269C>G	Missense_Mutation	1	0.11	OCIM1	N	5	0	0	N
FGFR2	LTKRVPLRR	LARGE_INTESTINE	419	p.I423V	c.1267A>G	Missense_Mutation	1	0.11	GP2D	N	6	0	0	N
FGFR2	LVTKNNVMK	SKIN	634	p.E637K	c.1909G>A	Missense_Mutation	1	0.11	A375	N	3	0	7	N
FGFR2	LYACTASST	UPPER_AERODIGESTIVE_TRACT	104	p.R111S	c.333G>C	Missense_Mutation	1	0.11	SNU899	N	1	0	0	Y
FGFR2	LYVVVEYAS	BILIARY_TRACT	561	p.I564V	c.1690A>G	Missense_Mutation	1	0.11	SNU245	N	2	0	0	N
FGFR2	MEHSYDINR	ENDOMETRIUM	585	p.Y587H	c.1759T>C	Missense_Mutation	1	0.11	EN	Y	0	9	0	N
FGFR2	MKNMTKKPD	PLEURA	401	p.T404M	c.1211C>T	Missense_Mutation	1	0.11	MSTO211H	N	0	0	17	N
FGFR2	MKTADFGLA	KIDNEY	641	p.I643T	c.1928T>C	Missense_Mutation	1	0.11	A498	N	2	0	0	N
FGFR2	MPLRRQVTV	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	423	p.I423M	c.1269C>G	Missense_Mutation	1	0.11	OCIM1	Y	15	9	0	N
FGFR2	MPYEPYLPQ	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	804	p.C809Y	c.2426G>A	Missense_Mutation	1	0.11	RCHACV	N	4	0	0	Y
FGFR2	MSTMRWLKN	LARGE_INTESTINE	186	p.P187S	c.559C>T	Missense_Mutation	1	0.11	SNU1040	N	0	0	0	N
FGFR2	MTKKPDFSS	PLEURA	404	p.T404M	c.1211C>T	Missense_Mutation	1	0.11	MSTO211H	N	0	0	0	Y
FGFR2	MVSWGRFIS	KIDNEY	1	p.C9S	c.25T>A	Missense_Mutation	1	0.11	A498	N	0	0	32	N
FGFR2	MVVTVILCQ	STOMACH	392	p.R400Q	c.1199G>A	Missense_Mutation	1	0.11	MKN74	N	0	0	35	N
FGFR2	NGPLYVIVE	SKIN	558	p.D558N	c.1672G>A	Missense_Mutation	1	0.11	COLO679	N	1	0	0	N
FGFR2	NIDYYKETT	BREAST	654	p.K660E	c.1978A>G	Missense_Mutation	1	0.11	EFM19	N	0	0	0	N
FGFR2	NLLGACTQN	SKIN	550	p.D558N	c.1672G>A	Missense_Mutation	1	0.11	COLO679	N	0	0	0	N
FGFR2	NMTKKPDFS	PLEURA	403	p.T404M	c.1211C>T	Missense_Mutation	1	0.11	MSTO211H	N	0	0	0	N
FGFR2	NNIDYYKET	BREAST	653	p.K660E	c.1978A>G	Missense_Mutation	1	0.11	EFM19	N	1	0	0	N
FGFR2	NNRTVLIVE	LUNG	82	p.G89V	c.266G>T	Missense_Mutation	1	0.11	CAL12T	N	0	0	0	Y
FGFR2	NNVMKTADF	KIDNEY	638	p.I643T	c.1928T>C	Missense_Mutation	1	0.11	A498	N	3	0	0	N
FGFR2	NPMSTMRWL	LARGE_INTESTINE	184	p.P187S	c.559C>T	Missense_Mutation	1	0.11	SNU1040	Y	20	9	0	N
FGFR2	NRTVLIVEY	LUNG	83	p.G89V	c.266G>T	Missense_Mutation	1	0.11	CAL12T	N	4	0	0	Y
FGFR2	NVLVTKNNV	SKIN	632	p.E637K	c.1909G>A	Missense_Mutation	1	0.11	A375	Y	4	10	0	N
FGFR2	NVMKTADFG	KIDNEY	639	p.I643T	c.1928T>C	Missense_Mutation	1	0.11	A498	N	0	0	0	N
FGFR2	NVSNYIGQA	ENDOMETRIUM	341	p.K341N	c.1023G>T	Missense_Mutation	1	0.11	HEC251	N	1	0	0	Y
FGFR2	PAGGNPMST	LARGE_INTESTINE	180	p.P187S	c.559C>T	Missense_Mutation	1	0.11	SNU1040	N	0	0	0	N
FGFR2	PCLPQYTHI	PANCREAS	808	p.P814T	c.2440C>A	Missense_Mutation	1	0.11	PSN1	N	1	0	0	N
FGFR2	PDGLPYLRV	ENDOMETRIUM	303	p.K310R	c.929A>G	Missense_Mutation	1	0.11	AN3CA	N	0	0	0	N
FGFR2	PDPMPYEPY	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	801	p.C809Y	c.2426G>A	Missense_Mutation	1	0.11	RCHACV	N	1	0	0	N
FGFR2	PGMEHSYDI	ENDOMETRIUM	583	p.Y587H	c.1759T>C	Missense_Mutation	1	0.11	EN	N	3	0	0	N
FGFR2	PGRKKEITA	LUNG	364	p.E367K	c.1099G>A	Missense_Mutation	1	0.11	SBC5	N	1	0	0	N
FGFR2	PKEAVTVVV	ENDOMETRIUM	509	p.A516V	c.1547C>T	Missense_Mutation	1	0.11	HEC59	N	1	0	0	N
FGFR2	PKETVTVAV	LARGE_INTESTINE	509	p.A512T	c.1534G>A	Missense_Mutation	1	0.11	SNU503	N	1	0	0	N
FGFR2	PKQQAPGRK	LUNG	359	p.E367K	c.1099G>A	Missense_Mutation	1	0.11	SBC5	N	1	0	0	N
FGFR2	PLGMEYSYD	LARGE_INTESTINE	582	p.P583L	c.1748C>T	Missense_Mutation	1	0.11	HCT116	N	0	0	0	N
FGFR2	PLYVVVEYA	BILIARY_TRACT	560	p.I564V	c.1690A>G	Missense_Mutation	1	0.11	SNU245	N	3	0	0	N
FGFR2	PMPYEPYLP	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	803	p.C809Y	c.2426G>A	Missense_Mutation	1	0.11	RCHACV	N	0	0	0	N
FGFR2	PMSTMRWLK	LARGE_INTESTINE	185	p.P187S	c.559C>T	Missense_Mutation	1	0.11	SNU1040	N	1	0	0	N
FGFR2	PNNRTVLIV	LUNG	81	p.G89V	c.266G>T	Missense_Mutation	1	0.11	CAL12T	Y	0	14	0	Y
FGFR2	PPGMEHSYD	ENDOMETRIUM	582	p.Y587H	c.1759T>C	Missense_Mutation	1	0.11	EN	N	0	0	0	N
FGFR2	PQYTHINGS	PANCREAS	811	p.P814T	c.2440C>A	Missense_Mutation	1	0.11	PSN1	N	0	0	0	N
FGFR2	PYEPYLPQY	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	805	p.C809Y	c.2426G>A	Missense_Mutation	1	0.11	RCHACV	N	2	0	0	Y
FGFR2	PYLPQYPHI	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	808	p.C809Y	c.2426G>A	Missense_Mutation	1	0.11	RCHACV	Y	3	11	0	N
FGFR2	PYLRVLKHS	ENDOMETRIUM	307	p.K310R	c.929A>G	Missense_Mutation	1	0.11	AN3CA	N	0	0	0	N
FGFR2	QAPGRKKEI	LUNG	362	p.E367K	c.1099G>A	Missense_Mutation	1	0.11	SBC5	N	7	0	0	N
FGFR2	QDGPLYVVV	BILIARY_TRACT	557	p.I564V	c.1690A>G	Missense_Mutation	1	0.11	SNU245	N	6	0	0	N
FGFR2	QEHCIGGYK	BREAST	200	p.R203C	c.607C>T	Missense_Mutation	1	0.11	HCC1143	N	1	0	0	N
FGFR2	QLATGMEYL	LUNG	610	p.R613T	c.1838G>C	Missense_Mutation	1	0.11	NCIH2009	Y	10	12	0	N
FGFR2	QMKNTTKKP	STOMACH	400	p.R400Q	c.1199G>A	Missense_Mutation	1	0.11	MKN74	N	0	0	0	N
FGFR2	QNGPLYVIV	SKIN	557	p.D558N	c.1672G>A	Missense_Mutation	1	0.11	COLO679	Y	2	17	0	N
FGFR2	QQAPGRKKE	LUNG	361	p.E367K	c.1099G>A	Missense_Mutation	1	0.11	SBC5	N	0	0	0	N
FGFR2	QYTHINGSV	PANCREAS	812	p.P814T	c.2440C>A	Missense_Mutation	1	0.11	PSN1	N	3	0	0	N
FGFR2	RARRPLGME	LARGE_INTESTINE	578	p.P583L	c.1748C>T	Missense_Mutation	1	0.11	HCT116	N	0	0	0	N
FGFR2	RFISLVVVT	KIDNEY	6	p.C9S	c.25T>A	Missense_Mutation	1	0.11	A498	N	1	0	0	N
FGFR2	RIGVFLIAC	ENDOMETRIUM	383	p.C383R	c.1147T>C	Missense_Mutation	1	0.11	JHUEM2	Y	3	10	0	N
FGFR2	RITTRLSLT	LUNG	447	p.S454L	c.1361C>T	Missense_Mutation	1	0.11	NCIH647	N	1	0	0	N
FGFR2	RKKEITASP	LUNG	366	p.E367K	c.1099G>A	Missense_Mutation	1	0.11	SBC5	N	0	0	0	N
FGFR2	RLSLTADTP	LUNG	451	p.S454L	c.1361C>T	Missense_Mutation	1	0.11	NCIH647	N	0	0	0	N
FGFR2	RLSSTAYTP	LARGE_INTESTINE	451	p.D457Y	c.1369G>T	Missense_Mutation	1	0.11	SNU175	N	1	0	0	N
FGFR2	RMKNMTKKP	PLEURA	400	p.T404M	c.1211C>T	Missense_Mutation	1	0.11	MSTO211H	N	0	0	0	N
FGFR2	RMPLRRQVT	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	422	p.I423M	c.1269C>G	Missense_Mutation	1	0.11	OCIM1	N	3	0	0	N
FGFR2	RNVLVTKNN	SKIN	631	p.E637K	c.1909G>A	Missense_Mutation	1	0.11	A375	N	0	0	0	N
FGFR2	RPLGMEYSY	LARGE_INTESTINE	581	p.P583L	c.1748C>T	Missense_Mutation	1	0.11	HCT116	N	12	0	0	N
FGFR2	RPPGMEHSY	ENDOMETRIUM	581	p.Y587H	c.1759T>C	Missense_Mutation	1	0.11	EN	N	11	0	0	Y
FGFR2	RRPLGMEYS	LARGE_INTESTINE	580	p.P583L	c.1748C>T	Missense_Mutation	1	0.11	HCT116	N	4	0	0	N
FGFR2	RRPPGMEHS	ENDOMETRIUM	580	p.Y587H	c.1759T>C	Missense_Mutation	1	0.11	EN	N	4	0	0	N
FGFR2	RTVLIVEYL	LUNG	84	p.G89V	c.266G>T	Missense_Mutation	1	0.11	CAL12T	Y	18	12	0	N
FGFR2	RVLKHSGIN	ENDOMETRIUM	310	p.K310R	c.929A>G	Missense_Mutation	1	0.11	AN3CA	N	0	0	0	N
FGFR2	RVPLRRQVT	LARGE_INTESTINE	422	p.I423V	c.1267A>G	Missense_Mutation	1	0.11	GP2D	N	3	0	0	N
FGFR2	SCTYQLATG	LUNG	606	p.R613T	c.1838G>C	Missense_Mutation	1	0.11	NCIH2009	N	0	0	0	N
FGFR2	SLTADTPML	LUNG	453	p.S454L	c.1361C>T	Missense_Mutation	1	0.11	NCIH647	N	12	0	0	N
FGFR2	SLVVVTMAT	KIDNEY	9	p.C9S	c.25T>A	Missense_Mutation	1	0.11	A498	N	3	0	0	N
FGFR2	SSTAYTPML	LARGE_INTESTINE	453	p.D457Y	c.1369G>T	Missense_Mutation	1	0.11	SNU175	N	10	0	0	N
FGFR2	SSTVDSETW	UPPER_AERODIGESTIVE_TRACT	110	p.R111S	c.333G>C	Missense_Mutation	1	0.11	SNU899	N	3	0	0	N
FGFR2	STAYTPMLA	LARGE_INTESTINE	454	p.D457Y	c.1369G>T	Missense_Mutation	1	0.11	SNU175	N	1	0	0	N
FGFR2	STMRWLKNG	LARGE_INTESTINE	187	p.P187S	c.559C>T	Missense_Mutation	1	0.11	SNU1040	N	0	0	0	N
FGFR2	STVDSETWY	UPPER_AERODIGESTIVE_TRACT	111	p.R111S	c.333G>C	Missense_Mutation	1	0.11	SNU899	N	5	0	0	N
FGFR2	SWGRFISLV	KIDNEY	3	p.C9S	c.25T>A	Missense_Mutation	1	0.11	A498	Y	3	9	0	N
FGFR2	TADFGLARD	KIDNEY	643	p.I643T	c.1928T>C	Missense_Mutation	1	0.11	A498	N	0	0	0	N
FGFR2	TASSTVDSE	UPPER_AERODIGESTIVE_TRACT	108	p.R111S	c.333G>C	Missense_Mutation	1	0.11	SNU899	N	0	0	0	N
FGFR2	TAYTPMLAG	LARGE_INTESTINE	455	p.D457Y	c.1369G>T	Missense_Mutation	1	0.11	SNU175	N	0	0	0	N
FGFR2	TDGAEVFVS	LARGE_INTESTINE	137	p.D142V	c.425A>T	Missense_Mutation	1	0.11	SNU283	N	2	0	0	Y
FGFR2	TENNVMKTA	KIDNEY	636	p.I643T	c.1928T>C	Missense_Mutation	1	0.11	A498	Y	6	9	0	N
FGFR2	TGMEYLASQ	LUNG	613	p.R613T	c.1838G>C	Missense_Mutation	1	0.11	NCIH2009	N	0	0	0	N
FGFR2	THINGSVKT	PANCREAS	814	p.P814T	c.2440C>A	Missense_Mutation	1	0.11	PSN1	N	1	0	0	N
FGFR2	TKNNVMKIA	SKIN	636	p.E637K	c.1909G>A	Missense_Mutation	1	0.11	A375	N	1	0	0	N
FGFR2	TKRMPLRRQ	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	420	p.I423M	c.1269C>G	Missense_Mutation	1	0.11	OCIM1	N	0	0	0	N
FGFR2	TKRVPLRRQ	LARGE_INTESTINE	420	p.I423V	c.1267A>G	Missense_Mutation	1	0.11	GP2D	N	0	0	0	N
FGFR2	TLGGLPYPG	ENDOMETRIUM	699	p.S703L	c.2108C>T	Missense_Mutation	1	0.11	HEC151	N	0	0	0	N
FGFR2	TQDGPLYVV	BILIARY_TRACT	556	p.I564V	c.1690A>G	Missense_Mutation	1	0.11	SNU245	N	4	0	0	N
FGFR2	TQNGPLYVI	SKIN	556	p.D558N	c.1672G>A	Missense_Mutation	1	0.11	COLO679	Y	6	13	0	N
FGFR2	TRLSLTADT	LUNG	450	p.S454L	c.1361C>T	Missense_Mutation	1	0.11	NCIH647	N	3	0	0	N
FGFR2	TRLSSTAYT	LARGE_INTESTINE	450	p.D457Y	c.1369G>T	Missense_Mutation	1	0.11	SNU175	N	3	0	0	N
FGFR2	TTRLSLTAD	LUNG	449	p.S454L	c.1361C>T	Missense_Mutation	1	0.11	NCIH647	N	0	0	0	N
FGFR2	TTRLSSTAY	LARGE_INTESTINE	449	p.D457Y	c.1369G>T	Missense_Mutation	1	0.11	SNU175	N	6	0	0	N
FGFR2	TVILCQMKN	STOMACH	395	p.R400Q	c.1199G>A	Missense_Mutation	1	0.11	MKN74	N	0	0	0	N
FGFR2	TVLIVEYLQ	LUNG	85	p.G89V	c.266G>T	Missense_Mutation	1	0.11	CAL12T	N	0	0	0	Y
FGFR2	TVTVAVKML	LARGE_INTESTINE	512	p.A512T	c.1534G>A	Missense_Mutation	1	0.11	SNU503	Y	7	9	0	N
FGFR2	TVVVKMLKD	ENDOMETRIUM	514	p.A516V	c.1547C>T	Missense_Mutation	1	0.11	HEC59	N	0	0	0	N
FGFR2	TYQLATGME	LUNG	608	p.R613T	c.1838G>C	Missense_Mutation	1	0.11	NCIH2009	N	0	0	0	N
FGFR2	VEYLQIKGA	LUNG	89	p.G89V	c.266G>T	Missense_Mutation	1	0.11	CAL12T	N	7	0	8	N
FGFR2	VFVSENSNN	LARGE_INTESTINE	142	p.D142V	c.425A>T	Missense_Mutation	1	0.11	SNU283	N	0	0	2	Y
FGFR2	VHKLTKRMP	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	416	p.I423M	c.1269C>G	Missense_Mutation	1	0.11	OCIM1	N	0	0	11	N
FGFR2	VHKLTKRVP	LARGE_INTESTINE	416	p.I423V	c.1267A>G	Missense_Mutation	1	0.11	GP2D	N	0	0	11	N
FGFR2	VILCQMKNT	STOMACH	396	p.R400Q	c.1199G>A	Missense_Mutation	1	0.11	MKN74	N	2	0	0	N
FGFR2	VILCRMKNM	PLEURA	396	p.T404M	c.1211C>T	Missense_Mutation	1	0.11	MSTO211H	N	8	0	0	N
FGFR2	VLIVEYLQI	LUNG	86	p.G89V	c.266G>T	Missense_Mutation	1	0.11	CAL12T	N	15	0	15	Y
FGFR2	VLVTKNNVM	SKIN	633	p.E637K	c.1909G>A	Missense_Mutation	1	0.11	A375	N	7	0	11	N
FGFR2	VMKTADFGL	KIDNEY	640	p.I643T	c.1928T>C	Missense_Mutation	1	0.11	A498	N	10	0	2	N
FGFR2	VPLRRQVTV	LARGE_INTESTINE	423	p.I423V	c.1267A>G	Missense_Mutation	1	0.11	GP2D	Y	15	10	0	N
FGFR2	VRITTRLSL	LUNG	446	p.S454L	c.1361C>T	Missense_Mutation	1	0.11	NCIH647	N	9	0	42	N
FGFR2	VSCTYQLAT	LUNG	605	p.R613T	c.1838G>C	Missense_Mutation	1	0.11	NCIH2009	N	1	0	0	N
FGFR2	VSWGRFISL	KIDNEY	2	p.C9S	c.25T>A	Missense_Mutation	1	0.11	A498	Y	21	11	0	N
FGFR2	VTENNVMKT	KIDNEY	635	p.I643T	c.1928T>C	Missense_Mutation	1	0.11	A498	N	2	0	0	N
FGFR2	VTKNNVMKI	SKIN	635	p.E637K	c.1909G>A	Missense_Mutation	1	0.11	A375	N	7	0	6	N
FGFR2	VTVILCQMK	STOMACH	394	p.R400Q	c.1199G>A	Missense_Mutation	1	0.11	MKN74	N	3	0	2	N
FGFR2	VTVVVKMLK	ENDOMETRIUM	513	p.A516V	c.1547C>T	Missense_Mutation	1	0.11	HEC59	N	5	0	12	N
FGFR2	VVEYASKGN	BILIARY_TRACT	564	p.I564V	c.1690A>G	Missense_Mutation	1	0.11	SNU245	N	1	0	2	N
FGFR2	VVKMLKDDA	ENDOMETRIUM	516	p.A516V	c.1547C>T	Missense_Mutation	1	0.11	HEC59	N	2	0	20	N
FGFR2	VVTVILCQM	STOMACH	393	p.R400Q	c.1199G>A	Missense_Mutation	1	0.11	MKN74	N	5	0	14	N
FGFR2	VVVEYASKG	BILIARY_TRACT	563	p.I564V	c.1690A>G	Missense_Mutation	1	0.11	SNU245	N	0	0	5	N
FGFR2	VVVKMLKDD	ENDOMETRIUM	515	p.A516V	c.1547C>T	Missense_Mutation	1	0.11	HEC59	N	0	0	12	N
FGFR2	WEIFTLGGL	ENDOMETRIUM	695	p.S703L	c.2108C>T	Missense_Mutation	1	0.11	HEC151	Y	13	11	7	N
FGFR2	WGRFISLVV	KIDNEY	4	p.C9S	c.25T>A	Missense_Mutation	1	0.11	A498	N	9	0	20	N
FGFR2	YACTASSTV	UPPER_AERODIGESTIVE_TRACT	105	p.R111S	c.333G>C	Missense_Mutation	1	0.11	SNU899	N	9	0	2	N
FGFR2	YEPCLPQYT	PANCREAS	806	p.P814T	c.2440C>A	Missense_Mutation	1	0.11	PSN1	N	8	0	1	N
FGFR2	YEPYLPQYP	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	806	p.C809Y	c.2426G>A	Missense_Mutation	1	0.11	RCHACV	N	2	0	0	Y
FGFR2	YICNVSNYI	ENDOMETRIUM	338	p.K341N	c.1023G>T	Missense_Mutation	1	0.11	HEC251	Y	10	10	8	N
FGFR2	YLEIAIYRI	ENDOMETRIUM	376	p.C383R	c.1147T>C	Missense_Mutation	1	0.11	JHUEM2	Y	11	13	2	N
FGFR2	YLPQYPHIN	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	809	p.C809Y	c.2426G>A	Missense_Mutation	1	0.11	RCHACV	N	4	0	4	N
FGFR2	YLRARRPLG	LARGE_INTESTINE	576	p.P583L	c.1748C>T	Missense_Mutation	1	0.11	HCT116	N	3	0	10	N
FGFR2	YLRVLKHSG	ENDOMETRIUM	308	p.K310R	c.929A>G	Missense_Mutation	1	0.11	AN3CA	N	2	0	16	N
FGFR2	YQLATGMEY	LUNG	609	p.R613T	c.1838G>C	Missense_Mutation	1	0.11	NCIH2009	N	9	0	12	N
FGFR2	YRIGVFLIA	ENDOMETRIUM	382	p.C383R	c.1147T>C	Missense_Mutation	1	0.11	JHUEM2	Y	6	10	17	N
FGFR2	YTHINGSVK	PANCREAS	813	p.P814T	c.2440C>A	Missense_Mutation	1	0.11	PSN1	N	3	0	2	N
FGFR2	YTPMLAGVS	LARGE_INTESTINE	457	p.D457Y	c.1369G>T	Missense_Mutation	1	0.11	SNU175	N	2	0	7	N
FGFR2	YVVVEYASK	BILIARY_TRACT	562	p.I564V	c.1690A>G	Missense_Mutation	1	0.11	SNU245	Y	6	15	6	N
FGFR2	DVVERWPHR	ENDOMETRIUM	247	p.S252W	c.755C>G	Missense_Mutation	1	0.22	MFE280	Y	5	9	0	Y
FGFR2	DVVERWPHR	ENDOMETRIUM	247	p.S252W	c.755C>G	Missense_Mutation	1	0.22	MFE319	Y	5	9	0	Y
FGFR2	ERWPHRPIL	ENDOMETRIUM	250	p.S252W	c.755C>G	Missense_Mutation	1	0.22	MFE280	Y	6	9	0	N
FGFR2	ERWPHRPIL	ENDOMETRIUM	250	p.S252W	c.755C>G	Missense_Mutation	1	0.22	MFE319	Y	6	9	0	N
FGFR2	GKHKNIIKL	ENDOMETRIUM	543	p.N550K	c.1650T>G	Missense_Mutation	1	0.22	AN3CA	Y	6	11	0	N
FGFR2	GKHKNIIKL	ENDOMETRIUM	543	p.N550K	c.1650T>G	Missense_Mutation	1	0.22	MFE296	Y	6	11	0	N
FGFR2	HKNIIKLLG	ENDOMETRIUM	545	p.N550K	c.1650T>G	Missense_Mutation	1	0.22	AN3CA	N	0	0	0	N
FGFR2	HKNIIKLLG	ENDOMETRIUM	545	p.N550K	c.1650T>G	Missense_Mutation	1	0.22	MFE296	N	0	0	0	N
FGFR2	HLDVVERWP	ENDOMETRIUM	245	p.S252W	c.755C>G	Missense_Mutation	1	0.22	MFE280	N	0	0	0	Y
FGFR2	HLDVVERWP	ENDOMETRIUM	245	p.S252W	c.755C>G	Missense_Mutation	1	0.22	MFE319	N	0	0	0	Y
FGFR2	IGKHKNIIK	ENDOMETRIUM	542	p.N550K	c.1650T>G	Missense_Mutation	1	0.22	AN3CA	N	0	0	3	N
FGFR2	IGKHKNIIK	ENDOMETRIUM	542	p.N550K	c.1650T>G	Missense_Mutation	1	0.22	MFE296	N	0	0	3	N
FGFR2	IIKLLGACT	ENDOMETRIUM	548	p.N550K	c.1650T>G	Missense_Mutation	1	0.22	AN3CA	N	1	0	2	N
FGFR2	IIKLLGACT	ENDOMETRIUM	548	p.N550K	c.1650T>G	Missense_Mutation	1	0.22	MFE296	N	1	0	2	N
FGFR2	IKLLGACTQ	ENDOMETRIUM	549	p.N550K	c.1650T>G	Missense_Mutation	1	0.22	AN3CA	N	0	0	35	N
FGFR2	IKLLGACTQ	ENDOMETRIUM	549	p.N550K	c.1650T>G	Missense_Mutation	1	0.22	MFE296	N	0	0	35	N
FGFR2	KHKNIIKLL	ENDOMETRIUM	544	p.N550K	c.1650T>G	Missense_Mutation	1	0.22	AN3CA	N	5	0	0	N
FGFR2	KHKNIIKLL	ENDOMETRIUM	544	p.N550K	c.1650T>G	Missense_Mutation	1	0.22	MFE296	N	5	0	0	N
FGFR2	KLLGACTQD	ENDOMETRIUM	550	p.N550K	c.1650T>G	Missense_Mutation	1	0.22	AN3CA	N	0	0	0	N
FGFR2	KLLGACTQD	ENDOMETRIUM	550	p.N550K	c.1650T>G	Missense_Mutation	1	0.22	MFE296	N	0	0	0	N
FGFR2	KNIIKLLGA	ENDOMETRIUM	546	p.N550K	c.1650T>G	Missense_Mutation	1	0.22	AN3CA	Y	3	13	0	N
FGFR2	KNIIKLLGA	ENDOMETRIUM	546	p.N550K	c.1650T>G	Missense_Mutation	1	0.22	MFE296	Y	3	13	0	N
FGFR2	LDVVERWPH	ENDOMETRIUM	246	p.S252W	c.755C>G	Missense_Mutation	1	0.22	MFE280	N	0	0	0	Y
FGFR2	LDVVERWPH	ENDOMETRIUM	246	p.S252W	c.755C>G	Missense_Mutation	1	0.22	MFE319	N	0	0	0	Y
FGFR2	NIIKLLGAC	ENDOMETRIUM	547	p.N550K	c.1650T>G	Missense_Mutation	1	0.22	AN3CA	N	0	0	0	N
FGFR2	NIIKLLGAC	ENDOMETRIUM	547	p.N550K	c.1650T>G	Missense_Mutation	1	0.22	MFE296	N	0	0	0	N
FGFR2	RWPHRPILQ	ENDOMETRIUM	251	p.S252W	c.755C>G	Missense_Mutation	1	0.22	MFE280	N	0	0	0	N
FGFR2	RWPHRPILQ	ENDOMETRIUM	251	p.S252W	c.755C>G	Missense_Mutation	1	0.22	MFE319	N	0	0	0	N
FGFR2	VERWPHRPI	ENDOMETRIUM	249	p.S252W	c.755C>G	Missense_Mutation	1	0.22	MFE280	N	8	0	11	Y
FGFR2	VERWPHRPI	ENDOMETRIUM	249	p.S252W	c.755C>G	Missense_Mutation	1	0.22	MFE319	N	8	0	11	Y
FGFR2	VVERWPHRP	ENDOMETRIUM	248	p.S252W	c.755C>G	Missense_Mutation	1	0.22	MFE280	N	0	0	0	Y
FGFR2	VVERWPHRP	ENDOMETRIUM	248	p.S252W	c.755C>G	Missense_Mutation	1	0.22	MFE319	N	0	0	0	Y
FGFR2	WPHRPILQA	ENDOMETRIUM	252	p.S252W	c.755C>G	Missense_Mutation	1	0.22	MFE280	Y	9	9	5	N
FGFR2	WPHRPILQA	ENDOMETRIUM	252	p.S252W	c.755C>G	Missense_Mutation	1	0.22	MFE319	Y	9	9	5	N
FGFR2	YHLDVVERW	ENDOMETRIUM	244	p.S252W	c.755C>G	Missense_Mutation	1	0.22	MFE280	Y	6	12	11	Y
FGFR2	YHLDVVERW	ENDOMETRIUM	244	p.S252W	c.755C>G	Missense_Mutation	1	0.22	MFE319	Y	6	12	11	Y
FGFR2	DYYKETTNG	BREAST	656	p.K660E	c.1978A>G	Missense_Mutation	1	0.33	EFM19	N	0	0	0	N
FGFR2	ETTNGRLPV	BREAST	660	p.K660E	c.1978A>G	Missense_Mutation	1	0.33	EFM19	N	2	0	0	N
FGFR2	KETTNGRLP	BREAST	659	p.K660E	c.1978A>G	Missense_Mutation	1	0.33	EFM19	N	0	0	0	N
FGFR2	YKETTNGRL	BREAST	658	p.K660E	c.1978A>G	Missense_Mutation	1	0.33	EFM19	N	7	0	2	N
FGFR2	YYKETTNGR	BREAST	657	p.K660E	c.1978A>G	Missense_Mutation	1	0.33	EFM19	N	3	0	4	N