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

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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 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:
CTNNB1	ADLMELEHG	SKIN	5	p.D11fs	c.31_32insA	Frame_Shift_Ins	3	0.11	HS936T	N	0	0	0	N
CTNNB1	DLMELEHGH	SKIN	6	p.D11fs	c.31_32insA	Frame_Shift_Ins	4	0.11	HS936T	N	0	0	0	N
CTNNB1	EHGHGTRQK	SKIN	11	p.D11fs	c.31_32insA	Frame_Shift_Ins	6	0.11	HS936T	N	0	0	0	N
CTNNB1	ELEHGHGTR	SKIN	9	p.D11fs	c.31_32insA	Frame_Shift_Ins	6	0.11	HS936T	N	5	0	0	N
CTNNB1	GHGTRQKSG	SKIN	13	p.D11fs	c.31_32insA	Frame_Shift_Ins	5	0.11	HS936T	N	0	0	0	Y
CTNNB1	HGHGTRQKS	SKIN	12	p.D11fs	c.31_32insA	Frame_Shift_Ins	6	0.11	HS936T	N	1	0	0	N
CTNNB1	HGTRQKSGC	SKIN	14	p.D11fs	c.31_32insA	Frame_Shift_Ins	6	0.11	HS936T	N	1	0	0	N
CTNNB1	LEHGHGTRQ	SKIN	10	p.D11fs	c.31_32insA	Frame_Shift_Ins	6	0.11	HS936T	N	0	0	0	N
CTNNB1	LMELEHGHG	SKIN	7	p.D11fs	c.31_32insA	Frame_Shift_Ins	5	0.11	HS936T	N	0	0	0	N
CTNNB1	MELEHGHGT	SKIN	8	p.D11fs	c.31_32insA	Frame_Shift_Ins	5	0.11	HS936T	N	7	0	0	N
CTNNB1	QADLMELEH	SKIN	4	p.D11fs	c.31_32insA	Frame_Shift_Ins	2	0.11	HS936T	N	1	0	0	N
CTNNB1	TQADLMELE	SKIN	3	p.D11fs	c.31_32insA	Frame_Shift_Ins	1	0.11	HS936T	N	0	0	0	N
CTNNB1	APLSGKGNP	SKIN	43	p.S45del	c.131_133delCTT	In_Frame_Del	2	0.22	COLO783	N	0	0	0	N
CTNNB1	APLSGKGNP	LARGE_INTESTINE	43	p.S45del	c.131_133delCTT	In_Frame_Del	2	0.22	HCT116	N	0	0	0	N
CTNNB1	ATTTAPLSG	SKIN	39	p.S45del	c.131_133delCTT	In_Frame_Del	3	0.22	COLO783	N	0	0	0	N
CTNNB1	ATTTAPLSG	LARGE_INTESTINE	39	p.S45del	c.131_133delCTT	In_Frame_Del	3	0.22	HCT116	N	0	0	0	N
CTNNB1	GATTTAPLS	SKIN	38	p.S45del	c.131_133delCTT	In_Frame_Del	2	0.22	COLO783	N	1	0	0	N
CTNNB1	GATTTAPLS	LARGE_INTESTINE	38	p.S45del	c.131_133delCTT	In_Frame_Del	2	0.22	HCT116	N	1	0	0	N
CTNNB1	SGATTTAPL	SKIN	37	p.S45del	c.131_133delCTT	In_Frame_Del	1	0.22	COLO783	N	10	0	0	N
CTNNB1	SGATTTAPL	LARGE_INTESTINE	37	p.S45del	c.131_133delCTT	In_Frame_Del	1	0.22	HCT116	N	10	0	0	N
CTNNB1	TAPLSGKGN	SKIN	42	p.S45del	c.131_133delCTT	In_Frame_Del	3	0.22	COLO783	N	1	0	0	N
CTNNB1	TAPLSGKGN	LARGE_INTESTINE	42	p.S45del	c.131_133delCTT	In_Frame_Del	3	0.22	HCT116	N	1	0	0	N
CTNNB1	TTAPLSGKG	SKIN	41	p.S45del	c.131_133delCTT	In_Frame_Del	3	0.22	COLO783	N	0	0	0	N
CTNNB1	TTAPLSGKG	LARGE_INTESTINE	41	p.S45del	c.131_133delCTT	In_Frame_Del	3	0.22	HCT116	N	0	0	0	N
CTNNB1	TTTAPLSGK	SKIN	40	p.S45del	c.131_133delCTT	In_Frame_Del	3	0.22	COLO783	N	2	0	0	N
CTNNB1	TTTAPLSGK	LARGE_INTESTINE	40	p.S45del	c.131_133delCTT	In_Frame_Del	3	0.22	HCT116	N	2	0	0	N
CTNNB1	PLSGKGNPE	SKIN	44	p.S45del	c.131_133delCTT	In_Frame_Del	1	0.33	COLO783	N	0	0	0	N
CTNNB1	PLSGKGNPE	LARGE_INTESTINE	44	p.S45del	c.131_133delCTT	In_Frame_Del	1	0.33	HCT116	N	0	0	0	N
CTNNB1	AAAVLFQMS	URINARY_TRACT	655	p.R661Q	c.1982G>A	Missense_Mutation	1	0.11	639V	N	1	0	0	N
CTNNB1	AAGVLCELS	UPPER_AERODIGESTIVE_TRACT	614	p.A622S	c.1864G>T	Missense_Mutation	1	0.11	HSC2	N	1	0	0	N
CTNNB1	AAVLFQMSE	URINARY_TRACT	656	p.R661Q	c.1982G>A	Missense_Mutation	1	0.11	639V	N	0	0	0	N
CTNNB1	AAVSHWRQQ	OVARY	20	p.Q26R	c.77A>G	Missense_Mutation	1	0.11	OVCAR8	N	0	0	0	N
CTNNB1	ADLMELGMA	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	5	p.D11G	c.32A>G	Missense_Mutation	1	0.11	HPBALL	N	4	0	0	N
CTNNB1	AGATTTAPS	OVARY	37	p.S37A	c.109T>G	Missense_Mutation	1	0.11	HS571T	N	0	0	0	N
CTNNB1	AGLMELDMA	LUNG	5	p.D6G	c.17A>G	Missense_Mutation	1	0.11	NCIH1092	N	2	0	0	N
CTNNB1	AGVLCELSQ	UPPER_AERODIGESTIVE_TRACT	615	p.A622S	c.1864G>T	Missense_Mutation	1	0.11	HSC2	N	0	0	0	N
CTNNB1	AKMAVRFAG	LARGE_INTESTINE	269	p.L275F	c.825A>T	Missense_Mutation	1	0.11	HT55	N	0	0	0	N
CTNNB1	ALHILAQDV	LARGE_INTESTINE	576	p.R582Q	c.1745G>A	Missense_Mutation	1	0.11	CW2	Y	5	10	0	N
CTNNB1	ALLNKTNVN	OVARY	284	p.K292N	c.876A>T	Missense_Mutation	1	0.11	TOV21G	N	0	0	0	N
CTNNB1	ALRHLTSQH	LARGE_INTESTINE	467	p.R474Q	c.1421G>A	Missense_Mutation	1	0.11	SNU81	N	0	0	0	N
CTNNB1	ALVHTVLRA	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	446	p.R449H	c.1346G>A	Missense_Mutation	1	0.11	CMLT1	Y	4	12	0	N
CTNNB1	ALVKMLASP	LARGE_INTESTINE	239	p.G245A	c.734G>C	Missense_Mutation	1	0.11	C2BBE1	N	0	0	0	N
CTNNB1	ANHAPLHEQ	ENDOMETRIUM	522	p.R528H	c.1583G>A	Missense_Mutation	1	0.11	HEC1A	N	0	0	0	N
CTNNB1	APCLSGKGN	STOMACH	43	p.S45C	c.134C>G	Missense_Mutation	1	0.11	OCUM1	N	3	0	0	N
CTNNB1	APLHEQGAI	ENDOMETRIUM	525	p.R528H	c.1583G>A	Missense_Mutation	1	0.11	HEC1A	N	15	0	0	N
CTNNB1	APPLSGKGN	BILIARY_TRACT	43	p.S45P	c.133T>C	Missense_Mutation	1	0.11	SNU869	N	3	0	0	N
CTNNB1	AQDVHNRIV	LARGE_INTESTINE	581	p.R582Q	c.1745G>A	Missense_Mutation	1	0.11	CW2	N	2	0	0	N
CTNNB1	AQEQVADID	LUNG	75	p.T75A	c.223A>G	Missense_Mutation	1	0.11	NCIH358	N	0	0	0	N
CTNNB1	ASGNQESKL	SKIN	305	p.Y306S	c.917A>C	Missense_Mutation	1	0.11	WM1799	Y	6	12	0	N
CTNNB1	ASPVDSVLF	LARGE_INTESTINE	245	p.G245A	c.734G>C	Missense_Mutation	1	0.11	C2BBE1	N	5	0	0	N
CTNNB1	ATQAGLMEL	LUNG	2	p.D6G	c.17A>G	Missense_Mutation	1	0.11	NCIH1092	Y	9	11	0	N
CTNNB1	ATTTAPCLS	STOMACH	39	p.S45C	c.134C>G	Missense_Mutation	1	0.11	OCUM1	N	0	0	0	N
CTNNB1	ATTTAPPLS	BILIARY_TRACT	39	p.S45P	c.133T>C	Missense_Mutation	1	0.11	SNU869	N	0	0	0	N
CTNNB1	AVLFQMSED	URINARY_TRACT	657	p.R661Q	c.1982G>A	Missense_Mutation	1	0.11	639V	N	0	0	0	N
CTNNB1	AVRFAGGLQ	LARGE_INTESTINE	272	p.L275F	c.825A>T	Missense_Mutation	1	0.11	HT55	N	0	0	0	N
CTNNB1	AVSHWRQQS	OVARY	21	p.Q26R	c.77A>G	Missense_Mutation	1	0.11	OVCAR8	N	0	0	0	N
CTNNB1	CALRHLTSQ	LARGE_INTESTINE	466	p.R474Q	c.1421G>A	Missense_Mutation	1	0.11	SNU81	N	0	0	0	N
CTNNB1	CELSQDKEA	UPPER_AERODIGESTIVE_TRACT	619	p.A622S	c.1864G>T	Missense_Mutation	1	0.11	HSC2	N	5	0	0	N
CTNNB1	CGIHSGATT	SKIN	33	p.S33C	c.98C>G	Missense_Mutation	1	0.11	SKMEL1	N	0	0	0	N
CTNNB1	CLQILASGN	SKIN	300	p.Y306S	c.917A>C	Missense_Mutation	1	0.11	WM1799	N	0	0	0	N
CTNNB1	CLQILGYGN	PROSTATE	300	p.A305G	c.914C>G	Missense_Mutation	1	0.11	DU145	N	0	0	0	N
CTNNB1	CLSGKGNPE	STOMACH	45	p.S45C	c.134C>G	Missense_Mutation	1	0.11	OCUM1	N	0	0	0	N
CTNNB1	CPANHAPLH	ENDOMETRIUM	520	p.R528H	c.1583G>A	Missense_Mutation	1	0.11	HEC1A	N	0	0	0	N
CTNNB1	DCGIHSGAT	SKIN	32	p.S33C	c.98C>G	Missense_Mutation	1	0.11	SKMEL1	N	0	0	0	N
CTNNB1	DCLQILASG	SKIN	299	p.Y306S	c.917A>C	Missense_Mutation	1	0.11	WM1799	N	0	0	0	N
CTNNB1	DCLQILGYG	PROSTATE	299	p.A305G	c.914C>G	Missense_Mutation	1	0.11	DU145	N	0	0	0	N
CTNNB1	DFGIHSGAT	LUNG	32	p.S33F	c.98C>T	Missense_Mutation	1	0.11	SW1573	N	1	0	0	N
CTNNB1	DGLPPGDSS	ENDOMETRIUM	764	p.N772S	c.2315A>G	Missense_Mutation	1	0.11	HEC59	N	1	0	0	N
CTNNB1	DGLPVLGHA	LARGE_INTESTINE	751	p.D755V	c.2264A>T	Missense_Mutation	1	0.11	GP2D	N	4	0	0	N
CTNNB1	DLGIHSGAT	LUNG	32	p.S33L	c.97_98TC>CT	Missense_Mutation	1	0.11	MORCPR	N	1	0	0	N
CTNNB1	DLMELGMAM	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	6	p.D11G	c.32A>G	Missense_Mutation	1	0.11	HPBALL	N	4	0	0	N
CTNNB1	DPMMEHEIG	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	732	p.M739I	c.2217G>A	Missense_Mutation	1	0.11	KYO1	N	0	0	0	N
CTNNB1	DSEIHSGAT	STOMACH	32	p.G34E	c.101G>A	Missense_Mutation	1	0.11	AGS	N	2	0	0	N
CTNNB1	DSGIHAGAT	OVARY	32	p.S37A	c.109T>G	Missense_Mutation	1	0.11	HS571T	N	1	0	0	N
CTNNB1	DSSQLAWFD	ENDOMETRIUM	770	p.N772S	c.2315A>G	Missense_Mutation	1	0.11	HEC59	N	0	0	0	N
CTNNB1	DYGIHSGAT	LARGE_INTESTINE	32	p.S33Y	c.98C>A	Missense_Mutation	1	0.11	SW48	N	2	0	0	N
CTNNB1	DYPVDGLPV	LARGE_INTESTINE	747	p.D755V	c.2264A>T	Missense_Mutation	1	0.11	GP2D	N	5	0	0	N
CTNNB1	EALVHTVLR	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	445	p.R449H	c.1346G>A	Missense_Mutation	1	0.11	CMLT1	N	3	0	0	N
CTNNB1	EGAKMAVRF	LARGE_INTESTINE	267	p.L275F	c.825A>T	Missense_Mutation	1	0.11	HT55	N	6	0	0	N
CTNNB1	EHEIGGHHP	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	736	p.M739I	c.2217G>A	Missense_Mutation	1	0.11	KYO1	N	0	0	0	Y
CTNNB1	EIGGHHPGA	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	738	p.M739I	c.2217G>A	Missense_Mutation	1	0.11	KYO1	N	1	0	0	N
CTNNB1	EIHSGATTT	STOMACH	34	p.G34E	c.101G>A	Missense_Mutation	1	0.11	AGS	N	1	0	0	N
CTNNB1	ELGMAMEPD	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	9	p.D11G	c.32A>G	Missense_Mutation	1	0.11	HPBALL	N	0	0	0	N
CTNNB1	ELSQDKEAA	UPPER_AERODIGESTIVE_TRACT	620	p.A622S	c.1864G>T	Missense_Mutation	1	0.11	HSC2	N	0	0	0	N
CTNNB1	EPSQMLKHV	LARGE_INTESTINE	127	p.A135V	c.404C>T	Missense_Mutation	1	0.11	SNU1040	N	13	0	0	N
CTNNB1	EQGFSQSFA	LUNG	67	p.T75A	c.223A>G	Missense_Mutation	1	0.11	NCIH358	N	1	0	0	Y
CTNNB1	FAGGLQKMV	LARGE_INTESTINE	275	p.L275F	c.825A>T	Missense_Mutation	1	0.11	HT55	N	8	0	0	N
CTNNB1	FAQEQVADI	LUNG	74	p.T75A	c.223A>G	Missense_Mutation	1	0.11	NCIH358	N	13	0	3	N
CTNNB1	FGIHSGATT	LUNG	33	p.S33F	c.98C>T	Missense_Mutation	1	0.11	SW1573	N	4	0	7	N
CTNNB1	FQMSEDKPQ	URINARY_TRACT	660	p.R661Q	c.1982G>A	Missense_Mutation	1	0.11	639V	N	2	0	2	N
CTNNB1	FSQSFAQEQ	LUNG	70	p.T75A	c.223A>G	Missense_Mutation	1	0.11	NCIH358	N	2	0	0	N
CTNNB1	GAKMAVRFA	LARGE_INTESTINE	268	p.L275F	c.825A>T	Missense_Mutation	1	0.11	HT55	N	4	0	0	N
CTNNB1	GALHILAQD	LARGE_INTESTINE	575	p.R582Q	c.1745G>A	Missense_Mutation	1	0.11	CW2	N	0	0	0	N
CTNNB1	GATTTAPCL	STOMACH	38	p.S45C	c.134C>G	Missense_Mutation	1	0.11	OCUM1	N	10	0	0	N
CTNNB1	GATTTAPPL	BILIARY_TRACT	38	p.S45P	c.133T>C	Missense_Mutation	1	0.11	SNU869	N	10	0	0	N
CTNNB1	GDSSQLAWF	ENDOMETRIUM	769	p.N772S	c.2315A>G	Missense_Mutation	1	0.11	HEC59	Y	4	10	0	N
CTNNB1	GFSQSFAQE	LUNG	69	p.T75A	c.223A>G	Missense_Mutation	1	0.11	NCIH358	N	0	0	0	N
CTNNB1	GGIEALVHT	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	442	p.R449H	c.1346G>A	Missense_Mutation	1	0.11	CMLT1	N	2	0	0	N
CTNNB1	GIEALVHTV	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	443	p.R449H	c.1346G>A	Missense_Mutation	1	0.11	CMLT1	Y	2	12	0	N
CTNNB1	GIHAGATTT	OVARY	34	p.S37A	c.109T>G	Missense_Mutation	1	0.11	HS571T	N	0	0	0	N
CTNNB1	GLMELDMAM	LUNG	6	p.D6G	c.17A>G	Missense_Mutation	1	0.11	NCIH1092	N	6	0	0	N
CTNNB1	GLPPGDSSQ	ENDOMETRIUM	765	p.N772S	c.2315A>G	Missense_Mutation	1	0.11	HEC59	N	0	0	0	N
CTNNB1	GLPVLGHAQ	LARGE_INTESTINE	752	p.D755V	c.2264A>T	Missense_Mutation	1	0.11	GP2D	N	0	0	0	N
CTNNB1	GMAMEPDRK	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	11	p.D11G	c.32A>G	Missense_Mutation	1	0.11	HPBALL	N	5	0	0	N
CTNNB1	GSHDINVVT	UPPER_AERODIGESTIVE_TRACT	410	p.D412H	c.1234G>C	Missense_Mutation	1	0.11	HSC4	N	1	0	0	N
CTNNB1	GVETARCTA	ENDOMETRIUM	207	p.D207G	c.620A>G	Missense_Mutation	1	0.11	HEC108	N	1	0	0	N
CTNNB1	GVLCELSQD	UPPER_AERODIGESTIVE_TRACT	616	p.A622S	c.1864G>T	Missense_Mutation	1	0.11	HSC2	N	0	0	0	N
CTNNB1	GYGNQESKL	PROSTATE	305	p.A305G	c.914C>G	Missense_Mutation	1	0.11	DU145	Y	6	10	0	N
CTNNB1	HAGATTTAP	OVARY	36	p.S37A	c.109T>G	Missense_Mutation	1	0.11	HS571T	N	0	0	0	N
CTNNB1	HAPLHEQGA	ENDOMETRIUM	524	p.R528H	c.1583G>A	Missense_Mutation	1	0.11	HEC1A	N	3	0	0	N
CTNNB1	HDINVVTCA	UPPER_AERODIGESTIVE_TRACT	412	p.D412H	c.1234G>C	Missense_Mutation	1	0.11	HSC4	N	5	0	0	N
CTNNB1	HEIGGHHPG	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	737	p.M739I	c.2217G>A	Missense_Mutation	1	0.11	KYO1	N	3	0	0	Y
CTNNB1	HEQGAIPRL	ENDOMETRIUM	528	p.R528H	c.1583G>A	Missense_Mutation	1	0.11	HEC1A	Y	10	9	0	N
CTNNB1	HILAQDVHN	LARGE_INTESTINE	578	p.R582Q	c.1745G>A	Missense_Mutation	1	0.11	CW2	N	0	0	0	N
CTNNB1	HLTSQHQEA	LARGE_INTESTINE	470	p.R474Q	c.1421G>A	Missense_Mutation	1	0.11	SNU81	N	2	0	0	N
CTNNB1	HTVLRAGDR	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	449	p.R449H	c.1346G>A	Missense_Mutation	1	0.11	CMLT1	N	5	0	0	N
CTNNB1	HVVVNLINY	LARGE_INTESTINE	134	p.A135V	c.404C>T	Missense_Mutation	1	0.11	SNU1040	Y	8	11	0	N
CTNNB1	HWQQQSYLN	STOMACH	24	p.D32N	c.94G>A	Missense_Mutation	1	0.11	KE39	N	0	0	0	N
CTNNB1	HWRQQSYLD	OVARY	24	p.Q26R	c.77A>G	Missense_Mutation	1	0.11	OVCAR8	N	0	0	0	N
CTNNB1	IEALVHTVL	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	444	p.R449H	c.1346G>A	Missense_Mutation	1	0.11	CMLT1	N	10	0	0	N
CTNNB1	IGGHHPGAD	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	739	p.M739I	c.2217G>A	Missense_Mutation	1	0.11	KYO1	N	0	0	0	N
CTNNB1	IHAGATTTA	OVARY	35	p.S37A	c.109T>G	Missense_Mutation	1	0.11	HS571T	N	2	0	1	N
CTNNB1	ILAQDVHNR	LARGE_INTESTINE	579	p.R582Q	c.1745G>A	Missense_Mutation	1	0.11	CW2	N	5	0	8	N
CTNNB1	ILASGNQES	SKIN	303	p.Y306S	c.917A>C	Missense_Mutation	1	0.11	WM1799	N	0	0	6	N
CTNNB1	ILGYGNQES	PROSTATE	303	p.A305G	c.914C>G	Missense_Mutation	1	0.11	DU145	N	1	0	10	N
CTNNB1	IMRTYTYKK	LARGE_INTESTINE	327	p.E334K	c.1000G>A	Missense_Mutation	1	0.11	SNU81	N	5	0	8	N
CTNNB1	IPALVKMLA	LARGE_INTESTINE	237	p.G245A	c.734G>C	Missense_Mutation	1	0.11	C2BBE1	N	9	0	8	N
CTNNB1	KAAVSHWRQ	OVARY	19	p.Q26R	c.77A>G	Missense_Mutation	1	0.11	OVCAR8	N	0	0	0	N
CTNNB1	KHVVVNLIN	LARGE_INTESTINE	133	p.A135V	c.404C>T	Missense_Mutation	1	0.11	SNU1040	N	1	0	0	N
CTNNB1	KKLLWTTSR	LARGE_INTESTINE	334	p.E334K	c.1000G>A	Missense_Mutation	1	0.11	SNU81	N	1	0	0	N
CTNNB1	KMAVRFAGG	LARGE_INTESTINE	270	p.L275F	c.825A>T	Missense_Mutation	1	0.11	HT55	N	0	0	0	N
CTNNB1	KMLASPVDS	LARGE_INTESTINE	242	p.G245A	c.734G>C	Missense_Mutation	1	0.11	C2BBE1	N	0	0	0	N
CTNNB1	KTNVNFLAI	OVARY	288	p.K292N	c.876A>T	Missense_Mutation	1	0.11	TOV21G	Y	7	14	0	N
CTNNB1	LAQDVHNRI	LARGE_INTESTINE	580	p.R582Q	c.1745G>A	Missense_Mutation	1	0.11	CW2	N	8	0	4	N
CTNNB1	LASGNQESK	SKIN	304	p.Y306S	c.917A>C	Missense_Mutation	1	0.11	WM1799	N	2	0	0	N
CTNNB1	LASPVDSVL	LARGE_INTESTINE	244	p.G245A	c.734G>C	Missense_Mutation	1	0.11	C2BBE1	N	15	0	0	N
CTNNB1	LCELSQDKE	UPPER_AERODIGESTIVE_TRACT	618	p.A622S	c.1864G>T	Missense_Mutation	1	0.11	HSC2	N	0	0	0	N
CTNNB1	LDCGIHSGA	SKIN	31	p.S33C	c.98C>G	Missense_Mutation	1	0.11	SKMEL1	N	4	0	0	N
CTNNB1	LDFGIHSGA	LUNG	31	p.S33F	c.98C>T	Missense_Mutation	1	0.11	SW1573	N	6	0	0	N
CTNNB1	LDLGIHSGA	LUNG	31	p.S33L	c.97_98TC>CT	Missense_Mutation	1	0.11	MORCPR	N	5	0	0	N
CTNNB1	LDSEIHSGA	STOMACH	31	p.G34E	c.101G>A	Missense_Mutation	1	0.11	AGS	N	4	0	0	N
CTNNB1	LDSGIHAGA	OVARY	31	p.S37A	c.109T>G	Missense_Mutation	1	0.11	HS571T	N	4	0	0	N
CTNNB1	LDYGIHSGA	LARGE_INTESTINE	31	p.S33Y	c.98C>A	Missense_Mutation	1	0.11	SW48	N	6	0	0	N
CTNNB1	LFQMSEDKP	URINARY_TRACT	659	p.R661Q	c.1982G>A	Missense_Mutation	1	0.11	639V	N	0	0	0	N
CTNNB1	LGIHSGATT	LUNG	33	p.S33L	c.97_98TC>CT	Missense_Mutation	1	0.11	MORCPR	N	0	0	3	N
CTNNB1	LGMAMEPDR	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	10	p.D11G	c.32A>G	Missense_Mutation	1	0.11	HPBALL	N	1	0	0	N
CTNNB1	LGSHDINVV	UPPER_AERODIGESTIVE_TRACT	409	p.D412H	c.1234G>C	Missense_Mutation	1	0.11	HSC4	N	7	0	11	N
CTNNB1	LGYGNQESK	PROSTATE	304	p.A305G	c.914C>G	Missense_Mutation	1	0.11	DU145	N	1	0	0	N
CTNNB1	LHEQGAIPR	ENDOMETRIUM	527	p.R528H	c.1583G>A	Missense_Mutation	1	0.11	HEC1A	N	2	0	0	N
CTNNB1	LHILAQDVH	LARGE_INTESTINE	577	p.R582Q	c.1745G>A	Missense_Mutation	1	0.11	CW2	N	0	0	0	N
CTNNB1	LKHVVVNLI	LARGE_INTESTINE	132	p.A135V	c.404C>T	Missense_Mutation	1	0.11	SNU1040	N	3	0	16	N
CTNNB1	LLGSHDINV	UPPER_AERODIGESTIVE_TRACT	408	p.D412H	c.1234G>C	Missense_Mutation	1	0.11	HSC4	Y	7	10	0	N
CTNNB1	LLNKTNVNF	OVARY	285	p.K292N	c.876A>T	Missense_Mutation	1	0.11	TOV21G	Y	7	9	1	N
CTNNB1	LMELGMAME	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	7	p.D11G	c.32A>G	Missense_Mutation	1	0.11	HPBALL	N	0	0	0	N
CTNNB1	LNKTNVNFL	OVARY	286	p.K292N	c.876A>T	Missense_Mutation	1	0.11	TOV21G	N	10	0	2	N
CTNNB1	LNSGIHSGA	STOMACH	31	p.D32N	c.94G>A	Missense_Mutation	1	0.11	KE39	N	1	0	0	N
CTNNB1	LPPGDSSQL	ENDOMETRIUM	766	p.N772S	c.2315A>G	Missense_Mutation	1	0.11	HEC59	N	15	0	0	N
CTNNB1	LPVLGHAQD	LARGE_INTESTINE	753	p.D755V	c.2264A>T	Missense_Mutation	1	0.11	GP2D	N	1	0	0	N
CTNNB1	LQILASGNQ	SKIN	301	p.Y306S	c.917A>C	Missense_Mutation	1	0.11	WM1799	N	0	0	26	N
CTNNB1	LQILGYGNQ	PROSTATE	301	p.A305G	c.914C>G	Missense_Mutation	1	0.11	DU145	N	0	0	12	N
CTNNB1	LRHLTSQHQ	LARGE_INTESTINE	468	p.R474Q	c.1421G>A	Missense_Mutation	1	0.11	SNU81	N	1	0	36	N
CTNNB1	LSQDKEAAE	UPPER_AERODIGESTIVE_TRACT	621	p.A622S	c.1864G>T	Missense_Mutation	1	0.11	HSC2	N	0	0	0	N
CTNNB1	LTSQHQEAE	LARGE_INTESTINE	471	p.R474Q	c.1421G>A	Missense_Mutation	1	0.11	SNU81	N	0	0	0	N
CTNNB1	LVHTVLRAG	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	447	p.R449H	c.1346G>A	Missense_Mutation	1	0.11	CMLT1	N	0	0	6	N
CTNNB1	LVKMLASPV	LARGE_INTESTINE	240	p.G245A	c.734G>C	Missense_Mutation	1	0.11	C2BBE1	N	3	0	12	N
CTNNB1	LVQLLGSHD	UPPER_AERODIGESTIVE_TRACT	405	p.D412H	c.1234G>C	Missense_Mutation	1	0.11	HSC4	N	0	0	2	N
CTNNB1	MATQAGLME	LUNG	1	p.D6G	c.17A>G	Missense_Mutation	1	0.11	NCIH1092	N	0	0	0	N
CTNNB1	MAVRFAGGL	LARGE_INTESTINE	271	p.L275F	c.825A>T	Missense_Mutation	1	0.11	HT55	N	19	0	0	N
CTNNB1	MDPMMEHEI	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	731	p.M739I	c.2217G>A	Missense_Mutation	1	0.11	KYO1	N	4	0	0	N
CTNNB1	MEHEIGGHH	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	735	p.M739I	c.2217G>A	Missense_Mutation	1	0.11	KYO1	N	0	0	0	N
CTNNB1	MELGMAMEP	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	8	p.D11G	c.32A>G	Missense_Mutation	1	0.11	HPBALL	N	1	0	0	N
CTNNB1	MLASPVDSV	LARGE_INTESTINE	243	p.G245A	c.734G>C	Missense_Mutation	1	0.11	C2BBE1	Y	8	11	0	N
CTNNB1	MLKHVVVNL	LARGE_INTESTINE	131	p.A135V	c.404C>T	Missense_Mutation	1	0.11	SNU1040	Y	12	13	14	N
CTNNB1	MMEHEIGGH	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	734	p.M739I	c.2217G>A	Missense_Mutation	1	0.11	KYO1	N	0	0	0	N
CTNNB1	MQNTNGVET	ENDOMETRIUM	202	p.D207G	c.620A>G	Missense_Mutation	1	0.11	HEC108	N	4	0	1	N
CTNNB1	MRTYTYKKL	LARGE_INTESTINE	328	p.E334K	c.1000G>A	Missense_Mutation	1	0.11	SNU81	Y	8	9	3	N
CTNNB1	NFLAITTDC	OVARY	292	p.K292N	c.876A>T	Missense_Mutation	1	0.11	TOV21G	N	1	0	0	N
CTNNB1	NGVETARCT	ENDOMETRIUM	206	p.D207G	c.620A>G	Missense_Mutation	1	0.11	HEC108	N	1	0	0	N
CTNNB1	NHAPLHEQG	ENDOMETRIUM	523	p.R528H	c.1583G>A	Missense_Mutation	1	0.11	HEC1A	N	0	0	0	N
CTNNB1	NIMRTYTYK	LARGE_INTESTINE	326	p.E334K	c.1000G>A	Missense_Mutation	1	0.11	SNU81	Y	4	10	0	N
CTNNB1	NKTNVNFLA	OVARY	287	p.K292N	c.876A>T	Missense_Mutation	1	0.11	TOV21G	N	2	0	0	N
CTNNB1	NSGIHSGAT	STOMACH	32	p.D32N	c.94G>A	Missense_Mutation	1	0.11	KE39	N	1	0	0	N
CTNNB1	NTNGVETAR	ENDOMETRIUM	204	p.D207G	c.620A>G	Missense_Mutation	1	0.11	HEC108	N	5	0	0	N
CTNNB1	NVNFLAITT	OVARY	290	p.K292N	c.876A>T	Missense_Mutation	1	0.11	TOV21G	N	1	0	0	N
CTNNB1	PALVKMLAS	LARGE_INTESTINE	238	p.G245A	c.734G>C	Missense_Mutation	1	0.11	C2BBE1	N	0	0	0	N
CTNNB1	PANHAPLHE	ENDOMETRIUM	521	p.R528H	c.1583G>A	Missense_Mutation	1	0.11	HEC1A	N	0	0	0	N
CTNNB1	PCLSGKGNP	STOMACH	44	p.S45C	c.134C>G	Missense_Mutation	1	0.11	OCUM1	N	0	0	0	N
CTNNB1	PGDSSQLAW	ENDOMETRIUM	768	p.N772S	c.2315A>G	Missense_Mutation	1	0.11	HEC59	N	0	0	0	N
CTNNB1	PLHEQGAIP	ENDOMETRIUM	526	p.R528H	c.1583G>A	Missense_Mutation	1	0.11	HEC1A	N	0	0	0	N
CTNNB1	PMMEHEIGG	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	733	p.M739I	c.2217G>A	Missense_Mutation	1	0.11	KYO1	N	0	0	0	N
CTNNB1	PPGDSSQLA	ENDOMETRIUM	767	p.N772S	c.2315A>G	Missense_Mutation	1	0.11	HEC59	N	3	0	0	N
CTNNB1	PPLSGKGNP	BILIARY_TRACT	44	p.S45P	c.133T>C	Missense_Mutation	1	0.11	SNU869	N	0	0	0	N
CTNNB1	PSQMLKHVV	LARGE_INTESTINE	128	p.A135V	c.404C>T	Missense_Mutation	1	0.11	SNU1040	N	0	0	0	N
CTNNB1	PVDGLPVLG	LARGE_INTESTINE	749	p.D755V	c.2264A>T	Missense_Mutation	1	0.11	GP2D	N	0	0	0	N
CTNNB1	PVLGHAQDL	LARGE_INTESTINE	754	p.D755V	c.2264A>T	Missense_Mutation	1	0.11	GP2D	N	3	0	0	N
CTNNB1	QADLMELGM	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	4	p.D11G	c.32A>G	Missense_Mutation	1	0.11	HPBALL	N	5	0	0	N
CTNNB1	QAGLMELDM	LUNG	4	p.D6G	c.17A>G	Missense_Mutation	1	0.11	NCIH1092	N	5	0	0	N
CTNNB1	QDVHNRIVI	LARGE_INTESTINE	582	p.R582Q	c.1745G>A	Missense_Mutation	1	0.11	CW2	N	8	0	0	N
CTNNB1	QGFSQSFAQ	LUNG	68	p.T75A	c.223A>G	Missense_Mutation	1	0.11	NCIH358	N	0	0	0	N
CTNNB1	QHQEAEMAQ	LARGE_INTESTINE	474	p.R474Q	c.1421G>A	Missense_Mutation	1	0.11	SNU81	N	0	0	0	N
CTNNB1	QILASGNQE	SKIN	302	p.Y306S	c.917A>C	Missense_Mutation	1	0.11	WM1799	N	0	0	0	N
CTNNB1	QILGYGNQE	PROSTATE	302	p.A305G	c.914C>G	Missense_Mutation	1	0.11	DU145	N	0	0	0	N
CTNNB1	QLLGSHDIN	UPPER_AERODIGESTIVE_TRACT	407	p.D412H	c.1234G>C	Missense_Mutation	1	0.11	HSC4	N	0	0	0	N
CTNNB1	QMLKHVVVN	LARGE_INTESTINE	130	p.A135V	c.404C>T	Missense_Mutation	1	0.11	SNU1040	N	0	0	0	N
CTNNB1	QMSEDKPQD	URINARY_TRACT	661	p.R661Q	c.1982G>A	Missense_Mutation	1	0.11	639V	N	0	0	0	N
CTNNB1	QNTNGVETA	ENDOMETRIUM	203	p.D207G	c.620A>G	Missense_Mutation	1	0.11	HEC108	N	0	0	0	N
CTNNB1	QQQSYLDCG	SKIN	26	p.S33C	c.98C>G	Missense_Mutation	1	0.11	SKMEL1	N	0	0	0	N
CTNNB1	QQQSYLDFG	LUNG	26	p.S33F	c.98C>T	Missense_Mutation	1	0.11	SW1573	N	0	0	0	N
CTNNB1	QQQSYLDLG	LUNG	26	p.S33L	c.97_98TC>CT	Missense_Mutation	1	0.11	MORCPR	N	0	0	0	N
CTNNB1	QQQSYLDSE	STOMACH	26	p.G34E	c.101G>A	Missense_Mutation	1	0.11	AGS	N	0	0	0	N
CTNNB1	QQQSYLDYG	LARGE_INTESTINE	26	p.S33Y	c.98C>A	Missense_Mutation	1	0.11	SW48	N	0	0	0	N
CTNNB1	QQQSYLNSG	STOMACH	26	p.D32N	c.94G>A	Missense_Mutation	1	0.11	KE39	N	0	0	0	N
CTNNB1	QQSYLDCGI	SKIN	27	p.S33C	c.98C>G	Missense_Mutation	1	0.11	SKMEL1	N	5	0	0	N
CTNNB1	QQSYLDFGI	LUNG	27	p.S33F	c.98C>T	Missense_Mutation	1	0.11	SW1573	N	7	0	0	N
CTNNB1	QQSYLDLGI	LUNG	27	p.S33L	c.97_98TC>CT	Missense_Mutation	1	0.11	MORCPR	N	5	0	0	N
CTNNB1	QQSYLDSEI	STOMACH	27	p.G34E	c.101G>A	Missense_Mutation	1	0.11	AGS	N	5	0	0	N
CTNNB1	QQSYLDYGI	LARGE_INTESTINE	27	p.S33Y	c.98C>A	Missense_Mutation	1	0.11	SW48	N	5	0	0	N
CTNNB1	QQSYLNSGI	STOMACH	27	p.D32N	c.94G>A	Missense_Mutation	1	0.11	KE39	N	6	0	0	N
CTNNB1	QSFAQEQVA	LUNG	72	p.T75A	c.223A>G	Missense_Mutation	1	0.11	NCIH358	N	3	0	0	N
CTNNB1	QSYLDCGIH	SKIN	28	p.S33C	c.98C>G	Missense_Mutation	1	0.11	SKMEL1	N	0	0	0	N
CTNNB1	QSYLDFGIH	LUNG	28	p.S33F	c.98C>T	Missense_Mutation	1	0.11	SW1573	N	0	0	0	N
CTNNB1	QSYLDLGIH	LUNG	28	p.S33L	c.97_98TC>CT	Missense_Mutation	1	0.11	MORCPR	N	0	0	0	N
CTNNB1	QSYLDSEIH	STOMACH	28	p.G34E	c.101G>A	Missense_Mutation	1	0.11	AGS	N	0	0	0	N
CTNNB1	QSYLDYGIH	LARGE_INTESTINE	28	p.S33Y	c.98C>A	Missense_Mutation	1	0.11	SW48	N	0	0	0	N
CTNNB1	QSYLNSGIH	STOMACH	28	p.D32N	c.94G>A	Missense_Mutation	1	0.11	KE39	N	1	0	0	N
CTNNB1	RFAGGLQKM	LARGE_INTESTINE	274	p.L275F	c.825A>T	Missense_Mutation	1	0.11	HT55	N	4	0	0	Y
CTNNB1	RHLTSQHQE	LARGE_INTESTINE	469	p.R474Q	c.1421G>A	Missense_Mutation	1	0.11	SNU81	N	0	0	0	N
CTNNB1	RKAAVSHWR	OVARY	18	p.Q26R	c.77A>G	Missense_Mutation	1	0.11	OVCAR8	N	1	0	0	N
CTNNB1	RQQSYLDSG	OVARY	26	p.Q26R	c.77A>G	Missense_Mutation	1	0.11	OVCAR8	N	0	0	0	N
CTNNB1	RTMQNTNGV	ENDOMETRIUM	200	p.D207G	c.620A>G	Missense_Mutation	1	0.11	HEC108	N	6	0	0	N
CTNNB1	RTYTYKKLL	LARGE_INTESTINE	329	p.E334K	c.1000G>A	Missense_Mutation	1	0.11	SNU81	N	16	0	0	N
CTNNB1	SEIHSGATT	STOMACH	33	p.G34E	c.101G>A	Missense_Mutation	1	0.11	AGS	N	5	0	0	N
CTNNB1	SFAQEQVAD	LUNG	73	p.T75A	c.223A>G	Missense_Mutation	1	0.11	NCIH358	N	0	0	0	N
CTNNB1	SGATTTAPC	STOMACH	37	p.S45C	c.134C>G	Missense_Mutation	1	0.11	OCUM1	N	1	0	0	N
CTNNB1	SGATTTAPP	BILIARY_TRACT	37	p.S45P	c.133T>C	Missense_Mutation	1	0.11	SNU869	N	0	0	0	N
CTNNB1	SGIHAGATT	OVARY	33	p.S37A	c.109T>G	Missense_Mutation	1	0.11	HS571T	N	2	0	0	N
CTNNB1	SGNQESKLI	SKIN	306	p.Y306S	c.917A>C	Missense_Mutation	1	0.11	WM1799	N	7	0	0	N
CTNNB1	SHDINVVTC	UPPER_AERODIGESTIVE_TRACT	411	p.D412H	c.1234G>C	Missense_Mutation	1	0.11	HSC4	Y	2	10	0	N
CTNNB1	SHWRQQSYL	OVARY	23	p.Q26R	c.77A>G	Missense_Mutation	1	0.11	OVCAR8	Y	4	9	0	N
CTNNB1	SQDKEAAEA	UPPER_AERODIGESTIVE_TRACT	622	p.A622S	c.1864G>T	Missense_Mutation	1	0.11	HSC2	N	1	0	0	N
CTNNB1	SQHQEAEMA	LARGE_INTESTINE	473	p.R474Q	c.1421G>A	Missense_Mutation	1	0.11	SNU81	N	2	0	0	N
CTNNB1	SQLAWFDTD	ENDOMETRIUM	772	p.N772S	c.2315A>G	Missense_Mutation	1	0.11	HEC59	N	0	0	0	N
CTNNB1	SQMLKHVVV	LARGE_INTESTINE	129	p.A135V	c.404C>T	Missense_Mutation	1	0.11	SNU1040	N	6	0	0	N
CTNNB1	SQSFAQEQV	LUNG	71	p.T75A	c.223A>G	Missense_Mutation	1	0.11	NCIH358	N	5	0	0	N
CTNNB1	SSQLAWFDT	ENDOMETRIUM	771	p.N772S	c.2315A>G	Missense_Mutation	1	0.11	HEC59	N	1	0	0	N
CTNNB1	SYLDCGIHS	SKIN	29	p.S33C	c.98C>G	Missense_Mutation	1	0.11	SKMEL1	N	2	0	0	N
CTNNB1	SYLDFGIHS	LUNG	29	p.S33F	c.98C>T	Missense_Mutation	1	0.11	SW1573	N	2	0	0	N
CTNNB1	SYLDLGIHS	LUNG	29	p.S33L	c.97_98TC>CT	Missense_Mutation	1	0.11	MORCPR	N	2	0	0	N
CTNNB1	SYLDSEIHS	STOMACH	29	p.G34E	c.101G>A	Missense_Mutation	1	0.11	AGS	N	2	0	0	N
CTNNB1	SYLDSGIHA	OVARY	29	p.S37A	c.109T>G	Missense_Mutation	1	0.11	HS571T	Y	3	10	0	N
CTNNB1	SYLDYGIHS	LARGE_INTESTINE	29	p.S33Y	c.98C>A	Missense_Mutation	1	0.11	SW48	N	2	0	0	N
CTNNB1	SYLNSGIHS	STOMACH	29	p.D32N	c.94G>A	Missense_Mutation	1	0.11	KE39	N	2	0	0	N
CTNNB1	TAPCLSGKG	STOMACH	42	p.S45C	c.134C>G	Missense_Mutation	1	0.11	OCUM1	N	0	0	0	N
CTNNB1	TAPPLSGKG	BILIARY_TRACT	42	p.S45P	c.133T>C	Missense_Mutation	1	0.11	SNU869	N	0	0	0	N
CTNNB1	TDCLQILAS	SKIN	298	p.Y306S	c.917A>C	Missense_Mutation	1	0.11	WM1799	N	1	0	0	N
CTNNB1	TDCLQILGY	PROSTATE	298	p.A305G	c.914C>G	Missense_Mutation	1	0.11	DU145	N	3	0	0	N
CTNNB1	TGALHILAQ	LARGE_INTESTINE	574	p.R582Q	c.1745G>A	Missense_Mutation	1	0.11	CW2	N	0	0	0	N
CTNNB1	TLVQLLGSH	UPPER_AERODIGESTIVE_TRACT	404	p.D412H	c.1234G>C	Missense_Mutation	1	0.11	HSC4	N	0	0	0	N
CTNNB1	TMQNTNGVE	ENDOMETRIUM	201	p.D207G	c.620A>G	Missense_Mutation	1	0.11	HEC108	N	0	0	0	N
CTNNB1	TNGVETARC	ENDOMETRIUM	205	p.D207G	c.620A>G	Missense_Mutation	1	0.11	HEC108	N	0	0	0	N
CTNNB1	TNVNFLAIT	OVARY	289	p.K292N	c.876A>T	Missense_Mutation	1	0.11	TOV21G	N	0	0	0	N
CTNNB1	TQADLMELG	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	3	p.D11G	c.32A>G	Missense_Mutation	1	0.11	HPBALL	N	0	0	0	N
CTNNB1	TQAGLMELD	LUNG	3	p.D6G	c.17A>G	Missense_Mutation	1	0.11	NCIH1092	N	0	0	0	N
CTNNB1	TSQHQEAEM	LARGE_INTESTINE	472	p.R474Q	c.1421G>A	Missense_Mutation	1	0.11	SNU81	Y	4	9	0	N
CTNNB1	TTAPCLSGK	STOMACH	41	p.S45C	c.134C>G	Missense_Mutation	1	0.11	OCUM1	N	3	0	0	N
CTNNB1	TTAPPLSGK	BILIARY_TRACT	41	p.S45P	c.133T>C	Missense_Mutation	1	0.11	SNU869	Y	3	14	0	N
CTNNB1	TTDCLQILG	PROSTATE	297	p.A305G	c.914C>G	Missense_Mutation	1	0.11	DU145	N	1	0	0	N
CTNNB1	TTTAPCLSG	STOMACH	40	p.S45C	c.134C>G	Missense_Mutation	1	0.11	OCUM1	N	0	0	0	N
CTNNB1	TTTAPPLSG	BILIARY_TRACT	40	p.S45P	c.133T>C	Missense_Mutation	1	0.11	SNU869	N	0	0	0	N
CTNNB1	TYAAAVLFQ	URINARY_TRACT	653	p.R661Q	c.1982G>A	Missense_Mutation	1	0.11	639V	N	0	0	0	N
CTNNB1	TYKKLLWTT	LARGE_INTESTINE	332	p.E334K	c.1000G>A	Missense_Mutation	1	0.11	SNU81	N	1	0	0	N
CTNNB1	TYTYKKLLW	LARGE_INTESTINE	330	p.E334K	c.1000G>A	Missense_Mutation	1	0.11	SNU81	N	1	0	0	N
CTNNB1	VDGLPVLGH	LARGE_INTESTINE	750	p.D755V	c.2264A>T	Missense_Mutation	1	0.11	GP2D	N	0	0	5	N
CTNNB1	VGGIEALVH	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	441	p.R449H	c.1346G>A	Missense_Mutation	1	0.11	CMLT1	N	0	0	13	N
CTNNB1	VHTVLRAGD	HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	448	p.R449H	c.1346G>A	Missense_Mutation	1	0.11	CMLT1	N	0	0	3	N
CTNNB1	VKMLASPVD	LARGE_INTESTINE	241	p.G245A	c.734G>C	Missense_Mutation	1	0.11	C2BBE1	N	0	0	10	N
CTNNB1	VLCELSQDK	UPPER_AERODIGESTIVE_TRACT	617	p.A622S	c.1864G>T	Missense_Mutation	1	0.11	HSC2	N	4	0	3	N
CTNNB1	VLFQMSEDK	URINARY_TRACT	658	p.R661Q	c.1982G>A	Missense_Mutation	1	0.11	639V	N	6	0	5	N
CTNNB1	VLGHAQDLM	LARGE_INTESTINE	755	p.D755V	c.2264A>T	Missense_Mutation	1	0.11	GP2D	N	5	0	0	N
CTNNB1	VNFLAITTD	OVARY	291	p.K292N	c.876A>T	Missense_Mutation	1	0.11	TOV21G	N	0	0	3	N
CTNNB1	VQLLGSHDI	UPPER_AERODIGESTIVE_TRACT	406	p.D412H	c.1234G>C	Missense_Mutation	1	0.11	HSC4	N	14	0	37	N
CTNNB1	VRFAGGLQK	LARGE_INTESTINE	273	p.L275F	c.825A>T	Missense_Mutation	1	0.11	HT55	N	2	0	25	N
CTNNB1	VRTMQNTNG	ENDOMETRIUM	199	p.D207G	c.620A>G	Missense_Mutation	1	0.11	HEC108	N	1	0	15	N
CTNNB1	VSHWRQQSY	OVARY	22	p.Q26R	c.77A>G	Missense_Mutation	1	0.11	OVCAR8	Y	7	13	0	N
CTNNB1	VVVNLINYQ	LARGE_INTESTINE	135	p.A135V	c.404C>T	Missense_Mutation	1	0.11	SNU1040	N	0	0	38	N
CTNNB1	WQQQSYLDC	SKIN	25	p.S33C	c.98C>G	Missense_Mutation	1	0.11	SKMEL1	N	7	0	0	N
CTNNB1	WQQQSYLDF	LUNG	25	p.S33F	c.98C>T	Missense_Mutation	1	0.11	SW1573	N	9	0	0	N
CTNNB1	WQQQSYLDL	LUNG	25	p.S33L	c.97_98TC>CT	Missense_Mutation	1	0.11	MORCPR	Y	16	13	2	N
CTNNB1	WQQQSYLDY	LARGE_INTESTINE	25	p.S33Y	c.98C>A	Missense_Mutation	1	0.11	SW48	N	10	0	0	N
CTNNB1	WQQQSYLNS	STOMACH	25	p.D32N	c.94G>A	Missense_Mutation	1	0.11	KE39	N	3	0	6	N
CTNNB1	WRQQSYLDS	OVARY	25	p.Q26R	c.77A>G	Missense_Mutation	1	0.11	OVCAR8	N	5	0	16	N
CTNNB1	YAAAVLFQM	URINARY_TRACT	654	p.R661Q	c.1982G>A	Missense_Mutation	1	0.11	639V	N	10	0	0	N
CTNNB1	YGIHSGATT	LARGE_INTESTINE	33	p.S33Y	c.98C>A	Missense_Mutation	1	0.11	SW48	N	3	0	6	N
CTNNB1	YKKLLWTTS	LARGE_INTESTINE	333	p.E334K	c.1000G>A	Missense_Mutation	1	0.11	SNU81	N	3	0	3	N
CTNNB1	YLDCGIHSG	SKIN	30	p.S33C	c.98C>G	Missense_Mutation	1	0.11	SKMEL1	N	3	0	0	N
CTNNB1	YLDFGIHSG	LUNG	30	p.S33F	c.98C>T	Missense_Mutation	1	0.11	SW1573	N	2	0	0	N
CTNNB1	YLDLGIHSG	LUNG	30	p.S33L	c.97_98TC>CT	Missense_Mutation	1	0.11	MORCPR	N	2	0	0	N
CTNNB1	YLDSEIHSG	STOMACH	30	p.G34E	c.101G>A	Missense_Mutation	1	0.11	AGS	N	3	0	0	N
CTNNB1	YLDSGIHAG	OVARY	30	p.S37A	c.109T>G	Missense_Mutation	1	0.11	HS571T	N	3	0	0	N
CTNNB1	YLDYGIHSG	LARGE_INTESTINE	30	p.S33Y	c.98C>A	Missense_Mutation	1	0.11	SW48	N	2	0	1	N
CTNNB1	YLNSGIHSG	STOMACH	30	p.D32N	c.94G>A	Missense_Mutation	1	0.11	KE39	Y	3	11	4	N
CTNNB1	YPVDGLPVL	LARGE_INTESTINE	748	p.D755V	c.2264A>T	Missense_Mutation	1	0.11	GP2D	Y	27	10	2	N
CTNNB1	YTYKKLLWT	LARGE_INTESTINE	331	p.E334K	c.1000G>A	Missense_Mutation	1	0.11	SNU81	N	5	0	4	N
CTNNB1	APFLSGKGN	LUNG	43	p.S45F	c.134C>T	Missense_Mutation	1	0.22	HCC15	N	5	0	0	N
CTNNB1	APFLSGKGN	LARGE_INTESTINE	43	p.S45F	c.134C>T	Missense_Mutation	1	0.22	LS180	N	5	0	0	N
CTNNB1	ATTTAPFLS	LUNG	39	p.S45F	c.134C>T	Missense_Mutation	1	0.22	HCC15	N	0	0	0	N
CTNNB1	ATTTAPFLS	LARGE_INTESTINE	39	p.S45F	c.134C>T	Missense_Mutation	1	0.22	LS180	N	0	0	0	N
CTNNB1	CGATTTAPS	ENDOMETRIUM	37	p.S37C	c.110C>G	Missense_Mutation	1	0.22	JHUEM2	N	0	0	0	N
CTNNB1	CGATTTAPS	LIVER	37	p.S37C	c.110C>G	Missense_Mutation	1	0.22	SNU398	N	0	0	0	N
CTNNB1	DSGIHCGAT	ENDOMETRIUM	32	p.S37C	c.110C>G	Missense_Mutation	1	0.22	JHUEM2	N	1	0	0	N
CTNNB1	DSGIHCGAT	LIVER	32	p.S37C	c.110C>G	Missense_Mutation	1	0.22	SNU398	N	1	0	0	N
CTNNB1	DSGIHPGAT	ENDOMETRIUM	32	p.S37P	c.109T>C	Missense_Mutation	1	0.22	HEC108	N	1	0	0	N
CTNNB1	DSGIHPGAT	ENDOMETRIUM	32	p.S37P	c.109T>C	Missense_Mutation	1	0.22	SNGM	N	1	0	0	N
CTNNB1	DSVIHSGAT	LIVER	32	p.G34V	c.101G>T	Missense_Mutation	1	0.22	HUH6	N	1	0	0	N
CTNNB1	DSVIHSGAT	STOMACH	32	p.G34V	c.101G>T	Missense_Mutation	1	0.22	SNU719	N	1	0	0	N
CTNNB1	FLSGKGNPE	LUNG	45	p.S45F	c.134C>T	Missense_Mutation	1	0.22	HCC15	N	1	0	0	N
CTNNB1	FLSGKGNPE	LARGE_INTESTINE	45	p.S45F	c.134C>T	Missense_Mutation	1	0.22	LS180	N	1	0	0	N
CTNNB1	GATTTAPFL	LUNG	38	p.S45F	c.134C>T	Missense_Mutation	1	0.22	HCC15	N	11	0	0	N
CTNNB1	GATTTAPFL	LARGE_INTESTINE	38	p.S45F	c.134C>T	Missense_Mutation	1	0.22	LS180	N	11	0	0	N
CTNNB1	GIHCGATTT	ENDOMETRIUM	34	p.S37C	c.110C>G	Missense_Mutation	1	0.22	JHUEM2	N	0	0	0	N
CTNNB1	GIHCGATTT	LIVER	34	p.S37C	c.110C>G	Missense_Mutation	1	0.22	SNU398	N	0	0	0	N
CTNNB1	GIHPGATTT	ENDOMETRIUM	34	p.S37P	c.109T>C	Missense_Mutation	1	0.22	HEC108	N	0	0	0	N
CTNNB1	GIHPGATTT	ENDOMETRIUM	34	p.S37P	c.109T>C	Missense_Mutation	1	0.22	SNGM	N	0	0	0	N
CTNNB1	HCGATTTAP	ENDOMETRIUM	36	p.S37C	c.110C>G	Missense_Mutation	1	0.22	JHUEM2	N	0	0	0	N
CTNNB1	HCGATTTAP	LIVER	36	p.S37C	c.110C>G	Missense_Mutation	1	0.22	SNU398	N	0	0	0	N
CTNNB1	HPGATTTAP	ENDOMETRIUM	36	p.S37P	c.109T>C	Missense_Mutation	1	0.22	HEC108	N	1	0	0	N
CTNNB1	HPGATTTAP	ENDOMETRIUM	36	p.S37P	c.109T>C	Missense_Mutation	1	0.22	SNGM	N	1	0	0	N
CTNNB1	HWQQQSYLV	ENDOMETRIUM	24	p.D32V	c.95A>T	Missense_Mutation	1	0.22	HEC265	N	1	0	0	N
CTNNB1	HWQQQSYLV	ENDOMETRIUM	24	p.D32V	c.95A>T	Missense_Mutation	1	0.22	HEC6	N	1	0	0	N
CTNNB1	IHCGATTTA	ENDOMETRIUM	35	p.S37C	c.110C>G	Missense_Mutation	1	0.22	JHUEM2	N	2	0	1	N
CTNNB1	IHCGATTTA	LIVER	35	p.S37C	c.110C>G	Missense_Mutation	1	0.22	SNU398	N	2	0	1	N
CTNNB1	IHPGATTTA	ENDOMETRIUM	35	p.S37P	c.109T>C	Missense_Mutation	1	0.22	HEC108	N	2	0	6	N
CTNNB1	IHPGATTTA	ENDOMETRIUM	35	p.S37P	c.109T>C	Missense_Mutation	1	0.22	SNGM	N	2	0	6	N
CTNNB1	LDSGIHCGA	ENDOMETRIUM	31	p.S37C	c.110C>G	Missense_Mutation	1	0.22	JHUEM2	N	4	0	0	N
CTNNB1	LDSGIHCGA	LIVER	31	p.S37C	c.110C>G	Missense_Mutation	1	0.22	SNU398	N	4	0	0	N
CTNNB1	LDSGIHPGA	ENDOMETRIUM	31	p.S37P	c.109T>C	Missense_Mutation	1	0.22	HEC108	N	4	0	0	N
CTNNB1	LDSGIHPGA	ENDOMETRIUM	31	p.S37P	c.109T>C	Missense_Mutation	1	0.22	SNGM	N	4	0	0	N
CTNNB1	LDSVIHSGA	LIVER	31	p.G34V	c.101G>T	Missense_Mutation	1	0.22	HUH6	N	4	0	0	N
CTNNB1	LDSVIHSGA	STOMACH	31	p.G34V	c.101G>T	Missense_Mutation	1	0.22	SNU719	N	4	0	0	N
CTNNB1	LVSGIHSGA	ENDOMETRIUM	31	p.D32V	c.95A>T	Missense_Mutation	1	0.22	HEC265	N	2	0	6	N
CTNNB1	LVSGIHSGA	ENDOMETRIUM	31	p.D32V	c.95A>T	Missense_Mutation	1	0.22	HEC6	N	2	0	6	N
CTNNB1	PFLSGKGNP	LUNG	44	p.S45F	c.134C>T	Missense_Mutation	1	0.22	HCC15	N	0	0	0	N
CTNNB1	PFLSGKGNP	LARGE_INTESTINE	44	p.S45F	c.134C>T	Missense_Mutation	1	0.22	LS180	N	0	0	0	N
CTNNB1	PGATTTAPS	ENDOMETRIUM	37	p.S37P	c.109T>C	Missense_Mutation	1	0.22	HEC108	N	0	0	0	N
CTNNB1	PGATTTAPS	ENDOMETRIUM	37	p.S37P	c.109T>C	Missense_Mutation	1	0.22	SNGM	N	0	0	0	N
CTNNB1	QQQSYLDSV	LIVER	26	p.G34V	c.101G>T	Missense_Mutation	1	0.22	HUH6	N	8	0	0	N
CTNNB1	QQQSYLDSV	STOMACH	26	p.G34V	c.101G>T	Missense_Mutation	1	0.22	SNU719	N	8	0	0	N
CTNNB1	QQQSYLVSG	ENDOMETRIUM	26	p.D32V	c.95A>T	Missense_Mutation	1	0.22	HEC265	N	0	0	0	N
CTNNB1	QQQSYLVSG	ENDOMETRIUM	26	p.D32V	c.95A>T	Missense_Mutation	1	0.22	HEC6	N	0	0	0	N
CTNNB1	QQSYLDSVI	LIVER	27	p.G34V	c.101G>T	Missense_Mutation	1	0.22	HUH6	N	5	0	0	N
CTNNB1	QQSYLDSVI	STOMACH	27	p.G34V	c.101G>T	Missense_Mutation	1	0.22	SNU719	N	5	0	0	N
CTNNB1	QQSYLVSGI	ENDOMETRIUM	27	p.D32V	c.95A>T	Missense_Mutation	1	0.22	HEC265	N	7	0	0	N
CTNNB1	QQSYLVSGI	ENDOMETRIUM	27	p.D32V	c.95A>T	Missense_Mutation	1	0.22	HEC6	N	7	0	0	N
CTNNB1	QSYLDSVIH	LIVER	28	p.G34V	c.101G>T	Missense_Mutation	1	0.22	HUH6	N	0	0	0	N
CTNNB1	QSYLDSVIH	STOMACH	28	p.G34V	c.101G>T	Missense_Mutation	1	0.22	SNU719	N	0	0	0	N
CTNNB1	QSYLVSGIH	ENDOMETRIUM	28	p.D32V	c.95A>T	Missense_Mutation	1	0.22	HEC265	N	0	0	0	N
CTNNB1	QSYLVSGIH	ENDOMETRIUM	28	p.D32V	c.95A>T	Missense_Mutation	1	0.22	HEC6	N	0	0	0	N
CTNNB1	SGATTTAPF	LUNG	37	p.S45F	c.134C>T	Missense_Mutation	1	0.22	HCC15	N	5	0	0	N
CTNNB1	SGATTTAPF	LARGE_INTESTINE	37	p.S45F	c.134C>T	Missense_Mutation	1	0.22	LS180	N	5	0	0	N
CTNNB1	SGIHCGATT	ENDOMETRIUM	33	p.S37C	c.110C>G	Missense_Mutation	1	0.22	JHUEM2	N	1	0	0	N
CTNNB1	SGIHCGATT	LIVER	33	p.S37C	c.110C>G	Missense_Mutation	1	0.22	SNU398	N	1	0	0	N
CTNNB1	SGIHPGATT	ENDOMETRIUM	33	p.S37P	c.109T>C	Missense_Mutation	1	0.22	HEC108	N	1	0	0	N
CTNNB1	SGIHPGATT	ENDOMETRIUM	33	p.S37P	c.109T>C	Missense_Mutation	1	0.22	SNGM	N	1	0	0	N
CTNNB1	SVIHSGATT	LIVER	33	p.G34V	c.101G>T	Missense_Mutation	1	0.22	HUH6	N	2	0	0	N
CTNNB1	SVIHSGATT	STOMACH	33	p.G34V	c.101G>T	Missense_Mutation	1	0.22	SNU719	N	2	0	0	N
CTNNB1	SYLDSGIHC	ENDOMETRIUM	29	p.S37C	c.110C>G	Missense_Mutation	1	0.22	JHUEM2	Y	3	10	0	N
CTNNB1	SYLDSGIHC	LIVER	29	p.S37C	c.110C>G	Missense_Mutation	1	0.22	SNU398	Y	3	10	0	N
CTNNB1	SYLDSGIHP	ENDOMETRIUM	29	p.S37P	c.109T>C	Missense_Mutation	1	0.22	HEC108	N	0	0	0	N
CTNNB1	SYLDSGIHP	ENDOMETRIUM	29	p.S37P	c.109T>C	Missense_Mutation	1	0.22	SNGM	N	0	0	0	N
CTNNB1	SYLDSVIHS	LIVER	29	p.G34V	c.101G>T	Missense_Mutation	1	0.22	HUH6	Y	2	10	0	N
CTNNB1	SYLDSVIHS	STOMACH	29	p.G34V	c.101G>T	Missense_Mutation	1	0.22	SNU719	Y	2	10	0	N
CTNNB1	SYLVSGIHS	ENDOMETRIUM	29	p.D32V	c.95A>T	Missense_Mutation	1	0.22	HEC265	N	2	0	0	N
CTNNB1	SYLVSGIHS	ENDOMETRIUM	29	p.D32V	c.95A>T	Missense_Mutation	1	0.22	HEC6	N	2	0	0	N
CTNNB1	TAPFLSGKG	LUNG	42	p.S45F	c.134C>T	Missense_Mutation	1	0.22	HCC15	N	0	0	0	N
CTNNB1	TAPFLSGKG	LARGE_INTESTINE	42	p.S45F	c.134C>T	Missense_Mutation	1	0.22	LS180	N	0	0	0	N
CTNNB1	TTAPFLSGK	LUNG	41	p.S45F	c.134C>T	Missense_Mutation	1	0.22	HCC15	Y	3	14	0	N
CTNNB1	TTAPFLSGK	LARGE_INTESTINE	41	p.S45F	c.134C>T	Missense_Mutation	1	0.22	LS180	Y	3	14	0	N
CTNNB1	TTTAPFLSG	LUNG	40	p.S45F	c.134C>T	Missense_Mutation	1	0.22	HCC15	N	0	0	0	N
CTNNB1	TTTAPFLSG	LARGE_INTESTINE	40	p.S45F	c.134C>T	Missense_Mutation	1	0.22	LS180	N	0	0	0	N
CTNNB1	VIHSGATTT	LIVER	34	p.G34V	c.101G>T	Missense_Mutation	1	0.22	HUH6	N	1	0	0	N
CTNNB1	VIHSGATTT	STOMACH	34	p.G34V	c.101G>T	Missense_Mutation	1	0.22	SNU719	N	1	0	0	N
CTNNB1	VSGIHSGAT	ENDOMETRIUM	32	p.D32V	c.95A>T	Missense_Mutation	1	0.22	HEC265	N	1	0	0	N
CTNNB1	VSGIHSGAT	ENDOMETRIUM	32	p.D32V	c.95A>T	Missense_Mutation	1	0.22	HEC6	N	1	0	0	N
CTNNB1	WQQQSYLVS	ENDOMETRIUM	25	p.D32V	c.95A>T	Missense_Mutation	1	0.22	HEC265	N	3	0	6	N
CTNNB1	WQQQSYLVS	ENDOMETRIUM	25	p.D32V	c.95A>T	Missense_Mutation	1	0.22	HEC6	N	3	0	6	N
CTNNB1	YLDSGIHCG	ENDOMETRIUM	30	p.S37C	c.110C>G	Missense_Mutation	1	0.22	JHUEM2	N	3	0	0	N
CTNNB1	YLDSGIHCG	LIVER	30	p.S37C	c.110C>G	Missense_Mutation	1	0.22	SNU398	N	3	0	0	N
CTNNB1	YLDSGIHPG	ENDOMETRIUM	30	p.S37P	c.109T>C	Missense_Mutation	1	0.22	HEC108	N	3	0	0	N
CTNNB1	YLDSGIHPG	ENDOMETRIUM	30	p.S37P	c.109T>C	Missense_Mutation	1	0.22	SNGM	N	3	0	0	N
CTNNB1	YLDSVIHSG	LIVER	30	p.G34V	c.101G>T	Missense_Mutation	1	0.22	HUH6	N	3	0	0	N
CTNNB1	YLDSVIHSG	STOMACH	30	p.G34V	c.101G>T	Missense_Mutation	1	0.22	SNU719	N	3	0	0	N
CTNNB1	YLVSGIHSG	ENDOMETRIUM	30	p.D32V	c.95A>T	Missense_Mutation	1	0.22	HEC265	N	3	0	4	N
CTNNB1	YLVSGIHSG	ENDOMETRIUM	30	p.D32V	c.95A>T	Missense_Mutation	1	0.22	HEC6	N	3	0	4	N
CTNNB1	ATAPSLSGK	LARGE_INTESTINE	41	p.T41A	c.121A>G	Missense_Mutation	1	0.33	CCK81	Y	3	15	0	N
CTNNB1	ATAPSLSGK	LUNG	41	p.T41A	c.121A>G	Missense_Mutation	1	0.33	LXF289	Y	3	15	0	N
CTNNB1	ATAPSLSGK	LARGE_INTESTINE	41	p.T41A	c.121A>G	Missense_Mutation	1	0.33	SNU407	Y	3	15	0	N
CTNNB1	ATATAPSLS	LARGE_INTESTINE	39	p.T41A	c.121A>G	Missense_Mutation	1	0.33	CCK81	N	0	0	0	N
CTNNB1	ATATAPSLS	LUNG	39	p.T41A	c.121A>G	Missense_Mutation	1	0.33	LXF289	N	0	0	0	N
CTNNB1	ATATAPSLS	LARGE_INTESTINE	39	p.T41A	c.121A>G	Missense_Mutation	1	0.33	SNU407	N	0	0	0	N
CTNNB1	GATATAPSL	LARGE_INTESTINE	38	p.T41A	c.121A>G	Missense_Mutation	1	0.33	CCK81	N	10	0	0	N
CTNNB1	GATATAPSL	LUNG	38	p.T41A	c.121A>G	Missense_Mutation	1	0.33	LXF289	N	10	0	0	N
CTNNB1	GATATAPSL	LARGE_INTESTINE	38	p.T41A	c.121A>G	Missense_Mutation	1	0.33	SNU407	N	10	0	0	N
CTNNB1	GIHSGATAT	LARGE_INTESTINE	34	p.T41A	c.121A>G	Missense_Mutation	1	0.33	CCK81	N	0	0	0	N
CTNNB1	GIHSGATAT	LUNG	34	p.T41A	c.121A>G	Missense_Mutation	1	0.33	LXF289	N	0	0	0	N
CTNNB1	GIHSGATAT	LARGE_INTESTINE	34	p.T41A	c.121A>G	Missense_Mutation	1	0.33	SNU407	N	0	0	0	N
CTNNB1	HSGATATAP	LARGE_INTESTINE	36	p.T41A	c.121A>G	Missense_Mutation	1	0.33	CCK81	N	0	0	0	N
CTNNB1	HSGATATAP	LUNG	36	p.T41A	c.121A>G	Missense_Mutation	1	0.33	LXF289	N	0	0	0	N
CTNNB1	HSGATATAP	LARGE_INTESTINE	36	p.T41A	c.121A>G	Missense_Mutation	1	0.33	SNU407	N	0	0	0	N
CTNNB1	IHSGATATA	LARGE_INTESTINE	35	p.T41A	c.121A>G	Missense_Mutation	1	0.33	CCK81	N	2	0	6	N
CTNNB1	IHSGATATA	LUNG	35	p.T41A	c.121A>G	Missense_Mutation	1	0.33	LXF289	N	2	0	6	N
CTNNB1	IHSGATATA	LARGE_INTESTINE	35	p.T41A	c.121A>G	Missense_Mutation	1	0.33	SNU407	N	2	0	6	N
CTNNB1	PLSGKGNPE	BILIARY_TRACT	45	p.S45P	c.133T>C	Missense_Mutation	1	0.33	SNU869	N	0	0	0	N
CTNNB1	SGATATAPS	LARGE_INTESTINE	37	p.T41A	c.121A>G	Missense_Mutation	1	0.33	CCK81	N	1	0	0	N
CTNNB1	SGATATAPS	LUNG	37	p.T41A	c.121A>G	Missense_Mutation	1	0.33	LXF289	N	1	0	0	N
CTNNB1	SGATATAPS	LARGE_INTESTINE	37	p.T41A	c.121A>G	Missense_Mutation	1	0.33	SNU407	N	1	0	0	N
CTNNB1	SGIHSGATA	LARGE_INTESTINE	33	p.T41A	c.121A>G	Missense_Mutation	1	0.33	CCK81	N	2	0	0	N
CTNNB1	SGIHSGATA	LUNG	33	p.T41A	c.121A>G	Missense_Mutation	1	0.33	LXF289	N	2	0	0	N
CTNNB1	SGIHSGATA	LARGE_INTESTINE	33	p.T41A	c.121A>G	Missense_Mutation	1	0.33	SNU407	N	2	0	0	N
CTNNB1	TATAPSLSG	LARGE_INTESTINE	40	p.T41A	c.121A>G	Missense_Mutation	1	0.33	CCK81	N	0	0	0	N
CTNNB1	TATAPSLSG	LUNG	40	p.T41A	c.121A>G	Missense_Mutation	1	0.33	LXF289	N	0	0	0	N
CTNNB1	TATAPSLSG	LARGE_INTESTINE	40	p.T41A	c.121A>G	Missense_Mutation	1	0.33	SNU407	N	0	0	0	N