Entrez Gene

Basic Information
Gene ID	153090
Name	DAB2IP

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.1918C>T; p.P640S; 9:121772818-121772818	skin	malignant_melanoma	Substitution - Missense
c.1753G>A; p.D585N; 9:121772653-121772653	lung	carcinoma; small_cell_carcinoma	Substitution - Missense
c.2302C>T; p.R768*; 9:121773202-121773202	oesophagus; lower_third	carcinoma; squamous_cell_carcinoma	Substitution - Nonsense
c.682A>G; p.I228V; 9:121760323-121760323	prostate	carcinoma	Substitution - Missense
c.2302C>T; p.R768*; 9:121773202-121773202	large_intestine	carcinoma; adenocarcinoma	Substitution - Nonsense
c.2711G>A; p.R904K; 9:121774375-121774375	haematopoietic_and_lymphoid_tissue	lymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma	Substitution - Missense
c.2549C>T; p.S850F; 9:121773449-121773449	skin	malignant_melanoma	Substitution - Missense
c.408C>T; p.F136F; 9:121760049-121760049	biliary_tract; gallbladder	carcinoma; adenocarcinoma	Substitution - coding silent
c.2591A>T; p.K864M; 9:121773491-121773491	liver	carcinoma	Substitution - Missense
c.3049T>C; p.L1017L; 9:121782349-121782349	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - coding silent
c.3090G>A; p.Q1030Q; 9:121782390-121782390	lung	carcinoma; adenocarcinoma	Substitution - coding silent
c.2591A>T; p.K864M; 9:121773491-121773491	liver	carcinoma	Substitution - Missense
c.1450G>A; p.E484K; 9:121768556-121768556	breast	carcinoma	Substitution - Missense
c.2980G>A; p.A994T; 9:121781501-121781501	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.39G>C; p.L13L; 9:121757061-121757061	upper_aerodigestive_tract; pharynx	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.259G>A; p.V87M; 9:121759900-121759900	breast	carcinoma; basal_(triple-negative)_carcinoma	Substitution - Missense
c.1706G>T; p.G569V; 9:121770724-121770724	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.1125G>A; p.S375S; 9:121766530-121766530	central_nervous_system; cerebellum	primitive_neuroectodermal_tumour-medulloblastoma; SHH_subtype	Substitution - coding silent
c.2661G>A; p.A887A; 9:121774325-121774325	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - coding silent
c.1731G>A; p.P577P; 9:121772631-121772631	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.1125G>A; p.S375S; 9:121766530-121766530	central_nervous_system; brain	primitive_neuroectodermal_tumour-medulloblastoma; medullomyoblastoma	Substitution - coding silent
c.1125G>A; p.S375S; 9:121766530-121766530	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - coding silent
c.106G>A; p.V36M; 9:121757128-121757128	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.862T>G; p.F288V; 9:121763568-121763568	oesophagus	carcinoma; adenocarcinoma	Substitution - Missense
c.3132C>T; p.S1044S; 9:121782432-121782432	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.2363G>A; p.G788D; 9:121773263-121773263	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.758C>G; p.S253C; 9:121760399-121760399	urinary_tract; bladder	carcinoma	Substitution - Missense
c.615C>T; p.R205R; 9:121760256-121760256	lung	carcinoma; adenocarcinoma	Substitution - coding silent
c.1869C>T; p.S623S; 9:121772769-121772769	skin	malignant_melanoma	Substitution - coding silent
c.2608G>A; p.V870M; 9:121774272-121774272	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - Missense
c.652A>G; p.M218V; 9:121760293-121760293	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.1149C>T; p.R383R; 9:121766554-121766554	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.1465C>A; p.L489M; 9:121768571-121768571	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.1465C>A; p.L489M; 9:121768571-121768571	large_intestine; colon	carcinoma	Substitution - Missense
c.3070C>T; p.L1024F; 9:121782370-121782370	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.1465C>A; p.L489M; 9:121768571-121768571	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.2052C>A; p.T684T; 9:121772952-121772952	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.1313C>T; p.A438V; 9:121766718-121766718	large_intestine; colon	carcinoma	Substitution - Missense
c.774C>T; p.I258I; 9:121760415-121760415	skin	malignant_melanoma	Substitution - coding silent
c.1443C>T; p.A481A; 9:121768549-121768549	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.1985C>T; p.P662L; 9:121772885-121772885	haematopoietic_and_lymphoid_tissue	lymphoid_neoplasm; acute_lymphoblastic_leukaemia	Substitution - Missense
c.2724G>A; p.K908K; 9:121774388-121774388	oesophagus	carcinoma; adenocarcinoma	Substitution - coding silent
c.3023A>G; p.D1008G; 9:121781544-121781544	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.1413C>A; p.I471I; 9:121768519-121768519	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.1061C>T; p.A354V; 9:121763852-121763852	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.2417delC; p.R808fs*9; 9:121773317-121773317	large_intestine	carcinoma; adenocarcinoma	Deletion - Frameshift
c.2073C>T; p.G691G; 9:121772973-121772973	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.398G>A; p.G133D; 9:121760039-121760039	breast	carcinoma	Substitution - Missense
c.1368C>T; p.F456F; 9:121768474-121768474	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.1053C>T; p.C351C; 9:121763844-121763844	oesophagus	carcinoma; adenocarcinoma	Substitution - coding silent
c.2467A>T; p.R823*; 9:121773367-121773367	lung	carcinoma; adenocarcinoma	Substitution - Nonsense
c.2360C>T; p.A787V; 9:121773260-121773260	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.342C>T; p.D114D; 9:121759983-121759983	oesophagus; lower_third	carcinoma; adenocarcinoma	Substitution - coding silent
c.1082C>T; p.S361F; 9:121763873-121763873	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.936C>T; p.D312D; 9:121763642-121763642	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.235C>T; p.P79S; 9:121758988-121758988	skin	malignant_melanoma	Substitution - Missense
c.223C>T; p.R75*; 9:121758976-121758976	ovary	carcinoma; serous_carcinoma	Substitution - Nonsense
c.1121C>T; p.A374V; 9:121766526-121766526	skin	malignant_melanoma	Substitution - Missense
c.2508_2514delGGTGGGC; p.W836fs*6; 9:121773408-121773414	large_intestine	carcinoma; adenocarcinoma	Deletion - Frameshift
c.1172G>A; p.R391Q; 9:121766577-121766577	breast	carcinoma	Substitution - Missense
c.221G>A; p.R74Q; 9:121758974-121758974	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.1396C>T; p.R466C; 9:121768502-121768502	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.819G>A; p.M273I; 9:121763525-121763525	skin	malignant_melanoma	Substitution - Missense
c.2449A>C; p.S817R; 9:121773349-121773349	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.1582_1583GC>CG; p.A528>?; 9:121770600-121770601	large_intestine; rectum	carcinoma; adenocarcinoma	Complex
c.1924G>A; p.G642S; 9:121772824-121772824	skin	malignant_melanoma	Substitution - Missense
c.1582G>A; p.A528T; 9:121770600-121770600	prostate	carcinoma; adenocarcinoma	Substitution - Missense
c.3048G>A; p.S1016S; 9:121782348-121782348	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.2529G>A; p.L843L; 9:121773429-121773429	urinary_tract; bladder	carcinoma	Substitution - coding silent
c.2752C>T; p.L918L; 9:121776201-121776201	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.399C>T; p.G133G; 9:121760040-121760040	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.2704A>T; p.R902W; 9:121774368-121774368	lung; left_upper_lobe	carcinoma; adenocarcinoma	Substitution - Missense
c.1887C>T; p.D629D; 9:121772787-121772787	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.433C>T; p.R145C; 9:121760074-121760074	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.193G>A; p.E65K; 9:121758946-121758946	breast	carcinoma	Substitution - Missense
c.2676C>T; p.D892D; 9:121774340-121774340	large_intestine; colon	NS	Substitution - coding silent
c.1780G>T; p.G594W; 9:121772680-121772680	lung; right_upper_lobe	carcinoma; adenocarcinoma	Substitution - Missense
c.3068G>A; p.R1023H; 9:121782368-121782368	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.937G>A; p.A313T; 9:121763643-121763643	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.2713C>T; p.L905L; 9:121774377-121774377	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.2894G>A; p.R965Q; 9:121776343-121776343	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.121C>A; p.L41I; 9:121757143-121757143	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.1640C>T; p.P547L; 9:121770658-121770658	oesophagus; middle_third	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.1759delT; p.F588fs*81; 9:121772659-121772659	large_intestine; colon	carcinoma; adenocarcinoma	Deletion - Frameshift
c.469_471delAAG; p.K161delK; 9:121760110-121760112	large_intestine; rectum	carcinoma; adenocarcinoma	Deletion - In frame
c.2693_2694insCC; p.H901fs*6; 9:121774357-121774358	large_intestine; colon	carcinoma; adenocarcinoma	Insertion - Frameshift
c.2660C>T; p.A887V; 9:121774324-121774324	stomach	carcinoma; intestinal_adenocarcinoma	Substitution - Missense
c.625C>T; p.R209C; 9:121760266-121760266	pancreas	carcinoma	Substitution - Missense
c.625C>T; p.R209C; 9:121760266-121760266	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.2953G>T; p.V985L; 9:121781474-121781474	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.256C>T; p.R86C; 9:121759897-121759897	stomach	carcinoma; intestinal_adenocarcinoma	Substitution - Missense
c.256C>T; p.R86C; 9:121759897-121759897	lung	carcinoma; small_cell_carcinoma	Substitution - Missense
c.2140G>A; p.G714S; 9:121773040-121773040	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.1675C>T; p.Q559*; 9:121770693-121770693	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Nonsense
c.1881C>A; p.L627L; 9:121772781-121772781	oesophagus; lower_third	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.1852G>A; p.G618S; 9:121772752-121772752	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.368G>T; p.G123V; 9:121760009-121760009	kidney	carcinoma; papillary_renal_cell_carcinoma	Substitution - Missense
c.271C>T; p.L91L; 9:121759912-121759912	cervix	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.2517C>A; p.P839P; 9:121773417-121773417	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.2776C>T; p.R926*; 9:121776225-121776225	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Nonsense
c.1882C>T; p.Q628*; 9:121772782-121772782	skin	malignant_melanoma	Substitution - Nonsense
c.2078C>T; p.P693L; 9:121772978-121772978	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Missense
c.2078C>T; p.P693L; 9:121772978-121772978	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Missense
c.3058G>A; p.A1020T; 9:121782358-121782358	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.225A>G; p.R75R; 9:121758978-121758978	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.1184C>T; p.A395V; 9:121766589-121766589	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.1100G>A; p.R367Q; 9:121766505-121766505	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.3067C>T; p.R1023C; 9:121782367-121782367	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.3067C>T; p.R1023C; 9:121782367-121782367	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.1273C>T; p.R425C; 9:121766678-121766678	skin	malignant_melanoma	Substitution - Missense
c.729C>T; p.L243L; 9:121760370-121760370	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.1422C>T; p.P474P; 9:121768528-121768528	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.2994G>A; p.A998A; 9:121781515-121781515	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.2994G>A; p.A998A; 9:121781515-121781515	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.2265G>A; p.A755A; 9:121773165-121773165	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.2229G>A; p.A743A; 9:121773129-121773129	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.1225C>G; p.P409A; 9:121766630-121766630	ovary	carcinoma; serous_carcinoma	Substitution - Missense
c.2245G>T; p.G749*; 9:121773145-121773145	large_intestine	carcinoma; adenocarcinoma	Substitution - Nonsense
c.1775C>T; p.S592F; 9:121772675-121772675	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.2135C>T; p.A712V; 9:121773035-121773035	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.1259A>G; p.D420G; 9:121766664-121766664	adrenal_gland; adrenal_gland	adrenal_cortical_carcinoma; functioning	Substitution - Missense
c.1744G>T; p.E582*; 9:121772644-121772644	skin	malignant_melanoma	Substitution - Nonsense
c.1933G>A; p.V645I; 9:121772833-121772833	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Missense
c.2103G>A; p.P701P; 9:121773003-121773003	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.2953G>A; p.V985M; 9:121781474-121781474	oesophagus	carcinoma; adenocarcinoma	Substitution - Missense
c.84G>T; p.E28D; 9:121757106-121757106	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.1171C>T; p.R391W; 9:121766576-121766576	haematopoietic_and_lymphoid_tissue	lymphoid_neoplasm; acute_lymphoblastic_leukaemia	Substitution - Missense
c.2076G>A; p.A692A; 9:121772976-121772976	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.785C>T; p.T262M; 9:121760426-121760426	pancreas	other; cystic_tumour	Substitution - Missense
c.626G>A; p.R209H; 9:121760267-121760267	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.1421C>T; p.P474L; 9:121768527-121768527	skin	malignant_melanoma	Substitution - Missense
c.2728G>A; p.E910K; 9:121774392-121774392	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.1449C>T; p.F483F; 9:121768555-121768555	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.1928C>T; p.P643L; 9:121772828-121772828	liver	carcinoma	Substitution - Missense
c.1976C>T; p.A659V; 9:121772876-121772876	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.1928C>T; p.P643L; 9:121772828-121772828	liver	carcinoma	Substitution - Missense
c.182G>A; p.R61Q; 9:121758935-121758935	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.2434delC; p.N814fs*3; 9:121773334-121773334	large_intestine	carcinoma; adenocarcinoma	Deletion - Frameshift
c.2693_2694insC; p.H901fs*4; 9:121774357-121774358	large_intestine; caecum	carcinoma; adenocarcinoma	Insertion - Frameshift
c.2693_2694insC; p.H901fs*4; 9:121774357-121774358	large_intestine; colon	carcinoma; adenocarcinoma	Insertion - Frameshift
c.2693_2694insC; p.H901fs*4; 9:121774357-121774358	large_intestine; colon	carcinoma; adenocarcinoma	Insertion - Frameshift
c.2693_2694insC; p.H901fs*4; 9:121774357-121774358	large_intestine	carcinoma; adenocarcinoma	Insertion - Frameshift
c.2419C>T; p.P807S; 9:121773319-121773319	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.1930G>A; p.D644N; 9:121772830-121772830	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.2906A>G; p.E969G; 9:121776355-121776355	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.393C>G; p.F131L; 9:121760034-121760034	breast	carcinoma	Substitution - Missense
c.367G>A; p.G123S; 9:121760008-121760008	skin	malignant_melanoma	Substitution - Missense
c.393C>T; p.F131F; 9:121760034-121760034	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.1509C>G; p.A503A; 9:121768615-121768615	breast	carcinoma	Substitution - coding silent
c.23G>A; p.R8H; 9:121757045-121757045	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.1641G>A; p.P547P; 9:121770659-121770659	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.2494G>A; p.A832T; 9:121773394-121773394	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.2082C>T; p.G694G; 9:121772982-121772982	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.968A>C; p.E323A; 9:121763759-121763759	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.1198C>T; p.R400C; 9:121766603-121766603	breast	carcinoma	Substitution - Missense
c.2694_2695insC; p.H901fs*4; 9:121774358-121774359	stomach	carcinoma; intestinal_adenocarcinoma	Insertion - Frameshift
c.18G>A; p.E6E; 9:121757040-121757040	breast	carcinoma	Substitution - coding silent
c.88G>C; p.E30Q; 9:121757110-121757110	urinary_tract; bladder	carcinoma	Substitution - Missense
c.1170G>A; p.E390E; 9:121766575-121766575	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.1993G>T; p.A665S; 9:121772893-121772893	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.149C>T; p.T50M; 9:121758902-121758902	liver	carcinoma	Substitution - Missense
c.2531G>C; p.R844T; 9:121773431-121773431	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.2403G>A; p.P801P; 9:121773303-121773303	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - coding silent
c.2102C>T; p.P701L; 9:121773002-121773002	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.2242C>T; p.L748L; 9:121773142-121773142	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.1199G>A; p.R400H; 9:121766604-121766604	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.2698C>T; p.P900S; 9:121774362-121774362	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.1524G>A; p.E508E; 9:121768630-121768630	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.6G>C; p.P2P; 9:121757028-121757028	meninges	meningioma	Substitution - coding silent
c.572C>T; p.T191M; 9:121760213-121760213	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.2694delC; p.H901fs*5; 9:121774358-121774358	large_intestine; caecum	carcinoma; adenocarcinoma	Deletion - Frameshift
c.2694delC; p.H901fs*5; 9:121774358-121774358	large_intestine; colon	carcinoma; adenocarcinoma	Deletion - Frameshift
c.2694delC; p.H901fs*5; 9:121774358-121774358	large_intestine; colon	carcinoma; adenocarcinoma	Deletion - Frameshift
c.2694delC; p.H901fs*5; 9:121774358-121774358	large_intestine; caecum	carcinoma; adenocarcinoma	Deletion - Frameshift
c.2694delC; p.H901fs*5; 9:121774358-121774358	large_intestine; caecum	carcinoma; adenocarcinoma	Deletion - Frameshift
c.2694delC; p.H901fs*5; 9:121774358-121774358	large_intestine; colon	carcinoma; adenocarcinoma	Deletion - Frameshift
c.2694delC; p.H901fs*5; 9:121774358-121774358	large_intestine; colon	carcinoma; adenocarcinoma	Deletion - Frameshift
c.2694delC; p.H901fs*5; 9:121774358-121774358	large_intestine	carcinoma; adenocarcinoma	Deletion - Frameshift
c.2694delC; p.H901fs*5; 9:121774358-121774358	large_intestine	carcinoma; adenocarcinoma	Deletion - Frameshift
c.2694delC; p.H901fs*5; 9:121774358-121774358	stomach	carcinoma; intestinal_adenocarcinoma	Deletion - Frameshift
c.2694delC; p.H901fs*5; 9:121774358-121774358	large_intestine; colon	carcinoma; adenocarcinoma	Deletion - Frameshift
c.2694delC; p.H901fs*5; 9:121774358-121774358	large_intestine	carcinoma; adenocarcinoma	Deletion - Frameshift
c.2694delC; p.H901fs*5; 9:121774358-121774358	large_intestine; colon	carcinoma; adenocarcinoma	Deletion - Frameshift
c.2694delC; p.H901fs*5; 9:121774358-121774358	large_intestine	carcinoma; adenocarcinoma	Deletion - Frameshift
c.1224G>A; p.S408S; 9:121766629-121766629	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.3136A>C; p.T1046P; 9:121782436-121782436	breast	carcinoma	Substitution - Missense
c.1158G>A; p.P386P; 9:121766563-121766563	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.1158G>A; p.P386P; 9:121766563-121766563	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.1158G>A; p.P386P; 9:121766563-121766563	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - coding silent
c.1012G>A; p.A338T; 9:121763803-121763803	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.364A>G; p.T122A; 9:121760005-121760005	skin	malignant_melanoma	Substitution - Missense
c.1441G>A; p.A481T; 9:121768547-121768547	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.3112C>T; p.Q1038*; 9:121782412-121782412	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Nonsense
c.565G>A; p.V189M; 9:121760206-121760206	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense

The somatic mutations from COSMIC database