Entrez Gene

Basic Information
Gene ID	6925
Name	TCF4

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.951C>A; p.S317R; 18:55261505-55261505	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.240G>C; p.M80I; 18:55461083-55461083	lung; right_lower_lobe	carcinoma; adenocarcinoma	Substitution - Missense
c.143C>T; p.S48L; 18:55585282-55585282	breast	carcinoma	Substitution - Missense
c.3G>A; p.M1I; 18:55587114-55587114	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.1785C>T; p.L595L; 18:55228929-55228929	breast	carcinoma	Substitution - coding silent
c.678T>A; p.P226P; 18:55275730-55275730	lung	carcinoma; adenocarcinoma	Substitution - coding silent
c.990G>A; p.S330S; 18:55261466-55261466	breast	carcinoma	Substitution - coding silent
c.520C>T; p.R174*; 18:55350388-55350388	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Nonsense
c.520C>T; p.R174*; 18:55350388-55350388	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Nonsense
c.215G>C; p.G72A; 18:55461108-55461108	breast	carcinoma	Substitution - Missense
c.718delG; p.G240fs*24; 18:55275690-55275690	prostate	carcinoma; adenocarcinoma	Deletion - Frameshift
c.520C>T; p.R174*; 18:55350388-55350388	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Nonsense
c.520C>T; p.R174*; 18:55350388-55350388	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Nonsense
c.473G>A; p.R158K; 18:55350900-55350900	skin; trunk	malignant_melanoma	Substitution - Missense
c.1876C>G; p.L626V; 18:55228353-55228353	lung	carcinoma; small_cell_carcinoma	Substitution - Missense
c.1117C>T; p.P373S; 18:55257344-55257344	skin; mucosal	malignant_melanoma	Substitution - Missense
c.1596G>A; p.K532K; 18:55232562-55232562	skin	malignant_melanoma	Substitution - coding silent
c.932G>A; p.G311E; 18:55261524-55261524	skin	malignant_melanoma	Substitution - Missense
c.1857G>C; p.Q619H; 18:55228857-55228857	breast	carcinoma	Substitution - Missense
c.470G>A; p.R157Q; 18:55350903-55350903	skin	malignant_melanoma	Substitution - Missense
c.114T>G; p.T38T; 18:55585311-55585311	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.1812C>G; p.L604L; 18:55228902-55228902	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm; chronic_myelomonocytic_leukaemia	Substitution - coding silent
c.1105G>A; p.A369T; 18:55257356-55257356	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm; myelodysplastic_syndrome	Substitution - Missense
c.1366G>A; p.E456K; 18:55234668-55234668	skin	malignant_melanoma	Substitution - Missense
c.337G>T; p.G113W; 18:55403486-55403486	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.61G>T; p.D21Y; 18:55587056-55587056	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.278C>T; p.P93L; 18:55461045-55461045	skin	malignant_melanoma	Substitution - Missense
c.278C>T; p.P93L; 18:55461045-55461045	oesophagus; middle_third	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.1786A>G; p.K596E; 18:55228928-55228928	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.842C>A; p.S281Y; 18:55269911-55269911	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.417T>G; p.L139L; 18:55350956-55350956	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.885C>T; p.S295S; 18:55269868-55269868	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - coding silent
c.557C>T; p.A186V; 18:55279649-55279649	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.557C>T; p.A186V; 18:55279649-55279649	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.1884G>A; p.P628P; 18:55228345-55228345	skin	malignant_melanoma	Substitution - coding silent
c.1883_1892del10; p.P628fs*3; 18:55228337-55228346	central_nervous_system; brainstem	glioma; astrocytoma_Grade_II	Deletion - Frameshift
c.418T>A; p.S140T; 18:55350955-55350955	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.1397C>A; p.S466Y; 18:55234637-55234637	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.1963C>T; p.P655S; 18:55228266-55228266	skin	malignant_melanoma	Substitution - Missense
c.1963C>T; p.P655S; 18:55228266-55228266	skin	malignant_melanoma	Substitution - Missense
c.509C>T; p.T170I; 18:55350399-55350399	oesophagus; lower_third	carcinoma; adenocarcinoma	Substitution - Missense
c.71C>T; p.A24V; 18:55587046-55587046	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.243C>T; p.T81T; 18:55461080-55461080	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - coding silent
c.1109C>T; p.S370L; 18:55257352-55257352	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.1978G>T; p.A660S; 18:55228251-55228251	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.9C>T; p.H3H; 18:55587108-55587108	urinary_tract; bladder	carcinoma	Substitution - coding silent
c.1041T>G; p.T347T; 18:55259977-55259977	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm; myelodysplastic_syndrome	Substitution - coding silent
c.323C>T; p.S108L; 18:55403500-55403500	skin	malignant_melanoma	Substitution - Missense
c.893C>T; p.P298L; 18:55269860-55269860	skin	malignant_melanoma	Substitution - Missense
c.1982C>T; p.S661L; 18:55228247-55228247	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.1982C>T; p.S661L; 18:55228247-55228247	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.1940C>T; p.P647L; 18:55228289-55228289	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - Missense
c.989C>T; p.S330L; 18:55261467-55261467	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.1465C>T; p.P489S; 18:55234569-55234569	skin	malignant_melanoma	Substitution - Missense
c.1864C>T; p.R622*; 18:55228850-55228850	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Nonsense
c.943G>A; p.A315T; 18:55261513-55261513	skin	malignant_melanoma	Substitution - Missense
c.1567C>G; p.L523V; 18:55232591-55232591	breast	carcinoma	Substitution - Missense
c.293C>T; p.S98F; 18:55461030-55461030	skin	malignant_melanoma	Substitution - Missense
c.943G>A; p.A315T; 18:55261513-55261513	skin	malignant_melanoma	Substitution - Missense
c.1743C>T; p.N581N; 18:55228971-55228971	breast	carcinoma	Substitution - coding silent
c.975G>A; p.G325G; 18:55261481-55261481	skin	malignant_melanoma	Substitution - coding silent
c.1054C>T; p.P352S; 18:55259964-55259964	skin; upper_leg	malignant_melanoma	Substitution - Missense
c.936C>T; p.S312S; 18:55261520-55261520	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.936C>T; p.S312S; 18:55261520-55261520	breast	carcinoma	Substitution - coding silent
c.1603G>C; p.D535H; 18:55232555-55232555	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.1249G>A; p.D417N; 18:55254598-55254598	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Missense
c.1249G>A; p.D417N; 18:55254598-55254598	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Missense
c.179G>T; p.G60V; 18:55464104-55464104	skin; extremity	malignant_melanoma	Substitution - Missense
c.1761C>T; p.L587L; 18:55228953-55228953	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - coding silent
c.998C>A; p.S333Y; 18:55260020-55260020	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.1100G>A; p.G367E; 18:55257361-55257361	skin	malignant_melanoma	Substitution - Missense
c.1697G>T; p.R566M; 18:55229017-55229017	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.1765C>T; p.R589C; 18:55228949-55228949	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.1972G>T; p.G658*; 18:55228257-55228257	ovary	carcinoma; serous_carcinoma	Substitution - Nonsense
c.1078G>T; p.A360S; 18:55257383-55257383	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.1141T>C; p.S381P; 18:55257320-55257320	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.1001C>T; p.P334L; 18:55260017-55260017	skin	malignant_melanoma	Substitution - Missense
c.30A>G; p.L10L; 18:55587087-55587087	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.867C>T; p.N289N; 18:55269886-55269886	skin; leg	malignant_melanoma; superficial_spreading	Substitution - coding silent
c.1591G>T; p.D531Y; 18:55232567-55232567	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.1816A>T; p.I606F; 18:55228898-55228898	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.937G>A; p.G313R; 18:55261519-55261519	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.912_913insC; p.S305fs*6; 18:55269840-55269841	central_nervous_system; brain	primitive_neuroectodermal_tumour-medulloblastoma	Insertion - Frameshift
c.650T>C; p.M217T; 18:55279556-55279556	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm; chronic_myelomonocytic_leukaemia	Substitution - Missense
c.656-1G>T; p.?; 18:55275753-55275753	liver	carcinoma; hepatocellular_carcinoma	Unknown
c.1862T>A; p.V621D; 18:55228852-55228852	haematopoietic_and_lymphoid_tissue; spleen	lymphoid_neoplasm; marginal_zone_lymphoma	Substitution - Missense
c.648C>T; p.F216F; 18:55279558-55279558	skin	malignant_melanoma	Substitution - coding silent
c.844delA; p.T282fs*25; 18:55269909-55269909	central_nervous_system; midbrain	glioma; oligoastrocytoma_Grade_III	Deletion - Frameshift
c.217G>A; p.D73N; 18:55461106-55461106	skin	malignant_melanoma	Substitution - Missense
c.684C>G; p.S228R; 18:55275724-55275724	skin	malignant_melanoma	Substitution - Missense
c.1829C>T; p.A610V; 18:55228885-55228885	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.1819C>T; p.L607F; 18:55228895-55228895	skin; face	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.1925C>T; p.S642F; 18:55228304-55228304	skin; head_neck	malignant_melanoma; superficial_spreading	Substitution - Missense
c.1720C>T; p.R574C; 18:55228994-55228994	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.421C>T; p.P141S; 18:55350952-55350952	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm; myelodysplastic_syndrome	Substitution - Missense
c.1940delC; p.P647fs*>21; 18:55228289-55228289	oesophagus	carcinoma; adenocarcinoma	Deletion - Frameshift
c.1520C>T; p.S507F; 18:55232638-55232638	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm; myelodysplastic_syndrome	Substitution - Missense
c.1940delC; p.P647fs*>21; 18:55228289-55228289	large_intestine; colon	carcinoma; adenocarcinoma	Deletion - Frameshift
c.153A>C; p.E51D; 18:55464130-55464130	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.1942C>T; p.L648F; 18:55228287-55228287	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.319G>A; p.G107S; 18:55403504-55403504	skin	malignant_melanoma	Substitution - Missense
c.1733G>T; p.R578L; 18:55228981-55228981	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.1608C>T; p.D536D; 18:55232550-55232550	pancreas	carcinoma	Substitution - coding silent
c.1042C>T; p.P348S; 18:55259976-55259976	skin	malignant_melanoma	Substitution - Missense
c.1258G>A; p.G420R; 18:55254589-55254589	skin	malignant_melanoma	Substitution - Missense
c.1530C>T; p.S510S; 18:55232628-55232628	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.1456G>T; p.D486Y; 18:55234578-55234578	breast	carcinoma	Substitution - Missense
c.1632T>A; p.I544I; 18:55232526-55232526	lung	carcinoma; adenocarcinoma	Substitution - coding silent
c.897T>A; p.P299P; 18:55269856-55269856	liver	carcinoma; hepatocellular_carcinoma	Substitution - coding silent
c.897T>A; p.P299P; 18:55269856-55269856	liver	carcinoma	Substitution - coding silent
c.1868-1G>A; p.?; 18:55228362-55228362	skin	malignant_melanoma	Unknown
c.953C>T; p.S318F; 18:55261503-55261503	skin	malignant_melanoma	Substitution - Missense
c.151G>T; p.E51*; 18:55464132-55464132	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Nonsense
c.1059A>G; p.P353P; 18:55259959-55259959	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.327C>T; p.Y109Y; 18:55403496-55403496	pancreas	carcinoma	Substitution - coding silent
c.1978G>A; p.A660T; 18:55228251-55228251	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.781G>A; p.E261K; 18:55275627-55275627	skin	malignant_melanoma	Substitution - Missense
c.1635T>G; p.T545T; 18:55232523-55232523	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.521G>A; p.R174Q; 18:55350387-55350387	skin	malignant_melanoma	Substitution - Missense
c.9C>A; p.H3Q; 18:55587108-55587108	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm; myelodysplastic_syndrome	Substitution - Missense
c.552C>T; p.V184V; 18:55279654-55279654	skin	malignant_melanoma	Substitution - coding silent
c.1269A>G; p.G423G; 18:55254578-55254578	pancreas	carcinoma	Substitution - coding silent
c.36G>A; p.T12T; 18:55587081-55587081	skin	malignant_melanoma	Substitution - coding silent
c.1855C>T; p.Q619*; 18:55228859-55228859	central_nervous_system; brain	primitive_neuroectodermal_tumour-medulloblastoma	Substitution - Nonsense
c.530C>A; p.P177H; 18:55350378-55350378	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.1637+6G>C; p.?; 18:55232515-55232515	breast	carcinoma; basal_(triple-negative)_carcinoma	Unknown
c.1025C>T; p.S342L; 18:55259993-55259993	skin	malignant_melanoma	Substitution - Missense
c.1458C>A; p.D486E; 18:55234576-55234576	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.1275T>C; p.S425S; 18:55254572-55254572	breast	carcinoma	Substitution - coding silent
c.1954G>A; p.G652S; 18:55228275-55228275	prostate	carcinoma	Substitution - Missense
c.1983G>A; p.S661S; 18:55228246-55228246	skin	malignant_melanoma	Substitution - coding silent
c.525A>C; p.K175N; 18:55350383-55350383	breast	carcinoma	Substitution - Missense
c.1484G>A; p.R495K; 18:55234550-55234550	prostate	carcinoma; adenocarcinoma	Substitution - Missense
c.651G>A; p.M217I; 18:55279555-55279555	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.658G>A; p.G220S; 18:55275750-55275750	skin	malignant_melanoma	Substitution - Missense
c.1266T>C; p.I422I; 18:55254581-55254581	kidney	carcinoma; papillary_renal_cell_carcinoma	Substitution - coding silent
c.726G>T; p.L242F; 18:55275682-55275682	lung; right_upper_lobe	carcinoma; adenocarcinoma	Substitution - Missense
c.135T>C; p.F45F; 18:55585290-55585290	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.510_513delAAAG; p.K172fs*61; 18:55350395-55350398	central_nervous_system; cerebellum	primitive_neuroectodermal_tumour-medulloblastoma; SHH_subtype	Deletion - Frameshift
c.532C>T; p.P178S; 18:55350376-55350376	skin	malignant_melanoma	Substitution - Missense
c.510_513delAAAG; p.K172fs*61; 18:55350395-55350398	central_nervous_system; brain	primitive_neuroectodermal_tumour-medulloblastoma; medullomyoblastoma	Deletion - Frameshift
c.958A>G; p.T320A; 18:55261498-55261498	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm; acute_myeloid_leukaemia	Substitution - Missense
c.1602A>G; p.L534L; 18:55232556-55232556	liver	carcinoma	Substitution - coding silent
c.941C>T; p.A314V; 18:55261515-55261515	breast	carcinoma	Substitution - Missense
c.1159G>A; p.E387K; 18:55254688-55254688	skin	malignant_melanoma	Substitution - Missense
c.1637+2T>A; p.?; 18:55232519-55232519	stomach	carcinoma; adenocarcinoma	Unknown
c.1495C>T; p.P499S; 18:55232663-55232663	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.1632T>G; p.I544M; 18:55232526-55232526	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.529C>T; p.P177S; 18:55350379-55350379	skin	malignant_melanoma	Substitution - Missense
c.529C>T; p.P177S; 18:55350379-55350379	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.1682G>T; p.R561L; 18:55229032-55229032	prostate	carcinoma; adenocarcinoma	Substitution - Missense
c.529C>T; p.P177S; 18:55350379-55350379	skin	malignant_melanoma	Substitution - Missense
c.1147C>T; p.Q383*; 18:55254700-55254700	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm; myelodysplastic_syndrome	Substitution - Nonsense
c.1126G>A; p.E376K; 18:55257335-55257335	skin	malignant_melanoma	Substitution - Missense
c.1836C>G; p.A612A; 18:55228878-55228878	bone	Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour	Substitution - coding silent
c.1201C>T; p.R401W; 18:55254646-55254646	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.899C>T; p.A300V; 18:55269854-55269854	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.611C>T; p.S204F; 18:55279595-55279595	skin	malignant_melanoma	Substitution - Missense
c.1835C>A; p.A612D; 18:55228879-55228879	liver	carcinoma; hepatocellular_carcinoma	Substitution - Missense
c.1776G>T; p.Q592H; 18:55228938-55228938	lung; right_upper_lobe	carcinoma; adenocarcinoma	Substitution - Missense
c.830T>G; p.L277R; 18:55269923-55269923	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.1812C>T; p.L604L; 18:55228902-55228902	skin	malignant_melanoma	Substitution - coding silent
c.1717G>A; p.E573K; 18:55228997-55228997	central_nervous_system; brain	glioma; astrocytoma_Grade_III	Substitution - Missense
c.1717G>A; p.E573K; 18:55228997-55228997	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm; polycythaemia_vera	Substitution - Missense
c.1198C>A; p.L400I; 18:55254649-55254649	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.1517T>A; p.V506D; 18:55232641-55232641	haematopoietic_and_lymphoid_tissue; tonsil	lymphoid_neoplasm; diffuse_large_B_cell_lymphoma	Substitution - Missense
c.1219C>T; p.P407S; 18:55254628-55254628	skin	malignant_melanoma	Substitution - Missense
c.469C>T; p.R157*; 18:55350904-55350904	central_nervous_system; brain	primitive_neuroectodermal_tumour-medulloblastoma	Substitution - Nonsense
c.1112C>T; p.S371L; 18:55257349-55257349	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.692G>A; p.S231N; 18:55275716-55275716	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm; myelodysplastic_syndrome	Substitution - Missense
c.1193A>G; p.H398R; 18:55254654-55254654	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.1418C>A; p.P473Q; 18:55234616-55234616	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.1578G>A; p.T526T; 18:55232580-55232580	breast	carcinoma	Substitution - coding silent
c.1694G>A; p.R565Q; 18:55229020-55229020	lung; right_upper_lobe	carcinoma; adenocarcinoma	Substitution - Missense
c.1726C>T; p.R576W; 18:55228988-55228988	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm; myelofibrosis	Substitution - Missense
c.1578G>A; p.T526T; 18:55232580-55232580	skin	malignant_melanoma	Substitution - coding silent
c.1544C>T; p.S515F; 18:55232614-55232614	skin	malignant_melanoma	Substitution - Missense
c.277C>T; p.P93S; 18:55461046-55461046	oesophagus; middle_third	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.1717G>T; p.E573*; 18:55228997-55228997	lung	carcinoma; adenocarcinoma	Substitution - Nonsense
c.1165C>T; p.R389C; 18:55254682-55254682	skin	malignant_melanoma	Substitution - Missense
c.1714C>T; p.R572*; 18:55229000-55229000	central_nervous_system; brain	primitive_neuroectodermal_tumour-medulloblastoma	Substitution - Nonsense
c.1417C>T; p.P473S; 18:55234617-55234617	skin	malignant_melanoma	Substitution - Missense
c.1714C>T; p.R572*; 18:55229000-55229000	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Nonsense
c.1278T>A; p.H426Q; 18:55254569-55254569	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense

The somatic mutations from COSMIC database