Entrez Gene

Basic Information
Gene ID	55810
Name	FOXJ2

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.242C>T; p.S81F; 12:8040074-8040074	skin	malignant_melanoma	Substitution - Missense
c.1088T>C; p.M363T; 12:8048152-8048152	oesophagus	carcinoma; adenocarcinoma	Substitution - Missense
c.838G>A; p.D280N; 12:8047902-8047902	autonomic_ganglia	neuroblastoma	Substitution - Missense
c.838G>A; p.D280N; 12:8047902-8047902	breast	carcinoma	Substitution - Missense
c.667C>T; p.R223*; 12:8044808-8044808	lung	carcinoma; squamous_cell_carcinoma	Substitution - Nonsense
c.751C>T; p.L251L; 12:8044892-8044892	skin	malignant_melanoma	Substitution - coding silent
c.667C>T; p.R223*; 12:8044808-8044808	skin; scalp	carcinoma; squamous_cell_carcinoma	Substitution - Nonsense
c.1163A>T; p.Q388L; 12:8048227-8048227	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.338C>T; p.S113L; 12:8042662-8042662	skin; neck	malignant_melanoma	Substitution - Missense
c.1270A>G; p.S424G; 12:8048741-8048741	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Missense
c.1270A>G; p.S424G; 12:8048741-8048741	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Missense
c.64G>A; p.A22T; 12:8039896-8039896	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Missense
c.1309G>C; p.E437Q; 12:8048780-8048780	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.1309G>C; p.E437Q; 12:8048780-8048780	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.920C>T; p.P307L; 12:8047984-8047984	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.1606A>C; p.T536P; 12:8050590-8050590	breast	carcinoma	Substitution - Missense
c.723C>A; p.F241L; 12:8044864-8044864	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.1317A>G; p.S439S; 12:8048788-8048788	liver	carcinoma	Substitution - coding silent
c.723C>A; p.F241L; 12:8044864-8044864	breast	carcinoma	Substitution - Missense
c.1317A>G; p.S439S; 12:8048788-8048788	liver	carcinoma	Substitution - coding silent
c.1289G>A; p.R430Q; 12:8048760-8048760	skin	malignant_melanoma	Substitution - Missense
c.1210A>G; p.N404D; 12:8048274-8048274	stomach	carcinoma; intestinal_adenocarcinoma	Substitution - Missense
c.425T>G; p.I142S; 12:8043717-8043717	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - Missense
c.425T>G; p.I142S; 12:8043717-8043717	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - Missense
c.425T>G; p.I142S; 12:8043717-8043717	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - Missense
c.836G>T; p.G279V; 12:8047900-8047900	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.425T>G; p.I142S; 12:8043717-8043717	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - Missense
c.425T>G; p.I142S; 12:8043717-8043717	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - Missense
c.425T>G; p.I142S; 12:8043717-8043717	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - Missense
c.75G>T; p.E25D; 12:8039907-8039907	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.115A>G; p.S39G; 12:8039947-8039947	bone	Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour	Substitution - Missense
c.1564C>T; p.P522S; 12:8050548-8050548	skin	malignant_melanoma	Substitution - Missense
c.852G>A; p.S284S; 12:8047916-8047916	central_nervous_system; brain	glioma	Substitution - coding silent
c.1419C>T; p.F473F; 12:8049453-8049453	skin	malignant_melanoma	Substitution - coding silent
c.1419C>T; p.F473F; 12:8049453-8049453	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.767G>A; p.R256H; 12:8044908-8044908	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.1080C>T; p.P360P; 12:8048144-8048144	breast	carcinoma	Substitution - coding silent
c.835G>A; p.G279R; 12:8047899-8047899	ovary	carcinoma; serous_carcinoma	Substitution - Missense
c.1090G>A; p.A364T; 12:8048154-8048154	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.835G>A; p.G279R; 12:8047899-8047899	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.1004C>A; p.P335Q; 12:8048068-8048068	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.164G>A; p.S55N; 12:8039996-8039996	stomach	carcinoma; intestinal_adenocarcinoma	Substitution - Missense
c.162G>C; p.L54L; 12:8039994-8039994	lung	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.765C>T; p.F255F; 12:8044906-8044906	breast	carcinoma	Substitution - coding silent
c.720A>C; p.K240N; 12:8044861-8044861	skin	malignant_melanoma	Substitution - Missense
c.1631G>A; p.R544H; 12:8050615-8050615	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.258G>C; p.K86N; 12:8040090-8040090	upper_aerodigestive_tract; mouth	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.258G>C; p.K86N; 12:8040090-8040090	upper_aerodigestive_tract; mouth	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.1058G>A; p.G353E; 12:8048122-8048122	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.649G>A; p.A217T; 12:8044790-8044790	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.1481G>A; p.R494H; 12:8049515-8049515	oesophagus	carcinoma	Substitution - Missense
c.758G>C; p.W253S; 12:8044899-8044899	prostate	carcinoma; adenocarcinoma	Substitution - Missense
c.772C>A; p.L258I; 12:8044913-8044913	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.898_900delCAG; p.Q306delQ; 12:8047962-8047964	endometrium	carcinoma; endometrioid_carcinoma	Deletion - In frame
c.520C>T; p.R174W; 12:8043993-8043993	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.1003C>G; p.P335A; 12:8048067-8048067	ovary	carcinoma; serous_carcinoma	Substitution - Missense
c.687C>G; p.P229P; 12:8044828-8044828	liver	carcinoma; hepatocellular_carcinoma	Substitution - coding silent
c.687C>G; p.P229P; 12:8044828-8044828	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.357T>C; p.S119S; 12:8042681-8042681	thyroid	other; neoplasm	Substitution - coding silent
c.832C>T; p.L278L; 12:8047896-8047896	skin	malignant_melanoma	Substitution - coding silent
c.1566C>T; p.P522P; 12:8050550-8050550	lung	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.345G>A; p.R115R; 12:8042669-8042669	skin	malignant_melanoma	Substitution - coding silent
c.692C>A; p.P231H; 12:8044833-8044833	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.1294A>G; p.N432D; 12:8048765-8048765	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.1415A>C; p.H472P; 12:8049449-8049449	breast	carcinoma	Substitution - Missense
c.870T>C; p.Y290Y; 12:8047934-8047934	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.192C>T; p.D64D; 12:8040024-8040024	skin	malignant_melanoma	Substitution - coding silent
c.713A>G; p.D238G; 12:8044854-8044854	haematopoietic_and_lymphoid_tissue	lymphoid_neoplasm; mantle_cell_lymphoma	Substitution - Missense
c.1338G>A; p.E446E; 12:8049372-8049372	lung	carcinoma; adenocarcinoma	Substitution - coding silent
c.1195G>T; p.G399C; 12:8048259-8048259	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.1195G>T; p.G399C; 12:8048259-8048259	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.1195G>T; p.G399C; 12:8048259-8048259	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.8C>T; p.S3F; 12:8039840-8039840	lung; right_lower_lobe	carcinoma; adenocarcinoma	Substitution - Missense
c.91T>C; p.S31P; 12:8039923-8039923	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.549C>T; p.A183A; 12:8044022-8044022	skin	malignant_melanoma	Substitution - coding silent
c.1288C>T; p.R430W; 12:8048759-8048759	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.343C>T; p.R115W; 12:8042667-8042667	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.1608C>T; p.T536T; 12:8050592-8050592	liver	carcinoma	Substitution - coding silent
c.1352C>T; p.A451V; 12:8049386-8049386	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.1608C>T; p.T536T; 12:8050592-8050592	liver	carcinoma	Substitution - coding silent
c.884C>A; p.P295Q; 12:8047948-8047948	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.1696G>C; p.D566H; 12:8052821-8052821	urinary_tract; bladder	carcinoma	Substitution - Missense
c.449G>A; p.R150Q; 12:8043741-8043741	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.679G>T; p.E227*; 12:8044820-8044820	lung	carcinoma; squamous_cell_carcinoma	Substitution - Nonsense
c.1636+2T>C; p.?; 12:8050622-8050622	large_intestine; colon	carcinoma; adenocarcinoma	Unknown
c.824C>A; p.S275Y; 12:8047888-8047888	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.1316C>G; p.S439*; 12:8048787-8048787	liver	carcinoma	Substitution - Nonsense
c.1316C>G; p.S439*; 12:8048787-8048787	liver	carcinoma	Substitution - Nonsense
c.518C>T; p.P173L; 12:8043991-8043991	skin; face	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.1685A>T; p.E562V; 12:8052810-8052810	ovary	carcinoma; serous_carcinoma	Substitution - Missense
c.1632C>T; p.R544R; 12:8050616-8050616	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.482C>T; p.S161F; 12:8043955-8043955	skin	malignant_melanoma	Substitution - Missense
c.1358A>G; p.Q453R; 12:8049392-8049392	lung	carcinoma; small_cell_carcinoma	Substitution - Missense
c.629C>T; p.S210F; 12:8044770-8044770	skin	malignant_melanoma	Substitution - Missense
c.1107G>A; p.P369P; 12:8048171-8048171	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.1613A>G; p.D538G; 12:8050597-8050597	breast	carcinoma	Substitution - Missense
c.413C>T; p.S138F; 12:8043705-8043705	skin	malignant_melanoma	Substitution - Missense
c.1145C>T; p.P382L; 12:8048209-8048209	skin	malignant_melanoma	Substitution - Missense
c.179_186delCAGTGCAC; p.V61fs*35; 12:8040011-8040018	ovary	carcinoma; serous_carcinoma	Deletion - Frameshift
c.344G>A; p.R115Q; 12:8042668-8042668	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.428A>G; p.D143G; 12:8043720-8043720	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.1537+3A>C; p.?; 12:8049574-8049574	thyroid	carcinoma	Unknown
c.1057G>A; p.G353R; 12:8048121-8048121	bone	Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour	Substitution - Missense
c.1475C>T; p.P492L; 12:8049509-8049509	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.1630C>T; p.R544C; 12:8050614-8050614	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.572C>T; p.P191L; 12:8044045-8044045	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.1704C>T; p.F568F; 12:8052829-8052829	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.1704C>T; p.F568F; 12:8052829-8052829	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.1346G>A; p.R449Q; 12:8049380-8049380	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.1346G>A; p.R449Q; 12:8049380-8049380	liver	carcinoma	Substitution - Missense
c.1346G>A; p.R449Q; 12:8049380-8049380	liver	carcinoma	Substitution - Missense
c.1042delG; p.G349fs*14; 12:8048106-8048106	large_intestine; colon	carcinoma; adenocarcinoma	Deletion - Frameshift
c.169G>C; p.D57H; 12:8040001-8040001	upper_aerodigestive_tract; mouth	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.169G>C; p.D57H; 12:8040001-8040001	upper_aerodigestive_tract; mouth	carcinoma; squamous_cell_carcinoma	Substitution - Missense

The somatic mutations from COSMIC database