Entrez Gene

Basic Information
Gene ID	57504
Name	MTA3

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.496G>C; p.E166Q; 2:42644241-42644241	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.1421A>C; p.Y474S; 2:42708992-42708992	stomach	carcinoma; diffuse_adenocarcinoma	Substitution - Missense
c.1130G>A; p.R377K; 2:42704298-42704298	breast	carcinoma	Substitution - Missense
c.729A>C; p.R243S; 2:42682427-42682427	breast	carcinoma	Substitution - Missense
c.1113G>A; p.Q371Q; 2:42704281-42704281	oesophagus; lower_third	carcinoma; adenocarcinoma	Substitution - coding silent
c.108C>T; p.G36G; 2:42579118-42579118	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.816A>T; p.S272S; 2:42682514-42682514	lung; right_upper_lobe	carcinoma; adenocarcinoma	Substitution - coding silent
c.779G>T; p.G260V; 2:42682477-42682477	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.1202G>A; p.R401K; 2:42707954-42707954	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.1039C>T; p.P347S; 2:42704207-42704207	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.871A>G; p.N291D; 2:42682569-42682569	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.409G>A; p.D137N; 2:42644154-42644154	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.405C>G; p.V135V; 2:42644150-42644150	lung	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.1098C>G; p.T366T; 2:42704266-42704266	autonomic_ganglia	neuroblastoma	Substitution - coding silent
c.1215T>G; p.I405M; 2:42707967-42707967	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.994A>T; p.S332C; 2:42697803-42697803	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - Missense
c.53C>A; p.S18Y; 2:42570461-42570461	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.970C>T; p.R324C; 2:42697779-42697779	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.557delG; p.S186fs*12; 2:42656257-42656257	lung	carcinoma; adenocarcinoma	Deletion - Frameshift
c.373G>C; p.D125H; 2:42640228-42640228	upper_aerodigestive_tract; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.1052C>T; p.S351F; 2:42704220-42704220	lung; right_upper_lobe	carcinoma; adenocarcinoma	Substitution - Missense
c.1052C>T; p.S351F; 2:42704220-42704220	skin	malignant_melanoma	Substitution - Missense
c.1156C>T; p.Q386*; 2:42707908-42707908	lung	carcinoma; adenocarcinoma	Substitution - Nonsense
c.709G>A; p.A237T; 2:42682407-42682407	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.1407C>T; p.F469F; 2:42708978-42708978	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.571C>T; p.R191*; 2:42656271-42656271	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Nonsense
c.571C>T; p.R191*; 2:42656271-42656271	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Nonsense
c.143G>A; p.R48Q; 2:42579153-42579153	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.922G>C; p.E308Q; 2:42695795-42695795	ovary	carcinoma; serous_carcinoma	Substitution - Missense
c.735C>T; p.S245S; 2:42682433-42682433	lung; right_lower_lobe	carcinoma; adenocarcinoma	Substitution - coding silent
c.393C>G; p.F131L; 2:42644138-42644138	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.461C>G; p.P154R; 2:42644206-42644206	upper_aerodigestive_tract; mouth	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.1300G>C; p.E434Q; 2:42708052-42708052	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.579T>C; p.I193I; 2:42656279-42656279	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - coding silent
c.1373C>A; p.P458Q; 2:42708944-42708944	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm; acute_myeloid_leukaemia	Substitution - Missense
c.1623T>A; p.P541P; 2:42722899-42722899	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm; acute_myeloid_leukaemia	Substitution - coding silent
c.1345G>A; p.G449R; 2:42708916-42708916	skin	malignant_melanoma	Substitution - Missense
c.1355T>C; p.V452A; 2:42708926-42708926	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm; acute_myeloid_leukaemia	Substitution - Missense
c.552A>T; p.P184P; 2:42656252-42656252	lung	carcinoma; adenocarcinoma	Substitution - coding silent
c.1374A>G; p.P458P; 2:42708945-42708945	lung	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.1083T>C; p.N361N; 2:42704251-42704251	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - coding silent
c.1106A>T; p.Q369L; 2:42704274-42704274	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.1380T>G; p.S460S; 2:42708951-42708951	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm; acute_myeloid_leukaemia	Substitution - coding silent
c.851delA; p.K285fs*19; 2:42682549-42682549	large_intestine; caecum	carcinoma; adenocarcinoma	Deletion - Frameshift
c.1456A>G; p.T486A; 2:42709027-42709027	oesophagus; lower_third	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.618C>A; p.F206L; 2:42659778-42659778	kidney	carcinoma; papillary_renal_cell_carcinoma	Substitution - Missense
c.752C>A; p.A251D; 2:42682450-42682450	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.1465C>T; p.L489L; 2:42709036-42709036	skin	malignant_melanoma	Substitution - coding silent
c.1441C>G; p.Q481E; 2:42709012-42709012	oesophagus; lower_third	carcinoma; adenocarcinoma	Substitution - Missense
c.417A>G; p.S139S; 2:42644162-42644162	lung	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.1457C>G; p.T486S; 2:42709028-42709028	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.235A>G; p.T79A; 2:42609502-42609502	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.567G>T; p.T189T; 2:42656267-42656267	lung	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.882_891+4delGCAAGATTTTGTAA; p.?; 2:42682580-42682593	stomach	carcinoma; intestinal_adenocarcinoma	Unknown
c.273C>G; p.L91L; 2:42609540-42609540	lung	carcinoma; adenocarcinoma	Substitution - coding silent
c.1468C>T; p.R490W; 2:42709039-42709039	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.918_919insA; p.I307fs*2; 2:42695791-42695792	large_intestine; rectum	carcinoma; adenocarcinoma	Insertion - Frameshift
c.1275G>T; p.E425D; 2:42708027-42708027	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.1690A>G; p.T564A; 2:42722966-42722966	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.1525+8G>T; p.?; 2:42709104-42709104	ovary	carcinoma; serous_carcinoma	Unknown
c.477C>T; p.D159D; 2:42644222-42644222	breast	carcinoma	Substitution - coding silent
c.55A>G; p.S19G; 2:42570463-42570463	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - Missense

The somatic mutations from COSMIC database