Entrez Gene

Basic Information
Gene ID	7593
Name	MZF1

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.58G>A; p.V20I; 19:58571332-58571332	kidney	carcinoma; papillary_renal_cell_carcinoma	Substitution - Missense
c.389G>A; p.R130Q; 19:58571001-58571001	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.1280T>C; p.L427P; 19:58562997-58562997	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.1013C>A; p.P338H; 19:58563264-58563264	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.945G>A; p.Q315Q; 19:58563332-58563332	skin	malignant_melanoma	Substitution - coding silent
c.118C>T; p.P40S; 19:58571272-58571272	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm; acute_myeloid_leukaemia	Substitution - Missense
c.778G>A; p.A260T; 19:58563499-58563499	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.82G>C; p.E28Q; 19:58571308-58571308	urinary_tract; bladder	carcinoma	Substitution - Missense
c.118C>T; p.P40S; 19:58571272-58571272	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm; acute_myeloid_leukaemia	Substitution - Missense
c.337G>A; p.E113K; 19:58571053-58571053	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.1747A>G; p.T583A; 19:58562530-58562530	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - Missense
c.1511A>T; p.Q504L; 19:58562766-58562766	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.1991A>G; p.Q664R; 19:58562286-58562286	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.2156A>G; p.H719R; 19:58562121-58562121	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.866C>G; p.S289C; 19:58563411-58563411	oesophagus; middle_third	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.1862G>A; p.G621D; 19:58562415-58562415	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.54G>A; p.G18G; 19:58571336-58571336	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.117C>T; p.G39G; 19:58571273-58571273	kidney	carcinoma; papillary_renal_cell_carcinoma	Substitution - coding silent
c.1723G>A; p.G575S; 19:58562554-58562554	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.592T>G; p.S198A; 19:58569575-58569575	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.1771C>T; p.H591Y; 19:58562506-58562506	lung; right_upper_lobe	carcinoma; adenocarcinoma	Substitution - Missense
c.1878C>A; p.H626Q; 19:58562399-58562399	kidney	carcinoma; papillary_renal_cell_carcinoma	Substitution - Missense
c.2048G>T; p.C683F; 19:58562229-58562229	oesophagus; lower_third	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.11C>T; p.A4V; 19:58571379-58571379	pancreas	carcinoma	Substitution - Missense
c.810A>C; p.P270P; 19:58563467-58563467	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.1171C>T; p.R391C; 19:58563106-58563106	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.2144G>A; p.G715D; 19:58562133-58562133	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.1035C>T; p.R345R; 19:58563242-58563242	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - coding silent
c.1848G>A; p.Q616Q; 19:58562429-58562429	liver	carcinoma	Substitution - coding silent
c.1611C>T; p.G537G; 19:58562666-58562666	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.490G>C; p.E164Q; 19:58570434-58570434	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Missense
c.490G>C; p.E164Q; 19:58570434-58570434	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Missense
c.991A>G; p.I331V; 19:58563286-58563286	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.991A>G; p.I331V; 19:58563286-58563286	liver	carcinoma; hepatocellular_carcinoma	Substitution - Missense
c.687C>T; p.H229H; 19:58569362-58569362	lung	carcinoma; adenocarcinoma	Substitution - coding silent
c.1271G>A; p.S424N; 19:58563006-58563006	liver	carcinoma; hepatocellular_carcinoma	Substitution - Missense
c.580G>A; p.D194N; 19:58570344-58570344	stomach	carcinoma; diffuse_adenocarcinoma	Substitution - Missense
c.1864G>A; p.E622K; 19:58562413-58562413	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm; acute_myeloid_leukaemia	Substitution - Missense
c.721G>T; p.E241*; 19:58569328-58569328	skin	malignant_melanoma	Substitution - Nonsense
c.664G>T; p.V222L; 19:58569385-58569385	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.939T>C; p.S313S; 19:58563338-58563338	lung	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.169G>T; p.G57W; 19:58571221-58571221	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.427C>G; p.L143V; 19:58570497-58570497	breast	carcinoma; basal_(triple-negative)_carcinoma	Substitution - Missense
c.2058_2059delTG; p.C686fs*>49; 19:58562218-58562219	large_intestine; colon	carcinoma; adenocarcinoma	Deletion - Frameshift
c.140T>C; p.F47S; 19:58571250-58571250	kidney	carcinoma; papillary_renal_cell_carcinoma	Substitution - Missense
c.1215G>A; p.T405T; 19:58563062-58563062	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.1215G>A; p.T405T; 19:58563062-58563062	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.1476G>A; p.E492E; 19:58562801-58562801	liver	carcinoma	Substitution - coding silent
c.1476G>A; p.E492E; 19:58562801-58562801	liver	carcinoma	Substitution - coding silent
c.280G>A; p.G94S; 19:58571110-58571110	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.209G>A; p.R70H; 19:58571181-58571181	liver	carcinoma	Substitution - Missense
c.1492G>C; p.A498P; 19:58562785-58562785	oesophagus; lower_third	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.204G>C; p.L68L; 19:58571186-58571186	liver	carcinoma; hepatocellular_carcinoma	Substitution - coding silent
c.1831_1832ins12; p.L610_K611insSQRL; 19:58562445-58562446	large_intestine; colon	carcinoma; adenocarcinoma	Insertion - In frame
c.1831_1832ins12; p.L610_K611insSQRL; 19:58562445-58562446	breast	carcinoma	Insertion - In frame
c.870C>T; p.G290G; 19:58563407-58563407	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.1906C>T; p.Q636*; 19:58562371-58562371	haematopoietic_and_lymphoid_tissue	lymphoid_neoplasm; acute_lymphoblastic_leukaemia	Substitution - Nonsense
c.2035C>T; p.R679W; 19:58562242-58562242	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.1270A>G; p.S424G; 19:58563007-58563007	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.220C>T; p.R74C; 19:58571170-58571170	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.1850_1852delGGA; p.R617delR; 19:58562425-58562427	endometrium	carcinoma; endometrioid_carcinoma	Deletion - In frame
c.212A>G; p.Q71R; 19:58571178-58571178	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.121G>A; p.E41K; 19:58571269-58571269	urinary_tract; bladder	carcinoma	Substitution - Missense
c.121G>A; p.E41K; 19:58571269-58571269	urinary_tract; bladder	carcinoma; transitional_cell_carcinoma	Substitution - Missense
c.1716C>T; p.A572A; 19:58562561-58562561	urinary_tract; bladder	carcinoma	Substitution - coding silent
c.2018G>A; p.R673H; 19:58562259-58562259	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.282C>T; p.G94G; 19:58571108-58571108	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.741G>A; p.W247*; 19:58569308-58569308	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Nonsense
c.1564T>C; p.F522L; 19:58562713-58562713	breast	carcinoma; ductal_carcinoma	Substitution - Missense
c.2053G>A; p.E685K; 19:58562224-58562224	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.563_564delAG; p.E188fs*26; 19:58570360-58570361	large_intestine; colon	carcinoma; adenocarcinoma	Deletion - Frameshift
c.964C>A; p.P322T; 19:58563313-58563313	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.173C>T; p.P58L; 19:58571217-58571217	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.1968C>T; p.P656P; 19:58562309-58562309	lung	carcinoma; adenocarcinoma	Substitution - coding silent
c.323G>T; p.R108L; 19:58571067-58571067	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.323G>T; p.R108L; 19:58571067-58571067	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.2079G>A; p.R693R; 19:58562198-58562198	urinary_tract; bladder	carcinoma	Substitution - coding silent
c.727C>T; p.P243S; 19:58569322-58569322	skin	malignant_melanoma	Substitution - Missense
c.304G>A; p.A102T; 19:58571086-58571086	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.2137G>A; p.D713N; 19:58562140-58562140	lung; right_upper_lobe	carcinoma; adenocarcinoma	Substitution - Missense
c.1055T>G; p.V352G; 19:58563222-58563222	ovary	other; neoplasm	Substitution - Missense
c.1191G>C; p.S397S; 19:58563086-58563086	lung	carcinoma; adenocarcinoma	Substitution - coding silent
c.13G>A; p.V5M; 19:58571377-58571377	skin; hand	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.1614G>C; p.E538D; 19:58562663-58562663	pancreas	carcinoma	Substitution - Missense
c.1877A>G; p.H626R; 19:58562400-58562400	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.133C>A; p.L45M; 19:58571257-58571257	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.1250G>T; p.C417F; 19:58563027-58563027	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.1295G>T; p.R432I; 19:58562982-58562982	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.143G>A; p.R48Q; 19:58571247-58571247	upper_aerodigestive_tract; mouth	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.612C>T; p.T204T; 19:58569555-58569555	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.612C>T; p.T204T; 19:58569555-58569555	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.137G>A; p.R46H; 19:58571253-58571253	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.1237G>T; p.V413L; 19:58563040-58563040	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.2150G>A; p.R717H; 19:58562127-58562127	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.375G>A; p.E125E; 19:58571015-58571015	ovary	carcinoma; serous_carcinoma	Substitution - coding silent
c.1678C>T; p.R560W; 19:58562599-58562599	breast	carcinoma	Substitution - Missense
c.2032G>A; p.E678K; 19:58562245-58562245	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.1934G>A; p.R645H; 19:58562343-58562343	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.2186G>A; p.R729H; 19:58562091-58562091	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.377C>T; p.P126L; 19:58571013-58571013	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense

The somatic mutations from COSMIC database