Entrez Gene

Basic Information
Gene ID	3162
Name	HMOX1

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.41C>A; p.S14*; 22:35383123-35383123	lung	carcinoma; adenocarcinoma	Substitution - Nonsense
c.785G>A; p.R262H; 22:35393516-35393516	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.275A>G; p.D92G; 22:35386815-35386815	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.580G>A; p.A194T; 22:35387120-35387120	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Missense
c.275A>G; p.D92G; 22:35386815-35386815	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.580G>A; p.A194T; 22:35387120-35387120	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Missense
c.222C>T; p.F74F; 22:35386762-35386762	skin	malignant_melanoma	Substitution - coding silent
c.222C>T; p.F74F; 22:35386762-35386762	prostate	carcinoma	Substitution - coding silent
c.453C>A; p.A151A; 22:35386993-35386993	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.597G>A; p.V199V; 22:35387137-35387137	lung	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.379G>A; p.E127K; 22:35386919-35386919	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.553C>A; p.R185S; 22:35387093-35387093	prostate	carcinoma; adenocarcinoma	Substitution - Missense
c.367C>T; p.R123C; 22:35386907-35386907	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.367C>T; p.R123C; 22:35386907-35386907	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.804C>T; p.L268L; 22:35393535-35393535	skin	malignant_melanoma	Substitution - coding silent
c.617C>T; p.A206V; 22:35387157-35387157	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.486G>A; p.E162E; 22:35387026-35387026	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.606G>T; p.E202D; 22:35387146-35387146	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - Missense
c.791A>T; p.Q264L; 22:35393522-35393522	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.797C>T; p.P266L; 22:35393528-35393528	central_nervous_system; brain	glioma; oligodendroglioma_Grade_III	Substitution - Missense
c.155C>A; p.A52D; 22:35386695-35386695	skin	malignant_melanoma	Substitution - Missense
c.342T>C; p.Y114Y; 22:35386882-35386882	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.765G>A; p.G255G; 22:35393496-35393496	breast	carcinoma	Substitution - coding silent
c.469C>T; p.L157L; 22:35387009-35387009	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.54G>T; p.K18N; 22:35383136-35383136	kidney	carcinoma; papillary_renal_cell_carcinoma	Substitution - Missense
c.487G>C; p.G163R; 22:35387027-35387027	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.291C>T; p.Y97Y; 22:35386831-35386831	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.553C>T; p.R185C; 22:35387093-35387093	skin	malignant_melanoma	Substitution - Missense
c.427delG; p.G144fs*43; 22:35386967-35386967	large_intestine; caecum	carcinoma; adenocarcinoma	Deletion - Frameshift
c.227C>A; p.P76H; 22:35386767-35386767	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.784C>A; p.R262S; 22:35393515-35393515	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.522T>A; p.S174R; 22:35387062-35387062	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.442A>G; p.K148E; 22:35386982-35386982	liver	carcinoma	Substitution - Missense
c.442A>G; p.K148E; 22:35386982-35386982	liver	carcinoma	Substitution - Missense
c.78C>T; p.T26T; 22:35383160-35383160	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.299G>A; p.R100H; 22:35386839-35386839	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.646G>C; p.E216Q; 22:35389873-35389873	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - Missense
c.415G>T; p.G139C; 22:35386955-35386955	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.709C>T; p.R237C; 22:35389936-35389936	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.171C>T; p.I57I; 22:35386711-35386711	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.180C>T; p.A60A; 22:35386720-35386720	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.180C>T; p.A60A; 22:35386720-35386720	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.159C>T; p.S53S; 22:35386699-35386699	lung	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.180C>T; p.A60A; 22:35386720-35386720	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.294G>A; p.G98G; 22:35386834-35386834	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.806G>A; p.R269Q; 22:35393537-35393537	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.48C>T; p.A16A; 22:35383130-35383130	breast	carcinoma	Substitution - coding silent
c.276C>T; p.D92D; 22:35386816-35386816	ovary	carcinoma; serous_carcinoma	Substitution - coding silent
c.518C>T; p.A173V; 22:35387058-35387058	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.183G>A; p.L61L; 22:35386723-35386723	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.761G>C; p.R254T; 22:35393492-35393492	urinary_tract; bladder	carcinoma	Substitution - Missense
c.761G>C; p.R254T; 22:35393492-35393492	urinary_tract; bladder	carcinoma; transitional_cell_carcinoma	Substitution - Missense
c.196G>C; p.E66Q; 22:35386736-35386736	cervix	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.131G>A; p.R44Q; 22:35383213-35383213	oesophagus	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.767A>G; p.K256R; 22:35393498-35393498	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.253C>T; p.R85C; 22:35386793-35386793	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.839C>A; p.T280K; 22:35393570-35393570	soft_tissue; fibrous_tissue_and_uncertain_o	gastrointestinal_stromal_tumour	Substitution - Missense
c.186G>T; p.E62D; 22:35386726-35386726	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.665C>A; p.T222N; 22:35389892-35389892	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - Missense
c.47C>T; p.A16V; 22:35383129-35383129	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.636G>T; p.Q212H; 22:35387176-35387176	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - Missense
c.452C>T; p.A151V; 22:35386992-35386992	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense

The somatic mutations from COSMIC database