Entrez Gene

Basic Information
Gene ID	3219
Name	HOXB9

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.672G>C; p.L224L; 17:48622981-48622981	breast	carcinoma	Substitution - coding silent
c.442C>A; p.L148M; 17:48625828-48625828	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.649G>A; p.E217K; 17:48623004-48623004	oesophagus	carcinoma	Substitution - Missense
c.504G>A; p.E168E; 17:48625766-48625766	lung; right_upper_lobe	carcinoma; adenocarcinoma	Substitution - coding silent
c.700C>T; p.Q234*; 17:48622953-48622953	skin	malignant_melanoma	Substitution - Nonsense
c.355G>A; p.E119K; 17:48625915-48625915	kidney	carcinoma; papillary_renal_cell_carcinoma	Substitution - Missense
c.644G>A; p.R215K; 17:48623009-48623009	liver	carcinoma; hepatocellular_carcinoma	Substitution - Missense
c.544G>A; p.A182T; 17:48623109-48623109	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.534C>G; p.N178K; 17:48623119-48623119	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.547C>T; p.R183C; 17:48623106-48623106	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.551C>G; p.S184C; 17:48623102-48623102	skin	malignant_melanoma	Substitution - Missense
c.440T>A; p.V147E; 17:48625830-48625830	prostate	carcinoma	Substitution - Missense
c.141C>G; p.F47L; 17:48626129-48626129	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Missense
c.342G>C; p.A114A; 17:48625928-48625928	lung	carcinoma; adenocarcinoma	Substitution - coding silent
c.413T>C; p.L138S; 17:48625857-48625857	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.334G>T; p.G112C; 17:48625936-48625936	lung; right_upper_lobe	carcinoma; adenocarcinoma	Substitution - Missense
c.706C>A; p.R236R; 17:48622947-48622947	lung; right_upper_lobe	carcinoma; adenocarcinoma	Substitution - coding silent
c.426G>T; p.A142A; 17:48625844-48625844	lung	carcinoma; adenocarcinoma	Substitution - coding silent
c.117G>A; p.P39P; 17:48626153-48626153	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.129G>C; p.E43D; 17:48626141-48626141	haematopoietic_and_lymphoid_tissue	lymphoid_neoplasm; plasma_cell_myeloma	Substitution - Missense
c.538C>T; p.L180L; 17:48623115-48623115	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.538C>T; p.L180L; 17:48623115-48623115	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.555C>T; p.S185S; 17:48623098-48623098	skin	malignant_melanoma	Substitution - coding silent
c.740A>G; p.Q247R; 17:48622913-48622913	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - Missense
c.477A>C; p.K159N; 17:48625793-48625793	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.518C>T; p.T173I; 17:48623135-48623135	adrenal_gland; adrenal_gland	adrenal_cortical_carcinoma; functioning	Substitution - Missense
c.455G>T; p.R152I; 17:48625815-48625815	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.92G>A; p.G31D; 17:48626178-48626178	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.94C>T; p.Q32*; 17:48626176-48626176	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Nonsense
c.636G>A; p.R212R; 17:48623017-48623017	skin	malignant_melanoma	Substitution - coding silent
c.604_606delAAG; p.K202delK; 17:48623047-48623049	large_intestine; caecum	carcinoma; adenocarcinoma	Deletion - In frame
c.11C>G; p.S4C; 17:48626259-48626259	breast	carcinoma	Substitution - Missense
c.31delT; p.Y11fs*6; 17:48626239-48626239	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Deletion - Frameshift
c.356A>G; p.E119G; 17:48625914-48625914	kidney	carcinoma; papillary_renal_cell_carcinoma	Substitution - Missense
c.706C>T; p.R236W; 17:48622947-48622947	breast	carcinoma	Substitution - Missense
c.706C>T; p.R236W; 17:48622947-48622947	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.706C>T; p.R236W; 17:48622947-48622947	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.444_462del19; p.S149fs*46; 17:48625808-48625826	peritoneum; appendix	other; pseudomyxoma_peritonei	Deletion - Frameshift
c.590C>T; p.T197M; 17:48623063-48623063	stomach	carcinoma; intestinal_adenocarcinoma	Substitution - Missense

The somatic mutations from COSMIC database