Entrez Gene

Basic Information
Gene ID	3217
Name	HOXB7

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.489G>T; p.T163T; 17:48608007-48608007	lung	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.191delG; p.G64fs*99; 17:48610728-48610728	large_intestine; colon	carcinoma; adenocarcinoma	Deletion - Frameshift
c.146C>T; p.A49V; 17:48610773-48610773	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm; acute_myeloid_leukaemia	Substitution - Missense
c.146C>T; p.A49V; 17:48610773-48610773	thyroid	other; neoplasm	Substitution - Missense
c.386G>A; p.W129*; 17:48610533-48610533	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Nonsense
c.604G>A; p.G202R; 17:48607892-48607892	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.92C>T; p.S31F; 17:48610827-48610827	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.229G>A; p.G77S; 17:48610690-48610690	kidney	carcinoma; papillary_renal_cell_carcinoma	Substitution - Missense
c.645G>A; p.E215E; 17:48607851-48607851	pancreas	carcinoma	Substitution - coding silent
c.532G>A; p.E178K; 17:48607964-48607964	kidney	other; neoplasm	Substitution - Missense
c.496C>T; p.R166W; 17:48608000-48608000	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.113C>A; p.P38H; 17:48610806-48610806	upper_aerodigestive_tract; mouth	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.113C>A; p.P38H; 17:48610806-48610806	upper_aerodigestive_tract; mouth	carcinoma	Substitution - Missense
c.485T>G; p.L162R; 17:48608011-48608011	skin	malignant_melanoma	Substitution - Missense
c.328G>A; p.A110T; 17:48610591-48610591	upper_aerodigestive_tract; mouth	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.512C>T; p.A171V; 17:48607984-48607984	oesophagus; lower_third	carcinoma; adenocarcinoma	Substitution - Missense
c.108C>T; p.S36S; 17:48610811-48610811	skin	malignant_melanoma	Substitution - coding silent
c.582G>A; p.K194K; 17:48607914-48607914	skin	malignant_melanoma	Substitution - coding silent
c.510C>T; p.I170I; 17:48607986-48607986	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - coding silent
c.225_238del14; p.A76fs*13; 17:48610681-48610694	large_intestine; rectum	carcinoma; adenocarcinoma	Deletion - Frameshift
c.620A>G; p.D207G; 17:48607876-48607876	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.462A>T; p.K154N; 17:48608034-48608034	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.21G>C; p.A7A; 17:48610898-48610898	NS	NS	Substitution - coding silent
c.103G>T; p.A35S; 17:48610816-48610816	liver	carcinoma	Substitution - Missense
c.103G>T; p.A35S; 17:48610816-48610816	liver	carcinoma	Substitution - Missense
c.178C>A; p.P60T; 17:48610741-48610741	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.191_192insG; p.M65fs*29; 17:48610727-48610728	large_intestine	carcinoma; adenocarcinoma	Insertion - Frameshift
c.436C>T; p.R146C; 17:48608060-48608060	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.478C>T; p.R160C; 17:48608018-48608018	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.406G>A; p.D136N; 17:48608090-48608090	urinary_tract; bladder	carcinoma	Substitution - Missense
c.406G>A; p.D136N; 17:48608090-48608090	urinary_tract; bladder	carcinoma; transitional_cell_carcinoma	Substitution - Missense
c.489G>A; p.T163T; 17:48608007-48608007	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - coding silent
c.169G>T; p.G57C; 17:48610750-48610750	central_nervous_system; brain	glioma	Substitution - Missense
c.169G>T; p.G57C; 17:48610750-48610750	lung	carcinoma; large_cell_carcinoma	Substitution - Missense
c.473A>G; p.Y158C; 17:48608023-48608023	lung	carcinoma; adenocarcinoma	Substitution - Missense

The somatic mutations from COSMIC database