Entrez Gene

Basic Information
Gene ID	3149
Name	HMGB3

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.117G>A; p.A39A; 23:150985716-150985716	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.515C>T; p.P172L; 23:150987826-150987826	skin; trunk	malignant_melanoma	Substitution - Missense
c.199G>T; p.D67Y; 23:150986099-150986099	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.90A>C; p.K30N; 23:150985689-150985689	breast	carcinoma	Substitution - Missense
c.217C>T; p.R73W; 23:150986117-150986117	skin	malignant_melanoma	Substitution - Missense
c.118G>A; p.E40K; 23:150985717-150985717	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.151-1G>C; p.?; 23:150986050-150986050	large_intestine; rectum	carcinoma; adenocarcinoma	Unknown
c.436G>A; p.A146T; 23:150987273-150987273	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.107T>C; p.V36A; 23:150985706-150985706	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - Missense
c.597T>C; p.D199D; 23:150987908-150987908	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.485C>T; p.S162L; 23:150987796-150987796	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.594G>T; p.E198D; 23:150987905-150987905	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.576G>A; p.E192E; 23:150987887-150987887	prostate	carcinoma; adenocarcinoma	Substitution - coding silent
c.576G>A; p.E192E; 23:150987887-150987887	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.576G>A; p.E192E; 23:150987887-150987887	biliary_tract; gallbladder	carcinoma; adenocarcinoma	Substitution - coding silent
c.576G>A; p.E192E; 23:150987887-150987887	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - coding silent
c.576G>A; p.E192E; 23:150987887-150987887	autonomic_ganglia	neuroblastoma	Substitution - coding silent
c.576G>A; p.E192E; 23:150987887-150987887	prostate	carcinoma; adenocarcinoma	Substitution - coding silent
c.576G>A; p.E192E; 23:150987887-150987887	central_nervous_system; brain	glioma	Substitution - coding silent
c.576G>A; p.E192E; 23:150987887-150987887	central_nervous_system; brain	glioma	Substitution - coding silent
c.576G>A; p.E192E; 23:150987887-150987887	prostate	carcinoma; adenocarcinoma	Substitution - coding silent
c.576G>A; p.E192E; 23:150987887-150987887	prostate	carcinoma; adenocarcinoma	Substitution - coding silent
c.576G>A; p.E192E; 23:150987887-150987887	skin	malignant_melanoma	Substitution - coding silent
c.576G>A; p.E192E; 23:150987887-150987887	prostate	carcinoma; adenocarcinoma	Substitution - coding silent
c.576G>A; p.E192E; 23:150987887-150987887	lung; right_upper_lobe	carcinoma; adenocarcinoma	Substitution - coding silent
c.486G>A; p.S162S; 23:150987797-150987797	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - coding silent
c.552T>A; p.D184E; 23:150987863-150987863	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.511G>C; p.G171R; 23:150987822-150987822	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.294T>C; p.S98S; 23:150987131-150987131	skin	malignant_melanoma	Substitution - coding silent
c.555A>G; p.E185E; 23:150987866-150987866	ovary	carcinoma; serous_carcinoma	Substitution - coding silent
c.369G>C; p.V123V; 23:150987206-150987206	thyroid	carcinoma	Substitution - coding silent
c.64A>G; p.T22A; 23:150985663-150985663	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.37A>T; p.M13L; 23:150985636-150985636	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.271A>T; p.N91Y; 23:150986171-150986171	ovary	carcinoma; serous_carcinoma	Substitution - Missense
c.284G>T; p.R95M; 23:150986184-150986184	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.518C>A; p.A173D; 23:150987829-150987829	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.139G>C; p.E47Q; 23:150985738-150985738	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.378G>T; p.K126N; 23:150987215-150987215	ovary	carcinoma; serous_carcinoma	Substitution - Missense
c.235G>T; p.G79*; 23:150986135-150986135	lung	carcinoma; adenocarcinoma	Substitution - Nonsense
c.535A>T; p.K179*; 23:150987846-150987846	breast	carcinoma	Substitution - Nonsense
c.483G>C; p.K161N; 23:150987794-150987794	oesophagus; lower_third	carcinoma; adenocarcinoma	Substitution - Missense
c.269C>A; p.P90H; 23:150986169-150986169	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.269C>A; p.P90H; 23:150986169-150986169	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.316G>A; p.E106K; 23:150987153-150987153	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.116C>T; p.A39V; 23:150985715-150985715	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.220G>T; p.E74*; 23:150986120-150986120	skin	malignant_melanoma	Substitution - Nonsense
c.465G>T; p.K155N; 23:150987302-150987302	breast	carcinoma	Substitution - Missense
c.568_570delGAA; p.E198delE; 23:150987879-150987881	endometrium	carcinoma; endometrioid_carcinoma	Deletion - In frame
c.598G>A; p.E200K; 23:150987909-150987909	breast	carcinoma	Substitution - Missense
c.506C>T; p.A169V; 23:150987817-150987817	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.367G>A; p.V123M; 23:150987204-150987204	liver	carcinoma	Substitution - Missense
c.125C>T; p.S42F; 23:150985724-150985724	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense

The somatic mutations from COSMIC database