Entrez Gene

Basic Information
Gene ID	7351
Name	UCP2

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.906C>A; p.C302*; 11:73975031-73975031	breast	carcinoma	Substitution - Nonsense
c.827C>T; p.S276F; 11:73975110-73975110	skin	malignant_melanoma	Substitution - Missense
c.410C>T; p.T137M; 11:73976945-73976945	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.410C>T; p.T137M; 11:73976945-73976945	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.410C>T; p.T137M; 11:73976945-73976945	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.397G>T; p.V133L; 11:73976958-73976958	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.452G>C; p.G151A; 11:73976903-73976903	breast	carcinoma	Substitution - Missense
c.118C>T; p.R40W; 11:73978261-73978261	oesophagus	carcinoma; adenocarcinoma	Substitution - Missense
c.708C>T; p.D236D; 11:73975598-73975598	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.277_278insCCTCTGT; p.R96fs*8; 11:73977945-73977946	prostate	carcinoma	Insertion - Frameshift
c.737C>T; p.A246V; 11:73975569-73975569	stomach	carcinoma; intestinal_adenocarcinoma	Substitution - Missense
c.432C>T; p.F144F; 11:73976923-73976923	skin	malignant_melanoma	Substitution - coding silent
c.212G>T; p.R71L; 11:73978011-73978011	urinary_tract; bladder	carcinoma	Substitution - Missense
c.78C>T; p.I26I; 11:73978301-73978301	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - coding silent
c.835C>T; p.R279C; 11:73975102-73975102	skin	malignant_melanoma	Substitution - Missense
c.252C>T; p.A84A; 11:73977971-73977971	liver	carcinoma	Substitution - coding silent
c.252C>T; p.A84A; 11:73977971-73977971	liver	carcinoma	Substitution - coding silent
c.853G>A; p.V285M; 11:73975084-73975084	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.154C>T; p.R52C; 11:73978069-73978069	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.212G>A; p.R71H; 11:73978011-73978011	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.287G>A; p.R96H; 11:73977936-73977936	upper_aerodigestive_tract; mouth	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.287G>A; p.R96H; 11:73977936-73977936	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.720G>A; p.T240T; 11:73975586-73975586	urinary_tract; bladder	carcinoma	Substitution - coding silent
c.913C>T; p.R305*; 11:73975024-73975024	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Nonsense
c.360C>T; p.L120L; 11:73976995-73976995	skin	malignant_melanoma	Substitution - coding silent
c.337+1G>A; p.?; 11:73977885-73977885	large_intestine; colon	carcinoma; adenocarcinoma	Unknown
c.22G>A; p.D8N; 11:73978357-73978357	breast	carcinoma	Substitution - Missense
c.484G>C; p.A162P; 11:73976871-73976871	salivary_gland	carcinoma; adenoid_cystic_carcinoma	Substitution - Missense
c.523C>T; p.L175F; 11:73976832-73976832	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.292G>A; p.G98S; 11:73977931-73977931	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.460C>T; p.R154W; 11:73976895-73976895	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.205A>G; p.M69V; 11:73978018-73978018	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.148C>A; p.P50T; 11:73978075-73978075	ovary	carcinoma; serous_carcinoma	Substitution - Missense
c.848G>A; p.W283*; 11:73975089-73975089	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Nonsense
c.94T>A; p.F32I; 11:73978285-73978285	breast	carcinoma	Substitution - Missense
c.439C>G; p.Q147E; 11:73976916-73976916	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.789G>A; p.K263K; 11:73975517-73975517	lung	carcinoma; adenocarcinoma	Substitution - coding silent
c.815G>A; p.G272E; 11:73975491-73975491	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.32delC; p.P11fs*5; 11:73978347-73978347	large_intestine; colon	carcinoma; adenocarcinoma	Deletion - Frameshift
c.291C>T; p.I97I; 11:73977932-73977932	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.865G>A; p.V289I; 11:73975072-73975072	liver	carcinoma	Substitution - Missense
c.865G>A; p.V289I; 11:73975072-73975072	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.865G>A; p.V289I; 11:73975072-73975072	liver	carcinoma	Substitution - Missense
c.79G>A; p.A27T; 11:73978300-73978300	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.79G>A; p.A27T; 11:73978300-73978300	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.912C>T; p.S304S; 11:73975025-73975025	skin	malignant_melanoma	Substitution - coding silent
c.79G>A; p.A27T; 11:73978300-73978300	upper_aerodigestive_tract; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.488A>T; p.Y163F; 11:73976867-73976867	breast	carcinoma	Substitution - Missense
c.643C>T; p.P215S; 11:73975663-73975663	skin	malignant_melanoma	Substitution - Missense
c.52C>A; p.L18I; 11:73978327-73978327	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.615G>A; p.L205L; 11:73976660-73976660	breast	carcinoma	Substitution - coding silent
c.262C>T; p.R88C; 11:73977961-73977961	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.615G>A; p.L205L; 11:73976660-73976660	breast	carcinoma	Substitution - coding silent
c.874G>T; p.E292*; 11:73975063-73975063	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - Nonsense
c.126G>T; p.Q42H; 11:73978253-73978253	oesophagus	carcinoma; adenocarcinoma	Substitution - Missense
c.169G>T; p.A57S; 11:73978054-73978054	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.238A>G; p.N80D; 11:73977985-73977985	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense

The somatic mutations from COSMIC database