Entrez Gene

Basic Information
Gene ID	29126
Name	CD274

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.256C>T; p.R86W; 9:5457282-5457282	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.820A>G; p.I274V; 9:5466799-5466799	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.741C>A; p.I247I; 9:5465557-5465557	oesophagus; lower_third	carcinoma; adenocarcinoma	Substitution - coding silent
c.373C>T; p.R125*; 9:5457399-5457399	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Nonsense
c.171G>A; p.W57*; 9:5457197-5457197	haematopoietic_and_lymphoid_tissue; spleen	lymphoid_neoplasm; marginal_zone_lymphoma	Substitution - Nonsense
c.826G>C; p.D276H; 9:5466805-5466805	breast	carcinoma	Substitution - Missense
c.468G>T; p.Q156H; 9:5462907-5462907	ovary	carcinoma; serous_carcinoma	Substitution - Missense
c.826G>T; p.D276Y; 9:5466805-5466805	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.778C>T; p.R260C; 9:5465594-5465594	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.869C>T; p.T290M; 9:5467858-5467858	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.535A>C; p.T179P; 9:5462974-5462974	skin	malignant_melanoma	Substitution - Missense
c.395C>G; p.A132G; 9:5462834-5462834	stomach	carcinoma; intestinal_adenocarcinoma	Substitution - Missense
c.490G>A; p.E164K; 9:5462929-5462929	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.822C>A; p.I274I; 9:5466801-5466801	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.562G>A; p.E188K; 9:5463001-5463001	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - Missense
c.720delC; p.L241fs*2; 9:5465536-5465536	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Deletion - Frameshift
c.674T>C; p.V225A; 9:5463113-5463113	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.589C>G; p.L197V; 9:5463028-5463028	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.593G>T; p.R198I; 9:5463032-5463032	breast	carcinoma	Substitution - Missense
c.822C>T; p.I274I; 9:5466801-5466801	lung	carcinoma; small_cell_carcinoma	Substitution - coding silent
c.822C>T; p.I274I; 9:5466801-5466801	lung	carcinoma; small_cell_carcinoma	Substitution - coding silent
c.822C>T; p.I274I; 9:5466801-5466801	lung	carcinoma; small_cell_carcinoma	Substitution - coding silent
c.390C>T; p.V130V; 9:5457416-5457416	skin	malignant_melanoma	Substitution - coding silent
c.217G>C; p.D73H; 9:5457243-5457243	liver	carcinoma; hepatocellular_carcinoma	Substitution - Missense
c.384G>A; p.V128V; 9:5457410-5457410	kidney	carcinoma; papillary_renal_cell_carcinoma	Substitution - coding silent
c.51C>T; p.N17N; 9:5456164-5456164	bone	Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour	Substitution - coding silent
c.52G>A; p.A18T; 9:5456165-5456165	skin	malignant_melanoma	Substitution - Missense
c.697C>T; p.H233Y; 9:5465513-5465513	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.829A>T; p.T277S; 9:5466808-5466808	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.58A>G; p.T20A; 9:5457084-5457084	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.114T>G; p.I38M; 9:5457140-5457140	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.629C>G; p.T210S; 9:5463068-5463068	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.404A>G; p.N135S; 9:5462843-5462843	liver	carcinoma	Substitution - Missense
c.404A>G; p.N135S; 9:5462843-5462843	liver	carcinoma	Substitution - Missense
c.726A>T; p.V242V; 9:5465542-5465542	lung	carcinoma; adenocarcinoma	Substitution - coding silent
c.102C>T; p.S34S; 9:5457128-5457128	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.278C>T; p.S93F; 9:5457304-5457304	skin	malignant_melanoma	Substitution - Missense
c.18C>A; p.V6V; 9:5456131-5456131	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.469G>A; p.A157T; 9:5462908-5462908	central_nervous_system; brain	glioma	Substitution - Missense
c.469G>A; p.A157T; 9:5462908-5462908	central_nervous_system; brain	glioma	Substitution - Missense
c.651G>A; p.E217E; 9:5463090-5463090	skin	malignant_melanoma	Substitution - coding silent

The somatic mutations from COSMIC database