Entrez Gene

Basic Information
Gene ID	967
Name	CD63

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.215G>A; p.C72Y; 12:55727191-55727191	skin	malignant_melanoma	Substitution - Missense
c.581_583delAGA; p.K194delK; 12:55725881-55725883	large_intestine; colon	carcinoma; adenocarcinoma	Deletion - In frame
c.635G>T; p.G212V; 12:55725829-55725829	breast	carcinoma	Substitution - Missense
c.451_452delTA; p.Y151fs*21; 12:55726236-55726237	oesophagus	carcinoma; adenocarcinoma	Deletion - Frameshift
c.451_452delTA; p.Y151fs*21; 12:55726236-55726237	oesophagus	carcinoma; adenocarcinoma	Deletion - Frameshift
c.513T>C; p.I171I; 12:55726175-55726175	lung	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.579G>T; p.E193D; 12:55725885-55725885	breast	carcinoma	Substitution - Missense
c.333G>A; p.V111V; 12:55726793-55726793	skin	malignant_melanoma	Substitution - coding silent
c.110T>G; p.L37R; 12:55727296-55727296	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.220G>A; p.G74R; 12:55727186-55727186	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.126C>T; p.T42T; 12:55727280-55727280	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - coding silent
c.175G>A; p.A59T; 12:55727231-55727231	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.298G>A; p.A100T; 12:55726922-55726922	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.717G>A; p.239; 12:55725561-55725561	breast	carcinoma	Substitution - coding silent
c.702C>T; p.G234G; 12:55725576-55725576	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.381G>A; p.P127P; 12:55726745-55726745	skin	malignant_melanoma	Substitution - coding silent
c.374A>G; p.N125S; 12:55726752-55726752	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.468A>C; p.K156N; 12:55726220-55726220	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.211G>A; p.G71S; 12:55727195-55727195	skin	malignant_melanoma	Substitution - Missense
c.472C>T; p.P158S; 12:55726216-55726216	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.139G>A; p.A47T; 12:55727267-55727267	skin	malignant_melanoma	Substitution - Missense
c.440G>A; p.G147E; 12:55726248-55726248	bone	Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour	Substitution - Missense
c.366G>A; p.Q122Q; 12:55726760-55726760	skin	malignant_melanoma	Substitution - coding silent
c.457G>T; p.D153Y; 12:55726231-55726231	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.71G>A; p.C24Y; 12:55727335-55727335	skin	malignant_melanoma	Substitution - Missense
c.482C>T; p.S161L; 12:55726206-55726206	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.171C>T; p.I57I; 12:55727235-55727235	skin	malignant_melanoma	Substitution - coding silent
c.291G>A; p.E97E; 12:55726929-55726929	skin	malignant_melanoma	Substitution - coding silent
c.401C>T; p.S134L; 12:55726725-55726725	urinary_tract; bladder	carcinoma	Substitution - Missense
c.358C>T; p.R120W; 12:55726768-55726768	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.358C>T; p.R120W; 12:55726768-55726768	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Missense
c.358C>T; p.R120W; 12:55726768-55726768	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.256-1G>A; p.?; 12:55726965-55726965	skin	malignant_melanoma	Unknown
c.310G>A; p.G104S; 12:55726910-55726910	skin	malignant_melanoma	Substitution - Missense
c.332T>C; p.V111A; 12:55726794-55726794	ovary	carcinoma; serous_carcinoma	Substitution - Missense

The somatic mutations from COSMIC database