Entrez Gene

Basic Information
Gene ID	9370
Name	ADIPOQ

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.161G>A; p.G54D; 3:186853219-186853219	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.585C>A; p.D195E; 3:186854554-186854554	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.729C>T; p.T243T; 3:186854698-186854698	oesophagus	carcinoma; adenocarcinoma	Substitution - coding silent
c.667G>T; p.G223*; 3:186854636-186854636	lung	carcinoma; squamous_cell_carcinoma	Substitution - Nonsense
c.502A>G; p.M168V; 3:186854471-186854471	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.382A>G; p.M128V; 3:186854351-186854351	stomach	carcinoma; intestinal_adenocarcinoma	Substitution - Missense
c.382A>G; p.M128V; 3:186854351-186854351	stomach	adenocarcinoma	Substitution - Missense
c.315A>G; p.G105G; 3:186854284-186854284	lung	carcinoma; adenocarcinoma	Substitution - coding silent
c.442G>T; p.G148C; 3:186854411-186854411	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.112G>T; p.G38C; 3:186853170-186853170	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.387C>A; p.P129P; 3:186854356-186854356	ovary	other; neoplasm	Substitution - coding silent
c.183C>T; p.T61T; 3:186853241-186853241	skin	malignant_melanoma	Substitution - coding silent
c.443G>T; p.G148V; 3:186854412-186854412	ovary	carcinoma; serous_carcinoma	Substitution - Missense
c.600T>C; p.S200S; 3:186854569-186854569	lung	carcinoma; small_cell_carcinoma	Substitution - coding silent
c.427T>G; p.Y143D; 3:186854396-186854396	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.70G>T; p.G24W; 3:186853128-186853128	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.43G>T; p.G15C; 3:186853101-186853101	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.549C>T; p.L183L; 3:186854518-186854518	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.140C>T; p.P47L; 3:186853198-186853198	stomach	carcinoma; intestinal_adenocarcinoma	Substitution - Missense
c.215-2A>G; p.?; 3:186854182-186854182	stomach	carcinoma; adenocarcinoma	Unknown
c.442G>A; p.G148S; 3:186854411-186854411	skin	malignant_melanoma	Substitution - Missense
c.443G>A; p.G148D; 3:186854412-186854412	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.244G>A; p.E82K; 3:186854213-186854213	skin	malignant_melanoma	Substitution - Missense
c.463C>T; p.P155S; 3:186854432-186854432	lung; middle_lobe	carcinoma; adenocarcinoma	Substitution - Missense
c.163C>A; p.R55S; 3:186853221-186853221	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.667G>A; p.G223R; 3:186854636-186854636	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.455G>A; p.C152Y; 3:186854424-186854424	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.353G>A; p.G118E; 3:186854322-186854322	skin	malignant_melanoma	Substitution - Missense
c.570G>A; p.Q190Q; 3:186854539-186854539	skin	malignant_melanoma	Substitution - coding silent
c.312T>G; p.P104P; 3:186854281-186854281	bone	Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour	Substitution - coding silent
c.175G>T; p.D59Y; 3:186853233-186853233	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.613C>A; p.L205M; 3:186854582-186854582	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.164G>A; p.R55H; 3:186853222-186853222	pleura	pulmonary_blastoma	Substitution - Missense
c.229A>G; p.K77E; 3:186854198-186854198	oesophagus	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.101G>A; p.G34E; 3:186853159-186853159	skin; leg	malignant_melanoma	Substitution - Missense
c.101G>A; p.G34E; 3:186853159-186853159	skin; leg	malignant_melanoma	Substitution - Missense
c.304G>A; p.G102R; 3:186854273-186854273	skin	malignant_melanoma	Substitution - Missense
c.304G>A; p.G102R; 3:186854273-186854273	skin	malignant_melanoma	Substitution - Missense
c.304G>A; p.G102R; 3:186854273-186854273	skin	malignant_melanoma	Substitution - Missense
c.63G>A; p.T21T; 3:186853121-186853121	skin	malignant_melanoma	Substitution - coding silent
c.163C>T; p.R55C; 3:186853221-186853221	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.44G>T; p.G15V; 3:186853102-186853102	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.283C>T; p.P95S; 3:186854252-186854252	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.366C>T; p.Y122Y; 3:186854335-186854335	breast	carcinoma	Substitution - coding silent
c.516G>T; p.K172N; 3:186854485-186854485	lung; right_lower_lobe	carcinoma; adenocarcinoma	Substitution - Missense
c.523C>T; p.L175F; 3:186854492-186854492	skin	malignant_melanoma	Substitution - Missense
c.661C>T; p.R221C; 3:186854630-186854630	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.215G>A; p.G72D; 3:186854184-186854184	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.246A>G; p.E82E; 3:186854215-186854215	skin	malignant_melanoma	Substitution - coding silent
c.265G>A; p.E89K; 3:186854234-186854234	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.469C>T; p.L157L; 3:186854438-186854438	lung	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.701T>G; p.F234C; 3:186854670-186854670	stomach	carcinoma; intestinal_adenocarcinoma	Substitution - Missense
c.717C>T; p.L239L; 3:186854686-186854686	breast	carcinoma	Substitution - coding silent
c.723T>C; p.H241H; 3:186854692-186854692	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.452A>T; p.H151L; 3:186854421-186854421	bone; pelvis	chondrosarcoma	Substitution - Missense
c.122C>T; p.A41V; 3:186853180-186853180	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.122C>T; p.A41V; 3:186853180-186853180	breast	carcinoma; ductal_carcinoma	Substitution - Missense
c.143G>A; p.G48D; 3:186853201-186853201	lung; right_upper_lobe	carcinoma; adenocarcinoma	Substitution - Missense

The somatic mutations from COSMIC database