Entrez Gene

Basic Information
Gene ID	4283
Name	CXCL9

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.110A>G; p.N37S; 4:76006229-76006229	pancreas	carcinoma	Substitution - Missense
c.99C>T; p.C33C; 4:76006240-76006240	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.188T>C; p.I63T; 4:76006151-76006151	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.30G>T; p.L10F; 4:76007420-76007420	skin	malignant_melanoma	Substitution - Missense
c.311A>G; p.K104R; 4:76003665-76003665	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.276+1G>T; p.?; 4:76004808-76004808	large_intestine; colon	carcinoma; adenocarcinoma	Unknown
c.124C>A; p.H42N; 4:76006215-76006215	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.300G>T; p.K100N; 4:76003676-76003676	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.31G>T; p.G11C; 4:76007419-76007419	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm; acute_myeloid_leukaemia	Substitution - Missense
c.236C>T; p.S79L; 4:76004849-76004849	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.312A>T; p.K104N; 4:76003664-76003664	ovary	carcinoma; serous_carcinoma	Substitution - Missense
c.305G>A; p.G102E; 4:76003671-76003671	skin	malignant_melanoma	Substitution - Missense
c.358C>T; p.R120C; 4:76003618-76003618	skin	malignant_melanoma	Substitution - Missense
c.142G>T; p.D48Y; 4:76006197-76006197	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.142G>T; p.D48Y; 4:76006197-76006197	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.323delA; p.K108fs*4; 4:76003653-76003653	large_intestine; colon	carcinoma; adenocarcinoma	Deletion - Frameshift
c.67A>G; p.T23A; 4:76006272-76006272	kidney	other; neoplasm	Substitution - Missense
c.340C>T; p.R114*; 4:76003636-76003636	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Nonsense
c.340C>T; p.R114*; 4:76003636-76003636	oesophagus	carcinoma; adenocarcinoma	Substitution - Nonsense
c.340C>T; p.R114*; 4:76003636-76003636	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Nonsense
c.135C>T; p.S45S; 4:76006204-76006204	skin; head_neck	malignant_melanoma; superficial_spreading	Substitution - coding silent
c.312A>G; p.K104K; 4:76003664-76003664	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.312A>G; p.K104K; 4:76003664-76003664	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.341G>A; p.R114Q; 4:76003635-76003635	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.341G>A; p.R114Q; 4:76003635-76003635	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.341G>A; p.R114Q; 4:76003635-76003635	prostate	carcinoma; adenocarcinoma	Substitution - Missense
c.105C>A; p.S35R; 4:76006234-76006234	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.366G>C; p.K122N; 4:76003610-76003610	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.70C>T; p.P24S; 4:76006269-76006269	skin	malignant_melanoma	Substitution - Missense
c.105C>T; p.S35S; 4:76006234-76006234	pancreas	carcinoma	Substitution - coding silent
c.93T>A; p.C31*; 4:76006246-76006246	lung	carcinoma; adenocarcinoma	Substitution - Nonsense
c.180A>C; p.K60N; 4:76006159-76006159	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.232G>T; p.D78Y; 4:76004853-76004853	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.232G>T; p.D78Y; 4:76004853-76004853	liver	carcinoma; hepatocellular_carcinoma	Substitution - Missense
c.306G>A; p.G102G; 4:76003670-76003670	skin	malignant_melanoma	Substitution - coding silent
c.276G>T; p.Q92H; 4:76004809-76004809	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.157G>T; p.A53S; 4:76006182-76006182	lung; right_lower_lobe	carcinoma; adenocarcinoma	Substitution - Missense
c.303T>C; p.N101N; 4:76003673-76003673	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.89G>A; p.R30H; 4:76006250-76006250	central_nervous_system; brain	glioma	Substitution - Missense
c.353G>A; p.R118H; 4:76003623-76003623	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.359G>A; p.R120H; 4:76003617-76003617	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.270G>T; p.E90D; 4:76004815-76004815	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.24C>T; p.F8F; 4:76007426-76007426	skin	malignant_melanoma	Substitution - coding silent
c.127C>G; p.L43V; 4:76006212-76006212	bone; extraskeletal	Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour	Substitution - Missense

The somatic mutations from COSMIC database