Entrez Gene

Basic Information
Gene ID	3589
Name	IL11

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.457C>A; p.P153T; 19:55366150-55366150	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.125C>T; p.T42I; 19:55368824-55368824	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.56C>T; p.A19V; 19:55368893-55368893	liver	carcinoma; hepatocellular_carcinoma	Substitution - Missense
c.104C>A; p.P35H; 19:55368845-55368845	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.10G>A; p.V4I; 19:55368939-55368939	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.16C>T; p.R6C; 19:55368933-55368933	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.571G>A; p.G191R; 19:55366036-55366036	skin	malignant_melanoma	Substitution - Missense
c.571G>A; p.G191R; 19:55366036-55366036	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.492delC; p.S165fs*19; 19:55366115-55366115	haematopoietic_and_lymphoid_tissue	lymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma	Deletion - Frameshift
c.17G>C; p.R6P; 19:55368932-55368932	breast	carcinoma	Substitution - Missense
c.317G>A; p.R106Q; 19:55368322-55368322	lung; right_upper_lobe	carcinoma; adenocarcinoma	Substitution - Missense
c.316C>T; p.R106W; 19:55368323-55368323	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.513C>A; p.I171I; 19:55366094-55366094	ovary	other; neoplasm	Substitution - coding silent
c.370C>T; p.P124S; 19:55368269-55368269	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.62C>T; p.A21V; 19:55368887-55368887	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.509_510insG; p.I171fs*16; 19:55366097-55366098	large_intestine; caecum	carcinoma; adenocarcinoma	Insertion - Frameshift
c.86_87insC; p.R30fs*38; 19:55368862-55368863	large_intestine; colon	carcinoma; adenocarcinoma	Insertion - Frameshift
c.404G>A; p.R135Q; 19:55368235-55368235	skin	malignant_melanoma	Substitution - Missense
c.540_541insG; p.L181fs*6; 19:55366066-55366067	large_intestine; caecum	carcinoma; adenocarcinoma	Insertion - Frameshift
c.202G>A; p.G68R; 19:55368548-55368548	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.70C>T; p.P24S; 19:55368879-55368879	central_nervous_system; brain	primitive_neuroectodermal_tumour-medulloblastoma	Substitution - Missense
c.509delG; p.G170fs*14; 19:55366098-55366098	large_intestine; colon	carcinoma; adenocarcinoma	Deletion - Frameshift
c.509delG; p.G170fs*14; 19:55366098-55366098	large_intestine; colon	carcinoma; adenocarcinoma	Deletion - Frameshift
c.509delG; p.G170fs*14; 19:55366098-55366098	large_intestine; caecum	carcinoma; adenocarcinoma	Deletion - Frameshift
c.246G>A; p.A82A; 19:55368504-55368504	liver	carcinoma; hepatocellular_carcinoma	Substitution - coding silent
c.246G>A; p.A82A; 19:55368504-55368504	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.227C>T; p.P76L; 19:55368523-55368523	skin; scalp	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.192C>T; p.F64F; 19:55368558-55368558	skin	malignant_melanoma	Substitution - coding silent
c.470C>T; p.P157L; 19:55366137-55366137	haematopoietic_and_lymphoid_tissue; lymph_node	lymphoid_neoplasm; follicular_lymphoma	Substitution - Missense
c.470C>T; p.P157L; 19:55366137-55366137	haematopoietic_and_lymphoid_tissue; spleen	lymphoid_neoplasm; diffuse_large_B_cell_lymphoma	Substitution - Missense

The somatic mutations from COSMIC database