| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 10875 |
Name | FGL2 |
Synonymous | fibrinogen-like 2;FGL2;fibrinogen-like 2 |
Definition | fibrinogen-like protein 2|fibroleukin |
Position | 7q11.23 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.1035C>T; p.F345F; 7:77196564-77196564 |
breast | carcinoma | Substitution - coding silent |
c.827G>A; p.G276E; 7:77196772-77196772 |
skin | malignant_melanoma | Substitution - Missense |
c.189delC; p.L64fs*1; 7:77199605-77199605 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.222G>A; p.R74R; 7:77199572-77199572 |
skin | malignant_melanoma | Substitution - coding silent |
c.583C>A; p.P195T; 7:77199211-77199211 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.433A>T; p.K145*; 7:77199361-77199361 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1198G>C; p.G400R; 7:77196401-77196401 |
pancreas | carcinoma | Substitution - Missense |
c.399A>C; p.L133F; 7:77199395-77199395 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.503A>C; p.N168T; 7:77199291-77199291 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.805C>T; p.Q269*; 7:77196794-77196794 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.22T>C; p.W8R; 7:77199772-77199772 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.189_190insC; p.T65fs*27; 7:77199604-77199605 |
large_intestine | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.465T>C; p.H155H; 7:77199329-77199329 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.399_400insA; p.E134fs*3; 7:77199394-77199395 |
oesophagus | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.651C>T; p.Y217Y; 7:77196948-77196948 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.541A>G; p.T181A; 7:77199253-77199253 |
skin | malignant_melanoma | Substitution - Missense |
c.1309T>G; p.F437V; 7:77196290-77196290 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.741G>A; p.M247I; 7:77196858-77196858 |
skin | malignant_melanoma | Substitution - Missense |
c.618A>G; p.Q206Q; 7:77196981-77196981 |
skin | malignant_melanoma | Substitution - coding silent |
c.259G>A; p.E87K; 7:77199535-77199535 |
skin | malignant_melanoma | Substitution - Missense |
c.259G>A; p.E87K; 7:77199535-77199535 |
skin | malignant_melanoma | Substitution - Missense |
c.85G>A; p.E29K; 7:77199709-77199709 |
skin; nipple | malignant_melanoma | Substitution - Missense |
c.961G>T; p.V321L; 7:77196638-77196638 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.961G>T; p.V321L; 7:77196638-77196638 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia_therapy_related | Substitution - Missense |
c.769C>T; p.R257C; 7:77196830-77196830 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1030C>T; p.R344C; 7:77196569-77196569 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.804G>A; p.W268*; 7:77196795-77196795 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.673G>C; p.E225Q; 7:77196926-77196926 |
breast | carcinoma | Substitution - Missense |
c.693T>G; p.P231P; 7:77196906-77196906 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.284C>A; p.S95Y; 7:77199510-77199510 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.458T>C; p.V153A; 7:77199336-77199336 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1238T>C; p.V413A; 7:77196361-77196361 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.508G>T; p.E170*; 7:77199286-77199286 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.33A>G; p.S11S; 7:77199761-77199761 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.858C>A; p.N286K; 7:77196741-77196741 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1050C>A; p.N350K; 7:77196549-77196549 |
breast | carcinoma | Substitution - Missense |
c.665G>T; p.R222I; 7:77196934-77196934 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.746delG; p.G249fs*44; 7:77196853-77196853 |
lung | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.53G>T; p.G18V; 7:77199741-77199741 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1175A>T; p.K392I; 7:77196424-77196424 |
skin | malignant_melanoma | Substitution - Missense |
c.762G>A; p.L254L; 7:77196837-77196837 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.475G>A; p.E159K; 7:77199319-77199319 |
skin | malignant_melanoma | Substitution - Missense |
c.226G>C; p.E76Q; 7:77199568-77199568 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1203C>T; p.V401V; 7:77196396-77196396 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.851T>C; p.L284P; 7:77196748-77196748 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1241G>T; p.S414I; 7:77196358-77196358 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.264C>T; p.I88I; 7:77199530-77199530 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.140G>A; p.G47E; 7:77199654-77199654 |
skin | malignant_melanoma | Substitution - Missense |
c.97G>A; p.E33K; 7:77199697-77199697 |
skin | malignant_melanoma | Substitution - Missense |
c.141G>A; p.G47G; 7:77199653-77199653 |
skin | malignant_melanoma | Substitution - coding silent |
c.1066T>C; p.F356L; 7:77196533-77196533 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.150A>G; p.E50E; 7:77199644-77199644 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.159G>A; p.G53G; 7:77199635-77199635 |
skin | malignant_melanoma | Substitution - coding silent |
c.575_576insA; p.C194fs*18; 7:77199218-77199219 |
lung | carcinoma; bronchioloalveolar_adenocarcinoma | Insertion - Frameshift |
c.874C>T; p.L292L; 7:77196725-77196725 |
central_nervous_system; brain | glioma | Substitution - coding silent |
c.206C>T; p.P69L; 7:77199588-77199588 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.985C>T; p.R329C; 7:77196614-77196614 |
skin | malignant_melanoma | Substitution - Missense |
c.985C>T; p.R329C; 7:77196614-77196614 |
skin | malignant_melanoma | Substitution - Missense |
c.986G>A; p.R329H; 7:77196613-77196613 |
breast | carcinoma | Substitution - Missense |
c.720T>G; p.V240V; 7:77196879-77196879 |
skin | malignant_melanoma | Substitution - coding silent |
c.836G>A; p.R279K; 7:77196763-77196763 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1094G>A; p.R365Q; 7:77196505-77196505 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.952C>T; p.Q318*; 7:77196647-77196647 |
skin | malignant_melanoma | Substitution - Nonsense |
c.607C>A; p.R203S; 7:77199187-77199187 |
prostate | carcinoma | Substitution - Missense |
c.686T>C; p.V229A; 7:77196913-77196913 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.707G>A; p.S236N; 7:77196892-77196892 |
kidney | other; neoplasm | Substitution - Missense |
c.728A>G; p.D243G; 7:77196871-77196871 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.931G>A; p.E311K; 7:77196668-77196668 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.931G>A; p.E311K; 7:77196668-77196668 |
skin | malignant_melanoma | Substitution - Missense |
c.1272C>T; p.S424S; 7:77196327-77196327 |
skin | malignant_melanoma | Substitution - coding silent |
c.907G>A; p.D303N; 7:77196692-77196692 |
skin | malignant_melanoma | Substitution - Missense |
c.673G>A; p.E225K; 7:77196926-77196926 |
skin | malignant_melanoma | Substitution - Missense |
c.788A>G; p.N263S; 7:77196811-77196811 |
skin | malignant_melanoma | Substitution - Missense |
c.859G>A; p.D287N; 7:77196740-77196740 |
skin | malignant_melanoma | Substitution - Missense |
c.1226C>T; p.T409I; 7:77196373-77196373 |
breast | carcinoma; basal_(triple-negative)_carcinoma | Substitution - Missense |
c.314A>G; p.D105G; 7:77199480-77199480 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1103C>A; p.S368Y; 7:77196496-77196496 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.989T>A; p.L330*; 7:77196610-77196610 |
meninges | meningioma | Substitution - Nonsense |
c.23G>T; p.W8L; 7:77199771-77199771 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.94G>A; p.D32N; 7:77199700-77199700 |
cervix | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.283T>C; p.S95P; 7:77199511-77199511 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.607C>G; p.R203G; 7:77199187-77199187 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.380A>G; p.D127G; 7:77199414-77199414 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |