| General information | Literature | Expression | lncRNA |Regulation | Mutation | Homolog | Interaction |
Basic Information | |||
|---|---|---|---|
Gene ID | 79626 | ||
Name | TNFAIP8L2 | ||
The somatic mutations from COSMIC database | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.246T>A; p.S82R; 1:151158943-151158943 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.24C>A; p.S8R; 1:151158721-151158721 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.182A>C; p.K61T; 1:151158879-151158879 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.370C>T; p.R124W; 1:151159067-151159067 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; acute_lymphoblastic_leukaemia | Substitution - Missense |
c.510G>C; p.K170N; 1:151159207-151159207 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.545G>A; p.G182E; 1:151159242-151159242 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.481delG; p.P162fs*18; 1:151159178-151159178 |
endometrium | carcinoma; endometrioid_carcinoma | Deletion - Frameshift |
c.146A>G; p.Y49C; 1:151158843-151158843 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.146A>G; p.Y49C; 1:151158843-151158843 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.189G>A; p.L63L; 1:151158886-151158886 |
skin; trunk | malignant_melanoma; nodular | Substitution - coding silent |
c.470C>T; p.T157M; 1:151159167-151159167 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.137C>T; p.S46F; 1:151158834-151158834 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - Missense |
c.285G>A; p.R95R; 1:151158982-151158982 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.130C>T; p.R44C; 1:151158827-151158827 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.71G>A; p.R24H; 1:151158768-151158768 |
breast | carcinoma | Substitution - Missense |
c.71G>A; p.R24H; 1:151158768-151158768 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.498G>A; p.Q166Q; 1:151159195-151159195 |
skin | malignant_melanoma | Substitution - coding silent |
c.112G>A; p.V38M; 1:151158809-151158809 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.59A>C; p.K20T; 1:151158756-151158756 |
skin | malignant_melanoma | Substitution - Missense |
c.212C>T; p.A71V; 1:151158909-151158909 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.184G>A; p.D62N; 1:151158881-151158881 |
skin; extremity | malignant_melanoma | Substitution - Missense |
c.333C>T; p.F111F; 1:151159030-151159030 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.399C>G; p.H133Q; 1:151159096-151159096 |
large_intestine; rectum | adenoma | Substitution - Missense |
c.289G>A; p.G97S; 1:151158986-151158986 |
skin | malignant_melanoma | Substitution - Missense |
c.87C>G; p.L29L; 1:151158784-151158784 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.268T>C; p.F90L; 1:151158965-151158965 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.521G>A; p.G174E; 1:151159218-151159218 |
skin | malignant_melanoma | Substitution - Missense |