| Gene ID | 7186 |
| Symbol | TRAF2 |
| Synonymous | MGC:45012|TRAP|TRAP3 |
| Full name | TNF receptor-associated factor 2 |
| Gene description | E3 ubiquitin-protein ligase TRAF2|tumor necrosis factor type 2 receptor associated protein 3|tumor necrosis factor type 2 receptor-associated protein 3 |
| Cytoband | 9q34 |
| Gene type | protein-coding |
| Synonymous | MIM:601895; HGNC:HGNC:12032; Ensembl:ENSG00000127191; HPRD:03538; Vega:OTTHUMG00000020952 |
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.25C>T; p.P9S; 9:136898765-136898765 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1362C>T; p.S454S; 9:136925757-136925757 |
skin | malignant_melanoma | Substitution - coding silent |
c.1288-2A>C; p.?; 9:136925681-136925681 |
stomach | carcinoma; adenocarcinoma | Unknown |
c.341G>A; p.W114*; 9:136900495-136900495 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; mantle_cell_lymphoma | Substitution - Nonsense |
c.125G>A; p.R42H; 9:136898865-136898865 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; mantle_cell_lymphoma | Substitution - Missense |
c.125G>A; p.R42H; 9:136898865-136898865 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.414G>T; p.A138A; 9:136908117-136908117 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.537C>T; p.H179H; 9:136909928-136909928 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.358G>T; p.E120*; 9:136900512-136900512 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1203C>T; p.T401T; 9:136923916-136923916 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.629G>C; p.G210A; 9:136916566-136916566 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1326C>T; p.H442H; 9:136925721-136925721 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.600G>T; p.E200D; 9:136909991-136909991 |
upper_aerodigestive_tract; larynx | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1251G>A; p.P417P; 9:136923964-136923964 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1223C>T; p.S408F; 9:136923936-136923936 |
skin | malignant_melanoma | Substitution - Missense |
c.270C>G; p.A90A; 9:136900424-136900424 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - coding silent |
c.363C>G; p.Y121*; 9:136900517-136900517 |
thyroid | other; neoplasm | Substitution - Nonsense |
c.309G>A; p.L103L; 9:136900463-136900463 |
bone; extraskeletal | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.1219C>A; p.L407M; 9:136923932-136923932 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.457G>C; p.E153Q; 9:136908160-136908160 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1376C>T; p.P459L; 9:136925771-136925771 |
skin | malignant_melanoma | Substitution - Missense |
c.1154G>C; p.R385T; 9:136923867-136923867 |
breast | carcinoma; lobular_carcinoma | Substitution - Missense |
c.1051G>A; p.D351N; 9:136921128-136921128 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.388C>T; p.P130S; 9:136908091-136908091 |
skin | malignant_melanoma | Substitution - Missense |
c.1015G>C; p.E339Q; 9:136921092-136921092 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.749C>T; p.S250L; 9:136920304-136920304 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1396G>A; p.A466T; 9:136925791-136925791 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1158C>T; p.Y386Y; 9:136923871-136923871 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.340T>C; p.W114R; 9:136900494-136900494 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.128G>T; p.R43M; 9:136898868-136898868 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.1134C>T; p.S378S; 9:136921211-136921211 |
skin | malignant_melanoma | Substitution - coding silent |
c.803T>C; p.L268P; 9:136920358-136920358 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.803T>C; p.L268P; 9:136920358-136920358 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.803T>C; p.L268P; 9:136920358-136920358 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1370_1371delAG; p.R458fs*>44; 9:136925765-136925766 |
lung | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1284G>A; p.Q428Q; 9:136923997-136923997 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.129G>T; p.R43S; 9:136898869-136898869 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.1120C>T; p.P374S; 9:136921197-136921197 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.493C>T; p.H165Y; 9:136908196-136908196 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.960G>T; p.K320N; 9:136920515-136920515 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1269G>A; p.R423R; 9:136923982-136923982 |
skin | malignant_melanoma | Substitution - coding silent |
c.1269G>A; p.R423R; 9:136923982-136923982 |
skin | malignant_melanoma | Substitution - coding silent |
c.861C>T; p.C287C; 9:136920416-136920416 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.790G>A; p.A264T; 9:136920345-136920345 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.1123G>A; p.A375T; 9:136921200-136921200 |
central_nervous_system; brain | primitive_neuroectodermal_tumour-medulloblastoma | Substitution - Missense |
c.448C>T; p.R150C; 9:136908151-136908151 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.266C>T; p.S89L; 9:136899671-136899671 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1370A>T; p.Q457L; 9:136925765-136925765 |
breast | carcinoma; ductal_carcinoma | Substitution - Missense |
c.1370A>T; p.Q457L; 9:136925765-136925765 |
breast | carcinoma; ductal_carcinoma | Substitution - Missense |
c.1370A>T; p.Q457L; 9:136925765-136925765 |
breast | carcinoma; HER-positive_carcinoma | Substitution - Missense |
c.821G>T; p.S274I; 9:136920376-136920376 |
thyroid | other; neoplasm | Substitution - Missense |
c.914G>T; p.R305L; 9:136920469-136920469 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1401C>T; p.S467S; 9:136925796-136925796 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.313G>A; p.A105T; 9:136900467-136900467 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.490C>T; p.R164W; 9:136908193-136908193 |
breast | carcinoma | Substitution - Missense |
c.1115G>A; p.R372H; 9:136921192-136921192 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.1257C>T; p.D419D; 9:136923970-136923970 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.538G>A; p.E180K; 9:136909929-136909929 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.789C>T; p.H263H; 9:136920344-136920344 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1268G>A; p.R423Q; 9:136923981-136923981 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1230C>T; p.F410F; 9:136923943-136923943 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1002G>A; p.A334A; 9:136921079-136921079 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.802C>T; p.L268F; 9:136920357-136920357 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.1250C>T; p.P417L; 9:136923963-136923963 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1197C>T; p.D399D; 9:136923910-136923910 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.223G>A; p.E75K; 9:136899628-136899628 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.223G>A; p.E75K; 9:136899628-136899628 |
lung | carcinoma; non_small_cell_carcinoma | Substitution - Missense |
c.223G>A; p.E75K; 9:136899628-136899628 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1159G>A; p.G387S; 9:136923872-136923872 |
large_intestine; colon | carcinoma | Substitution - Missense |
c.315C>T; p.A105A; 9:136900469-136900469 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1009G>T; p.D337Y; 9:136921086-136921086 |
pancreas | carcinoma | Substitution - Missense |
c.20delC; p.P9fs*77; 9:136898760-136898760 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.20delC; p.P9fs*77; 9:136898760-136898760 |
stomach | carcinoma; intestinal_adenocarcinoma | Deletion - Frameshift |
c.20delC; p.P9fs*77; 9:136898760-136898760 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.127A>T; p.R43W; 9:136898867-136898867 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.757G>C; p.E253Q; 9:136920312-136920312 |
lung; middle_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.757G>C; p.E253Q; 9:136920312-136920312 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1348G>A; p.D450N; 9:136925743-136925743 |
eye; uveal_tract | malignant_melanoma; spindle | Substitution - Missense |
c.106G>A; p.A36T; 9:136898846-136898846 |
pancreas | carcinoma | Substitution - Missense |
c.449G>A; p.R150H; 9:136908152-136908152 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1118T>C; p.I373T; 9:136921195-136921195 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; acute_lymphoblastic_leukaemia | Substitution - Missense |
c.1462G>A; p.D488N; 9:136925857-136925857 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1491C>T; p.D497D; 9:136925886-136925886 |
pancreas | carcinoma | Substitution - coding silent |
c.1491C>T; p.D497D; 9:136925886-136925886 |
pancreas | carcinoma | Substitution - coding silent |
c.767C>T; p.P256L; 9:136920322-136920322 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |