| Gene information | Literature | Expression | lncRNA | Mutation | Homolog |
Basic Information | |
|---|---|
Gene ID | 3660 |
Name | IRF2 |
Synonymous | interferon regulatory factor 2;IRF2;interferon regulatory factor 2 |
Definition | - |
Position | 4q34.1-q35.1 |
Gene Type | protein-coding |
COSMIC confirmed somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.678C>T; p.P226P; 4:184398931-184398931 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.989C>T; p.T330I; 4:184388819-184388819 |
breast | carcinoma | Substitution - Missense |
c.746G>A; p.R249Q; 4:184389062-184389062 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.249C>T; p.C83C; 4:184418647-184418647 |
central_nervous_system; brain | glioma | Substitution - coding silent |
c.88-5_88-4delTT; p.?; 4:184419572-184419573 |
central_nervous_system; brain | glioma; astrocytoma_Grade_III | Unknown |
c.128G>C; p.R43T; 4:184419528-184419528 |
cervix | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.538C>T; p.Q180*; 4:184399071-184399071 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.476C>T; p.A159V; 4:184408211-184408211 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.639G>A; p.P213P; 4:184398970-184398970 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.236C>T; p.A79V; 4:184418660-184418660 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1012A>G; p.T338A; 4:184388796-184388796 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.108C>T; p.I36I; 4:184419548-184419548 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.683C>T; p.S228F; 4:184398926-184398926 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.249C>T; p.C83C; 4:184418647-184418647 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.327C>T; p.Y109Y; 4:184418569-184418569 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.250G>C; p.A84P; 4:184418646-184418646 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.702_706delAACGA; p.E234fs*2; 4:184390738-184390742 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma | Deletion - Frameshift |
c.783G>C; p.Q261H; 4:184389025-184389025 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.827G>A; p.G276D; 4:184388981-184388981 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.408C>G; p.I136M; 4:184418170-184418170 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.820C>T; p.L274L; 4:184388988-184388988 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.826G>A; p.G276S; 4:184388982-184388982 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.58A>T; p.T20S; 4:184429007-184429007 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.122C>T; p.A41V; 4:184419534-184419534 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.858G>A; p.P286P; 4:184388950-184388950 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.532G>A; p.V178I; 4:184399077-184399077 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.857C>T; p.P286L; 4:184388951-184388951 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.102_103insT; p.Q35fs*9; 4:184419553-184419554 |
large_intestine; caecum | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.300G>T; p.K100N; 4:184418596-184418596 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.638C>T; p.P213L; 4:184398971-184398971 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.349C>T; p.R117W; 4:184418547-184418547 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.339C>T; p.P113P; 4:184418557-184418557 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.991C>T; p.R331W; 4:184388817-184388817 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.323T>G; p.V108G; 4:184418573-184418573 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1000G>A; p.V334I; 4:184388808-184388808 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.250G>A; p.A84T; 4:184418646-184418646 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.67G>T; p.G23W; 4:184428998-184428998 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.234G>A; p.K78K; 4:184418662-184418662 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.234G>A; p.K78K; 4:184418662-184418662 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.952A>G; p.T318A; 4:184388856-184388856 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1034G>A; p.R345H; 4:184388774-184388774 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.952A>G; p.T318A; 4:184388856-184388856 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.234G>A; p.K78K; 4:184418662-184418662 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.704C>T; p.T235M; 4:184390740-184390740 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.388G>T; p.E130*; 4:184418190-184418190 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.25C>T; p.R9C; 4:184429040-184429040 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.25C>T; p.R9C; 4:184429040-184429040 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.66G>A; p.P22P; 4:184428999-184428999 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.172T>C; p.W58R; 4:184419484-184419484 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.38A>G; p.E13G; 4:184429027-184429027 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.914G>A; p.W305*; 4:184388894-184388894 |
liver | carcinoma | Substitution - Nonsense |
c.312delT; p.N104fs*48; 4:184418584-184418584 |
liver | carcinoma | Deletion - Frameshift |
c.412-6_419delTCCTAGCAAGAACC; p.?; 4:184408268-184408281 |
liver | carcinoma; hepatocellular_carcinoma | Unknown |
c.409A>C; p.K137Q; 4:184418169-184418169 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.1004T>G; p.I335S; 4:184388804-184388804 |
liver | carcinoma | Substitution - Missense |
c.1004T>G; p.I335S; 4:184388804-184388804 |
liver | carcinoma | Substitution - Missense |
c.238A>T; p.N80Y; 4:184418658-184418658 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.477G>T; p.A159A; 4:184408210-184408210 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.248G>T; p.C83F; 4:184418648-184418648 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.711T>C; p.D237D; 4:184390733-184390733 |
lung | carcinoma; small_cell_carcinoma | Substitution - coding silent |
c.638C>T; p.P213L; 4:184398971-184398971 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.26G>T; p.R9L; 4:184429039-184429039 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.639G>A; p.P213P; 4:184398970-184398970 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.880G>C; p.E294Q; 4:184388928-184388928 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.914G>T; p.W305L; 4:184388894-184388894 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.610G>T; p.E204*; 4:184398999-184398999 |
lung | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.622G>A; p.E208K; 4:184398987-184398987 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1028A>T; p.Q343L; 4:184388780-184388780 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.825C>G; p.P275P; 4:184388983-184388983 |
meninges | meningioma | Substitution - coding silent |
c.679G>A; p.V227M; 4:184398930-184398930 |
oesophagus; middle_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.358A>T; p.K120*; 4:184418538-184418538 |
ovary | carcinoma; serous_carcinoma | Substitution - Nonsense |
c.172T>C; p.W58R; 4:184419484-184419484 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.541_549delTCCCATCTG; p.S181_L183delSHL; 4:184399060-184399068 |
ovary | carcinoma; serous_carcinoma | Deletion - In frame |
c.758G>A; p.R253Q; 4:184389050-184389050 |
pancreas | carcinoma | Substitution - Missense |
c.758G>A; p.R253Q; 4:184389050-184389050 |
pancreas | carcinoma | Substitution - Missense |
c.892C>G; p.P298A; 4:184388916-184388916 |
pancreas | carcinoma | Substitution - Missense |
c.758G>T; p.R253L; 4:184389050-184389050 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.694+4A>T; p.?; 4:184398911-184398911 |
prostate | carcinoma | Unknown |
c.676C>G; p.P226A; 4:184398933-184398933 |
skin | malignant_melanoma | Substitution - Missense |
c.935C>T; p.P312L; 4:184388873-184388873 |
skin | malignant_melanoma | Substitution - Missense |
c.940T>G; p.S314A; 4:184388868-184388868 |
skin | malignant_melanoma | Substitution - Missense |
c.700G>A; p.E234K; 4:184390744-184390744 |
skin | malignant_melanoma | Substitution - Missense |
c.962C>T; p.S321F; 4:184388846-184388846 |
skin; scalp | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.187+2T>C; p.?; 4:184419467-184419467 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Unknown |
c.469G>A; p.E157K; 4:184408218-184408218 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.250G>A; p.A84T; 4:184418646-184418646 |
skin; sole | malignant_melanoma; acral_lentiginous | Substitution - Missense |
c.529G>A; p.V177I; 4:184408158-184408158 |
skin | malignant_melanoma | Substitution - Missense |
c.108C>T; p.I36I; 4:184419548-184419548 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.108C>T; p.I36I; 4:184419548-184419548 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.948C>T; p.S316S; 4:184388860-184388860 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.93G>A; p.K31K; 4:184419563-184419563 |
skin | malignant_melanoma | Substitution - coding silent |
c.359A>C; p.K120T; 4:184418537-184418537 |
skin; leg | malignant_melanoma | Substitution - Missense |
c.674C>T; p.S225F; 4:184398935-184398935 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.103C>T; p.Q35*; 4:184419553-184419553 |
skin | malignant_melanoma | Substitution - Nonsense |
c.338C>T; p.P113L; 4:184418558-184418558 |
skin; trunk | malignant_melanoma | Substitution - Missense |
c.1032C>T; p.A344A; 4:184388776-184388776 |
skin | malignant_melanoma | Substitution - coding silent |
c.122C>T; p.A41V; 4:184419534-184419534 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.122C>T; p.A41V; 4:184419534-184419534 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.363A>G; p.K121K; 4:184418533-184418533 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.191A>C; p.K64T; 4:184418705-184418705 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.349C>T; p.R117W; 4:184418547-184418547 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.174G>T; p.W58C; 4:184419482-184419482 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.236C>T; p.A79V; 4:184418660-184418660 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1000G>A; p.V334I; 4:184388808-184388808 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.321G>T; p.R107S; 4:184418575-184418575 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.500delA; p.N167fs*7; 4:184408187-184408187 |
stomach | carcinoma; intestinal_adenocarcinoma | Deletion - Frameshift |
c.868G>A; p.V290I; 4:184388940-184388940 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.744G>A; p.G248G; 4:184389064-184389064 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.365-2A>T; p.?; 4:184418215-184418215 |
stomach | carcinoma; adenocarcinoma | Unknown |
c.160C>G; p.L54V; 4:184419496-184419496 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.103C>T; p.Q35*; 4:184419553-184419553 |
stomach | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.250G>C; p.A84P; 4:184418646-184418646 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.412-1G>A; p.?; 4:184408276-184408276 |
stomach | carcinoma; adenocarcinoma | Unknown |
c.37G>T; p.E13*; 4:184429028-184429028 |
stomach | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1008G>A; p.K336K; 4:184388800-184388800 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.745C>T; p.R249W; 4:184389063-184389063 |
thyroid | carcinoma; anaplastic_carcinoma | Substitution - Missense |
c.187G>A; p.G63R; 4:184419469-184419469 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.37G>C; p.E13Q; 4:184429028-184429028 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - Missense |
c.37G>C; p.E13Q; 4:184429028-184429028 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.37G>C; p.E13Q; 4:184429028-184429028 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.236C>T; p.A79V; 4:184418660-184418660 |
urinary_tract; bladder | carcinoma | Substitution - Missense |