| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 1960 |
Name | EGR3 |
Synonymous | early growth response 3;EGR3;early growth response 3 |
Definition | early growth response protein 3|zinc finger protein pilot |
Position | 8p23-p21 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.931A>C; p.M311L; 8:22690706-22690706 |
pancreas | carcinoma | Substitution - Missense |
c.125C>A; p.S42*; 8:22692820-22692820 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.851G>A; p.R284H; 8:22690786-22690786 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.851G>A; p.R284H; 8:22690786-22690786 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.851G>A; p.R284H; 8:22690786-22690786 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.732C>A; p.G244G; 8:22690905-22690905 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.603C>T; p.N201N; 8:22691034-22691034 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.776G>A; p.R259H; 8:22690861-22690861 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.38T>C; p.M13T; 8:22692907-22692907 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.597C>A; p.H199Q; 8:22691040-22691040 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.533C>T; p.S178L; 8:22691104-22691104 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.655C>G; p.R219G; 8:22690982-22690982 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.457_464delCTCTACTC; p.L153fs*38; 8:22691173-22691180 |
breast | carcinoma | Deletion - Frameshift |
c.747G>A; p.P249P; 8:22690890-22690890 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.137A>G; p.Y46C; 8:22692808-22692808 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.156G>T; p.E52D; 8:22691481-22691481 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.362G>A; p.S121N; 8:22691275-22691275 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.41G>A; p.S14N; 8:22692904-22692904 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.806C>T; p.P269L; 8:22690831-22690831 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1048C>T; p.R350C; 8:22690589-22690589 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.546G>A; p.A182A; 8:22691091-22691091 |
breast | carcinoma | Substitution - coding silent |
c.769C>G; p.R257G; 8:22690868-22690868 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.156G>C; p.E52D; 8:22691481-22691481 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.590A>T; p.Y197F; 8:22691047-22691047 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.96G>A; p.A32A; 8:22692849-22692849 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.198G>A; p.P66P; 8:22691439-22691439 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1029G>A; p.A343A; 8:22690608-22690608 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1029G>A; p.A343A; 8:22690608-22690608 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1015G>T; p.G339W; 8:22690622-22690622 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.860G>A; p.S287N; 8:22690777-22690777 |
skin | malignant_melanoma | Substitution - Missense |
c.544G>A; p.A182T; 8:22691093-22691093 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1028C>T; p.A343V; 8:22690609-22690609 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.457C>A; p.L153I; 8:22691180-22691180 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.428C>T; p.A143V; 8:22691209-22691209 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.402G>T; p.Q134H; 8:22691235-22691235 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.371C>T; p.T124M; 8:22691266-22691266 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1143C>A; p.P381P; 8:22690494-22690494 |
prostate | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1143C>A; p.P381P; 8:22690494-22690494 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.268G>T; p.A90S; 8:22691369-22691369 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.16G>T; p.A6S; 8:22692929-22692929 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.206_207delCT; p.S69fs*35; 8:22691430-22691431 |
central_nervous_system; brain | glioma; astrocytoma_Grade_III | Deletion - Frameshift |
c.438delC; p.Y147fs*44; 8:22691199-22691199 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.870C>T; p.D290D; 8:22690767-22690767 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.647A>G; p.D216G; 8:22690990-22690990 |
oesophagus | carcinoma | Substitution - Missense |
c.724G>A; p.G242S; 8:22690913-22690913 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1100G>T; p.G367V; 8:22690537-22690537 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1057A>G; p.K353E; 8:22690580-22690580 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.377C>T; p.T126M; 8:22691260-22691260 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.867G>A; p.S289S; 8:22690770-22690770 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.867G>A; p.S289S; 8:22690770-22690770 |
pancreas | carcinoma | Substitution - coding silent |
c.867G>A; p.S289S; 8:22690770-22690770 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1128_1129insC; p.V377fs*>12; 8:22690508-22690509 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.490delC; p.Q164fs*27; 8:22691147-22691147 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.987C>T; p.G329G; 8:22690650-22690650 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.416C>T; p.A139V; 8:22691221-22691221 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.267C>T; p.F89F; 8:22691370-22691370 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.285delC; p.N96fs*11; 8:22691352-22691352 |
breast | carcinoma | Deletion - Frameshift |
c.1122G>A; p.A374A; 8:22690515-22690515 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.197C>A; p.P66Q; 8:22691440-22691440 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.144G>T; p.Q48H; 8:22692801-22692801 |
central_nervous_system; brain | primitive_neuroectodermal_tumour-medulloblastoma | Substitution - Missense |
c.147G>A; p.M49I; 8:22692798-22692798 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.415G>A; p.A139T; 8:22691222-22691222 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.520delC; p.Q174fs*17; 8:22691117-22691117 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1038_1040delCGA; p.D346delD; 8:22690597-22690599 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Deletion - In frame |
c.579C>T; p.D193D; 8:22691058-22691058 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.690delC; p.I231fs*62; 8:22690947-22690947 |
breast | carcinoma | Deletion - Frameshift |
c.542C>T; p.P181L; 8:22691095-22691095 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.378G>A; p.T126T; 8:22691259-22691259 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.306C>T; p.I102I; 8:22691331-22691331 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1141C>T; p.P381S; 8:22690496-22690496 |
skin | malignant_melanoma | Substitution - Missense |
c.935G>A; p.R312Q; 8:22690702-22690702 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1015_1016GG>AA; p.G339K; 8:22690621-22690622 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1133C>T; p.S378L; 8:22690504-22690504 |
skin | malignant_melanoma | Substitution - Missense |
c.640G>A; p.G214S; 8:22690997-22690997 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1036G>C; p.D346H; 8:22690601-22690601 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1049G>A; p.R350H; 8:22690588-22690588 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |