| Gene information | Literature | Expression | lncRNA | Mutation | Homolog |
Basic Information | |
|---|---|
Gene ID | 10276 |
Name | NET1 |
Synonymous | neuroepithelial cell transforming 1;NET1;neuroepithelial cell transforming 1 |
Definition | Rho guanine nucleotide exchange factor (GEF) 8|guanine nucleotide regulatory protein (oncogene)|neuroepithelial cell-transforming gene 1 protein|neuroepithelioma transforming gene 1|p65 Net1 proto-oncogene protein|small GTP-binding protein regulator |
Position | 10p15 |
Gene Type | protein-coding |
COSMIC confirmed somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.490A>G; p.I164V; 10:5453307-5453307 |
bone; pelvis | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.442G>A; p.D148N; 10:5453259-5453259 |
breast | carcinoma; ductal_carcinoma | Substitution - Missense |
c.1129A>G; p.I377V; 10:5456180-5456180 |
breast | carcinoma; basal_(triple-negative)_carcinoma | Substitution - Missense |
c.565G>A; p.D189N; 10:5453519-5453519 |
breast | carcinoma | Substitution - Missense |
c.1396G>A; p.E466K; 10:5456761-5456761 |
breast | carcinoma | Substitution - Missense |
c.919G>A; p.E307K; 10:5455002-5455002 |
breast | carcinoma | Substitution - Missense |
c.134C>T; p.T45M; 10:5451870-5451870 |
breast | carcinoma | Substitution - Missense |
c.1159C>A; p.L387M; 10:5456210-5456210 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.820C>T; p.H274Y; 10:5454478-5454478 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.399G>T; p.Q133H; 10:5452887-5452887 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1419C>A; p.P473P; 10:5456784-5456784 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.918C>T; p.S306S; 10:5455001-5455001 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1619C>A; p.T540N; 10:5456984-5456984 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1365A>G; p.P455P; 10:5456730-5456730 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.1482A>G; p.E494E; 10:5456847-5456847 |
kidney | other; neoplasm | Substitution - coding silent |
c.1046T>C; p.I349T; 10:5456097-5456097 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.361C>T; p.R121W; 10:5452517-5452517 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.656C>T; p.A219V; 10:5454314-5454314 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.65T>C; p.V22A; 10:5446830-5446830 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.155C>T; p.S52F; 10:5451891-5451891 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.387C>T; p.S129S; 10:5452875-5452875 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.11A>G; p.H4R; 10:5446776-5446776 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.279C>T; p.P93P; 10:5452435-5452435 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1086C>T; p.V362V; 10:5456137-5456137 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.718C>A; p.L240I; 10:5454376-5454376 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.500A>G; p.D167G; 10:5453317-5453317 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1339_1340insC; p.F449fs*9; 10:5456704-5456705 |
large_intestine; rectum | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.857A>G; p.E286G; 10:5454515-5454515 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.203C>A; p.S68*; 10:5452359-5452359 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.391_393delGGT; p.G131delG; 10:5452879-5452881 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - In frame |
c.1243C>T; p.R415C; 10:5456608-5456608 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1243C>T; p.R415C; 10:5456608-5456608 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1503A>T; p.R501S; 10:5456868-5456868 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.649C>T; p.L217L; 10:5454307-5454307 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.586G>A; p.G196S; 10:5453540-5453540 |
liver | carcinoma | Substitution - Missense |
c.607-1G>T; p.?; 10:5454264-5454264 |
liver | carcinoma | Unknown |
c.607-1G>T; p.?; 10:5454264-5454264 |
liver | carcinoma | Unknown |
c.1593C>T; p.A531A; 10:5456958-5456958 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.227G>C; p.R76T; 10:5452383-5452383 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.597C>A; p.L199L; 10:5453551-5453551 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.906G>C; p.K302N; 10:5454989-5454989 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.106_107delAA; p.R37fs*37; 10:5451842-5451843 |
lung | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.475G>C; p.E159Q; 10:5453292-5453292 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.310G>A; p.E104K; 10:5452466-5452466 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.921G>T; p.E307D; 10:5455004-5455004 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.624C>G; p.A208A; 10:5454282-5454282 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1386G>A; p.P462P; 10:5456751-5456751 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.918C>T; p.S306S; 10:5455001-5455001 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1405G>A; p.E469K; 10:5456770-5456770 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.49A>G; p.I17V; 10:5446814-5446814 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.33A>G; p.L11L; 10:5446798-5446798 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.107A>C; p.K36T; 10:5451843-5451843 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.808G>T; p.E270*; 10:5454466-5454466 |
prostate | carcinoma | Substitution - Nonsense |
c.864+9T>C; p.?; 10:5454531-5454531 |
prostate | carcinoma | Unknown |
c.1524G>A; p.M508I; 10:5456889-5456889 |
skin | malignant_melanoma | Substitution - Missense |
c.345C>A; p.T115T; 10:5452501-5452501 |
skin | malignant_melanoma | Substitution - coding silent |
c.1211A>T; p.N404I; 10:5456262-5456262 |
skin; head_neck | malignant_melanoma; superficial_spreading | Substitution - Missense |
c.721G>A; p.E241K; 10:5454379-5454379 |
skin | malignant_melanoma | Substitution - Missense |
c.1243C>T; p.R415C; 10:5456608-5456608 |
skin | malignant_melanoma | Substitution - Missense |
c.230C>T; p.S77F; 10:5452386-5452386 |
skin | malignant_melanoma | Substitution - Missense |
c.759C>T; p.F253F; 10:5454417-5454417 |
skin | malignant_melanoma | Substitution - coding silent |
c.101G>T; p.S34I; 10:5451837-5451837 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.510T>C; p.S170S; 10:5453327-5453327 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1435A>G; p.T479A; 10:5456800-5456800 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.1435A>G; p.T479A; 10:5456800-5456800 |
stomach | adenocarcinoma | Substitution - Missense |
c.428G>A; p.R143K; 10:5452916-5452916 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.1095C>T; p.N365N; 10:5456146-5456146 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1095C>T; p.N365N; 10:5456146-5456146 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1059A>G; p.Q353Q; 10:5456110-5456110 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.929A>G; p.Y310C; 10:5455012-5455012 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.329T>C; p.M110T; 10:5452485-5452485 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1031G>A; p.G344E; 10:5455114-5455114 |
thyroid | other; neoplasm | Substitution - Missense |
c.1006C>A; p.H336N; 10:5455089-5455089 |
thyroid | other; neoplasm | Substitution - Missense |
c.1286C>T; p.A429V; 10:5456651-5456651 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1190C>G; p.S397C; 10:5456241-5456241 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.763G>C; p.D255H; 10:5454421-5454421 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.156_175del20; p.P53fs*15; 10:5451892-5451911 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Deletion - Frameshift |