| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 7555 |
Name | CNBP |
Synonymous | CCHC-type zinc finger, nucleic acid binding protein;CNBP;CCHC-type zinc finger, nucleic acid binding protein |
Definition | cellular nucleic acid binding protein|cellular nucleic acid-binding protein|erythroid differentiation-related|sterol regulatory element-binding protein|zinc finger protein 273|zinc finger protein 9 (a cellular retroviral nucleic acid binding protein) |
Position | 3q21 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.117G>A; p.S39S; 3:129171641-129171641 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.334G>A; p.D112N; 3:129171161-129171161 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.486C>T; p.G162G; 3:129170501-129170501 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.280C>T; p.R94*; 3:129171215-129171215 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.125-2A>G; p.?; 3:129171540-129171540 |
lung | carcinoma; squamous_cell_carcinoma | Unknown |
c.512G>T; p.C171F; 3:129170475-129170475 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.428C>G; p.T143S; 3:129170559-129170559 |
thyroid | other; neoplasm | Substitution - Missense |
c.218-1G>T; p.?; 3:129171278-129171278 |
endometrium | carcinoma; endometrioid_carcinoma | Unknown |
c.393C>T; p.D131D; 3:129171102-129171102 |
skin | malignant_melanoma | Substitution - coding silent |
c.333C>T; p.C111C; 3:129171162-129171162 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.362C>T; p.S121F; 3:129171133-129171133 |
biliary_tract; bile_duct | carcinoma; adenocarcinoma | Substitution - Missense |
c.170G>T; p.C57F; 3:129171493-129171493 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.529G>A; p.A177T; 3:129170458-129170458 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.82G>T; p.G28*; 3:129171676-129171676 |
stomach | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.129C>T; p.F43F; 3:129171534-129171534 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.239G>A; p.G80D; 3:129171256-129171256 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.376G>A; p.G126R; 3:129171119-129171119 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.140C>T; p.S47F; 3:129171523-129171523 |
skin | malignant_melanoma | Substitution - Missense |
c.148C>G; p.L50V; 3:129171515-129171515 |
central_nervous_system; brain | glioma; astrocytoma_Grade_II | Substitution - Missense |
c.315C>T; p.G105G; 3:129171180-129171180 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.48C>T; p.A16A; 3:129171710-129171710 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.166C>T; p.R56C; 3:129171497-129171497 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.166C>T; p.R56C; 3:129171497-129171497 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |