| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 53635 |
Name | PTOV1 |
Synonymous | prostate tumor overexpressed 1;PTOV1;prostate tumor overexpressed 1 |
Definition | activator interaction domain-containing protein 2|prostate tumor-overexpressed gene 1 protein |
Position | 19q13.33 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.657C>G; p.P219P; 19:49857073-49857073 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.997C>T; p.L333L; 19:49858609-49858609 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1174C>T; p.R392C; 19:49860118-49860118 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1076G>T; p.C359F; 19:49860020-49860020 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.1174C>T; p.R392C; 19:49860118-49860118 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1174C>T; p.R392C; 19:49860118-49860118 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1021C>T; p.R341W; 19:49858633-49858633 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.754A>G; p.I252V; 19:49857732-49857732 |
thyroid | other; neoplasm | Substitution - Missense |
c.517G>A; p.D173N; 19:49855036-49855036 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.659A>C; p.Y220S; 19:49857075-49857075 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.703A>C; p.T235P; 19:49857119-49857119 |
breast | carcinoma | Substitution - Missense |
c.411G>A; p.P137P; 19:49854849-49854849 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.744C>T; p.G248G; 19:49857722-49857722 |
kidney | other; neoplasm | Substitution - coding silent |
c.1134C>T; p.L378L; 19:49860078-49860078 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.804+2T>G; p.?; 19:49857784-49857784 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Unknown |
c.215C>T; p.S72F; 19:49854449-49854449 |
skin | malignant_melanoma | Substitution - Missense |
c.879G>A; p.L293L; 19:49858057-49858057 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.466C>G; p.L156V; 19:49854985-49854985 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.466C>G; p.L156V; 19:49854985-49854985 |
liver | carcinoma | Substitution - Missense |
c.1129G>T; p.G377C; 19:49860073-49860073 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1242delG; p.*417fs?; 19:49860270-49860270 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1242delG; p.*417fs?; 19:49860270-49860270 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1242delG; p.*417fs?; 19:49860270-49860270 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1242delG; p.*417fs?; 19:49860270-49860270 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1242delG; p.*417fs?; 19:49860270-49860270 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.644T>C; p.M215T; 19:49857060-49857060 |
stomach | adenocarcinoma | Substitution - Missense |
c.535T>A; p.C179S; 19:49855054-49855054 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.972G>C; p.L324L; 19:49858584-49858584 |
liver | carcinoma | Substitution - coding silent |
c.1085G>A; p.R362H; 19:49860029-49860029 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.972G>C; p.L324L; 19:49858584-49858584 |
liver | carcinoma | Substitution - coding silent |
c.656C>A; p.P219H; 19:49857072-49857072 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.350G>A; p.R117Q; 19:49854692-49854692 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.951G>A; p.P317P; 19:49858563-49858563 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.631A>C; p.K211Q; 19:49857047-49857047 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.437C>T; p.P146L; 19:49854875-49854875 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1098C>T; p.L366L; 19:49860042-49860042 |
pancreas | carcinoma; ductal_carcinoma | Substitution - coding silent |
c.682G>A; p.A228T; 19:49857098-49857098 |
liver | carcinoma | Substitution - Missense |
c.682G>A; p.A228T; 19:49857098-49857098 |
liver | carcinoma | Substitution - Missense |
c.1022G>T; p.R341L; 19:49858634-49858634 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1084C>T; p.R362C; 19:49860028-49860028 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.234C>T; p.L78L; 19:49854468-49854468 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.817C>T; p.P273S; 19:49857916-49857916 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.841C>T; p.L281L; 19:49857940-49857940 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.966G>A; p.S322S; 19:49858578-49858578 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.314G>A; p.R105H; 19:49854656-49854656 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.438T>G; p.P146P; 19:49854876-49854876 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.384C>T; p.G128G; 19:49854726-49854726 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.601C>T; p.R201C; 19:49857017-49857017 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1047C>T; p.G349G; 19:49859991-49859991 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.601C>T; p.R201C; 19:49857017-49857017 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1164C>T; p.N388N; 19:49860108-49860108 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.735C>G; p.V245V; 19:49857713-49857713 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.735C>G; p.V245V; 19:49857713-49857713 |
breast | carcinoma | Substitution - coding silent |
c.624G>A; p.S208S; 19:49857040-49857040 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.225G>A; p.G75G; 19:49854459-49854459 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.636G>T; p.K212N; 19:49857052-49857052 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.759_761delCAA; p.N255delN; 19:49857737-49857739 |
central_nervous_system; thalamus | glioma; astrocytoma_Grade_IV | Deletion - In frame |
c.462delC; p.L156fs*132; 19:49854981-49854981 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.857A>T; p.Y286F; 19:49857956-49857956 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.410C>T; p.P137L; 19:49854848-49854848 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.867G>A; p.Q289Q; 19:49857966-49857966 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.642C>A; p.F214L; 19:49857058-49857058 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.439C>T; p.Q147*; 19:49854877-49854877 |
thyroid | other; neoplasm | Substitution - Nonsense |
c.289G>A; p.G97S; 19:49854523-49854523 |
skin | malignant_melanoma | Substitution - Missense |
c.289G>A; p.G97S; 19:49854523-49854523 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.210T>C; p.G70G; 19:49854444-49854444 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.660C>T; p.Y220Y; 19:49857076-49857076 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.660C>T; p.Y220Y; 19:49857076-49857076 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.660C>T; p.Y220Y; 19:49857076-49857076 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.728G>A; p.G243D; 19:49857706-49857706 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.182G>A; p.R61Q; 19:49854416-49854416 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.873G>C; p.E291D; 19:49857972-49857972 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.602G>A; p.R201H; 19:49857018-49857018 |
pancreas | carcinoma | Substitution - Missense |
c.696C>T; p.V232V; 19:49857112-49857112 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.696C>T; p.V232V; 19:49857112-49857112 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - coding silent |
c.604G>A; p.V202M; 19:49857020-49857020 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.602G>A; p.R201H; 19:49857018-49857018 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.604G>A; p.V202M; 19:49857020-49857020 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1208G>A; p.R403Q; 19:49860152-49860152 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.313C>T; p.R105C; 19:49854655-49854655 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.434T>C; p.I145T; 19:49854872-49854872 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.642C>T; p.F214F; 19:49857058-49857058 |
skin | malignant_melanoma | Substitution - coding silent |
c.562G>T; p.G188C; 19:49856978-49856978 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.235delG; p.G80fs*4; 19:49854469-49854469 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.628_630delAAG; p.K212delK; 19:49857044-49857046 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - In frame |