General information | Literature | Expression | Regulation | Variant | Interaction |
Basic Information |
|
---|---|
Gene ID | 7270 |
Name | TTF1 |
Synonymous | transcription termination factor, RNA polymerase I;TTF1;transcription termination factor, RNA polymerase I |
Definition | transcription termination factor 1 |
Position | 9q34.13 |
Gene Type | protein-coding |
Mutation summary: | Mutations in domains Mutational pattern in 17 major cancer types LoF vs missense mutations All the copy number variations from COSMIC database V72 All the mutations from COSMIC database V72 |
Mutation summary in protein domains | Top |
The non-synonymous (top) and synonymous (bottom) mutational percentage for various cancers | Top |
Loss of Function mutations compare to missense mutations | Top |
The ratio of the loss-of-function mutations over missense mutations is 0.23. |
The copy number variations for various cancers | Top |
The copy number variations in 17 major cancer types: 1; Breast, 2; Central nervous system, 3; Cervix, 4; Endometrium, 5; Haematopoietic and lymphoid_tissue, 6; Kidney, 7; Large intestine, 8; Liver, 9; Lung, 10; Not specific, 11; Ovary, 12; Pancreas, 13; Prostate, 14; Skin, 15; Stomach, 16; Thyroid, 17; Urinary tract |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) |
Site |
Histology |
Mutation Type |
---|---|---|---|
c.1187C>T; p.S396F; 9:132401635-132401635 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1811A>G; p.Y604C; 9:132396478-132396478 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.2090T>G; p.V697G; 9:132390729-132390729 |
breast | carcinoma | Substitution - Missense |
c.1811A>G; p.Y604C; 9:132396478-132396478 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - Missense |
c.949C>T; p.H317Y; 9:132401873-132401873 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.312T>G; p.V104V; 9:132402510-132402510 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - coding silent |
c.312T>G; p.V104V; 9:132402510-132402510 |
liver | carcinoma | Substitution - coding silent |
c.127G>T; p.V43L; 9:132402695-132402695 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.10G>T; p.E4*; 9:132402812-132402812 |
lung | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.442C>A; p.L148I; 9:132402380-132402380 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2287C>T; p.R763W; 9:132388164-132388164 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.2303T>C; p.L768P; 9:132388148-132388148 |
skin | malignant_melanoma | Substitution - Missense |
c.896T>G; p.V299G; 9:132401926-132401926 |
breast | carcinoma | Substitution - Missense |
c.1233T>A; p.S411R; 9:132401589-132401589 |
skin; mucosal | malignant_melanoma | Substitution - Missense |
c.1476T>C; p.G492G; 9:132400150-132400150 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1288G>A; p.E430K; 9:132401534-132401534 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1288G>A; p.E430K; 9:132401534-132401534 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.1477T>G; p.S493A; 9:132400149-132400149 |
skin | malignant_melanoma | Substitution - Missense |
c.1792C>G; p.R598G; 9:132396497-132396497 |
skin | malignant_melanoma | Substitution - Missense |
c.1071C>T; p.Y357Y; 9:132401751-132401751 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1209T>C; p.S403S; 9:132401613-132401613 |
pancreas | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1146delC; p.N383fs*40; 9:132401676-132401676 |
thyroid | carcinoma; anaplastic_carcinoma | Deletion - Frameshift |
c.1892A>G; p.Y631C; 9:132392171-132392171 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1475G>C; p.G492A; 9:132400151-132400151 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1415C>T; p.S472F; 9:132400211-132400211 |
skin | malignant_melanoma | Substitution - Missense |
c.2397C>T; p.Y799Y; 9:132379126-132379126 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2412T>C; p.F804F; 9:132379111-132379111 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.832A>C; p.K278Q; 9:132401990-132401990 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.2704C>G; p.R902G; 9:132375929-132375929 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.2714T>C; p.I905T; 9:132375919-132375919 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.2714T>C; p.I905T; 9:132375919-132375919 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.718T>C; p.S240P; 9:132402104-132402104 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.718T>C; p.S240P; 9:132402104-132402104 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.493_495delGAG; p.E165delE; 9:132402327-132402329 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - In frame |
c.1466C>T; p.A489V; 9:132400160-132400160 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.836delA; p.K279fs*144; 9:132401986-132401986 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.836delA; p.K279fs*144; 9:132401986-132401986 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.836delA; p.K279fs*144; 9:132401986-132401986 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1287G>A; p.M429I; 9:132401535-132401535 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1287G>A; p.M429I; 9:132401535-132401535 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.438G>A; p.Q146Q; 9:132402384-132402384 |
skin | malignant_melanoma | Substitution - coding silent |
c.2590G>A; p.D864N; 9:132376043-132376043 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.684C>T; p.N228N; 9:132402138-132402138 |
skin | malignant_melanoma | Substitution - coding silent |
c.1060G>A; p.E354K; 9:132401762-132401762 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.904G>C; p.E302Q; 9:132401918-132401918 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.517_518delAG; p.R173fs*33; 9:132402304-132402305 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1088T>G; p.V363G; 9:132401734-132401734 |
thyroid | other; neoplasm | Substitution - Missense |
c.2137C>T; p.R713W; 9:132390682-132390682 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2137C>T; p.R713W; 9:132390682-132390682 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.2137C>T; p.R713W; 9:132390682-132390682 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2071C>T; p.P691S; 9:132390748-132390748 |
skin | malignant_melanoma | Substitution - Missense |
c.1707G>A; p.T569T; 9:132398211-132398211 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.2129C>T; p.S710L; 9:132390690-132390690 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.607C>T; p.P203S; 9:132402215-132402215 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.998A>C; p.K333T; 9:132401824-132401824 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2141A>G; p.E714G; 9:132390678-132390678 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.553G>A; p.D185N; 9:132402269-132402269 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.2473G>A; p.D825N; 9:132376160-132376160 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.891A>G; p.S297S; 9:132401931-132401931 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.545G>T; p.R182L; 9:132402277-132402277 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma | Substitution - Missense |
c.821_822insA; p.S275fs*2; 9:132402000-132402001 |
oesophagus | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.150T>A; p.T50T; 9:132402672-132402672 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.1202G>A; p.R401Q; 9:132401620-132401620 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1202G>A; p.R401Q; 9:132401620-132401620 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1202G>A; p.R401Q; 9:132401620-132401620 |
upper_aerodigestive_tract; tonsil | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.291C>T; p.D97D; 9:132402531-132402531 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.2643C>T; p.S881S; 9:132375990-132375990 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1039G>T; p.V347L; 9:132401783-132401783 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1833C>T; p.F611F; 9:132396456-132396456 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2461C>T; p.P821S; 9:132379062-132379062 |
skin | malignant_melanoma | Substitution - Missense |
c.1872T>C; p.D624D; 9:132392191-132392191 |
bone; fibula | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.1687G>A; p.A563T; 9:132398231-132398231 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2610C>T; p.D870D; 9:132376023-132376023 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2610C>T; p.D870D; 9:132376023-132376023 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.1555G>T; p.D519Y; 9:132400071-132400071 |
pancreas | carcinoma | Substitution - Missense |
c.1555G>T; p.D519Y; 9:132400071-132400071 |
pancreas | NS | Substitution - Missense |
c.677C>T; p.S226F; 9:132402145-132402145 |
skin | malignant_melanoma | Substitution - Missense |
c.677C>T; p.S226F; 9:132402145-132402145 |
skin | malignant_melanoma | Substitution - Missense |
c.677C>T; p.S226F; 9:132402145-132402145 |
skin | malignant_melanoma | Substitution - Missense |
c.1718C>A; p.P573H; 9:132398200-132398200 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1079G>T; p.G360V; 9:132401743-132401743 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.914C>T; p.A305V; 9:132401908-132401908 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1079G>T; p.G360V; 9:132401743-132401743 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.1312C>T; p.R438*; 9:132401510-132401510 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.1777+10G>A; p.?; 9:132398131-132398131 |
stomach | carcinoma; adenocarcinoma | Unknown |
c.1561T>C; p.L521L; 9:132400065-132400065 |
thyroid | carcinoma | Substitution - coding silent |
c.2680T>C; p.S894P; 9:132375953-132375953 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.2113C>T; p.P705S; 9:132390706-132390706 |
skin | malignant_melanoma | Substitution - Missense |
c.1437A>C; p.A479A; 9:132400189-132400189 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1821A>T; p.A607A; 9:132396468-132396468 |
liver | carcinoma | Substitution - coding silent |
c.2077G>C; p.E693Q; 9:132390742-132390742 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.916G>C; p.D306H; 9:132401906-132401906 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1181T>G; p.L394R; 9:132401641-132401641 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1305T>C; p.S435S; 9:132401517-132401517 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.102C>T; p.H34H; 9:132402720-132402720 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2046A>T; p.E682D; 9:132390773-132390773 |
kidney | carcinoma; renal_cell_carcinoma | Substitution - Missense |
c.2241G>T; p.K747N; 9:132388210-132388210 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.821delA; p.K274fs*149; 9:132402001-132402001 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.821delA; p.K274fs*149; 9:132402001-132402001 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.821delA; p.K274fs*149; 9:132402001-132402001 |
pancreas | carcinoma; acinar_carcinoma | Deletion - Frameshift |
c.821delA; p.K274fs*149; 9:132402001-132402001 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.821delA; p.K274fs*149; 9:132402001-132402001 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.821delA; p.K274fs*149; 9:132402001-132402001 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.821delA; p.K274fs*149; 9:132402001-132402001 |
stomach | carcinoma; intestinal_adenocarcinoma | Deletion - Frameshift |
c.821delA; p.K274fs*149; 9:132402001-132402001 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.821delA; p.K274fs*149; 9:132402001-132402001 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.2676T>G; p.C892W; 9:132375957-132375957 |
thyroid | other; neoplasm | Substitution - Missense |
c.2472C>T; p.I824I; 9:132376161-132376161 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1886_1887insA; p.M630fs*9; 9:132392176-132392177 |
lung | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.1997G>A; p.R666H; 9:132390822-132390822 |
bone; rib | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.1997G>A; p.R666H; 9:132390822-132390822 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.1996C>T; p.R666C; 9:132390823-132390823 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1996C>T; p.R666C; 9:132390823-132390823 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1463A>G; p.D488G; 9:132400163-132400163 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.406T>C; p.L136L; 9:132402416-132402416 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1996C>T; p.R666C; 9:132390823-132390823 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1770A>T; p.L590F; 9:132398148-132398148 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.2072C>T; p.P691L; 9:132390747-132390747 |
skin | malignant_melanoma | Substitution - Missense |
c.1844A>G; p.N615S; 9:132396445-132396445 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2704C>T; p.R902W; 9:132375929-132375929 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1007delA; p.K336fs*87; 9:132401815-132401815 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1007delA; p.K336fs*87; 9:132401815-132401815 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.2145delA; p.K715fs*9; 9:132390674-132390674 |
oesophagus | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.2145delA; p.K715fs*9; 9:132390674-132390674 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1007delA; p.K336fs*87; 9:132401815-132401815 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1007delA; p.K336fs*87; 9:132401815-132401815 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1007delA; p.K336fs*87; 9:132401815-132401815 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1973C>G; p.S658*; 9:132392090-132392090 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.1286T>A; p.M429K; 9:132401536-132401536 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1893C>G; p.Y631*; 9:132392170-132392170 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Nonsense |
c.1286T>A; p.M429K; 9:132401536-132401536 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.1361C>T; p.A454V; 9:132401461-132401461 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1361C>T; p.A454V; 9:132401461-132401461 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2150A>G; p.Y717C; 9:132390669-132390669 |
skin | malignant_melanoma | Substitution - Missense |
c.1838T>C; p.V613A; 9:132396451-132396451 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1515C>G; p.I505M; 9:132400111-132400111 |
pancreas | carcinoma | Substitution - Missense |
c.1515C>G; p.I505M; 9:132400111-132400111 |
pancreas | carcinoma; ductal_carcinoma | Substitution - Missense |
c.351G>T; p.K117N; 9:132402471-132402471 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1737C>T; p.I579I; 9:132398181-132398181 |
skin | malignant_melanoma | Substitution - coding silent |
c.1686T>C; p.S562S; 9:132398232-132398232 |
skin | malignant_melanoma | Substitution - coding silent |
c.1313G>A; p.R438Q; 9:132401509-132401509 |
prostate | adenoma | Substitution - Missense |
c.527C>T; p.A176V; 9:132402295-132402295 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.527C>T; p.A176V; 9:132402295-132402295 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.527C>T; p.A176V; 9:132402295-132402295 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1803A>C; p.K601N; 9:132396486-132396486 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.668delA; p.K223fs*45; 9:132402154-132402154 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.668delA; p.K223fs*45; 9:132402154-132402154 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.368T>A; p.V123D; 9:132402454-132402454 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.668delA; p.K223fs*45; 9:132402154-132402154 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1580T>G; p.F527C; 9:132400046-132400046 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1816C>T; p.R606*; 9:132396473-132396473 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.56A>G; p.K19R; 9:132402766-132402766 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.719C>G; p.S240W; 9:132402103-132402103 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.584A>G; p.E195G; 9:132402238-132402238 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.990C>A; p.N330K; 9:132401832-132401832 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; plasma_cell_myeloma | Substitution - Missense |
c.75T>C; p.H25H; 9:132402747-132402747 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2655G>A; p.A885A; 9:132375978-132375978 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1551C>T; p.Y517Y; 9:132400075-132400075 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1007_1008insA; p.K337fs*9; 9:132401814-132401815 |
large_intestine; caecum | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.1007_1008insA; p.K337fs*9; 9:132401814-132401815 |
large_intestine | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.2587C>T; p.R863*; 9:132376046-132376046 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.2587C>T; p.R863*; 9:132376046-132376046 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.634G>A; p.A212T; 9:132402188-132402188 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1597G>A; p.A533T; 9:132398321-132398321 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.547G>T; p.A183S; 9:132402275-132402275 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.2675G>A; p.C892Y; 9:132375958-132375958 |
thyroid | other; neoplasm | Substitution - Missense |
c.2209T>G; p.C737G; 9:132390610-132390610 |
skin; mucosal | malignant_melanoma | Substitution - Missense |
c.2541C>T; p.G847G; 9:132376092-132376092 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1324A>G; p.T442A; 9:132401498-132401498 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1008_1009insA; p.S339fs*7; 9:132401813-132401814 |
stomach | carcinoma; intestinal_adenocarcinoma | Insertion - Frameshift |
c.1596C>T; p.V532V; 9:132398322-132398322 |
breast | carcinoma | Substitution - coding silent |
c.1086G>C; p.Q362H; 9:132401736-132401736 |
thyroid | other; neoplasm | Substitution - Missense |
c.771_772GG>AA; p.G258S; 9:132402050-132402051 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1927G>T; p.G643C; 9:132392136-132392136 |
lung; middle_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.1291G>T; p.E431*; 9:132401531-132401531 |
breast | carcinoma | Substitution - Nonsense |
c.1248C>T; p.S416S; 9:132401574-132401574 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.2172A>C; p.E724D; 9:132390647-132390647 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1699C>A; p.L567M; 9:132398219-132398219 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2685T>C; p.S895S; 9:132375948-132375948 |
cervix | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.2685T>C; p.S895S; 9:132375948-132375948 |
cervix | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |