General information | Literature | Expression | Regulation | Variant | Interaction |
Basic Information |
|
---|---|
Gene ID | 6934 |
Name | TCF7L2 |
Synonymous | transcription factor 7-like 2 (T-cell specific, HMG-box);TCF7L2;transcription factor 7-like 2 (T-cell specific, HMG-box) |
Definition | HMG box transcription factor 4|T-cell factor 4|T-cell factor-4 variant A|T-cell factor-4 variant B|T-cell factor-4 variant C|T-cell factor-4 variant D|T-cell factor-4 variant E|T-cell factor-4 variant F|T-cell factor-4 variant G|T-cell factor-4 variant H| |
Position | 10q25.3 |
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 |
There is no record for TCF7L2 |
The non-synonymous (top) and synonymous (bottom) mutational percentage for various cancers | Top |
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Loss of Function mutations compare to missense mutations | Top |
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The ratio of the loss-of-function mutations over missense mutations is 0.32. |
The copy number variations for various cancers | Top |
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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.1465C>G; p.P489A; 10:113165646-113165646 |
haematopoietic_and_lymphoid_tissue; lymph_node | lymphoid_neoplasm; acute_lymphoblastic_leukaemia | Substitution - Missense |
c.1035C>A; p.V345V; 10:113151827-113151827 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.866C>T; p.P289L; 10:113151057-113151057 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.932+1G>A; p.?; 10:113151124-113151124 |
large_intestine; rectum | carcinoma; adenocarcinoma | Unknown |
c.546G>C; p.T182T; 10:113141246-113141246 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.332T>C; p.L111P; 10:112951558-112951558 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.1458G>A; p.S486S; 10:113165639-113165639 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.187G>A; p.E63K; 10:112950943-112950943 |
biliary_tract; gallbladder | carcinoma; adenocarcinoma | Substitution - Missense |
c.80_82delAGG; p.E29delE; 10:112950836-112950838 |
endometrium | carcinoma; endometrioid_carcinoma | Deletion - In frame |
c.1185C>A; p.S395S; 10:113152425-113152425 |
lung | carcinoma; small_cell_carcinoma | Substitution - coding silent |
c.916G>A; p.G306S; 10:113151107-113151107 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1380A>G; p.K460K; 10:113165561-113165561 |
pancreas | carcinoma; ductal_carcinoma | Substitution - coding silent |
c.1472C>T; p.P491L; 10:113165653-113165653 |
skin | malignant_melanoma | Substitution - Missense |
c.1380A>G; p.K460K; 10:113165561-113165561 |
pancreas | pancreatic_intraepithelial_neoplasia_(PanIN) | Substitution - coding silent |
c.1380A>G; p.K460K; 10:113165561-113165561 |
pancreas | pancreatic_intraepithelial_neoplasia_(PanIN) | Substitution - coding silent |
c.49G>T; p.E17*; 10:112950805-112950805 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1393C>T; p.R465C; 10:113165574-113165574 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1393C>T; p.R465C; 10:113165574-113165574 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1393C>T; p.R465C; 10:113165574-113165574 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1393C>T; p.R465C; 10:113165574-113165574 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.754G>T; p.G252*; 10:113146045-113146045 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1393C>T; p.R465C; 10:113165574-113165574 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1393C>T; p.R465C; 10:113165574-113165574 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.590_591insA; p.P198fs*107; 10:113141290-113141291 |
large_intestine | NS | Insertion - Frameshift |
c.1393C>A; p.R465S; 10:113165574-113165574 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.458G>A; p.R153Q; 10:113040101-113040101 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1087C>A; p.R363R; 10:113151879-113151879 |
thyroid | carcinoma | Substitution - coding silent |
c.503T>C; p.V168A; 10:113141203-113141203 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1289C>T; p.P430L; 10:113158706-113158706 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.1488C>T; p.S496S; 10:113165669-113165669 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1488C>T; p.S496S; 10:113165669-113165669 |
skin | malignant_melanoma | Substitution - coding silent |
c.439C>T; p.Q147*; 10:113040082-113040082 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1606G>A; p.E536K; 10:113165787-113165787 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1063G>A; p.A355T; 10:113151855-113151855 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; acute_lymphoblastic_leukaemia | Substitution - Missense |
c.381+1G>A; p.?; 10:112951608-112951608 |
large_intestine; rectum | carcinoma; adenocarcinoma | Unknown |
c.1288C>T; p.P430S; 10:113158705-113158705 |
breast | carcinoma | Substitution - Missense |
c.439C>T; p.Q147*; 10:113040082-113040082 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.818_834del17; p.H273fs*26; 10:113151009-113151025 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.698C>T; p.P233L; 10:113144004-113144004 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.835C>T; p.H279Y; 10:113151026-113151026 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1462C>T; p.P488S; 10:113165643-113165643 |
skin | malignant_melanoma | Substitution - Missense |
c.1187C>T; p.A396V; 10:113152427-113152427 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1187C>T; p.A396V; 10:113152427-113152427 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1186G>A; p.A396T; 10:113152426-113152426 |
breast | carcinoma | Substitution - Missense |
c.740C>T; p.P247L; 10:113146031-113146031 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.137C>A; p.S46*; 10:112950893-112950893 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1131C>T; p.Y377Y; 10:113152371-113152371 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.994A>G; p.N332D; 10:113151786-113151786 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.152A>G; p.E51G; 10:112950908-112950908 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.904C>T; p.Q302*; 10:113151095-113151095 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.303C>A; p.P101P; 10:112951529-112951529 |
prostate | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1204_1206delAAG; p.K405delK; 10:113158024-113158026 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - In frame |
c.1377delA; p.K462fs*23; 10:113165558-113165558 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1377delA; p.K462fs*23; 10:113165558-113165558 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1377delA; p.K462fs*23; 10:113165558-113165558 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1377delA; p.K462fs*23; 10:113165558-113165558 |
large_intestine; rectum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1377delA; p.K462fs*23; 10:113165558-113165558 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1377delA; p.K462fs*23; 10:113165558-113165558 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1377delA; p.K462fs*23; 10:113165558-113165558 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1377delA; p.K462fs*23; 10:113165558-113165558 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1377delA; p.K462fs*23; 10:113165558-113165558 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1377delA; p.K462fs*23; 10:113165558-113165558 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1377delA; p.K462fs*23; 10:113165558-113165558 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1377delA; p.K462fs*23; 10:113165558-113165558 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1377delA; p.K462fs*23; 10:113165558-113165558 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1377delA; p.K462fs*23; 10:113165558-113165558 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1377delA; p.K462fs*23; 10:113165558-113165558 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1377delA; p.K462fs*23; 10:113165558-113165558 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1377delA; p.K462fs*23; 10:113165558-113165558 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1377delA; p.K462fs*23; 10:113165558-113165558 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1377delA; p.K462fs*23; 10:113165558-113165558 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1377delA; p.K462fs*23; 10:113165558-113165558 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1377delA; p.K462fs*23; 10:113165558-113165558 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1377delA; p.K462fs*23; 10:113165558-113165558 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1377delA; p.K462fs*23; 10:113165558-113165558 |
stomach | carcinoma; intestinal_adenocarcinoma | Deletion - Frameshift |
c.1377delA; p.K462fs*23; 10:113165558-113165558 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1377delA; p.K462fs*23; 10:113165558-113165558 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1377delA; p.K462fs*23; 10:113165558-113165558 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1377delA; p.K462fs*23; 10:113165558-113165558 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1377delA; p.K462fs*23; 10:113165558-113165558 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.932_932+1insGT; p.K312fs*1; 10:113151123-113151124 |
large_intestine | carcinoma; adenocarcinoma | Unknown |
c.1471C>T; p.P491S; 10:113165652-113165652 |
skin | malignant_melanoma | Substitution - Missense |
c.1738C>G; p.L580V; 10:113165919-113165919 |
biliary_tract; gallbladder | carcinoma; adenocarcinoma | Substitution - Missense |
c.1738C>G; p.L580V; 10:113165919-113165919 |
biliary_tract; gallbladder | carcinoma; adenocarcinoma | Substitution - Missense |
c.1292C>T; p.P431L; 10:113158709-113158709 |
skin | malignant_melanoma | Substitution - Missense |
c.140C>T; p.S47F; 10:112950896-112950896 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.622C>T; p.P208S; 10:113143928-113143928 |
skin | malignant_melanoma | Substitution - Missense |
c.1000delT; p.F334fs*5; 10:113151792-113151792 |
skin; trunk | malignant_melanoma | Deletion - Frameshift |
c.398G>A; p.W133*; 10:113040041-113040041 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.398G>A; p.W133*; 10:113040041-113040041 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.622C>A; p.P208T; 10:113143928-113143928 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.458G>T; p.R153L; 10:113040101-113040101 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.218A>C; p.E73A; 10:112951235-112951235 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.461C>A; p.S154Y; 10:113040104-113040104 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1201-2A>G; p.?; 10:113158019-113158019 |
large_intestine; colon | carcinoma; adenocarcinoma | Unknown |
c.860C>T; p.P287L; 10:113151051-113151051 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.774C>A; p.P258P; 10:113146065-113146065 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1002C>A; p.F334L; 10:113151794-113151794 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1362C>T; p.C454C; 10:113159981-113159981 |
central_nervous_system; brain | primitive_neuroectodermal_tumour-medulloblastoma | Substitution - coding silent |
c.1002C>A; p.F334L; 10:113151794-113151794 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1002C>A; p.F334L; 10:113151794-113151794 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1025G>T; p.R342I; 10:113151817-113151817 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1200+2T>C; p.?; 10:113152442-113152442 |
large_intestine | carcinoma; adenocarcinoma | Unknown |
c.1766C>T; p.S589L; 10:113165947-113165947 |
liver | carcinoma | Substitution - Missense |
c.1468T>C; p.S490P; 10:113165649-113165649 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1394G>A; p.R465H; 10:113165575-113165575 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1741G>T; p.A581S; 10:113165922-113165922 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1394G>A; p.R465H; 10:113165575-113165575 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1394G>A; p.R465H; 10:113165575-113165575 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.469C>T; p.P157S; 10:113040112-113040112 |
skin | malignant_melanoma | Substitution - Missense |
c.657T>G; p.Y219*; 10:113143963-113143963 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1240G>T; p.E414*; 10:113158060-113158060 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Nonsense |
c.1081C>T; p.L361F; 10:113151873-113151873 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.746C>T; p.T249M; 10:113146037-113146037 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1473G>A; p.P491P; 10:113165654-113165654 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.416delA; p.Q139fs*63; 10:113040059-113040059 |
liver | carcinoma; hepatocellular_carcinoma | Deletion - Frameshift |
c.1457C>T; p.S486L; 10:113165638-113165638 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.76G>C; p.E26Q; 10:112950832-112950832 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.616G>A; p.G206R; 10:113141316-113141316 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.616G>A; p.G206R; 10:113141316-113141316 |
large_intestine; caecum | adenoma | Substitution - Missense |
c.1068C>A; p.A356A; 10:113151860-113151860 |
ovary | other; neoplasm | Substitution - coding silent |
c.932C>T; p.S311L; 10:113151123-113151123 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1163_1164insT; p.M388fs*12; 10:113152403-113152404 |
liver | carcinoma; hepatocellular_carcinoma | Insertion - Frameshift |
c.1552G>A; p.D518N; 10:113165733-113165733 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.1163_1164insT; p.M388fs*12; 10:113152403-113152404 |
liver | carcinoma; hepatocellular_carcinoma | Insertion - Frameshift |
c.1552G>A; p.D518N; 10:113165733-113165733 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.1767G>A; p.S589S; 10:113165948-113165948 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1329G>A; p.A443A; 10:113159948-113159948 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1680C>T; p.A560A; 10:113165861-113165861 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - coding silent |
c.1157T>G; p.L386R; 10:113152397-113152397 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.1330C>T; p.R444C; 10:113159949-113159949 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.747G>A; p.T249T; 10:113146038-113146038 |
skin | malignant_melanoma | Substitution - coding silent |
c.1379_1400del22; p.K460fs*18; 10:113165560-113165581 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.888C>T; p.V296V; 10:113151079-113151079 |
large_intestine; rectum | adenoma | Substitution - coding silent |
c.1379_1400del22; p.K460fs*18; 10:113165560-113165581 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.690delC; p.H232fs*3; 10:113143996-113143996 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1093-2A>T; p.?; 10:113152331-113152331 |
liver | carcinoma; hepatocellular_carcinoma | Unknown |
c.566C>T; p.T189M; 10:113141266-113141266 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.1775C>A; p.T592N; 10:113165956-113165956 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.699G>A; p.P233P; 10:113144005-113144005 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1009T>C; p.Y337H; 10:113151801-113151801 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.865C>T; p.P289S; 10:113151056-113151056 |
pancreas | carcinoid-endocrine_tumour | Substitution - Missense |
c.1159C>A; p.H387N; 10:113152399-113152399 |
breast | carcinoma; ductal_carcinoma | Substitution - Missense |
c.1159C>A; p.H387N; 10:113152399-113152399 |
liver | carcinoma | Substitution - Missense |
c.70G>T; p.E24*; 10:112950826-112950826 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1584G>A; p.P528P; 10:113165765-113165765 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1494C>T; p.P498P; 10:113165675-113165675 |
skin | malignant_melanoma | Substitution - coding silent |
c.1584G>A; p.P528P; 10:113165765-113165765 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.221G>C; p.S74T; 10:112951238-112951238 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.542T>C; p.I181T; 10:113141242-113141242 |
central_nervous_system; brainstem | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.1465C>T; p.P489S; 10:113165646-113165646 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1176C>T; p.P392P; 10:113152416-113152416 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1388G>A; p.C463Y; 10:113165569-113165569 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1376_1377insA; p.C463fs*8; 10:113165557-113165558 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.1376_1377insA; p.C463fs*8; 10:113165557-113165558 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.1376_1377insA; p.C463fs*8; 10:113165557-113165558 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.1376_1377insA; p.C463fs*8; 10:113165557-113165558 |
large_intestine; rectum | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.1293G>A; p.P431P; 10:113158710-113158710 |
central_nervous_system; brain | primitive_neuroectodermal_tumour-medulloblastoma | Substitution - coding silent |
c.1192G>T; p.D398Y; 10:113152432-113152432 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.525delC; p.L177fs*25; 10:113141225-113141225 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.772C>A; p.P258T; 10:113146063-113146063 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.772C>A; p.P258T; 10:113146063-113146063 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.525delC; p.L177fs*25; 10:113141225-113141225 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1121C>T; p.A374V; 10:113152361-113152361 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1122G>A; p.A374A; 10:113152362-113152362 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1121C>T; p.A374V; 10:113152361-113152361 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.601G>A; p.V201I; 10:113141301-113141301 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.862C>T; p.H288Y; 10:113151053-113151053 |
breast | carcinoma | Substitution - Missense |
c.1158T>C; p.L386L; 10:113152398-113152398 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1189C>T; p.R397W; 10:113152429-113152429 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1189C>T; p.R397W; 10:113152429-113152429 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.604G>T; p.D202Y; 10:113141304-113141304 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1013T>G; p.M338R; 10:113151805-113151805 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.26G>A; p.G9E; 10:112950782-112950782 |
skin | malignant_melanoma | Substitution - Missense |
c.1338C>T; p.G446G; 10:113159957-113159957 |
liver | carcinoma | Substitution - coding silent |
c.840G>A; p.T280T; 10:113151031-113151031 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.598G>A; p.D200N; 10:113141298-113141298 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.771C>A; p.Y257*; 10:113146062-113146062 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1201-1G>C; p.?; 10:113158020-113158020 |
large_intestine; colon | carcinoma; adenocarcinoma | Unknown |
c.771C>A; p.Y257*; 10:113146062-113146062 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1755C>T; p.P585P; 10:113165936-113165936 |
skin | malignant_melanoma | Substitution - coding silent |
c.1536G>A; p.S512S; 10:113165717-113165717 |
large_intestine; colon | NS | Substitution - coding silent |
c.1556C>T; p.P519L; 10:113165737-113165737 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1150C>T; p.R384*; 10:113152390-113152390 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1150C>T; p.R384*; 10:113152390-113152390 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1150C>T; p.R384*; 10:113152390-113152390 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.238C>A; p.R80R; 10:112951255-112951255 |
prostate | carcinoma; adenocarcinoma | Substitution - coding silent |
c.584C>T; p.P195L; 10:113141284-113141284 |
skin | malignant_melanoma | Substitution - Missense |
c.1626C>T; p.S542S; 10:113165807-113165807 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1199A>G; p.Y400C; 10:113152439-113152439 |
liver | carcinoma | Substitution - Missense |
c.1199A>G; p.Y400C; 10:113152439-113152439 |
liver | carcinoma | Substitution - Missense |
c.1199A>G; p.Y400C; 10:113152439-113152439 |
liver | carcinoma | Substitution - Missense |
c.1199A>G; p.Y400C; 10:113152439-113152439 |
liver | carcinoma | Substitution - Missense |
c.1694C>T; p.S565L; 10:113165875-113165875 |
fallopian_tube | carcinoma; serous_carcinoma | Substitution - Missense |
c.692C>T; p.P231L; 10:113143998-113143998 |
skin | malignant_melanoma | Substitution - Missense |
c.143T>C; p.L48P; 10:112950899-112950899 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1389C>T; p.C463C; 10:113165570-113165570 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.551_552GC>TT; p.S184>?; 10:113141251-113141252 |
large_intestine; rectum | carcinoma; adenocarcinoma | Complex |
c.1077G>T; p.Q359H; 10:113151869-113151869 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.545C>T; p.T182M; 10:113141245-113141245 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1132G>T; p.E378*; 10:113152372-113152372 |
pancreas | pancreatic_intraepithelial_neoplasia_(PanIN) | Substitution - Nonsense |
c.1132G>T; p.E378*; 10:113152372-113152372 |
pancreas | carcinoma; ductal_carcinoma | Substitution - Nonsense |
c.1191G>T; p.R397R; 10:113152431-113152431 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.505C>T; p.Q169*; 10:113141205-113141205 |
liver | carcinoma | Substitution - Nonsense |
c.1692A>G; p.S564S; 10:113165873-113165873 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.505C>T; p.Q169*; 10:113141205-113141205 |
liver | carcinoma | Substitution - Nonsense |
c.1401A>G; p.I467M; 10:113165582-113165582 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1682C>T; p.A561V; 10:113165863-113165863 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.259G>A; p.A87T; 10:112951485-112951485 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - Missense |
c.259G>A; p.A87T; 10:112951485-112951485 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.534G>A; p.T178T; 10:113141234-113141234 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1140C>T; p.A380A; 10:113152380-113152380 |
skin; head_neck | malignant_melanoma; superficial_spreading | Substitution - coding silent |
c.1140C>T; p.A380A; 10:113152380-113152380 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1430C>T; p.P477L; 10:113165611-113165611 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1062C>T; p.S354S; 10:113151854-113151854 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.556G>T; p.E186*; 10:113141256-113141256 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1561G>A; p.A521T; 10:113165742-113165742 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1378A>C; p.K460Q; 10:113165559-113165559 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.915C>T; p.V305V; 10:113151106-113151106 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.915C>T; p.V305V; 10:113151106-113151106 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.774C>T; p.P258P; 10:113146065-113146065 |
skin | malignant_melanoma | Substitution - coding silent |
c.567G>A; p.T189T; 10:113141267-113141267 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1505A>G; p.K502R; 10:113165686-113165686 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.1703A>G; p.Q568R; 10:113165884-113165884 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1375_1376insG; p.C463fs*8; 10:113165556-113165557 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.1182G>T; p.W394C; 10:113152422-113152422 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |