Pulmonary Arterial Hypertension KnowledgeBase (bioinfom_tsdb)
bioinfom_tsdb
Pulmonary Arterial Hypertension KnowledgeBase
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

The non-synonymous mutational pattern in 17 major cancer types.
The synonymous mutational pattern in 17 major cancer types.

Loss of Function mutations compare to missense mutations

Top

Loss of Function mutations compare to missense mutation.
The ratio of the loss-of-function mutations over missense mutations is 0.32.

The copy number variations for various cancers

Top

The copy number variations in 17 major cancer groups: 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; NS, 11; Ovary, 12; Pancreas, 13; Prostate, 14; Skin, 15; Stomach, 16; Thyroid, 17; Urinary tract

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_nodelymphoid_neoplasm; acute_lymphoblastic_leukaemiaSubstitution - Missense

c.1035C>A; p.V345V; 10:113151827-113151827

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.866C>T; p.P289L; 10:113151057-113151057

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.932+1G>A; p.?; 10:113151124-113151124

large_intestine; rectumcarcinoma; adenocarcinomaUnknown

c.546G>C; p.T182T; 10:113141246-113141246

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.332T>C; p.L111P; 10:112951558-112951558

central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.1458G>A; p.S486S; 10:113165639-113165639

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.187G>A; p.E63K; 10:112950943-112950943

biliary_tract; gallbladdercarcinoma; adenocarcinomaSubstitution - Missense

c.80_82delAGG; p.E29delE; 10:112950836-112950838

endometriumcarcinoma; endometrioid_carcinomaDeletion - In frame

c.1185C>A; p.S395S; 10:113152425-113152425

lungcarcinoma; small_cell_carcinomaSubstitution - coding silent

c.916G>A; p.G306S; 10:113151107-113151107

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.1380A>G; p.K460K; 10:113165561-113165561

pancreascarcinoma; ductal_carcinomaSubstitution - coding silent

c.1472C>T; p.P491L; 10:113165653-113165653

skinmalignant_melanomaSubstitution - Missense

c.1380A>G; p.K460K; 10:113165561-113165561

pancreaspancreatic_intraepithelial_neoplasia_(PanIN)Substitution - coding silent

c.1380A>G; p.K460K; 10:113165561-113165561

pancreaspancreatic_intraepithelial_neoplasia_(PanIN)Substitution - coding silent

c.49G>T; p.E17*; 10:112950805-112950805

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.1393C>T; p.R465C; 10:113165574-113165574

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.1393C>T; p.R465C; 10:113165574-113165574

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1393C>T; p.R465C; 10:113165574-113165574

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1393C>T; p.R465C; 10:113165574-113165574

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.754G>T; p.G252*; 10:113146045-113146045

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.1393C>T; p.R465C; 10:113165574-113165574

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1393C>T; p.R465C; 10:113165574-113165574

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.590_591insA; p.P198fs*107; 10:113141290-113141291

large_intestineNSInsertion - Frameshift

c.1393C>A; p.R465S; 10:113165574-113165574

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.458G>A; p.R153Q; 10:113040101-113040101

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1087C>A; p.R363R; 10:113151879-113151879

thyroidcarcinomaSubstitution - coding silent

c.503T>C; p.V168A; 10:113141203-113141203

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.1289C>T; p.P430L; 10:113158706-113158706

lungcarcinoma; small_cell_carcinomaSubstitution - Missense

c.1488C>T; p.S496S; 10:113165669-113165669

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.1488C>T; p.S496S; 10:113165669-113165669

skinmalignant_melanomaSubstitution - coding silent

c.439C>T; p.Q147*; 10:113040082-113040082

large_intestinecarcinoma; adenocarcinomaSubstitution - Nonsense

c.1606G>A; p.E536K; 10:113165787-113165787

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.1063G>A; p.A355T; 10:113151855-113151855

haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; acute_lymphoblastic_leukaemiaSubstitution - Missense

c.381+1G>A; p.?; 10:112951608-112951608

large_intestine; rectumcarcinoma; adenocarcinomaUnknown

c.1288C>T; p.P430S; 10:113158705-113158705

breastcarcinomaSubstitution - Missense

c.439C>T; p.Q147*; 10:113040082-113040082

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.818_834del17; p.H273fs*26; 10:113151009-113151025

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.698C>T; p.P233L; 10:113144004-113144004

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.835C>T; p.H279Y; 10:113151026-113151026

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1462C>T; p.P488S; 10:113165643-113165643

skinmalignant_melanomaSubstitution - Missense

c.1187C>T; p.A396V; 10:113152427-113152427

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.1187C>T; p.A396V; 10:113152427-113152427

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.1186G>A; p.A396T; 10:113152426-113152426

breastcarcinomaSubstitution - Missense

c.740C>T; p.P247L; 10:113146031-113146031

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.137C>A; p.S46*; 10:112950893-112950893

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Nonsense

c.1131C>T; p.Y377Y; 10:113152371-113152371

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.994A>G; p.N332D; 10:113151786-113151786

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.152A>G; p.E51G; 10:112950908-112950908

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.904C>T; p.Q302*; 10:113151095-113151095

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Nonsense

c.303C>A; p.P101P; 10:112951529-112951529

prostatecarcinoma; adenocarcinomaSubstitution - coding silent

c.1204_1206delAAG; p.K405delK; 10:113158024-113158026

large_intestine; coloncarcinoma; adenocarcinomaDeletion - In frame

c.1377delA; p.K462fs*23; 10:113165558-113165558

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.1377delA; p.K462fs*23; 10:113165558-113165558

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.1377delA; p.K462fs*23; 10:113165558-113165558

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.1377delA; p.K462fs*23; 10:113165558-113165558

large_intestine; rectumcarcinoma; adenocarcinomaDeletion - Frameshift

c.1377delA; p.K462fs*23; 10:113165558-113165558

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.1377delA; p.K462fs*23; 10:113165558-113165558

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.1377delA; p.K462fs*23; 10:113165558-113165558

large_intestinecarcinoma; adenocarcinomaDeletion - Frameshift

c.1377delA; p.K462fs*23; 10:113165558-113165558

large_intestine; caecumcarcinoma; adenocarcinomaDeletion - Frameshift

c.1377delA; p.K462fs*23; 10:113165558-113165558

large_intestinecarcinoma; adenocarcinomaDeletion - Frameshift

c.1377delA; p.K462fs*23; 10:113165558-113165558

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.1377delA; p.K462fs*23; 10:113165558-113165558

large_intestinecarcinoma; adenocarcinomaDeletion - Frameshift

c.1377delA; p.K462fs*23; 10:113165558-113165558

large_intestinecarcinoma; adenocarcinomaDeletion - Frameshift

c.1377delA; p.K462fs*23; 10:113165558-113165558

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.1377delA; p.K462fs*23; 10:113165558-113165558

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.1377delA; p.K462fs*23; 10:113165558-113165558

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.1377delA; p.K462fs*23; 10:113165558-113165558

large_intestine; caecumcarcinoma; adenocarcinomaDeletion - Frameshift

c.1377delA; p.K462fs*23; 10:113165558-113165558

large_intestine; caecumcarcinoma; adenocarcinomaDeletion - Frameshift

c.1377delA; p.K462fs*23; 10:113165558-113165558

large_intestinecarcinoma; adenocarcinomaDeletion - Frameshift

c.1377delA; p.K462fs*23; 10:113165558-113165558

large_intestinecarcinoma; adenocarcinomaDeletion - Frameshift

c.1377delA; p.K462fs*23; 10:113165558-113165558

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.1377delA; p.K462fs*23; 10:113165558-113165558

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.1377delA; p.K462fs*23; 10:113165558-113165558

large_intestinecarcinoma; adenocarcinomaDeletion - Frameshift

c.1377delA; p.K462fs*23; 10:113165558-113165558

stomachcarcinoma; intestinal_adenocarcinomaDeletion - Frameshift

c.1377delA; p.K462fs*23; 10:113165558-113165558

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.1377delA; p.K462fs*23; 10:113165558-113165558

large_intestinecarcinoma; adenocarcinomaDeletion - Frameshift

c.1377delA; p.K462fs*23; 10:113165558-113165558

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.1377delA; p.K462fs*23; 10:113165558-113165558

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.1377delA; p.K462fs*23; 10:113165558-113165558

large_intestinecarcinoma; adenocarcinomaDeletion - Frameshift

c.932_932+1insGT; p.K312fs*1; 10:113151123-113151124

large_intestinecarcinoma; adenocarcinomaUnknown

c.1471C>T; p.P491S; 10:113165652-113165652

skinmalignant_melanomaSubstitution - Missense

c.1738C>G; p.L580V; 10:113165919-113165919

biliary_tract; gallbladdercarcinoma; adenocarcinomaSubstitution - Missense

c.1738C>G; p.L580V; 10:113165919-113165919

biliary_tract; gallbladdercarcinoma; adenocarcinomaSubstitution - Missense

c.1292C>T; p.P431L; 10:113158709-113158709

skinmalignant_melanomaSubstitution - Missense

c.140C>T; p.S47F; 10:112950896-112950896

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.622C>T; p.P208S; 10:113143928-113143928

skinmalignant_melanomaSubstitution - Missense

c.1000delT; p.F334fs*5; 10:113151792-113151792

skin; trunkmalignant_melanomaDeletion - Frameshift

c.398G>A; p.W133*; 10:113040041-113040041

large_intestinecarcinoma; adenocarcinomaSubstitution - Nonsense

c.398G>A; p.W133*; 10:113040041-113040041

large_intestinecarcinoma; adenocarcinomaSubstitution - Nonsense

c.622C>A; p.P208T; 10:113143928-113143928

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.458G>T; p.R153L; 10:113040101-113040101

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.218A>C; p.E73A; 10:112951235-112951235

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.461C>A; p.S154Y; 10:113040104-113040104

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.1201-2A>G; p.?; 10:113158019-113158019

large_intestine; coloncarcinoma; adenocarcinomaUnknown

c.860C>T; p.P287L; 10:113151051-113151051

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.774C>A; p.P258P; 10:113146065-113146065

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.1002C>A; p.F334L; 10:113151794-113151794

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.1362C>T; p.C454C; 10:113159981-113159981

central_nervous_system; brainprimitive_neuroectodermal_tumour-medulloblastomaSubstitution - coding silent

c.1002C>A; p.F334L; 10:113151794-113151794

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.1002C>A; p.F334L; 10:113151794-113151794

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1025G>T; p.R342I; 10:113151817-113151817

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1200+2T>C; p.?; 10:113152442-113152442

large_intestinecarcinoma; adenocarcinomaUnknown

c.1766C>T; p.S589L; 10:113165947-113165947

livercarcinomaSubstitution - Missense

c.1468T>C; p.S490P; 10:113165649-113165649

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.1394G>A; p.R465H; 10:113165575-113165575

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1741G>T; p.A581S; 10:113165922-113165922

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.1394G>A; p.R465H; 10:113165575-113165575

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1394G>A; p.R465H; 10:113165575-113165575

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.469C>T; p.P157S; 10:113040112-113040112

skinmalignant_melanomaSubstitution - Missense

c.657T>G; p.Y219*; 10:113143963-113143963

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.1240G>T; p.E414*; 10:113158060-113158060

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - Nonsense

c.1081C>T; p.L361F; 10:113151873-113151873

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.746C>T; p.T249M; 10:113146037-113146037

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.1473G>A; p.P491P; 10:113165654-113165654

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.416delA; p.Q139fs*63; 10:113040059-113040059

livercarcinoma; hepatocellular_carcinomaDeletion - Frameshift

c.1457C>T; p.S486L; 10:113165638-113165638

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.76G>C; p.E26Q; 10:112950832-112950832

central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.616G>A; p.G206R; 10:113141316-113141316

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.616G>A; p.G206R; 10:113141316-113141316

large_intestine; caecumadenomaSubstitution - Missense

c.1068C>A; p.A356A; 10:113151860-113151860

ovaryother; neoplasmSubstitution - coding silent

c.932C>T; p.S311L; 10:113151123-113151123

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.1163_1164insT; p.M388fs*12; 10:113152403-113152404

livercarcinoma; hepatocellular_carcinomaInsertion - Frameshift

c.1552G>A; p.D518N; 10:113165733-113165733

stomachcarcinoma; intestinal_adenocarcinomaSubstitution - Missense

c.1163_1164insT; p.M388fs*12; 10:113152403-113152404

livercarcinoma; hepatocellular_carcinomaInsertion - Frameshift

c.1552G>A; p.D518N; 10:113165733-113165733

prostatecarcinoma; adenocarcinomaSubstitution - Missense

c.1767G>A; p.S589S; 10:113165948-113165948

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.1329G>A; p.A443A; 10:113159948-113159948

upper_aerodigestive_tract; mouthcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.1680C>T; p.A560A; 10:113165861-113165861

kidneycarcinoma; papillary_renal_cell_carcinomaSubstitution - coding silent

c.1157T>G; p.L386R; 10:113152397-113152397

central_nervous_system; braingliomaSubstitution - Missense

c.1330C>T; p.R444C; 10:113159949-113159949

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.747G>A; p.T249T; 10:113146038-113146038

skinmalignant_melanomaSubstitution - coding silent

c.1379_1400del22; p.K460fs*18; 10:113165560-113165581

large_intestinecarcinoma; adenocarcinomaDeletion - Frameshift

c.888C>T; p.V296V; 10:113151079-113151079

large_intestine; rectumadenomaSubstitution - coding silent

c.1379_1400del22; p.K460fs*18; 10:113165560-113165581

large_intestinecarcinoma; adenocarcinomaDeletion - Frameshift

c.690delC; p.H232fs*3; 10:113143996-113143996

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.1093-2A>T; p.?; 10:113152331-113152331

livercarcinoma; hepatocellular_carcinomaUnknown

c.566C>T; p.T189M; 10:113141266-113141266

oesophaguscarcinoma; adenocarcinomaSubstitution - Missense

c.1775C>A; p.T592N; 10:113165956-113165956

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.699G>A; p.P233P; 10:113144005-113144005

large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.1009T>C; p.Y337H; 10:113151801-113151801

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.865C>T; p.P289S; 10:113151056-113151056

pancreascarcinoid-endocrine_tumourSubstitution - Missense

c.1159C>A; p.H387N; 10:113152399-113152399

breastcarcinoma; ductal_carcinomaSubstitution - Missense

c.1159C>A; p.H387N; 10:113152399-113152399

livercarcinomaSubstitution - Missense

c.70G>T; p.E24*; 10:112950826-112950826

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Nonsense

c.1584G>A; p.P528P; 10:113165765-113165765

large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.1494C>T; p.P498P; 10:113165675-113165675

skinmalignant_melanomaSubstitution - coding silent

c.1584G>A; p.P528P; 10:113165765-113165765

large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.221G>C; p.S74T; 10:112951238-112951238

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.542T>C; p.I181T; 10:113141242-113141242

central_nervous_system; brainstemglioma; astrocytoma_Grade_IVSubstitution - Missense

c.1465C>T; p.P489S; 10:113165646-113165646

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1176C>T; p.P392P; 10:113152416-113152416

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.1388G>A; p.C463Y; 10:113165569-113165569

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1376_1377insA; p.C463fs*8; 10:113165557-113165558

large_intestine; coloncarcinoma; adenocarcinomaInsertion - Frameshift

c.1376_1377insA; p.C463fs*8; 10:113165557-113165558

large_intestine; coloncarcinoma; adenocarcinomaInsertion - Frameshift

c.1376_1377insA; p.C463fs*8; 10:113165557-113165558

large_intestine; coloncarcinoma; adenocarcinomaInsertion - Frameshift

c.1376_1377insA; p.C463fs*8; 10:113165557-113165558

large_intestine; rectumcarcinoma; adenocarcinomaInsertion - Frameshift

c.1293G>A; p.P431P; 10:113158710-113158710

central_nervous_system; brainprimitive_neuroectodermal_tumour-medulloblastomaSubstitution - coding silent

c.1192G>T; p.D398Y; 10:113152432-113152432

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.525delC; p.L177fs*25; 10:113141225-113141225

large_intestine; caecumcarcinoma; adenocarcinomaDeletion - Frameshift

c.772C>A; p.P258T; 10:113146063-113146063

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.772C>A; p.P258T; 10:113146063-113146063

ovarycarcinoma; serous_carcinomaSubstitution - Missense

c.525delC; p.L177fs*25; 10:113141225-113141225

large_intestine; caecumcarcinoma; adenocarcinomaDeletion - Frameshift

c.1121C>T; p.A374V; 10:113152361-113152361

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1122G>A; p.A374A; 10:113152362-113152362

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - coding silent

c.1121C>T; p.A374V; 10:113152361-113152361

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.601G>A; p.V201I; 10:113141301-113141301

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.862C>T; p.H288Y; 10:113151053-113151053

breastcarcinomaSubstitution - Missense

c.1158T>C; p.L386L; 10:113152398-113152398

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.1189C>T; p.R397W; 10:113152429-113152429

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.1189C>T; p.R397W; 10:113152429-113152429

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.604G>T; p.D202Y; 10:113141304-113141304

kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.1013T>G; p.M338R; 10:113151805-113151805

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.26G>A; p.G9E; 10:112950782-112950782

skinmalignant_melanomaSubstitution - Missense

c.1338C>T; p.G446G; 10:113159957-113159957

livercarcinomaSubstitution - coding silent

c.840G>A; p.T280T; 10:113151031-113151031

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.598G>A; p.D200N; 10:113141298-113141298

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.771C>A; p.Y257*; 10:113146062-113146062

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.1201-1G>C; p.?; 10:113158020-113158020

large_intestine; coloncarcinoma; adenocarcinomaUnknown

c.771C>A; p.Y257*; 10:113146062-113146062

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.1755C>T; p.P585P; 10:113165936-113165936

skinmalignant_melanomaSubstitution - coding silent

c.1536G>A; p.S512S; 10:113165717-113165717

large_intestine; colonNSSubstitution - coding silent

c.1556C>T; p.P519L; 10:113165737-113165737

upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1150C>T; p.R384*; 10:113152390-113152390

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.1150C>T; p.R384*; 10:113152390-113152390

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.1150C>T; p.R384*; 10:113152390-113152390

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Nonsense

c.238C>A; p.R80R; 10:112951255-112951255

prostatecarcinoma; adenocarcinomaSubstitution - coding silent

c.584C>T; p.P195L; 10:113141284-113141284

skinmalignant_melanomaSubstitution - Missense

c.1626C>T; p.S542S; 10:113165807-113165807

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.1199A>G; p.Y400C; 10:113152439-113152439

livercarcinomaSubstitution - Missense

c.1199A>G; p.Y400C; 10:113152439-113152439

livercarcinomaSubstitution - Missense

c.1199A>G; p.Y400C; 10:113152439-113152439

livercarcinomaSubstitution - Missense

c.1199A>G; p.Y400C; 10:113152439-113152439

livercarcinomaSubstitution - Missense

c.1694C>T; p.S565L; 10:113165875-113165875

fallopian_tubecarcinoma; serous_carcinomaSubstitution - Missense

c.692C>T; p.P231L; 10:113143998-113143998

skinmalignant_melanomaSubstitution - Missense

c.143T>C; p.L48P; 10:112950899-112950899

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1389C>T; p.C463C; 10:113165570-113165570

large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.551_552GC>TT; p.S184>?; 10:113141251-113141252

large_intestine; rectumcarcinoma; adenocarcinomaComplex

c.1077G>T; p.Q359H; 10:113151869-113151869

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.545C>T; p.T182M; 10:113141245-113141245

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1132G>T; p.E378*; 10:113152372-113152372

pancreaspancreatic_intraepithelial_neoplasia_(PanIN)Substitution - Nonsense

c.1132G>T; p.E378*; 10:113152372-113152372

pancreascarcinoma; ductal_carcinomaSubstitution - Nonsense

c.1191G>T; p.R397R; 10:113152431-113152431

lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.505C>T; p.Q169*; 10:113141205-113141205

livercarcinomaSubstitution - Nonsense

c.1692A>G; p.S564S; 10:113165873-113165873

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - coding silent

c.505C>T; p.Q169*; 10:113141205-113141205

livercarcinomaSubstitution - Nonsense

c.1401A>G; p.I467M; 10:113165582-113165582

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.1682C>T; p.A561V; 10:113165863-113165863

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.259G>A; p.A87T; 10:112951485-112951485

urinary_tract; bladdercarcinoma; transitional_cell_carcinomaSubstitution - Missense

c.259G>A; p.A87T; 10:112951485-112951485

urinary_tract; bladdercarcinomaSubstitution - Missense

c.534G>A; p.T178T; 10:113141234-113141234

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.1140C>T; p.A380A; 10:113152380-113152380

skin; head_neckmalignant_melanoma; superficial_spreadingSubstitution - coding silent

c.1140C>T; p.A380A; 10:113152380-113152380

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.1430C>T; p.P477L; 10:113165611-113165611

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1062C>T; p.S354S; 10:113151854-113151854

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.556G>T; p.E186*; 10:113141256-113141256

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Nonsense

c.1561G>A; p.A521T; 10:113165742-113165742

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.1378A>C; p.K460Q; 10:113165559-113165559

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.915C>T; p.V305V; 10:113151106-113151106

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.915C>T; p.V305V; 10:113151106-113151106

large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.774C>T; p.P258P; 10:113146065-113146065

skinmalignant_melanomaSubstitution - coding silent

c.567G>A; p.T189T; 10:113141267-113141267

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.1505A>G; p.K502R; 10:113165686-113165686

livercarcinoma; hepatocellular_carcinomaSubstitution - Missense

c.1703A>G; p.Q568R; 10:113165884-113165884

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.1375_1376insG; p.C463fs*8; 10:113165556-113165557

large_intestine; coloncarcinoma; adenocarcinomaInsertion - Frameshift

c.1182G>T; p.W394C; 10:113152422-113152422

oesophaguscarcinoma; adenocarcinomaSubstitution - Missense


')