Epithelial-Mesenchymal Transition gene database (dbEMT) Home
dbEMT
dbEMT 2.0
General information | Literature | Expression | lncRNA |Regulation | Mutation | Homolog | Interaction

Basic Information

Gene ID

2296

Name

FOXC1

The somatic mutations from COSMIC database

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.1462_1467delGCGGCG; p.A494_A495delAA; 6:1611907-1611912

upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaDeletion - In frame

c.440G>T; p.G147V; 6:1610885-1610885

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1077C>T; p.S359S; 6:1611522-1611522

lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.1457C>T; p.A486V; 6:1611902-1611902

oesophaguscarcinoma; adenocarcinomaSubstitution - Missense

c.1454T>C; p.L485S; 6:1611899-1611899

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.1661G>A; p.*554*; 6:1612106-1612106

urinary_tract; bladdercarcinomaSubstitution - coding silent

c.534C>G; p.D178E; 6:1610979-1610979

lung; right_lower_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.404G>A; p.C135Y; 6:1610849-1610849

haematopoietic_and_lymphoid_tissue; central_nervous_systemlymphoid_neoplasm; primary_central_nervous_system_lymphomaSubstitution - Missense

c.234G>T; p.K78N; 6:1610679-1610679

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.525G>A; p.K175K; 6:1610970-1610970

lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.501C>T; p.F167F; 6:1610946-1610946

lungcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.187G>A; p.A63T; 6:1610632-1610632

urinary_tract; bladdercarcinomaSubstitution - Missense

c.1638C>T; p.F546F; 6:1612083-1612083

urinary_tract; bladdercarcinomaSubstitution - coding silent

c.515G>A; p.R172Q; 6:1610960-1610960

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.403T>C; p.C135R; 6:1610848-1610848

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.1621C>T; p.R541C; 6:1612066-1612066

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.441C>T; p.G147G; 6:1610886-1610886

ovarycarcinoma; serous_carcinomaSubstitution - coding silent

c.469G>T; p.D157Y; 6:1610914-1610914

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.258C>A; p.L86L; 6:1610703-1610703

breastcarcinomaSubstitution - coding silent

c.458C>T; p.T153M; 6:1610903-1610903

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1595C>T; p.A532V; 6:1612040-1612040

skinmalignant_melanomaSubstitution - Missense

c.1123_1124insGGC; p.G375_G376insR; 6:1611568-1611569

biliary_tract; bile_ductcarcinoma; adenocarcinomaInsertion - In frame

c.474C>T; p.S158S; 6:1610919-1610919

prostatecarcinoma; adenocarcinomaSubstitution - coding silent

c.218C>A; p.P73H; 6:1610663-1610663

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.327G>A; p.M109I; 6:1610772-1610772

thyroidother; neoplasmSubstitution - Missense

c.513G>A; p.R171R; 6:1610958-1610958

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.532G>A; p.D178N; 6:1610977-1610977

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1020G>A; p.S340S; 6:1611465-1611465

livercarcinomaSubstitution - coding silent

c.1020G>A; p.S340S; 6:1611465-1611465

livercarcinomaSubstitution - coding silent

c.153G>A; p.A51A; 6:1610598-1610598

large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.524A>C; p.K175T; 6:1610969-1610969

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.779C>T; p.P260L; 6:1611224-1611224

NSmalignant_melanomaSubstitution - Missense

c.1554G>T; p.L518F; 6:1611999-1611999

livercarcinoma; hepatocellular_carcinomaSubstitution - Missense

c.1554G>T; p.L518F; 6:1611999-1611999

upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1600C>T; p.P534S; 6:1612045-1612045

oesophaguscarcinomaSubstitution - Missense

c.1554G>T; p.L518F; 6:1611999-1611999

upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1554G>T; p.L518F; 6:1611999-1611999

upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1554G>T; p.L518F; 6:1611999-1611999

upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1554G>T; p.L518F; 6:1611999-1611999

upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1554G>T; p.L518F; 6:1611999-1611999

upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1554G>T; p.L518F; 6:1611999-1611999

upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.373A>G; p.S125G; 6:1610818-1610818

breastcarcinomaSubstitution - Missense

c.503T>A; p.L168Q; 6:1610948-1610948

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.368A>C; p.Q123P; 6:1610813-1610813

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.600G>C; p.Q200H; 6:1611045-1611045

upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1122_1123insGGC; p.S374_G375insG; 6:1611567-1611568

lungcarcinoma; adenocarcinomaInsertion - In frame

c.893_894delCC; p.S298fs*7; 6:1611338-1611339

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift


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