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

Basic Information

Gene ID

1366

Name

CLDN7

The somatic mutations from COSMIC database

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.90G>A; p.W30*; 17:7261954-7261954

large_intestinecarcinoma; adenocarcinomaSubstitution - Nonsense

c.90G>A; p.W30*; 17:7261954-7261954

large_intestine; coloncarcinomaSubstitution - Nonsense

c.378C>T; p.F126F; 17:7260831-7260831

lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.315G>A; p.T105T; 17:7260894-7260894

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.19C>A; p.Q7K; 17:7262025-7262025

autonomic_ganglianeuroblastomaSubstitution - Missense

c.528C>T; p.I176I; 17:7260482-7260482

central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - coding silent

c.517G>A; p.A173T; 17:7260493-7260493

kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.587G>C; p.R196P; 17:7260423-7260423

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.350G>A; p.R117H; 17:7260859-7260859

haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; acute_lymphoblastic_leukaemiaSubstitution - Missense

c.271G>A; p.G91S; 17:7260938-7260938

skinmalignant_melanomaSubstitution - Missense

c.339G>T; p.V113V; 17:7260870-7260870

ovarycarcinoma; serous_carcinomaSubstitution - coding silent

c.606T>A; p.P202P; 17:7260404-7260404

oesophaguscarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.439G>T; p.D147Y; 17:7260676-7260676

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.622A>G; p.K208E; 17:7260388-7260388

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - Missense

c.633G>A; p.V211V; 17:7260377-7260377

central_nervous_system; braingliomaSubstitution - coding silent

c.203A>G; p.D68G; 17:7261841-7261841

haematopoietic_and_lymphoid_tissuelymphoid_neoplasmSubstitution - Missense

c.537T>G; p.G179G; 17:7260473-7260473

ovaryother; neoplasmSubstitution - coding silent

c.514T>G; p.S172A; 17:7260496-7260496

prostatecarcinoma; adenocarcinomaSubstitution - Missense

c.514T>G; p.S172A; 17:7260496-7260496

kidneycarcinoma; papillary_renal_cell_carcinomaSubstitution - Missense

c.514T>G; p.S172A; 17:7260496-7260496

kidneycarcinoma; papillary_renal_cell_carcinomaSubstitution - Missense

c.514T>G; p.S172A; 17:7260496-7260496

skinmalignant_melanomaSubstitution - Missense

c.373A>C; p.I125L; 17:7260836-7260836

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.603C>T; p.Y201Y; 17:7260407-7260407

lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - coding silent

c.606T>G; p.P202P; 17:7260404-7260404

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - coding silent


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