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

Basic Information

Gene ID

1437

Name

CSF2

The somatic mutations from COSMIC database

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.121C>G; p.R41G; 5:132073944-132073944

soft_tissue; striated_musclerhabdomyosarcoma; embryonalSubstitution - Missense

c.121C>G; p.R41G; 5:132073944-132073944

soft_tissue; striated_musclerhabdomyosarcomaSubstitution - Missense

c.309G>T; p.Q103H; 5:132074917-132074917

haematopoietic_and_lymphoid_tissuelymphoid_neoplasmSubstitution - Missense

c.319C>A; p.P107T; 5:132074927-132074927

stomachcarcinoma; intestinal_adenocarcinomaSubstitution - Missense

c.253G>A; p.G85S; 5:132074861-132074861

skinmalignant_melanomaSubstitution - Missense

c.409G>C; p.D137H; 5:132075826-132075826

pancreascarcinomaSubstitution - Missense

c.99G>C; p.V33V; 5:132073922-132073922

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - coding silent

c.298C>A; p.H100N; 5:132074906-132074906

skin; earcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.184G>T; p.E62*; 5:132074105-132074105

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Nonsense

c.387C>G; p.D129E; 5:132075804-132075804

ovaryother; neoplasmSubstitution - Missense

c.24C>T; p.L8L; 5:132073847-132073847

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.388T>C; p.F130L; 5:132075805-132075805

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemia_associated_with_MDSSubstitution - Missense

c.104C>T; p.A35V; 5:132073927-132073927

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.323C>T; p.T108I; 5:132074931-132074931

urinary_tract; bladdercarcinomaSubstitution - Missense

c.323C>T; p.T108I; 5:132074931-132074931

urinary_tract; bladdercarcinoma; transitional_cell_carcinomaSubstitution - Missense

c.350T>C; p.I117T; 5:132075767-132075767

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.350T>C; p.I117T; 5:132075767-132075767

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - Missense

c.170T>C; p.V57A; 5:132074091-132074091

central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.135G>A; p.L45L; 5:132073958-132073958

skinmalignant_melanomaSubstitution - coding silent

c.365G>A; p.S122N; 5:132075782-132075782

skinmalignant_melanomaSubstitution - Missense


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