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

Basic Information

Gene ID

6273

Name

S100A2

The somatic mutations from COSMIC database

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.260A>G; p.N87S; 1:153561473-153561473

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.260A>G; p.N87S; 1:153561473-153561473

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.260A>G; p.N87S; 1:153561473-153561473

ovarycarcinoma; serous_carcinomaSubstitution - Missense

c.259A>G; p.N87D; 1:153561474-153561474

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.259A>G; p.N87D; 1:153561474-153561474

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.259A>G; p.N87D; 1:153561474-153561474

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.62G>A; p.C21Y; 1:153563813-153563813

lungcarcinoma; small_cell_carcinomaSubstitution - Missense

c.41C>T; p.T14I; 1:153563834-153563834

breastcarcinomaSubstitution - Missense

c.211G>A; p.D71N; 1:153561522-153561522

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.73G>A; p.D25N; 1:153563802-153563802

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.261T>C; p.N87N; 1:153561472-153561472

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - coding silent

c.189T>G; p.D63E; 1:153561544-153561544

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.89G>T; p.S30I; 1:153563786-153563786

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.49C>T; p.H17Y; 1:153563826-153563826

skinmalignant_melanomaSubstitution - Missense

c.77A>C; p.K26T; 1:153563798-153563798

haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphomaSubstitution - Missense

c.77A>C; p.K26T; 1:153563798-153563798

haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; peripheral_T_cell_lymphoma_unspecifiedSubstitution - Missense

c.142G>A; p.E48K; 1:153561591-153561591

skinmalignant_melanomaSubstitution - Missense

c.220G>T; p.E74*; 1:153561513-153561513

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.209T>G; p.V70G; 1:153561524-153561524

breastcarcinomaSubstitution - Missense

c.72C>T; p.G24G; 1:153563803-153563803

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.241C>T; p.L81F; 1:153561492-153561492

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.234C>T; p.F78F; 1:153561499-153561499

skinmalignant_melanomaSubstitution - coding silent

c.59_61delCCT; p.S20delS; 1:153563814-153563816

large_intestine; coloncarcinoma; adenocarcinomaDeletion - In frame

c.76A>C; p.K26Q; 1:153563799-153563799

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.50A>C; p.H17P; 1:153563825-153563825

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense


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