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

Basic Information

Gene ID

6700

Name

SPRR2A

The somatic mutations from COSMIC database

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.216G>T; p.K72N; 1:153056520-153056520

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.197A>C; p.K66T; 1:153056539-153056539

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.31C>A; p.P11T; 1:153056705-153056705

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.164C>T; p.P55L; 1:153056572-153056572

skinmalignant_melanomaSubstitution - Missense

c.75G>A; p.E25E; 1:153056661-153056661

upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.163C>T; p.P55S; 1:153056573-153056573

skinmalignant_melanomaSubstitution - Missense

c.103C>T; p.P35S; 1:153056633-153056633

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.207G>A; p.P69P; 1:153056529-153056529

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.202C>T; p.P68S; 1:153056534-153056534

kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.213C>A; p.S71R; 1:153056523-153056523

ovarycarcinoma; serous_carcinomaSubstitution - Missense

c.132C>A; p.P44P; 1:153056604-153056604

autonomic_ganglianeuroblastomaSubstitution - coding silent

c.205C>T; p.P69S; 1:153056531-153056531

skinmalignant_melanomaSubstitution - Missense

c.54C>T; p.C18C; 1:153056682-153056682

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.62C>A; p.P21Q; 1:153056674-153056674

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.156G>T; p.Q52H; 1:153056580-153056580

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense


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