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

Basic Information

Gene ID

10563

Name

CXCL13

The somatic mutations from COSMIC database

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.20C>T; p.S7F; 4:77605885-77605885

skin; trunkmalignant_melanomaSubstitution - Missense

c.78C>A; p.V26V; 4:77607716-77607716

autonomic_ganglianeuroblastomaSubstitution - coding silent

c.185G>T; p.R62I; 4:77607823-77607823

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.15G>A; p.S5S; 4:77605880-77605880

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.14C>T; p.S5L; 4:77605879-77605879

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.149G>A; p.R50Q; 4:77607787-77607787

urinary_tract; bladdercarcinomaSubstitution - Missense

c.159C>A; p.I53I; 4:77607797-77607797

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.305C>T; p.P102L; 4:77611014-77611014

skinmalignant_melanomaSubstitution - Missense

c.157A>T; p.I53F; 4:77607795-77607795

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.279A>T; p.K93N; 4:77610988-77610988

thyroidcarcinomaSubstitution - Missense

c.145G>A; p.D49N; 4:77607783-77607783

skinmalignant_melanomaSubstitution - Missense

c.295C>G; p.L99V; 4:77611004-77611004

oesophaguscarcinomaSubstitution - Missense

c.136C>T; p.R46C; 4:77607774-77607774

bone; femurchondrosarcomaSubstitution - Missense

c.136C>T; p.R46C; 4:77607774-77607774

oesophaguscarcinoma; adenocarcinomaSubstitution - Missense

c.197+2T>G; p.?; 4:77607837-77607837

ovarycarcinoma; serous_carcinomaUnknown

c.30C>T; p.L10L; 4:77605895-77605895

urinary_tract; bladdercarcinomaSubstitution - coding silent

c.141C>A; p.F47L; 4:77607779-77607779

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.166C>T; p.R56C; 4:77607804-77607804

central_nervous_system; braingliomaSubstitution - Missense

c.138C>A; p.R46R; 4:77607776-77607776

lungcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.116G>A; p.S39N; 4:77607754-77607754

central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense


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