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

Basic Information

Gene ID

6347

Name

CCL2

The somatic mutations from COSMIC database

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.147G>A; p.A49A; 17:34256292-34256292

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.104G>A; p.C35Y; 17:34256249-34256249

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.250C>A; p.Q84K; 17:34256777-34256777

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.180C>A; p.P60P; 17:34256325-34256325

 lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.262G>C; p.D88H; 17:34256789-34256789

 kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.194T>A; p.I65N; 17:34256339-34256339

 central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.62G>A; p.G21E; 17:34255411-34255411

 skin; mucosalmalignant_melanomaSubstitution - Missense

c.231C>T; p.D77D; 17:34256758-34256758

 lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.55C>T; p.P19S; 17:34255404-34255404

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.273C>A; p.D91E; 17:34256800-34256800

 lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.157A>T; p.R53*; 17:34256302-34256302

 pancreasNSSubstitution - Nonsense

c.200A>G; p.K67R; 17:34256727-34256727

 breastcarcinomaSubstitution - Missense

c.157A>T; p.R53*; 17:34256302-34256302

 pancreascarcinomaSubstitution - Nonsense

c.291G>A; p.P97P; 17:34256818-34256818

 pancreascarcinomaSubstitution - coding silent

c.253G>A; p.D85N; 17:34256780-34256780

 skinmalignant_melanomaSubstitution - Missense

c.250C>T; p.Q84*; 17:34256777-34256777

 skinmalignant_melanomaSubstitution - Nonsense

c.280A>G; p.T94A; 17:34256807-34256807

 skinmalignant_melanomaSubstitution - Missense

c.172A>T; p.K58*; 17:34256317-34256317

 upper_aerodigestive_tract; larynxcarcinoma; squamous_cell_carcinomaSubstitution - Nonsense

c.158G>T; p.R53I; 17:34256303-34256303

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.229G>T; p.D77Y; 17:34256756-34256756

 oesophaguscarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.140G>C; p.R47T; 17:34256285-34256285

 kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.290C>T; p.P97L; 17:34256817-34256817

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.7G>A; p.V3I; 17:34255356-34255356

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.119A>G; p.N40S; 17:34256264-34256264

 pancreascarcinomaSubstitution - Missense

c.16G>A; p.A6T; 17:34255365-34255365

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.70C>T; p.Q24*; 17:34255419-34255419

 biliary_tract; gallbladdercarcinoma; adenocarcinomaSubstitution - Nonsense

c.146C>T; p.A49V; 17:34256291-34256291

 oesophaguscarcinomaSubstitution - Missense

c.146C>T; p.A49V; 17:34256291-34256291

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.146C>T; p.A49V; 17:34256291-34256291

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

')