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

Basic Information

Gene ID

3956

Name

LGALS1

The somatic mutations from COSMIC database

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.146G>A; p.R49H; 22:37678539-37678539

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.299A>G; p.K100R; 22:37679640-37679640

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.382A>C; p.K128Q; 22:37679723-37679723

oesophagus; lower_thirdcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.276C>T; p.F92F; 22:37679617-37679617

endometriumcarcinoma; serous_carcinomaSubstitution - coding silent

c.276C>T; p.F92F; 22:37679617-37679617

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.295G>A; p.V99I; 22:37679636-37679636

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.316G>A; p.E106K; 22:37679657-37679657

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.171C>T; p.N57N; 22:37678564-37678564

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.213C>T; p.T71T; 22:37678606-37678606

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.93C>T; p.F31F; 22:37678486-37678486

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.62G>A; p.R21Q; 22:37677038-37677038

breastcarcinomaSubstitution - Missense

c.292A>G; p.T98A; 22:37679633-37679633

livercarcinomaSubstitution - Missense

c.292A>G; p.T98A; 22:37679633-37679633

livercarcinomaSubstitution - Missense

c.307G>T; p.D103Y; 22:37679648-37679648

breastcarcinomaSubstitution - Missense

c.244_245CC>TT; p.P82F; 22:37678637-37678638

skin; mucosalmalignant_melanomaSubstitution - Missense

c.259G>C; p.E87Q; 22:37678652-37678652

breastcarcinomaSubstitution - Missense

c.262-7delC; p.?; 22:37679596-37679596

oesophagus; lower_thirdcarcinoma; adenocarcinomaUnknown

c.219G>A; p.Q73Q; 22:37678612-37678612

large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.262G>T; p.V88L; 22:37679603-37679603

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.23G>T; p.S8I; 22:37676999-37676999

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.108C>T; p.G36G; 22:37678501-37678501

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.335G>A; p.R112H; 22:37679676-37679676

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.128G>A; p.C43Y; 22:37678521-37678521

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense


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