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

Basic Information

Gene ID

5133

Name

PDCD1

The somatic mutations from COSMIC database

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.657C>T; p.F219F; 2:241851268-241851268

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.657C>T; p.F219F; 2:241851268-241851268

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.811C>T; p.P271S; 2:241851114-241851114

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.624C>A; p.P208P; 2:241851952-241851952

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.69G>A; p.W23*; 2:241858770-241858770

skinmalignant_melanomaSubstitution - Nonsense

c.237G>A; p.L79L; 2:241852820-241852820

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.809G>A; p.G270D; 2:241851116-241851116

haematopoietic_and_lymphoid_tissuelymphoid_neoplasmSubstitution - Missense

c.659C>T; p.S220F; 2:241851266-241851266

skinmalignant_melanomaSubstitution - Missense

c.561C>A; p.V187V; 2:241852229-241852229

livercarcinoma; hepatocellular_carcinomaSubstitution - coding silent

c.807C>T; p.D269D; 2:241851118-241851118

breastcarcinomaSubstitution - coding silent

c.606_607insGGAGCC; p.A202_R203insGA; 2:241851969-241851970

large_intestinecarcinoma; adenocarcinomaInsertion - In frame

c.766_767GG>AA; p.G256K; 2:241851158-241851159

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.739G>A; p.E247K; 2:241851186-241851186

skinmalignant_melanomaSubstitution - Missense

c.416G>A; p.R139Q; 2:241852641-241852641

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.390delC; p.K131fs*14; 2:241852667-241852667

stomachcarcinoma; intestinal_adenocarcinomaDeletion - Frameshift

c.328G>A; p.V110M; 2:241852729-241852729

prostatecarcinoma; adenocarcinomaSubstitution - Missense

c.328G>A; p.V110M; 2:241852729-241852729

breastcarcinomaSubstitution - Missense

c.344G>A; p.R115H; 2:241852713-241852713

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.740A>G; p.E247G; 2:241851185-241851185

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.804T>C; p.A268A; 2:241851121-241851121

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.436G>T; p.E146*; 2:241852621-241852621

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Nonsense

c.631G>A; p.E211K; 2:241851294-241851294

skinmalignant_melanomaSubstitution - Missense

c.631G>A; p.E211K; 2:241851294-241851294

skinmalignant_melanomaSubstitution - Missense

c.382C>T; p.L128L; 2:241852675-241852675

skinmalignant_melanomaSubstitution - coding silent

c.772G>A; p.G258S; 2:241851153-241851153

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.520G>A; p.V174M; 2:241852270-241852270

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.17C>A; p.A6E; 2:241858822-241858822

livercarcinomaSubstitution - Missense

c.105delC; p.T36fs*9; 2:241852952-241852952

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.771G>A; p.M257I; 2:241851154-241851154

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.525C>T; p.G175G; 2:241852265-241852265

central_nervous_system; brainprimitive_neuroectodermal_tumour-medulloblastomaSubstitution - coding silent

c.783C>T; p.S261S; 2:241851142-241851142

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.783C>T; p.S261S; 2:241851142-241851142

skinmalignant_melanomaSubstitution - coding silent

c.692G>A; p.R231Q; 2:241851233-241851233

skinmalignant_melanomaSubstitution - Missense

c.692G>A; p.R231Q; 2:241851233-241851233

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.646G>A; p.V216M; 2:241851279-241851279

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.815_816GG>AA; p.R272Q; 2:241851109-241851110

skinmalignant_melanomaSubstitution - Missense

c.265C>A; p.P89T; 2:241852792-241852792

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.265C>A; p.P89T; 2:241852792-241852792

prostatecarcinoma; adenocarcinomaSubstitution - Missense

c.265C>A; p.P89T; 2:241852792-241852792

prostatecarcinoma; adenocarcinomaSubstitution - Missense

c.252G>A; p.E84E; 2:241852805-241852805

lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.262C>T; p.Q88*; 2:241852795-241852795

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Nonsense

c.611G>T; p.R204L; 2:241851965-241851965

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.760C>T; p.P254S; 2:241851165-241851165

skin; trunkmalignant_melanomaSubstitution - Missense

c.127G>A; p.V43M; 2:241852930-241852930

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.766_767GG>CT; p.G256>?; 2:241851158-241851159

lungcarcinoma; adenocarcinomaComplex

c.610C>T; p.R204C; 2:241851966-241851966

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.257G>C; p.R86P; 2:241852800-241852800

ovarycarcinoma; serous_carcinomaSubstitution - Missense

c.58C>T; p.R20W; 2:241858781-241858781

central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.268G>A; p.G90S; 2:241852789-241852789

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.458C>T; p.T153I; 2:241852332-241852332

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.306C>T; p.N102N; 2:241852751-241852751

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.395C>T; p.A132V; 2:241852662-241852662

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.206G>A; p.R69H; 2:241852851-241852851

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.710C>T; p.P237L; 2:241851215-241851215

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.448G>A; p.E150K; 2:241852342-241852342

urinary_tract; bladdercarcinomaSubstitution - Missense

c.448G>A; p.E150K; 2:241852342-241852342

thyroidcarcinomaSubstitution - Missense

c.270C>A; p.G90G; 2:241852787-241852787

prostatecarcinoma; adenocarcinomaSubstitution - coding silent

c.499C>T; p.Q167*; 2:241852291-241852291

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Nonsense

c.805G>A; p.D269N; 2:241851120-241851120

urinary_tract; bladdercarcinoma; transitional_cell_carcinomaSubstitution - Missense

c.805G>A; p.D269N; 2:241851120-241851120

urinary_tract; bladdercarcinomaSubstitution - Missense

c.499C>T; p.Q167*; 2:241852291-241852291

skin; mucosalmalignant_melanomaSubstitution - Nonsense

c.162C>T; p.C54C; 2:241852895-241852895

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - coding silent

c.130G>C; p.V44L; 2:241852927-241852927

kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.795_796GG>AA; p.G266S; 2:241851129-241851130

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.537C>T; p.G179G; 2:241852253-241852253

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.310C>T; p.R104C; 2:241852747-241852747

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.61C>T; p.P21S; 2:241858778-241858778

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.696G>A; p.E232E; 2:241851229-241851229

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.200G>A; p.W67*; 2:241852857-241852857

skinmalignant_melanomaSubstitution - Nonsense

c.705G>A; p.P235P; 2:241851220-241851220

stomachcarcinoma; adenocarcinomaSubstitution - coding silent


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