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

Basic Information

Gene ID

5524

Name

PPP2R4

The somatic mutations from COSMIC database

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.91C>A; p.H31N; 9:129120572-129120572

 stomachcarcinoma; diffuse_adenocarcinomaSubstitution - Missense

c.402_405delGTTT; p.F135fs*39; 9:129129065-129129068

 breastcarcinomaDeletion - Frameshift

c.214G>A; p.E72K; 9:129123136-129123136

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.583G>T; p.A195S; 9:129134812-129134812

 breastcarcinomaSubstitution - Missense

c.430T>C; p.Y144H; 9:129129093-129129093

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1061C>A; p.P354H; 9:129147448-129147448

 kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.892-3C>A; p.?; 9:129142442-129142442

 adrenal_gland; adrenal_glandadrenal_cortical_carcinoma; functioningUnknown

c.383C>T; p.P128L; 9:129129046-129129046

 skinmalignant_melanomaSubstitution - Missense

c.49C>G; p.P17A; 9:129120530-129120530

 central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.352A>G; p.T118A; 9:129129015-129129015

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.888C>T; p.T296T; 9:129137689-129137689

 skinmalignant_melanomaSubstitution - coding silent

c.565G>T; p.G189W; 9:129131639-129131639

 prostatecarcinoma; adenocarcinomaSubstitution - Missense

c.426C>T; p.T142T; 9:129129089-129129089

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.548G>T; p.R183L; 9:129131622-129131622

 lungcarcinoma; non_small_cell_carcinomaSubstitution - Missense

c.203A>G; p.Y68C; 9:129123125-129123125

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.691C>T; p.Q231*; 9:129136496-129136496

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Nonsense

c.133T>C; p.Y45H; 9:129123055-129123055

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.63G>T; p.Q21H; 9:129120544-129120544

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.357G>A; p.L119L; 9:129129020-129129020

 skinmalignant_melanomaSubstitution - coding silent

c.352A>T; p.T118S; 9:129129015-129129015

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.596G>A; p.C199Y; 9:129134825-129134825

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.1070C>T; p.S357L; 9:129147457-129147457

 haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - Missense

c.582C>T; p.F194F; 9:129134811-129134811

 urinary_tract; bladdercarcinomaSubstitution - coding silent

c.582C>T; p.F194F; 9:129134811-129134811

 urinary_tract; bladdercarcinoma; transitional_cell_carcinomaSubstitution - coding silent

c.244G>T; p.E82*; 9:129127991-129127991

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Nonsense

c.1056C>T; p.I352I; 9:129147443-129147443

 oesophaguscarcinomaSubstitution - coding silent

c.353C>T; p.T118M; 9:129129016-129129016

 ovarycarcinoma; serous_carcinomaSubstitution - Missense

c.198C>T; p.F66F; 9:129123120-129123120

 skinmalignant_melanomaSubstitution - coding silent

c.682C>T; p.R228W; 9:129136487-129136487

 livercarcinoma; hepatocellular_carcinomaSubstitution - Missense

c.682C>T; p.R228W; 9:129136487-129136487

 livercarcinomaSubstitution - Missense

c.281G>C; p.C94S; 9:129128028-129128028

 breastcarcinomaSubstitution - Missense

c.148G>A; p.G50R; 9:129123070-129123070

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.943G>A; p.A315T; 9:129142496-129142496

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.910G>A; p.A304T; 9:129142463-129142463

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.718G>A; p.G240S; 9:129136523-129136523

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.718G>A; p.G240S; 9:129136523-129136523

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.295C>T; p.R99C; 9:129128042-129128042

 pancreascarcinomaSubstitution - Missense

c.760C>T; p.P254S; 9:129136565-129136565

 breastcarcinomaSubstitution - Missense

c.728G>T; p.G243V; 9:129136533-129136533

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.683G>A; p.R228Q; 9:129136488-129136488

 stomachcarcinoma; diffuse_adenocarcinomaSubstitution - Missense

c.339C>T; p.V113V; 9:129129002-129129002

 skinmalignant_melanomaSubstitution - coding silent

c.946G>T; p.V316F; 9:129142499-129142499

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.286C>G; p.P96A; 9:129128033-129128033

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.936C>A; p.N312K; 9:129142489-129142489

 pancreasNSSubstitution - Missense

c.615G>T; p.G205G; 9:129134844-129134844

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.865C>T; p.L289L; 9:129137666-129137666

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.396_397delCT; p.R134fs*4; 9:129129059-129129060

 breastcarcinomaDeletion - Frameshift

c.525G>T; p.K175N; 9:129131599-129131599

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.400C>T; p.R134W; 9:129129063-129129063

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.400C>T; p.R134W; 9:129129063-129129063

 breastcarcinoma; basal_(triple-negative)_carcinomaSubstitution - Missense

c.834C>T; p.A278A; 9:129137635-129137635

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.574G>A; p.A192T; 9:129134803-129134803

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.790_790+11delGGTACTAGAGCG; p.?; 9:129136595-129136606

 breastcarcinomaUnknown

c.328G>A; p.E110K; 9:129128991-129128991

 breastcarcinomaSubstitution - Missense

c.122G>A; p.R41H; 9:129120603-129120603

 upper_aerodigestive_tract; mouthcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.122G>A; p.R41H; 9:129120603-129120603

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.168C>T; p.N56N; 9:129123090-129123090

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.940A>T; p.S314C; 9:129142493-129142493

 skin; scalpcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.183G>T; p.G61G; 9:129123105-129123105

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.77_78insA; p.E29fs*19; 9:129120558-129120559

 large_intestine; coloncarcinoma; adenocarcinomaInsertion - Frameshift

c.566-1G>A; p.?; 9:129134794-129134794

 skinmalignant_melanomaUnknown

c.195C>T; p.T65T; 9:129123117-129123117

 skinmalignant_melanomaSubstitution - coding silent

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