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

Basic Information

Gene ID

1948

Name

EFNB2

The somatic mutations from COSMIC database

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.834C>T; p.S278S; 13:106493208-106493208

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.118T>G; p.S40A; 13:106534847-106534847

central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.118T>G; p.S40A; 13:106534847-106534847

central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.876G>A; p.P292P; 13:106493166-106493166

endometriumcarcinoma; serous_carcinomaSubstitution - coding silent

c.572G>T; p.G191V; 13:106494922-106494922

urinary_tract; bladdercarcinomaSubstitution - Missense

c.384_386delGAA; p.K128delK; 13:106512549-106512551

stomachadenocarcinomaDeletion - In frame

c.516A>T; p.G172G; 13:106494978-106494978

central_nervous_system; braingliomaSubstitution - coding silent

c.63A>G; p.R21R; 13:106534902-106534902

lungcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.813A>G; p.T271T; 13:106493229-106493229

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.614-1G>T; p.?; 13:106493429-106493429

pancreascarcinomaUnknown

c.762G>T; p.R254S; 13:106493280-106493280

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.586A>G; p.T196A; 13:106494908-106494908

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.381G>A; p.Q127Q; 13:106512554-106512554

kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - coding silent

c.24G>T; p.V8V; 13:106534941-106534941

central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - coding silent

c.24G>T; p.V8V; 13:106534941-106534941

central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - coding silent

c.835G>A; p.G279S; 13:106493207-106493207

urinary_tract; bladdercarcinomaSubstitution - Missense

c.835G>A; p.G279S; 13:106493207-106493207

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.989A>G; p.Y330C; 13:106493053-106493053

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.963G>T; p.M321I; 13:106493079-106493079

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.955C>T; p.Q319*; 13:106493087-106493087

skin; scalpcarcinoma; squamous_cell_carcinomaSubstitution - Nonsense

c.637G>A; p.A213T; 13:106493405-106493405

stomachcarcinoma; diffuse_adenocarcinomaSubstitution - Missense

c.747G>A; p.L249L; 13:106493295-106493295

urinary_tract; bladdercarcinomaSubstitution - coding silent

c.441C>T; p.N147N; 13:106495806-106495806

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - coding silent

c.614-2A>C; p.?; 13:106493430-106493430

pancreascarcinomaUnknown

c.783G>A; p.P261P; 13:106493259-106493259

haematopoietic_and_lymphoid_tissuelymphoid_neoplasmSubstitution - coding silent

c.783G>A; p.P261P; 13:106493259-106493259

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.195G>T; p.V65V; 13:106512740-106512740

lungcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.16G>T; p.D6Y; 13:106534949-106534949

breastcarcinomaSubstitution - Missense

c.826A>T; p.K276*; 13:106493216-106493216

lungcarcinoma; squamous_cell_carcinomaSubstitution - Nonsense

c.791C>T; p.T264M; 13:106493251-106493251

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.79T>A; p.S27T; 13:106534886-106534886

livercarcinomaSubstitution - Missense

c.791C>T; p.T264M; 13:106493251-106493251

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.79T>A; p.S27T; 13:106534886-106534886

livercarcinomaSubstitution - Missense

c.791C>T; p.T264M; 13:106493251-106493251

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.933C>T; p.Y311Y; 13:106493109-106493109

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.394T>G; p.Y132D; 13:106512541-106512541

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.639C>T; p.A213A; 13:106493403-106493403

skinmalignant_melanomaSubstitution - coding silent

c.259G>T; p.D87Y; 13:106512676-106512676

lung; right_lower_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.547C>T; p.P183S; 13:106494947-106494947

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.782C>T; p.P261L; 13:106493260-106493260

breastcarcinomaSubstitution - Missense

c.782C>T; p.P261L; 13:106493260-106493260

ovarycarcinoma; serous_carcinomaSubstitution - Missense

c.474G>A; p.M158I; 13:106495773-106495773

lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.499G>A; p.D167N; 13:106495748-106495748

kidneycarcinoma; papillary_renal_cell_carcinomaSubstitution - Missense

c.507T>C; p.S169S; 13:106494987-106494987

oesophagus; lower_thirdcarcinoma; adenocarcinomaSubstitution - coding silent

c.552A>C; p.E184D; 13:106494942-106494942

haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; diffuse_large_B_cell_lymphomaSubstitution - Missense

c.895G>A; p.V299I; 13:106493147-106493147

pancreascarcinomaSubstitution - Missense

c.669C>T; p.S223S; 13:106493373-106493373

stomachcarcinoma; diffuse_adenocarcinomaSubstitution - coding silent

c.663C>T; p.L221L; 13:106493379-106493379

skinmalignant_melanomaSubstitution - coding silent

c.442C>A; p.Q148K; 13:106495805-106495805

livercarcinomaSubstitution - Missense

c.738G>T; p.V246V; 13:106493304-106493304

livercarcinomaSubstitution - coding silent

c.500-6A>T; p.?; 13:106495000-106495000

livercarcinomaUnknown

c.500-6A>T; p.?; 13:106495000-106495000

livercarcinomaUnknown

c.829C>T; p.R277C; 13:106493213-106493213

oesophaguscarcinoma; adenocarcinomaSubstitution - Missense

c.479T>A; p.I160N; 13:106495768-106495768

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.772A>G; p.K258E; 13:106493270-106493270

livercarcinomaSubstitution - Missense

c.748C>T; p.L250L; 13:106493294-106493294

large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.398A>G; p.Y133C; 13:106512537-106512537

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.923G>T; p.S308I; 13:106493119-106493119

haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; plasma_cell_myelomaSubstitution - Missense

c.146T>C; p.V49A; 13:106512789-106512789

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.981G>A; p.A327A; 13:106493061-106493061

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.386_395del10; p.N129fs*27; 13:106512540-106512549

skin; chestmalignant_melanomaDeletion - Frameshift

c.804G>A; p.S268S; 13:106493238-106493238

lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.925G>A; p.G309S; 13:106493117-106493117

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.941C>T; p.P314L; 13:106493101-106493101

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.925G>A; p.G309S; 13:106493117-106493117

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.141A>G; p.G47G; 13:106512794-106512794

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.894C>T; p.S298S; 13:106493148-106493148

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.617C>G; p.S206C; 13:106493425-106493425

livercarcinoma; hepatocellular_carcinomaSubstitution - Missense

c.113C>A; p.S38*; 13:106534852-106534852

livercarcinomaSubstitution - Nonsense

c.113C>A; p.S38*; 13:106534852-106534852

livercarcinomaSubstitution - Nonsense

c.887C>T; p.A296V; 13:106493155-106493155

haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; plasma_cell_myelomaSubstitution - Missense

c.846C>T; p.N282N; 13:106493196-106493196

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.365G>T; p.W122L; 13:106512570-106512570

stomachcarcinoma; adenocarcinomaSubstitution - Missense


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