| 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; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.118T>G; p.S40A; 13:106534847-106534847 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.118T>G; p.S40A; 13:106534847-106534847 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.876G>A; p.P292P; 13:106493166-106493166 |
endometrium | carcinoma; serous_carcinoma | Substitution - coding silent |
c.572G>T; p.G191V; 13:106494922-106494922 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.384_386delGAA; p.K128delK; 13:106512549-106512551 |
stomach | adenocarcinoma | Deletion - In frame |
c.516A>T; p.G172G; 13:106494978-106494978 |
central_nervous_system; brain | glioma | Substitution - coding silent |
c.63A>G; p.R21R; 13:106534902-106534902 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.813A>G; p.T271T; 13:106493229-106493229 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.614-1G>T; p.?; 13:106493429-106493429 |
pancreas | carcinoma | Unknown |
c.762G>T; p.R254S; 13:106493280-106493280 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.586A>G; p.T196A; 13:106494908-106494908 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.381G>A; p.Q127Q; 13:106512554-106512554 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.24G>T; p.V8V; 13:106534941-106534941 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.24G>T; p.V8V; 13:106534941-106534941 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.835G>A; p.G279S; 13:106493207-106493207 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.835G>A; p.G279S; 13:106493207-106493207 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.989A>G; p.Y330C; 13:106493053-106493053 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.963G>T; p.M321I; 13:106493079-106493079 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.955C>T; p.Q319*; 13:106493087-106493087 |
skin; scalp | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.637G>A; p.A213T; 13:106493405-106493405 |
stomach | carcinoma; diffuse_adenocarcinoma | Substitution - Missense |
c.747G>A; p.L249L; 13:106493295-106493295 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.441C>T; p.N147N; 13:106495806-106495806 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.614-2A>C; p.?; 13:106493430-106493430 |
pancreas | carcinoma | Unknown |
c.783G>A; p.P261P; 13:106493259-106493259 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm | Substitution - coding silent |
c.783G>A; p.P261P; 13:106493259-106493259 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.195G>T; p.V65V; 13:106512740-106512740 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.16G>T; p.D6Y; 13:106534949-106534949 |
breast | carcinoma | Substitution - Missense |
c.826A>T; p.K276*; 13:106493216-106493216 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.791C>T; p.T264M; 13:106493251-106493251 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.79T>A; p.S27T; 13:106534886-106534886 |
liver | carcinoma | Substitution - Missense |
c.791C>T; p.T264M; 13:106493251-106493251 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.79T>A; p.S27T; 13:106534886-106534886 |
liver | carcinoma | Substitution - Missense |
c.791C>T; p.T264M; 13:106493251-106493251 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.933C>T; p.Y311Y; 13:106493109-106493109 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.394T>G; p.Y132D; 13:106512541-106512541 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.639C>T; p.A213A; 13:106493403-106493403 |
skin | malignant_melanoma | Substitution - coding silent |
c.259G>T; p.D87Y; 13:106512676-106512676 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.547C>T; p.P183S; 13:106494947-106494947 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.782C>T; p.P261L; 13:106493260-106493260 |
breast | carcinoma | Substitution - Missense |
c.782C>T; p.P261L; 13:106493260-106493260 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.474G>A; p.M158I; 13:106495773-106495773 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.499G>A; p.D167N; 13:106495748-106495748 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.507T>C; p.S169S; 13:106494987-106494987 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - coding silent |
c.552A>C; p.E184D; 13:106494942-106494942 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; diffuse_large_B_cell_lymphoma | Substitution - Missense |
c.895G>A; p.V299I; 13:106493147-106493147 |
pancreas | carcinoma | Substitution - Missense |
c.669C>T; p.S223S; 13:106493373-106493373 |
stomach | carcinoma; diffuse_adenocarcinoma | Substitution - coding silent |
c.663C>T; p.L221L; 13:106493379-106493379 |
skin | malignant_melanoma | Substitution - coding silent |
c.442C>A; p.Q148K; 13:106495805-106495805 |
liver | carcinoma | Substitution - Missense |
c.738G>T; p.V246V; 13:106493304-106493304 |
liver | carcinoma | Substitution - coding silent |
c.500-6A>T; p.?; 13:106495000-106495000 |
liver | carcinoma | Unknown |
c.500-6A>T; p.?; 13:106495000-106495000 |
liver | carcinoma | Unknown |
c.829C>T; p.R277C; 13:106493213-106493213 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.479T>A; p.I160N; 13:106495768-106495768 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.772A>G; p.K258E; 13:106493270-106493270 |
liver | carcinoma | Substitution - Missense |
c.748C>T; p.L250L; 13:106493294-106493294 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.398A>G; p.Y133C; 13:106512537-106512537 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.923G>T; p.S308I; 13:106493119-106493119 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; plasma_cell_myeloma | Substitution - Missense |
c.146T>C; p.V49A; 13:106512789-106512789 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.981G>A; p.A327A; 13:106493061-106493061 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.386_395del10; p.N129fs*27; 13:106512540-106512549 |
skin; chest | malignant_melanoma | Deletion - Frameshift |
c.804G>A; p.S268S; 13:106493238-106493238 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.925G>A; p.G309S; 13:106493117-106493117 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.941C>T; p.P314L; 13:106493101-106493101 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.925G>A; p.G309S; 13:106493117-106493117 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.141A>G; p.G47G; 13:106512794-106512794 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.894C>T; p.S298S; 13:106493148-106493148 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.617C>G; p.S206C; 13:106493425-106493425 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.113C>A; p.S38*; 13:106534852-106534852 |
liver | carcinoma | Substitution - Nonsense |
c.113C>A; p.S38*; 13:106534852-106534852 |
liver | carcinoma | Substitution - Nonsense |
c.887C>T; p.A296V; 13:106493155-106493155 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; plasma_cell_myeloma | Substitution - Missense |
c.846C>T; p.N282N; 13:106493196-106493196 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.365G>T; p.W122L; 13:106512570-106512570 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |