| General information | Literature | Expression | lncRNA |Regulation | Mutation | Homolog | Interaction |
Basic Information | |||
|---|---|---|---|
Gene ID | 682 | ||
Name | BSG | ||
The somatic mutations from COSMIC database | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.771G>C; p.K257N; 19:580761-580761 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.715A>G; p.M239V; 19:580705-580705 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.461T>C; p.L154P; 19:579545-579545 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.934G>A; p.A312T; 19:581456-581456 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.889G>A; p.G297S; 19:581411-581411 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.350A>C; p.N117T; 19:578056-578056 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1138C>A; p.R380S; 19:582557-582557 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.525C>T; p.G175G; 19:579609-579609 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.525C>T; p.G175G; 19:579609-579609 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.526G>A; p.V176M; 19:579610-579610 |
pancreas | carcinoma | Substitution - Missense |
c.213G>C; p.W71C; 19:577919-577919 |
thyroid | carcinoma | Substitution - Missense |
c.1045C>T; p.R349W; 19:581567-581567 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.285C>T; p.I95I; 19:577991-577991 |
skin | malignant_melanoma | Substitution - coding silent |
c.940A>G; p.I314V; 19:581462-581462 |
pancreas | carcinoma | Substitution - Missense |
c.750C>G; p.V250V; 19:580740-580740 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.55G>T; p.A19S; 19:572689-572689 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.55G>T; p.A19S; 19:572689-572689 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.55G>T; p.A19S; 19:572689-572689 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.55G>T; p.A19S; 19:572689-572689 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.933G>C; p.Q311H; 19:581455-581455 |
liver | carcinoma | Substitution - Missense |
c.933G>C; p.Q311H; 19:581455-581455 |
liver | carcinoma | Substitution - Missense |
c.1042C>T; p.R348C; 19:581564-581564 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.519delG; p.G175fs*4; 19:579603-579603 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.519delG; p.G175fs*4; 19:579603-579603 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.552C>A; p.P184P; 19:579636-579636 |
prostate | carcinoma; adenocarcinoma | Substitution - coding silent |
c.149C>T; p.P50L; 19:577855-577855 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.487G>A; p.A163T; 19:579571-579571 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.654C>T; p.H218H; 19:580460-580460 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - coding silent |
c.493G>C; p.E165Q; 19:579577-579577 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.543C>T; p.D181D; 19:579627-579627 |
thyroid | other; neoplasm | Substitution - coding silent |
c.543C>T; p.D181D; 19:579627-579627 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.922G>A; p.G308S; 19:581444-581444 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.790A>T; p.K264*; 19:580780-580780 |
thyroid | other; neoplasm | Substitution - Nonsense |
c.738C>T; p.S246S; 19:580728-580728 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.789C>T; p.D263D; 19:580779-580779 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.724T>G; p.C242G; 19:580714-580714 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - Missense |
c.645C>T; p.I215I; 19:580451-580451 |
breast | carcinoma | Substitution - coding silent |
c.716T>A; p.M239K; 19:580706-580706 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.791A>G; p.K264R; 19:580781-580781 |
thyroid | other; neoplasm | Substitution - Missense |
c.662C>T; p.P221L; 19:580652-580652 |
skin | malignant_melanoma | Substitution - Missense |
c.967G>A; p.A323T; 19:581489-581489 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.209T>C; p.L70P; 19:577915-577915 |
pancreas | carcinoma | Substitution - Missense |
c.811G>A; p.E271K; 19:581333-581333 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.675T>C; p.A225A; 19:580665-580665 |
breast | carcinoma | Substitution - coding silent |
c.330C>T; p.A110A; 19:578036-578036 |
skin | malignant_melanoma | Substitution - coding silent |
c.675T>C; p.A225A; 19:580665-580665 |
breast | carcinoma | Substitution - coding silent |
c.473C>T; p.S158F; 19:579557-579557 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.951C>T; p.R317R; 19:581473-581473 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.133G>A; p.E45K; 19:577839-577839 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1076A>G; p.D359G; 19:582312-582312 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1076A>G; p.D359G; 19:582312-582312 |
large_intestine; colon | carcinoma | Substitution - Missense |
c.1070-1G>A; p.?; 19:582305-582305 |
skin | malignant_melanoma | Unknown |
c.174T>C; p.F58F; 19:577880-577880 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.499A>T; p.T167S; 19:579583-579583 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.949C>T; p.R317C; 19:581471-581471 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.332G>A; p.S111N; 19:578038-578038 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.943A>G; p.T315A; 19:581465-581465 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.362G>C; p.R121P; 19:578068-578068 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.216C>T; p.D72D; 19:577922-577922 |
central_nervous_system; brain | primitive_neuroectodermal_tumour-medulloblastoma | Substitution - coding silent |
c.968C>T; p.A323V; 19:581490-581490 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.493G>A; p.E165K; 19:579577-579577 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.213G>A; p.W71*; 19:577919-577919 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.344A>T; p.D115V; 19:578050-578050 |
kidney | other; neoplasm | Substitution - Missense |
c.634A>G; p.T212A; 19:580440-580440 |
oesophagus; middle_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.620C>T; p.P207L; 19:580426-580426 |
breast | carcinoma | Substitution - Missense |
c.620C>T; p.P207L; 19:580426-580426 |
skin | malignant_melanoma | Substitution - Missense |
c.270C>A; p.A90A; 19:577976-577976 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |