| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 7482 |
Name | WNT2B |
Synonymous | wingless-type MMTV integration site family, member 2B;WNT2B;wingless-type MMTV integration site family, member 2B |
Definition | XWNT2, Xenopus, homolog of|protein Wnt-2b|wingless-type MMTV integration site family, member 13 |
Position | 1p13 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.539G>A; p.R180H; 1:112516275-112516275 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.539G>A; p.R180H; 1:112516275-112516275 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.112C>T; p.R38C; 1:112509374-112509374 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.112C>T; p.R38C; 1:112509374-112509374 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.335G>A; p.R112H; 1:112515026-112515026 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.335G>A; p.R112H; 1:112515026-112515026 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.335G>A; p.R112H; 1:112515026-112515026 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.811G>A; p.G271R; 1:112517250-112517250 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.507C>T; p.D169D; 1:112516243-112516243 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.811G>A; p.G271R; 1:112517250-112517250 |
liver | carcinoma | Substitution - Missense |
c.301C>T; p.R101*; 1:112514992-112514992 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.457G>A; p.A153T; 1:112516193-112516193 |
liver | carcinoma | Substitution - Missense |
c.780C>T; p.R260R; 1:112517219-112517219 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.379G>A; p.V127I; 1:112515070-112515070 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.379G>A; p.V127I; 1:112515070-112515070 |
breast | carcinoma | Substitution - Missense |
c.724G>A; p.V242M; 1:112517163-112517163 |
ovary | other; neoplasm | Substitution - Missense |
c.150G>C; p.L50L; 1:112509412-112509412 |
breast | carcinoma | Substitution - coding silent |
c.800G>A; p.R267Q; 1:112517239-112517239 |
skin | malignant_melanoma | Substitution - Missense |
c.242G>A; p.R81Q; 1:112514933-112514933 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.706G>A; p.E236K; 1:112517145-112517145 |
skin | malignant_melanoma | Substitution - Missense |
c.749C>A; p.T250N; 1:112517188-112517188 |
central_nervous_system; brain | primitive_neuroectodermal_tumour-medulloblastoma | Substitution - Missense |
c.515C>A; p.T172N; 1:112516251-112516251 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.196C>T; p.L66L; 1:112514887-112514887 |
skin | malignant_melanoma | Substitution - coding silent |
c.292G>A; p.E98K; 1:112514983-112514983 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.692G>A; p.R231Q; 1:112517131-112517131 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.641G>A; p.R214Q; 1:112516377-112516377 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.531T>A; p.H177Q; 1:112516267-112516267 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.641G>A; p.R214Q; 1:112516377-112516377 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.892G>A; p.D298N; 1:112517331-112517331 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.404-9T>C; p.?; 1:112516131-112516131 |
ovary | other; neoplasm | Unknown |
c.802C>T; p.R268C; 1:112517241-112517241 |
skin | malignant_melanoma | Substitution - Missense |
c.404-9T>C; p.?; 1:112516131-112516131 |
ovary | other; neoplasm | Unknown |
c.802C>T; p.R268C; 1:112517241-112517241 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.668G>A; p.R223H; 1:112516404-112516404 |
breast | carcinoma | Substitution - Missense |
c.803G>A; p.R268H; 1:112517242-112517242 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.789T>C; p.D263D; 1:112517228-112517228 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.803G>A; p.R268H; 1:112517242-112517242 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.789T>C; p.D263D; 1:112517228-112517228 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1104G>T; p.K368N; 1:112520437-112520437 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.689G>A; p.R230Q; 1:112517128-112517128 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.986C>T; p.S329L; 1:112520319-112520319 |
breast | carcinoma; HER-positive_carcinoma | Substitution - Missense |
c.713A>C; p.K238T; 1:112517152-112517152 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1125C>T; p.D375D; 1:112520458-112520458 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.590G>A; p.R197H; 1:112516326-112516326 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.304G>A; p.E102K; 1:112514995-112514995 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.814G>T; p.A272S; 1:112517253-112517253 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.322C>T; p.Q108*; 1:112515013-112515013 |
lung | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.354T>C; p.C118C; 1:112515045-112515045 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.253_254delCT; p.L85fs*51; 1:112514944-112514945 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Deletion - Frameshift |
c.205C>T; p.R69*; 1:112514896-112514896 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.731G>A; p.G244D; 1:112517170-112517170 |
breast | carcinoma; basal_(triple-negative)_carcinoma | Substitution - Missense |
c.956G>A; p.G319D; 1:112520289-112520289 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.93C>G; p.D31E; 1:112509355-112509355 |
pancreas | carcinoma | Substitution - Missense |
c.509C>T; p.P170L; 1:112516245-112516245 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.313C>A; p.R105R; 1:112515004-112515004 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.396G>A; p.M132I; 1:112515087-112515087 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.323A>G; p.Q108R; 1:112515014-112515014 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.302G>A; p.R101Q; 1:112514993-112514993 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.302G>A; p.R101Q; 1:112514993-112514993 |
breast | carcinoma | Substitution - Missense |
c.165C>T; p.R55R; 1:112509427-112509427 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.618G>A; p.K206K; 1:112516354-112516354 |
skin | malignant_melanoma | Substitution - coding silent |
c.406A>G; p.S136G; 1:112516142-112516142 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.878G>A; p.R293H; 1:112517317-112517317 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1042C>T; p.R348*; 1:112520375-112520375 |
oesophagus | carcinoma | Substitution - Nonsense |
c.1042C>T; p.R348*; 1:112520375-112520375 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.523C>T; p.R175*; 1:112516259-112516259 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.166G>A; p.V56I; 1:112509428-112509428 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.399C>T; p.L133L; 1:112515090-112515090 |
breast | carcinoma | Substitution - coding silent |
c.815C>A; p.A272D; 1:112517254-112517254 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.874C>T; p.R292C; 1:112517313-112517313 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.386G>C; p.G129A; 1:112515077-112515077 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.583G>A; p.G195S; 1:112516319-112516319 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.673G>T; p.G225C; 1:112516409-112516409 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.584G>A; p.G195D; 1:112516320-112516320 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.584G>A; p.G195D; 1:112516320-112516320 |
skin | malignant_melanoma | Substitution - Missense |
c.344G>A; p.R115H; 1:112515035-112515035 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.830C>T; p.A277V; 1:112517269-112517269 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.619G>A; p.E207K; 1:112516355-112516355 |
skin; abdomen | malignant_melanoma | Substitution - Missense |
c.988A>C; p.K330Q; 1:112520321-112520321 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.107C>T; p.S36L; 1:112509369-112509369 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - Missense |
c.582C>T; p.Y194Y; 1:112516318-112516318 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.107C>T; p.S36L; 1:112509369-112509369 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.877C>T; p.R293C; 1:112517316-112517316 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.907G>C; p.D303H; 1:112517346-112517346 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.682-1G>C; p.?; 1:112517120-112517120 |
skin | malignant_melanoma | Unknown |
c.453C>A; p.V151V; 1:112516189-112516189 |
breast | carcinoma | Substitution - coding silent |
c.381C>T; p.V127V; 1:112515072-112515072 |
breast | carcinoma | Substitution - coding silent |
c.1009A>G; p.I337V; 1:112520342-112520342 |
skin | malignant_melanoma | Substitution - Missense |
c.757C>T; p.R253C; 1:112517196-112517196 |
breast | carcinoma | Substitution - Missense |
c.282T>C; p.R94R; 1:112514973-112514973 |
liver | carcinoma | Substitution - coding silent |
c.282T>C; p.R94R; 1:112514973-112514973 |
liver | carcinoma | Substitution - coding silent |
c.606C>T; p.F202F; 1:112516342-112516342 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |