ONGene
Top
Scroll To Top
Gene information | Literature | Expression | lncRNA | Mutation | Homolog

Basic Information

Gene ID

7473

Name

WNT3

Synonymous

wingless-type MMTV integration site family, member 3;WNT3;wingless-type MMTV integration site family, member 3

Definition

WNT-3 proto-oncogene protein|proto-oncogene Int-4 homolog|proto-oncogene Wnt-3

Position

17q21

Gene Type

protein-coding

COSMIC confirmed somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.683G>A; p.R228H; 17:46768705-46768705

bone; pelvisEwings_sarcoma-peripheral_primitive_neuroectodermal_tumourSubstitution - Missense

c.198G>T; p.M66I; 17:46773792-46773792

breastcarcinomaSubstitution - Missense

c.1050C>T; p.D350D; 17:46768338-46768338

central_nervous_system; braingliomaSubstitution - coding silent

c.181A>G; p.N61D; 17:46773809-46773809

central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.853G>A; p.E285K; 17:46768535-46768535

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.690C>T; p.I230I; 17:46768698-46768698

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.690C>T; p.I230I; 17:46768698-46768698

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.642C>T; p.S214S; 17:46768746-46768746

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.921C>T; p.I307I; 17:46768467-46768467

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.720C>T; p.S240S; 17:46768668-46768668

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.624C>T; p.C208C; 17:46768764-46768764

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.16C>T; p.L6F; 17:46818582-46818582

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.95G>A; p.G32D; 17:46773895-46773895

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.768G>A; p.V256V; 17:46768620-46768620

kidneycarcinoma; papillary_renal_cell_carcinomaSubstitution - coding silent

c.648G>A; p.E216E; 17:46768740-46768740

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - coding silent

c.707A>G; p.D236G; 17:46768681-46768681

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.962C>T; p.T321M; 17:46768426-46768426

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.322+2T>C; p.?; 17:46773666-46773666

large_intestine; caecumcarcinoma; adenocarcinomaUnknown

c.212A>G; p.E71G; 17:46773778-46773778

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.20G>T; p.G7V; 17:46818578-46818578

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.892C>T; p.R298W; 17:46768496-46768496

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.976C>T; p.R326W; 17:46768412-46768412

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.210C>T; p.A70A; 17:46773780-46773780

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.367G>A; p.V123M; 17:46770004-46770004

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.636G>A; p.S212S; 17:46768752-46768752

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.527G>A; p.R176H; 17:46769844-46769844

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.915C>T; p.H305H; 17:46768473-46768473

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.628G>A; p.G210R; 17:46768760-46768760

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.870G>A; p.T290T; 17:46768518-46768518

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.516C>T; p.F172F; 17:46769855-46769855

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - coding silent

c.668C>T; p.A223V; 17:46768720-46768720

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.189C>T; p.I63I; 17:46773801-46773801

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - coding silent

c.355G>A; p.A119T; 17:46770016-46770016

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.792G>A; p.S264S; 17:46768596-46768596

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.529G>A; p.E177K; 17:46769842-46769842

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.240C>G; p.C80W; 17:46773750-46773750

livercarcinomaSubstitution - Missense

c.240C>G; p.C80W; 17:46773750-46773750

livercarcinomaSubstitution - Missense

c.240C>G; p.C80W; 17:46773750-46773750

livercarcinomaSubstitution - Missense

c.240C>G; p.C80W; 17:46773750-46773750

livercarcinomaSubstitution - Missense

c.13C>A; p.L5M; 17:46818585-46818585

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.91C>G; p.L31V; 17:46773899-46773899

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.682C>T; p.R228C; 17:46768706-46768706

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.213G>A; p.E71E; 17:46773777-46773777

lungcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.159C>A; p.P53P; 17:46773831-46773831

lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.385C>T; p.R129C; 17:46769986-46769986

oesophaguscarcinoma; adenocarcinomaSubstitution - Missense

c.198G>A; p.M66I; 17:46773792-46773792

oesophagus; lower_thirdcarcinoma; adenocarcinomaSubstitution - Missense

c.962C>T; p.T321M; 17:46768426-46768426

oesophaguscarcinoma; adenocarcinomaSubstitution - Missense

c.869C>T; p.T290M; 17:46768519-46768519

oesophaguscarcinoma; adenocarcinomaSubstitution - Missense

c.892C>T; p.R298W; 17:46768496-46768496

oesophaguscarcinoma; adenocarcinomaSubstitution - Missense

c.749G>A; p.R250H; 17:46768639-46768639

oesophaguscarcinoma; adenocarcinomaSubstitution - Missense

c.478G>T; p.E160*; 17:46769893-46769893

pancreascarcinomaSubstitution - Nonsense

c.367G>A; p.V123M; 17:46770004-46770004

pancreascarcinoma; acinar_carcinomaSubstitution - Missense

c.778C>A; p.R260R; 17:46768610-46768610

prostatecarcinoma; adenocarcinomaSubstitution - coding silent

c.950G>A; p.R317Q; 17:46768438-46768438

prostatecarcinomaSubstitution - Missense

c.1039C>T; p.R347C; 17:46768349-46768349

skinmalignant_melanomaSubstitution - Missense

c.889G>A; p.D297N; 17:46768499-46768499

skinmalignant_melanomaSubstitution - Missense

c.777_778CC>TT; p.R260W; 17:46768610-46768611

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.286G>A; p.D96N; 17:46773704-46773704

skinmalignant_melanomaSubstitution - Missense

c.511G>A; p.E171K; 17:46769860-46769860

skinmalignant_melanomaSubstitution - Missense

c.209C>T; p.A70V; 17:46773781-46773781

skinmalignant_melanomaSubstitution - Missense

c.950G>A; p.R317Q; 17:46768438-46768438

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.588+5G>A; p.?; 17:46769778-46769778

soft_tissue; striated_musclerhabdomyosarcoma; alveolarUnknown

c.62C>T; p.A21V; 17:46818536-46818536

soft_tissue; striated_musclerhabdomyosarcoma; alveolarSubstitution - Missense

c.893G>A; p.R298Q; 17:46768495-46768495

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.170G>A; p.R57H; 17:46773820-46773820

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.831C>T; p.Y277Y; 17:46768557-46768557

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.1009T>C; p.C337R; 17:46768379-46768379

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.468C>T; p.G156G; 17:46769903-46769903

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.669G>A; p.A223A; 17:46768719-46768719

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.668C>T; p.A223V; 17:46768720-46768720

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.485C>T; p.A162V; 17:46769886-46769886

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.931G>C; p.D311H; 17:46768457-46768457

thyroidother; neoplasmSubstitution - Missense