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Gene information | Literature | Expression | lncRNA | Mutation | Homolog

Basic Information

Gene ID

7480

Name

WNT10B

Synonymous

wingless-type MMTV integration site family, member 10B;WNT10B;wingless-type MMTV integration site family, member 10B

Definition

WNT-10B protein|protein Wnt-10b

Position

12q13

Gene Type

protein-coding

COSMIC confirmed somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.416G>A; p.G139D; 12:48968241-48968241

 biliary_tract; bile_ductcarcinoma; adenocarcinomaSubstitution - Missense

c.373G>A; p.A125T; 12:48968284-48968284

 breastcarcinomaSubstitution - Missense

c.466C>A; p.R156R; 12:48968191-48968191

 central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - coding silent

c.706C>T; p.R236C; 12:48967951-48967951

 central_nervous_system; brainglioma; oligodendroglioma_Grade_IIISubstitution - Missense

c.1034G>A; p.G345D; 12:48966231-48966231

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.705G>A; p.G235G; 12:48967952-48967952

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.102G>T; p.L34L; 12:48970324-48970324

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.829G>A; p.E277K; 12:48966436-48966436

 haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; hairy_cell_leukaemiaSubstitution - Missense

c.359C>A; p.S120Y; 12:48968298-48968298

 kidneycarcinoma; papillary_renal_cell_carcinomaSubstitution - Missense

c.363C>T; p.F121F; 12:48968294-48968294

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.953G>A; p.C318Y; 12:48966312-48966312

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.836T>C; p.L279P; 12:48966429-48966429

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.816G>T; p.G272G; 12:48966449-48966449

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.958C>T; p.R320*; 12:48966307-48966307

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.682C>T; p.R228*; 12:48967975-48967975

 large_intestine; coloncarcinomaSubstitution - Nonsense

c.682C>T; p.R228*; 12:48967975-48967975

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.1031G>A; p.C344Y; 12:48966234-48966234

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.832C>T; p.R278W; 12:48966433-48966433

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1063G>A; p.V355M; 12:48966202-48966202

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.904C>T; p.R302C; 12:48966361-48966361

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.903C>A; p.P301P; 12:48966362-48966362

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.346G>T; p.E116*; 12:48968311-48968311

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Nonsense

c.827G>A; p.R276K; 12:48966438-48966438

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.55T>C; p.F19L; 12:48970475-48970475

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1059C>T; p.H353H; 12:48966206-48966206

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.813G>A; p.V271V; 12:48966452-48966452

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.1070G>A; p.R357Q; 12:48966195-48966195

 livercarcinomaSubstitution - Missense

c.1070G>A; p.R357Q; 12:48966195-48966195

 livercarcinomaSubstitution - Missense

c.380G>A; p.G127E; 12:48968277-48968277

 livercarcinomaSubstitution - Missense

c.380G>A; p.G127E; 12:48968277-48968277

 livercarcinomaSubstitution - Missense

c.437G>T; p.C146F; 12:48968220-48968220

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.454G>C; p.G152R; 12:48968203-48968203

 lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.798A>T; p.P266P; 12:48966467-48966467

 lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.878G>T; p.G293V; 12:48966387-48966387

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1115G>T; p.C372F; 12:48966150-48966150

 lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.1069C>G; p.R357G; 12:48966196-48966196

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.674C>T; p.A225V; 12:48967983-48967983

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.504C>A; p.S168S; 12:48968153-48968153

 lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - coding silent

c.702G>T; p.V234V; 12:48967955-48967955

 lungcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.551C>G; p.S184*; 12:48968106-48968106

 lung; right_lower_lobecarcinoma; adenocarcinomaSubstitution - Nonsense

c.46G>A; p.G16S; 12:48970484-48970484

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.364T>A; p.S122T; 12:48968293-48968293

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.706C>A; p.R236S; 12:48967951-48967951

 lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.95T>C; p.L32P; 12:48970331-48970331

 lungcarcinoma; small_cell_carcinomaSubstitution - Missense

c.1006A>C; p.K336Q; 12:48966259-48966259

 lungcarcinoma; undifferentiated_carcinomaSubstitution - Missense

c.583delG; p.E195fs*45; 12:48968074-48968074

 lungcarcinoma; adenocarcinomaDeletion - Frameshift

c.391G>T; p.A131S; 12:48968266-48968266

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.393A>G; p.A131A; 12:48968264-48968264

 pancreascarcinoma; ductal_carcinomaSubstitution - coding silent

c.393A>G; p.A131A; 12:48968264-48968264

 pancreascarcinomaSubstitution - coding silent

c.958C>G; p.R320G; 12:48966307-48966307

 prostatecarcinomaSubstitution - Missense

c.878G>A; p.G293E; 12:48966387-48966387

 skinmalignant_melanomaSubstitution - Missense

c.678A>C; p.R226R; 12:48967979-48967979

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.699G>A; p.R233R; 12:48967958-48967958

 skin; handmalignant_melanomaSubstitution - coding silent

c.917G>A; p.G306E; 12:48966348-48966348

 skinmalignant_melanomaSubstitution - Missense

c.1051C>T; p.R351C; 12:48966214-48966214

 skinmalignant_melanomaSubstitution - Missense

c.698G>A; p.R233K; 12:48967959-48967959

 skin; handmalignant_melanomaSubstitution - Missense

c.583G>A; p.E195K; 12:48968074-48968074

 skinmalignant_melanomaSubstitution - Missense

c.583G>A; p.E195K; 12:48968074-48968074

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1023_1024GG>AA; p.D342N; 12:48966241-48966242

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.467G>A; p.R156Q; 12:48968190-48968190

 skinmalignant_melanomaSubstitution - Missense

c.829G>A; p.E277K; 12:48966436-48966436

 skinmalignant_melanomaSubstitution - Missense

c.669C>T; p.I223I; 12:48967988-48967988

 skinmalignant_melanomaSubstitution - coding silent

c.790G>A; p.A264T; 12:48966475-48966475

 skinmalignant_melanomaSubstitution - Missense

c.828G>A; p.R276R; 12:48966437-48966437

 skinmalignant_melanomaSubstitution - coding silent

c.1151G>A; p.W384*; 12:48966114-48966114

 skinmalignant_melanomaSubstitution - Nonsense

c.806G>C; p.R269P; 12:48966459-48966459

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.519C>T; p.F173F; 12:48968138-48968138

 skinmalignant_melanomaSubstitution - coding silent

c.1141G>A; p.V381I; 12:48966124-48966124

 skinmalignant_melanomaSubstitution - Missense

c.307_308insCCCC; p.L103fs*52; 12:48970118-48970119

 skin; extremitymalignant_melanomaInsertion - Frameshift

c.570C>T; p.P190P; 12:48968087-48968087

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.707G>A; p.R236H; 12:48967950-48967950

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.537C>T; p.S179S; 12:48968120-48968120

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.617G>C; p.G206A; 12:48968040-48968040

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.36G>A; p.S12S; 12:48970494-48970494

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.955G>T; p.E319*; 12:48966310-48966310

 thyroidother; neoplasmSubstitution - Nonsense

c.1059C>T; p.H353H; 12:48966206-48966206

 thyroidother; neoplasmSubstitution - coding silent

c.707G>A; p.R236H; 12:48967950-48967950

 urinary_tract; bladdercarcinoma; transitional_cell_carcinomaSubstitution - Missense

c.707G>A; p.R236H; 12:48967950-48967950

 urinary_tract; bladdercarcinomaSubstitution - Missense

c.35C>T; p.S12L; 12:48970495-48970495

 urinary_tract; bladdercarcinomaSubstitution - Missense

c.35C>T; p.S12L; 12:48970495-48970495

 urinary_tract; bladdercarcinoma; transitional_cell_carcinomaSubstitution - Missense