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

Basic Information

Gene ID

7471

Name

WNT1

Synonymous

wingless-type MMTV integration site family, member 1;WNT1;wingless-type MMTV integration site family, member 1

Definition

proto-oncogene Int-1 homolog|proto-oncogene Wnt-1|wingless-type MMTV integration site family, member 1 (oncogene INT1)

Position

12q13

Gene Type

protein-coding

COSMIC confirmed somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.465C>T; p.Y155Y; 12:48980530-48980530

 breastcarcinomaSubstitution - coding silent

c.490G>A; p.D164N; 12:48980555-48980555

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.855C>A; p.S285S; 12:48981382-48981382

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.258G>T; p.L86L; 12:48979621-48979621

 kidneycarcinomaSubstitution - coding silent

c.358+3G>A; p.?; 12:48979724-48979724

 kidneyother; neoplasmUnknown

c.244G>A; p.V82M; 12:48979607-48979607

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.500delG; p.G169fs*30; 12:48980565-48980565

 large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.500delG; p.G169fs*30; 12:48980565-48980565

 large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.500delG; p.G169fs*30; 12:48980565-48980565

 large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.500delG; p.G169fs*30; 12:48980565-48980565

 large_intestine; caecumcarcinoma; adenocarcinomaDeletion - Frameshift

c.250delG; p.L86fs*113; 12:48979613-48979613

 large_intestine; rectumcarcinoma; adenocarcinomaDeletion - Frameshift

c.783C>T; p.R261R; 12:48981310-48981310

 large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.689G>A; p.R230H; 12:48981216-48981216

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.371C>A; p.T124K; 12:48980436-48980436

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.274G>C; p.E92Q; 12:48979637-48979637

 lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.261G>C; p.Q87H; 12:48979624-48979624

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.750C>A; p.F250L; 12:48981277-48981277

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.208C>A; p.R70S; 12:48979571-48979571

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.125C>T; p.S42F; 12:48979488-48979488

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.195C>A; p.S65R; 12:48979558-48979558

 lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.591C>T; p.L197L; 12:48980656-48980656

 lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.714G>A; p.T238T; 12:48981241-48981241

 oesophaguscarcinoma; adenocarcinomaSubstitution - coding silent

c.1101C>T; p.H367H; 12:48981628-48981628

 oesophaguscarcinoma; adenocarcinomaSubstitution - coding silent

c.197G>A; p.R66H; 12:48979560-48979560

 prostatecarcinoma; adenocarcinomaSubstitution - Missense

c.991G>A; p.G331S; 12:48981518-48981518

 skinmalignant_melanomaSubstitution - Missense

c.114G>A; p.V38V; 12:48979477-48979477

 skinmalignant_melanomaSubstitution - coding silent

c.396C>T; p.S132S; 12:48980461-48980461

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.542G>C; p.G181A; 12:48980607-48980607

 skinmalignant_melanomaSubstitution - Missense

c.455C>T; p.T152M; 12:48980520-48980520

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.466C>T; p.R156W; 12:48980531-48980531

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.302G>T; p.R101L; 12:48979665-48979665

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.319G>A; p.A107T; 12:48979682-48979682

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.176C>T; p.P59L; 12:48979539-48979539

 urinary_tract; bladdercarcinomaSubstitution - Missense