Epithelial-Mesenchymal Transition gene database (dbEMT) Home
dbEMT
dbEMT 2.0
General information | Literature | Expression | lncRNA |Regulation | Mutation | Homolog | Interaction

Basic Information

Gene ID

9444

Name

QKI

The somatic mutations from COSMIC database

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.810A>T; p.P270P; 6:163563595-163563595

 ovarycarcinoma; serous_carcinomaSubstitution - coding silent

c.1007G>A; p.R336Q; 6:163566793-163566793

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1007G>A; p.R336Q; 6:163566793-163566793

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.188G>T; p.G63V; 6:163455324-163455324

 lungcarcinoma; non_small_cell_carcinomaSubstitution - Missense

c.725G>A; p.R242H; 6:163563510-163563510

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.725G>A; p.R242H; 6:163563510-163563510

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.542C>G; p.P181R; 6:163535121-163535121

 central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.93G>T; p.L31L; 6:163415286-163415286

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.274G>T; p.E92*; 6:163455410-163455410

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Nonsense

c.699G>A; p.A233A; 6:163563484-163563484

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.211G>T; p.E71*; 6:163455347-163455347

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.252G>A; p.E84E; 6:163455388-163455388

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.934+4A>C; p.?; 6:163563723-163563723

 stomachcarcinoma; diffuse_adenocarcinomaUnknown

c.380G>T; p.G127V; 6:163478874-163478874

 oesophagus; lower_thirdcarcinoma; adenocarcinomaSubstitution - Missense

c.968T>G; p.M323R; 6:163566754-163566754

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.360A>C; p.K120N; 6:163478854-163478854

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.970C>T; p.R324C; 6:163566756-163566756

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.935-8T>G; p.?; 6:163566713-163566713

 large_intestine; coloncarcinoma; adenocarcinomaUnknown

c.810A>G; p.P270P; 6:163563595-163563595

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.1012G>A; p.A338T; 6:163570696-163570696

 prostatecarcinomaSubstitution - Missense

c.860C>T; p.P287L; 6:163563645-163563645

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.795C>T; p.N265N; 6:163563580-163563580

 bone; tibiaEwings_sarcoma-peripheral_primitive_neuroectodermal_tumourSubstitution - coding silent

c.970C>A; p.R324S; 6:163566756-163566756

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.970C>A; p.R324S; 6:163566756-163566756

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.394_395delAA; p.K134fs*5; 6:163478888-163478889

 oesophaguscarcinoma; adenocarcinomaDeletion - Frameshift

c.970C>A; p.R324S; 6:163566756-163566756

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.465C>T; p.I155I; 6:163535044-163535044

 lungcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.700C>T; p.P234S; 6:163563485-163563485

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.354A>T; p.G118G; 6:163478848-163478848

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.956G>A; p.R319Q; 6:163566742-163566742

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.956G>A; p.R319Q; 6:163566742-163566742

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.956G>A; p.R319Q; 6:163566742-163566742

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.1017C>T; p.T339T; 6:163570701-163570701

 oesophaguscarcinoma; adenocarcinomaSubstitution - coding silent

c.393_394insA; p.E135fs*5; 6:163478887-163478888

 large_intestine; coloncarcinoma; adenocarcinomaInsertion - Frameshift

c.553G>T; p.G185*; 6:163561988-163561988

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.938C>T; p.A313V; 6:163566724-163566724

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1004A>C; p.D335A; 6:163566790-163566790

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.335A>C; p.Q112P; 6:163478829-163478829

 central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.335A>C; p.Q112P; 6:163478829-163478829

 central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.261T>A; p.Y87*; 6:163455397-163455397

 skinmalignant_melanomaSubstitution - Nonsense

c.1008A>G; p.R336R; 6:163566794-163566794

 large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.261T>A; p.Y87*; 6:163455397-163455397

 skinmalignant_melanomaSubstitution - Nonsense

c.490G>A; p.A164T; 6:163535069-163535069

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.780C>T; p.T260T; 6:163563565-163563565

 oesophagus; lower_thirdcarcinoma; adenocarcinomaSubstitution - coding silent

c.1010-1G>A; p.?; 6:163570693-163570693

 central_nervous_system; brainprimitive_neuroectodermal_tumour-medulloblastomaUnknown

c.902T>G; p.L301R; 6:163563687-163563687

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.40A>T; p.T14S; 6:163415233-163415233

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.830C>T; p.P277L; 6:163563615-163563615

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.394delA; p.K134fs*14; 6:163478888-163478888

 stomachcarcinoma; intestinal_adenocarcinomaDeletion - Frameshift

c.394delA; p.K134fs*14; 6:163478888-163478888

 large_intestinecarcinoma; adenocarcinomaDeletion - Frameshift

c.394delA; p.K134fs*14; 6:163478888-163478888

 large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.394delA; p.K134fs*14; 6:163478888-163478888

 large_intestinecarcinoma; adenocarcinomaDeletion - Frameshift

c.394delA; p.K134fs*14; 6:163478888-163478888

 large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.394delA; p.K134fs*14; 6:163478888-163478888

 pancreascarcinoma; acinar_carcinomaDeletion - Frameshift

c.394delA; p.K134fs*14; 6:163478888-163478888

 large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.394delA; p.K134fs*14; 6:163478888-163478888

 large_intestinecarcinoma; adenocarcinomaDeletion - Frameshift

c.394delA; p.K134fs*14; 6:163478888-163478888

 large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.394delA; p.K134fs*14; 6:163478888-163478888

 large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.394delA; p.K134fs*14; 6:163478888-163478888

 stomachcarcinoma; intestinal_adenocarcinomaDeletion - Frameshift

c.394delA; p.K134fs*14; 6:163478888-163478888

 large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.394delA; p.K134fs*14; 6:163478888-163478888

 large_intestinecarcinoma; adenocarcinomaDeletion - Frameshift

c.394delA; p.K134fs*14; 6:163478888-163478888

 large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.394delA; p.K134fs*14; 6:163478888-163478888

 stomachadenocarcinomaDeletion - Frameshift

c.394delA; p.K134fs*14; 6:163478888-163478888

 large_intestinecarcinoma; adenocarcinomaDeletion - Frameshift

c.165C>G; p.D55E; 6:163455301-163455301

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.363C>T; p.I121I; 6:163478857-163478857

 lungcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.939G>A; p.A313A; 6:163566725-163566725

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - coding silent

c.352G>A; p.G118R; 6:163478846-163478846

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.391G>T; p.D131Y; 6:163478885-163478885

 upper_aerodigestive_tract; mouthcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.391G>T; p.D131Y; 6:163478885-163478885

 upper_aerodigestive_tract; mouthcarcinomaSubstitution - Missense

c.439C>T; p.L147L; 6:163535018-163535018

 skinmalignant_melanomaSubstitution - coding silent

c.3G>A; p.M1I; 6:163415196-163415196

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.3G>A; p.M1I; 6:163415196-163415196

 skinmalignant_melanomaSubstitution - Missense

c.659C>G; p.A220G; 6:163563444-163563444

 central_nervous_system; braingliomaSubstitution - Missense

c.955C>T; p.R319*; 6:163566741-163566741

 skinmalignant_melanomaSubstitution - Nonsense

c.955C>T; p.R319*; 6:163566741-163566741

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.602A>G; p.N201S; 6:163562037-163562037

 prostatecarcinoma; adenocarcinomaSubstitution - Missense

c.766A>G; p.R256G; 6:163563551-163563551

 breastcarcinomaSubstitution - Missense

c.520G>A; p.E174K; 6:163535099-163535099

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.550G>T; p.E184*; 6:163561985-163561985

 large_intestinecarcinoma; adenocarcinomaSubstitution - Nonsense

c.984C>A; p.Y328*; 6:163566770-163566770

 prostatecarcinomaSubstitution - Nonsense

c.1014C>T; p.A338A; 6:163570698-163570698

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.613A>G; p.R205G; 6:163562048-163562048

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.848T>A; p.L283*; 6:163563633-163563633

 skinmalignant_melanomaSubstitution - Nonsense

c.649T>C; p.S217P; 6:163563434-163563434

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.734C>T; p.T245M; 6:163563519-163563519

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.634+2T>C; p.?; 6:163562071-163562071

 large_intestine; coloncarcinoma; adenocarcinomaUnknown

c.845G>A; p.G282D; 6:163563630-163563630

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.837C>T; p.P279P; 6:163563622-163563622

 urinary_tract; bladdercarcinomaSubstitution - coding silent

c.889G>A; p.A297T; 6:163563674-163563674

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.159G>T; p.R53R; 6:163455295-163455295

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - coding silent

c.317G>C; p.R106T; 6:163478811-163478811

 urinary_tract; bladdercarcinomaSubstitution - Missense

c.155T>C; p.V52A; 6:163455291-163455291

 central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.155T>C; p.V52A; 6:163455291-163455291

 central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.650C>A; p.S217Y; 6:163563435-163563435

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.402+1G>T; p.?; 6:163478897-163478897

 prostatecarcinoma; adenocarcinomaUnknown

c.870C>T; p.Y290Y; 6:163563655-163563655

 large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.661A>G; p.T221A; 6:163563446-163563446

 livercarcinomaSubstitution - Missense

c.897A>G; p.S299S; 6:163563682-163563682

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.351C>T; p.T117T; 6:163478845-163478845

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.989G>T; p.R330M; 6:163566775-163566775

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.991A>T; p.I331F; 6:163566777-163566777

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.20C>T; p.T7M; 6:163415213-163415213

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.638C>G; p.A213G; 6:163563423-163563423

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.169T>C; p.Y57H; 6:163455305-163455305

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

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