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

Basic Information

Gene ID

8856

Name

NR1I2

The somatic mutations from COSMIC database

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.980T>G; p.F327C; 3:119815047-119815047

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.913G>A; p.D305N; 3:119814980-119814980

breastcarcinomaSubstitution - Missense

c.762G>A; p.L254L; 3:119812811-119812811

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.68G>T; p.S23I; 3:119782825-119782825

lungcarcinoma; small_cell_carcinomaSubstitution - Missense

c.180G>T; p.E60D; 3:119807313-119807313

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.369C>A; p.C123*; 3:119810115-119810115

kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Nonsense

c.999G>A; p.A333A; 3:119815066-119815066

biliary_tract; bile_ductcarcinoma; adenocarcinomaSubstitution - coding silent

c.1159C>A; p.L387I; 3:119815427-119815427

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.584A>T; p.D195V; 3:119811674-119811674

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.1129G>A; p.E377K; 3:119815397-119815397

NSmalignant_melanomaSubstitution - Missense

c.538C>A; p.Q180K; 3:119811628-119811628

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.799C>A; p.P267T; 3:119812848-119812848

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.764G>A; p.R255Q; 3:119812813-119812813

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.764G>A; p.R255Q; 3:119812813-119812813

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.144G>T; p.W48C; 3:119807277-119807277

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.182C>G; p.S61C; 3:119807315-119807315

skin; facecarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.766G>T; p.G256W; 3:119812815-119812815

ovarycarcinoma; serous_carcinomaSubstitution - Missense

c.645G>T; p.G215G; 3:119812694-119812694

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.1254C>T; p.C418C; 3:119815808-119815808

livercarcinomaSubstitution - coding silent

c.1388T>C; p.L463P; 3:119817178-119817178

central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.1372C>T; p.P458S; 3:119817162-119817162

breastcarcinomaSubstitution - Missense

c.949G>A; p.G317R; 3:119815016-119815016

skinmalignant_melanomaSubstitution - Missense

c.1326C>G; p.I442M; 3:119817116-119817116

pancreascarcinomaSubstitution - Missense

c.20A>C; p.H7P; 3:119782777-119782777

prostatecarcinomaSubstitution - Missense

c.997G>T; p.A333S; 3:119815064-119815064

lungcarcinoma; small_cell_carcinomaSubstitution - Missense

c.853A>G; p.M285V; 3:119812902-119812902

livercarcinomaSubstitution - Missense

c.333C>T; p.N111N; 3:119810079-119810079

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.214G>A; p.E72K; 3:119807347-119807347

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1256A>G; p.N419S; 3:119815810-119815810

livercarcinoma; hepatocellular_carcinomaSubstitution - Missense

c.1055-10C>T; p.?; 3:119815313-119815313

oesophaguscarcinoma; adenocarcinomaUnknown

c.364G>A; p.A122T; 3:119810110-119810110

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.364G>A; p.A122T; 3:119810110-119810110

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.530T>A; p.L177Q; 3:119811620-119811620

lung; right_lower_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.1333C>T; p.Q445*; 3:119817123-119817123

breastcarcinomaSubstitution - Nonsense

c.1312G>A; p.E438K; 3:119817102-119817102

upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.144G>A; p.W48*; 3:119807277-119807277

skinmalignant_melanomaSubstitution - Nonsense

c.659G>A; p.G220D; 3:119812708-119812708

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.175A>G; p.T59A; 3:119807308-119807308

urinary_tract; bladdercarcinomaSubstitution - Missense

c.207C>T; p.N69N; 3:119807340-119807340

kidneyother; neoplasmSubstitution - coding silent

c.1306C>A; p.L436I; 3:119817096-119817096

urinary_tract; bladdercarcinomaSubstitution - Missense

c.953C>G; p.A318G; 3:119815020-119815020

stomachcarcinoma; intestinal_adenocarcinomaSubstitution - Missense

c.953C>G; p.A318G; 3:119815020-119815020

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.878T>G; p.I293S; 3:119812927-119812927

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.643G>A; p.G215R; 3:119812692-119812692

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.372G>A; p.E124E; 3:119810118-119810118

kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - coding silent

c.765G>C; p.R255R; 3:119812814-119812814

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.825C>T; p.I275I; 3:119812874-119812874

breastcarcinomaSubstitution - coding silent

c.257A>C; p.K86T; 3:119807390-119807390

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.257A>C; p.K86T; 3:119807390-119807390

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.167G>A; p.C56Y; 3:119807300-119807300

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.764delG; p.E257fs*59; 3:119812813-119812813

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.190G>A; p.G64R; 3:119807323-119807323

urinary_tract; bladdercarcinoma; transitional_cell_carcinomaSubstitution - Missense

c.190G>A; p.G64R; 3:119807323-119807323

urinary_tract; bladdercarcinomaSubstitution - Missense

c.716G>A; p.S239N; 3:119812765-119812765

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.1161C>T; p.L387L; 3:119815429-119815429

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.351C>T; p.P117P; 3:119810097-119810097

skinmalignant_melanomaSubstitution - coding silent

c.1007G>A; p.G336E; 3:119815074-119815074

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1371delC; p.F459fs*>15; 3:119817161-119817161

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.74C>T; p.A25V; 3:119782831-119782831

lungcarcinoma; small_cell_carcinomaSubstitution - Missense

c.1084A>G; p.M362V; 3:119815352-119815352

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.839C>T; p.P280L; 3:119812888-119812888

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.241C>T; p.R81C; 3:119807374-119807374

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.1404C>T; p.F468F; 3:119817194-119817194

skinmalignant_melanomaSubstitution - coding silent

c.924C>T; p.I308I; 3:119814991-119814991

NSmalignant_melanomaSubstitution - coding silent

c.924C>T; p.I308I; 3:119814991-119814991

NSmalignant_melanomaSubstitution - coding silent

c.1345C>T; p.R449W; 3:119817135-119817135

kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.912-1G>T; p.?; 3:119814978-119814978

lungcarcinoma; adenocarcinomaUnknown

c.351C>A; p.P117P; 3:119810097-119810097

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.227G>A; p.G76D; 3:119807360-119807360

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.251G>A; p.G84E; 3:119807384-119807384

skinmalignant_melanomaSubstitution - Missense

c.684G>A; p.Q228Q; 3:119812733-119812733

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.477G>C; p.E159D; 3:119811567-119811567

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.464A>T; p.E155V; 3:119811554-119811554

lungcarcinoma; small_cell_carcinomaSubstitution - Missense

c.1259G>A; p.R420Q; 3:119815813-119815813

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.770A>G; p.E257G; 3:119812819-119812819

prostatecarcinoma; adenocarcinomaSubstitution - Missense

c.1175G>A; p.R392H; 3:119815729-119815729

central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.1175G>A; p.R392H; 3:119815729-119815729

kidneyother; neoplasmSubstitution - Missense

c.1025G>A; p.R342Q; 3:119815092-119815092

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.863A>T; p.Y288F; 3:119812912-119812912

livercarcinomaSubstitution - Missense

c.863A>T; p.Y288F; 3:119812912-119812912

livercarcinomaSubstitution - Missense

c.863A>T; p.Y288F; 3:119812912-119812912

livercarcinomaSubstitution - Missense

c.1130A>C; p.E377A; 3:119815398-119815398

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1253G>T; p.C418F; 3:119815807-119815807

livercarcinomaSubstitution - Missense

c.585C>T; p.D195D; 3:119811675-119811675

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.585C>T; p.D195D; 3:119811675-119811675

large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.1198G>A; p.V400M; 3:119815752-119815752

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.845T>C; p.M282T; 3:119812894-119812894

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.1089G>T; p.L363L; 3:119815357-119815357

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.104G>A; p.G35D; 3:119807237-119807237

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.1318C>T; p.R440C; 3:119817108-119817108

skinmalignant_melanomaSubstitution - Missense

c.786G>A; p.W262*; 3:119812835-119812835

skin; trunkmalignant_melanomaSubstitution - Nonsense

c.955G>A; p.A319T; 3:119815022-119815022

pancreascarcinomaSubstitution - Missense

c.884G>A; p.S295N; 3:119812933-119812933

ovarycarcinoma; clear_cell_carcinomaSubstitution - Missense


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