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

Basic Information

Gene ID

3182

Name

HNRNPAB

The somatic mutations from COSMIC database

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.880G>A; p.D294N; 5:178210224-178210224

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.240T>C; p.D80D; 5:178205872-178205872

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.247delA; p.D85fs*2; 5:178205879-178205879

 large_intestinecarcinoma; adenocarcinomaDeletion - Frameshift

c.427_431delAAAAA; p.K143fs*20; 5:178206780-178206784

 urinary_tract; bladdercarcinoma; transitional_cell_carcinomaDeletion - Frameshift

c.480T>C; p.G160G; 5:178206833-178206833

 pancreascarcinomaSubstitution - coding silent

c.480T>C; p.G160G; 5:178206833-178206833

 pancreascarcinomaSubstitution - coding silent

c.480T>C; p.G160G; 5:178206833-178206833

 pancreascarcinomaSubstitution - coding silent

c.251A>C; p.K84T; 5:178205883-178205883

 pancreascarcinomaSubstitution - Missense

c.722G>A; p.G241D; 5:178209382-178209382

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.997T>G; p.*333G; 5:178210621-178210621

 large_intestine; coloncarcinoma; adenocarcinomaNonstop extension

c.398A>G; p.H133R; 5:178206751-178206751

 lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.992C>G; p.P331R; 5:178210616-178210616

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.840_841insA; p.G281fs*33; 5:178210184-178210185

 livercarcinomaInsertion - Frameshift

c.447G>T; p.K149N; 5:178206800-178206800

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.813C>G; p.G271G; 5:178210157-178210157

 ovaryother; neoplasmSubstitution - coding silent

c.604T>G; p.F202V; 5:178207160-178207160

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.706_707insC; p.Q236fs*78; 5:178209366-178209367

 lungcarcinoma; adenocarcinomaInsertion - Frameshift

c.879C>T; p.Y293Y; 5:178210223-178210223

 pancreascarcinoma; ductal_carcinomaSubstitution - coding silent

c.832_849del18; p.Y282_G287delYQQGYG; 5:178210176-178210193

 urinary_tract; bladdercarcinoma; transitional_cell_carcinomaDeletion - In frame

c.995A>C; p.Y332S; 5:178210619-178210619

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.904G>A; p.G302S; 5:178210248-178210248

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.966T>C; p.R322R; 5:178210590-178210590

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.896G>T; p.G299V; 5:178210240-178210240

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.327G>A; p.R109R; 5:178205959-178205959

 large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.389_391delAGA; p.K131delK; 5:178206742-178206744

 large_intestine; rectumcarcinoma; adenocarcinomaDeletion - In frame

c.888G>A; p.S296S; 5:178210232-178210232

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.702_703insT; p.Y235fs*79; 5:178209362-178209363

 endometriumcarcinoma; endometrioid_carcinomaInsertion - Frameshift

c.265T>C; p.Y89H; 5:178205897-178205897

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.978_979insA; p.N327fs*2; 5:178210602-178210603

 large_intestine; rectumcarcinoma; adenocarcinomaInsertion - Frameshift

c.697G>T; p.E233*; 5:178209357-178209357

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.697G>T; p.E233*; 5:178209357-178209357

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Nonsense

c.922G>A; p.D308N; 5:178210266-178210266

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.553T>C; p.L185L; 5:178207109-178207109

 breastcarcinomaSubstitution - coding silent

c.732C>T; p.G244G; 5:178209392-178209392

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.931C>T; p.Q311*; 5:178210555-178210555

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.991C>T; p.P331S; 5:178210615-178210615

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.494C>A; p.A165D; 5:178206847-178206847

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.256T>G; p.L86V; 5:178205888-178205888

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.928+1G>A; p.?; 5:178210273-178210273

 urinary_tract; bladdercarcinomaUnknown

c.733C>T; p.R245C; 5:178209393-178209393

 prostatecarcinoma; adenocarcinomaSubstitution - Missense

c.715C>T; p.Q239*; 5:178209375-178209375

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Nonsense

c.351G>A; p.L117L; 5:178205983-178205983

 kidneycarcinoma; papillary_renal_cell_carcinomaSubstitution - coding silent

c.909C>T; p.Y303Y; 5:178210253-178210253

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.450G>A; p.K150K; 5:178206803-178206803

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.380T>C; p.V127A; 5:178206733-178206733

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.602C>T; p.T201I; 5:178207158-178207158

 skinmalignant_melanomaSubstitution - Missense

c.737G>A; p.G246E; 5:178209397-178209397

 skinmalignant_melanomaSubstitution - Missense

c.899A>G; p.Y300C; 5:178210243-178210243

 prostatecarcinomaSubstitution - Missense

c.512delG; p.E172fs*20; 5:178206865-178206865

 skinmalignant_melanomaDeletion - Frameshift

c.818G>A; p.G273D; 5:178210162-178210162

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.841G>A; p.G281S; 5:178210185-178210185

 boneEwings_sarcoma-peripheral_primitive_neuroectodermal_tumourSubstitution - Missense

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