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

Basic Information

Gene ID

3178

Name

HNRNPA1

Synonymous

heterogeneous nuclear ribonucleoprotein A1;HNRNPA1;heterogeneous nuclear ribonucleoprotein A1

Definition

Putative heterogeneous nuclear ribonucleoprotein A1-like 3|helix-destabilizing protein|heterogeneous nuclear ribonucleoprotein A1B protein|heterogeneous nuclear ribonucleoprotein B2 protein|heterogeneous nuclear ribonucleoprotein core protein A1|hnRNP A1-

Position

12q13.1

Gene Type

protein-coding

COSMIC confirmed somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.910G>C; p.G304R; 12:54284260-54284260

 biliary_tract; gallbladdercarcinoma; adenocarcinomaSubstitution - Missense

c.919G>A; p.G307S; 12:54284269-54284269

 breastcarcinomaSubstitution - Missense

c.367G>T; p.D123Y; 12:54282177-54282177

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.677-2A>T; p.?; 12:54282798-54282798

 endometriumcarcinoma; endometrioid_carcinomaUnknown

c.456C>A; p.T152T; 12:54282266-54282266

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.89T>C; p.L30P; 12:54281459-54281459

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.789T>G; p.F263L; 12:54283849-54283849

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.178G>C; p.V60L; 12:54281840-54281840

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.702T>G; p.G234G; 12:54282825-54282825

 haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; diffuse_large_B_cell_lymphomaSubstitution - coding silent

c.534A>G; p.R178R; 12:54282437-54282437

 haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; acute_lymphoblastic_T_cell_leukaemiaSubstitution - coding silent

c.65G>C; p.S22T; 12:54281435-54281435

 haematopoietic_and_lymphoid_tissue; lymph_nodelymphoid_neoplasm; diffuse_large_B_cell_lymphomaSubstitution - Missense

c.648C>T; p.F216F; 12:54282637-54282637

 haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; acute_lymphoblastic_T_cell_leukaemiaSubstitution - coding silent

c.413C>G; p.T138S; 12:54282223-54282223

 haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; acute_lymphoblastic_T_cell_leukaemiaSubstitution - Missense

c.272C>G; p.S91C; 12:54281934-54281934

 kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.561T>G; p.A187A; 12:54282464-54282464

 kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - coding silent

c.6T>G; p.S2S; 12:54280813-54280813

 kidneyother; neoplasmSubstitution - coding silent

c.56G>T; p.G19V; 12:54281426-54281426

 kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.329G>A; p.G110D; 12:54282139-54282139

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.372T>G; p.Y124*; 12:54282182-54282182

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Nonsense

c.147A>C; p.P49P; 12:54281809-54281809

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - coding silent

c.437G>A; p.R146K; 12:54282247-54282247

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.534A>G; p.R178R; 12:54282437-54282437

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.731A>G; p.Y244C; 12:54282854-54282854

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.898C>T; p.R300*; 12:54283958-54283958

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.80A>G; p.D27G; 12:54281450-54281450

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.555G>C; p.E185D; 12:54282458-54282458

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.55G>A; p.G19R; 12:54281425-54281425

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.818T>G; p.F273C; 12:54283878-54283878

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.124G>A; p.D42N; 12:54281494-54281494

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.930C>T; p.S310S; 12:54284280-54284280

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.125A>G; p.D42G; 12:54281495-54281495

 livercarcinomaSubstitution - Missense

c.956G>C; p.R319T; 12:54284306-54284306

 lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.328G>T; p.G110C; 12:54282138-54282138

 lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.328G>T; p.G110C; 12:54282138-54282138

 lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.216G>C; p.M72I; 12:54281878-54281878

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.183A>G; p.T61T; 12:54281845-54281845

 lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.20C>G; p.P7R; 12:54281390-54281390

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.581G>C; p.R194T; 12:54282484-54282484

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.755G>T; p.S252I; 12:54283815-54283815

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.768T>C; p.G256G; 12:54283828-54283828

 lungcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.464A>G; p.D155G; 12:54282274-54282274

 oesophagus; middle_thirdcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.804T>A; p.N268K; 12:54283864-54283864

 oesophagus; lower_thirdcarcinoma; adenocarcinomaSubstitution - Missense

c.82G>A; p.E28K; 12:54281452-54281452

 ovarycarcinoma; serous_carcinomaSubstitution - Missense

c.592G>T; p.G198C; 12:54282581-54282581

 ovarycarcinoma; serous_carcinomaSubstitution - Missense

c.17C>A; p.S6Y; 12:54281387-54281387

 pancreaspancreatic_intraepithelial_neoplasia_(PanIN)Substitution - Missense

c.17C>A; p.S6Y; 12:54281387-54281387

 pancreascarcinoma; ductal_carcinomaSubstitution - Missense

c.607G>T; p.G203C; 12:54282596-54282596

 prostatecarcinoma; adenocarcinomaSubstitution - Missense

c.636G>A; p.G212G; 12:54282625-54282625

 skin; neckmalignant_melanomaSubstitution - coding silent

c.924C>T; p.S308S; 12:54284274-54284274

 skin; neckmalignant_melanomaSubstitution - coding silent

c.437G>T; p.R146M; 12:54282247-54282247

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.539C>A; p.A180D; 12:54282442-54282442

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.835G>A; p.G279R; 12:54283895-54283895

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.79G>T; p.D27Y; 12:54281449-54281449

 upper_aerodigestive_tract; mouthcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.70G>T; p.E24*; 12:54281440-54281440

 upper_aerodigestive_tract; mouthcarcinoma; squamous_cell_carcinomaSubstitution - Nonsense

c.124G>C; p.D42H; 12:54281494-54281494

 upper_aerodigestive_tract; sinonasal_and_nasal_cavitycarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.352G>C; p.E118Q; 12:54282162-54282162

 urinary_tract; bladdercarcinomaSubstitution - Missense

c.161C>G; p.S54C; 12:54281823-54281823

 urinary_tract; bladdercarcinomaSubstitution - Missense

c.190A>G; p.T64A; 12:54281852-54281852

 urinary_tract; bladdercarcinomaSubstitution - Missense

c.216G>A; p.M72I; 12:54281878-54281878

 urinary_tract; bladdercarcinomaSubstitution - Missense