Cancer metastasis gene database Home
Cancer metastasis database
General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction

Basic Information

Gene ID

3592

Name

IL12A

Synonymous

interleukin 12A;IL12A;interleukin 12A

Definition

CLMF p35|IL-12, subunit p35|IL35 subunit|NF cell stimulatory factor chain 1|NK cell stimulatory factor chain 1|cytotoxic lymphocyte maturation factor 1, p35|cytotoxic lymphocyte maturation factor 35 kDa subunit|interleukin 12, p35|interleukin 12A (natural

Position

3q25.33

Gene Type

protein-coding

COSMIC somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.554G>A; p.R185K; 3:159993792-159993792

 skinmalignant_melanomaSubstitution - Missense

c.629C>T; p.T210I; 3:159995426-159995426

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.264G>A; p.K88K; 3:159990312-159990312

 skinmalignant_melanomaSubstitution - coding silent

c.181G>A; p.V61M; 3:159990229-159990229

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.504C>T; p.Y168Y; 3:159993742-159993742

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.180C>T; p.P60P; 3:159990228-159990228

 bone; femurEwings_sarcoma-peripheral_primitive_neuroectodermal_tumourSubstitution - coding silent

c.147C>T; p.L49L; 3:159990195-159990195

 skinmalignant_melanomaSubstitution - coding silent

c.490G>A; p.D164N; 3:159993728-159993728

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.200G>A; p.G67E; 3:159990248-159990248

 skin; mucosalmalignant_melanomaSubstitution - Missense

c.79G>A; p.V27M; 3:159989135-159989135

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.618C>T; p.F206F; 3:159995415-159995415

 breastcarcinomaSubstitution - coding silent

c.691A>T; p.I231L; 3:159995488-159995488

 urinary_tract; bladdercarcinomaSubstitution - Missense

c.691A>T; p.I231L; 3:159995488-159995488

 urinary_tract; bladdercarcinoma; transitional_cell_carcinomaSubstitution - Missense

c.559A>G; p.I187V; 3:159993797-159993797

 livercarcinomaSubstitution - Missense

c.559A>G; p.I187V; 3:159993797-159993797

 livercarcinomaSubstitution - Missense

c.414C>T; p.F138F; 3:159993486-159993486

 autonomic_ganglianeuroblastomaSubstitution - coding silent

c.74G>C; p.R25P; 3:159989130-159989130

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.591_595delTGATG; p.D198fs*10; 3:159993829-159993833

 breastcarcinomaDeletion - Frameshift

c.606+1G>C; p.?; 3:159993845-159993845

 lungcarcinoma; squamous_cell_carcinomaUnknown

c.436G>A; p.A146T; 3:159993583-159993583

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.667T>C; p.Y223H; 3:159995464-159995464

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.116G>A; p.R39H; 3:159989172-159989172

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.282A>C; p.E94D; 3:159993029-159993029

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.39A>C; p.S13S; 3:159989095-159989095

 kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - coding silent

c.620A>G; p.N207S; 3:159995417-159995417

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.552G>T; p.K184N; 3:159993790-159993790

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.552G>T; p.K184N; 3:159993790-159993790

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.715C>T; p.R239W; 3:159995512-159995512

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.715C>T; p.R239W; 3:159995512-159995512

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.715C>T; p.R239W; 3:159995512-159995512

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.715C>T; p.R239W; 3:159995512-159995512

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.600G>T; p.L200L; 3:159993838-159993838

 lung; right_lower_lobecarcinoma; adenocarcinomaSubstitution - coding silent

c.209C>T; p.P70L; 3:159990257-159990257

 skinmalignant_melanomaSubstitution - Missense

c.669T>C; p.Y223Y; 3:159995466-159995466

 livercarcinomaSubstitution - coding silent

c.669T>C; p.Y223Y; 3:159995466-159995466

 livercarcinomaSubstitution - coding silent

c.67G>T; p.A23S; 3:159989123-159989123

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.640A>G; p.K214E; 3:159995437-159995437

 skin; mucosalmalignant_melanomaSubstitution - Missense

c.698T>G; p.L233R; 3:159995495-159995495

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.327A>G; p.T109T; 3:159993074-159993074

 prostatecarcinoma; adenocarcinomaSubstitution - coding silent

c.700C>T; p.H234Y; 3:159995497-159995497

 urinary_tract; bladdercarcinoma; transitional_cell_carcinomaSubstitution - Missense

c.700C>T; p.H234Y; 3:159995497-159995497

 urinary_tract; bladdercarcinomaSubstitution - Missense

c.135_136insA; p.T46fs*56; 3:159990183-159990184

 skin; solemalignant_melanoma; acral_lentiginousInsertion - Frameshift

c.135_136insA; p.T46fs*56; 3:159990183-159990184

 oesophagus; lower_thirdcarcinoma; adenocarcinomaInsertion - Frameshift

c.516C>A; p.F172L; 3:159993754-159993754

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.708C>T; p.F236F; 3:159995505-159995505

 thyroidcarcinomaSubstitution - coding silent

c.346G>A; p.V116M; 3:159993093-159993093

 skinmalignant_melanomaSubstitution - Missense

c.123C>T; p.L41L; 3:159990171-159990171

 skinmalignant_melanomaSubstitution - coding silent

c.136_137insA; p.T46fs*56; 3:159990184-159990185

 prostatecarcinoma; adenocarcinomaInsertion - Frameshift

c.136_137insA; p.T46fs*56; 3:159990184-159990185

 lungcarcinoma; adenocarcinomaInsertion - Frameshift

c.655G>A; p.E219K; 3:159995452-159995452

 skinmalignant_melanomaSubstitution - Missense

c.421-1G>A; p.?; 3:159993567-159993567

 prostatecarcinoma; adenocarcinomaUnknown