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

Basic Information

Gene ID

7133

Name

TNFRSF1B

Synonymous

tumor necrosis factor receptor superfamily, member 1B;TNFRSF1B;tumor necrosis factor receptor superfamily, member 1B

Definition

TNF-R2|TNF-RII|p75 TNF receptor|p80 TNF-alpha receptor|soluble TNFR1B variant 1|tumor necrosis factor beta receptor|tumor necrosis factor binding protein 2|tumor necrosis factor receptor 2|tumor necrosis factor receptor superfamily member 1B|tumor necrosi

Position

1p36.22

Gene Type

protein-coding

COSMIC confirmed somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.824T>C; p.I275T; 1:12193991-12193991

 boneEwings_sarcoma-peripheral_primitive_neuroectodermal_tumourSubstitution - Missense

c.1308G>A; p.T436T; 1:12206942-12206942

 boneEwings_sarcoma-peripheral_primitive_neuroectodermal_tumourSubstitution - coding silent

c.1291C>T; p.R431W; 1:12206925-12206925

 breastcarcinomaSubstitution - Missense

c.1299G>A; p.Q433Q; 1:12206933-12206933

 breastcarcinomaSubstitution - coding silent

c.643C>T; p.H215Y; 1:12192954-12192954

 breastcarcinomaSubstitution - Missense

c.664A>C; p.T222P; 1:12192975-12192975

 central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.664A>C; p.T222P; 1:12192975-12192975

 central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.609G>A; p.T203T; 1:12192920-12192920

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.475G>A; p.V159M; 1:12192448-12192448

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.109G>A; p.G37R; 1:12188826-12188826

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.694G>A; p.E232K; 1:12193005-12193005

 haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - Missense

c.1295C>T; p.S432L; 1:12206929-12206929

 kidneycarcinoma; papillary_renal_cell_carcinomaSubstitution - Missense

c.251C>T; p.T84I; 1:12191029-12191029

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.528G>A; p.T176T; 1:12192501-12192501

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.1371G>A; p.G457G; 1:12207005-12207005

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.783A>C; p.P261P; 1:12193094-12193094

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.788-1G>T; p.?; 1:12193954-12193954

 large_intestine; rectumcarcinoma; adenocarcinomaUnknown

c.665C>A; p.T222K; 1:12192976-12192976

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.666A>G; p.T222T; 1:12192977-12192977

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.1239G>A; p.S413S; 1:12206873-12206873

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - coding silent

c.769G>A; p.D257N; 1:12193080-12193080

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.916G>A; p.D306N; 1:12201982-12201982

 livercarcinomaSubstitution - Missense

c.916G>A; p.D306N; 1:12201982-12201982

 livercarcinoma; hepatocellular_carcinomaSubstitution - Missense

c.641T>C; p.V214A; 1:12192952-12192952

 livercarcinomaSubstitution - Missense

c.641T>C; p.V214A; 1:12192952-12192952

 livercarcinomaSubstitution - Missense

c.641T>C; p.V214A; 1:12192952-12192952

 livercarcinomaSubstitution - Missense

c.1153G>T; p.V385L; 1:12206787-12206787

 livercarcinomaSubstitution - Missense

c.587T>G; p.M196R; 1:12192898-12192898

 livercarcinoma; hepatocellular_carcinomaSubstitution - Missense

c.694G>A; p.E232K; 1:12193005-12193005

 livercarcinoma; hepatocellular_carcinomaSubstitution - Missense

c.168A>G; p.K56K; 1:12188885-12188885

 livercarcinoma; hepatocellular_carcinomaSubstitution - coding silent

c.303C>A; p.S101R; 1:12191081-12191081

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.436G>C; p.G146R; 1:12191902-12191902

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.609G>T; p.T203T; 1:12192920-12192920

 lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - coding silent

c.425A>T; p.K142M; 1:12191891-12191891

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.147A>T; p.T49T; 1:12188864-12188864

 lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.134A>T; p.Y45F; 1:12188851-12188851

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.927G>T; p.R309R; 1:12201993-12201993

 lungcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.1150_1164del15; p.I384_C388delIVNVC; 1:12206784-12206798

 oesophaguscarcinoma; adenocarcinomaDeletion - In frame

c.178+8C>A; p.?; 1:12188903-12188903

 oesophaguscarcinoma; adenocarcinomaUnknown

c.1291C>T; p.R431W; 1:12206925-12206925

 oesophaguscarcinoma; adenocarcinomaSubstitution - Missense

c.1270T>G; p.S424A; 1:12206904-12206904

 skinmalignant_melanomaSubstitution - Missense

c.1215G>A; p.M405I; 1:12206849-12206849

 skinmalignant_melanomaSubstitution - Missense

c.1270_1271TC>GT; p.S424V; 1:12206904-12206905

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1275G>A; p.K425K; 1:12206909-12206909

 skin; nipplemalignant_melanomaSubstitution - coding silent

c.781C>T; p.P261S; 1:12193092-12193092

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.457G>A; p.G153R; 1:12191923-12191923

 skinmalignant_melanomaSubstitution - Missense

c.499G>A; p.G167R; 1:12192472-12192472

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1225G>C; p.D409H; 1:12206859-12206859

 skinmalignant_melanomaSubstitution - Missense

c.720C>T; p.S240S; 1:12193031-12193031

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.671C>T; p.S224F; 1:12192982-12192982

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1325G>A; p.G442E; 1:12206959-12206959

 skinmalignant_melanomaSubstitution - Missense

c.1014G>A; p.L338L; 1:12202080-12202080

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.774C>T; p.F258F; 1:12193085-12193085

 skinmalignant_melanomaSubstitution - coding silent

c.416C>T; p.P139L; 1:12191882-12191882

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.942C>T; p.P314P; 1:12202008-12202008

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.173C>T; p.S58L; 1:12188890-12188890

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.429C>T; p.C143C; 1:12191895-12191895

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.1382G>A; p.S461N; 1:12207016-12207016

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.587T>G; p.M196R; 1:12192898-12192898

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.1026G>A; p.A342A; 1:12202092-12202092

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.905A>T; p.H302L; 1:12201971-12201971

 thyroidother; neoplasmSubstitution - Missense

c.168A>G; p.K56K; 1:12188885-12188885

 thyroidother; neoplasmSubstitution - coding silent

c.1239G>T; p.S413S; 1:12206873-12206873

 upper_aerodigestive_tract; mouthcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.436G>T; p.G146C; 1:12191902-12191902

 urinary_tract; bladdercarcinomaSubstitution - Missense

c.637G>C; p.A213P; 1:12192948-12192948

 urinary_tract; bladdercarcinomaSubstitution - Missense

c.422G>A; p.R141H; 1:12191888-12191888

 urinary_tract; bladdercarcinomaSubstitution - Missense