| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 8771 |
Name | TNFRSF6B |
Synonymous | tumor necrosis factor receptor superfamily, member 6b, decoy;TNFRSF6B;tumor necrosis factor receptor superfamily, member 6b, decoy |
Definition | decoy receptor 3|decoy receptor for Fas ligand|tumor necrosis factor receptor superfamily member 6B |
Position | 20q13.3 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.130G>A; p.G44R; 20:63696897-63696897 |
skin | malignant_melanoma | Substitution - Missense |
c.783C>G; p.L261L; 20:63698443-63698443 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.147C>T; p.C49C; 20:63696914-63696914 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.147C>T; p.C49C; 20:63696914-63696914 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.147C>T; p.C49C; 20:63696914-63696914 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.800C>T; p.A267V; 20:63698460-63698460 |
skin | malignant_melanoma | Substitution - Missense |
c.9G>A; p.A3A; 20:63696776-63696776 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.756C>T; p.A252A; 20:63698416-63698416 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.756C>T; p.A252A; 20:63698416-63698416 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.812C>T; p.A271V; 20:63698472-63698472 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.515G>A; p.R172H; 20:63697418-63697418 |
liver | carcinoma | Substitution - Missense |
c.515G>A; p.R172H; 20:63697418-63697418 |
liver | carcinoma | Substitution - Missense |
c.471_473delCTT; p.F158delF; 20:63697374-63697376 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - In frame |
c.507G>A; p.Q169Q; 20:63697410-63697410 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.749G>A; p.R250H; 20:63698409-63698409 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.573C>G; p.T191T; 20:63697476-63697476 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.573C>G; p.T191T; 20:63697476-63697476 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.573C>G; p.T191T; 20:63697476-63697476 |
thyroid | other; neoplasm | Substitution - coding silent |
c.200C>T; p.P67L; 20:63696967-63696967 |
skin | malignant_melanoma | Substitution - Missense |
c.312T>C; p.A104A; 20:63697079-63697079 |
breast | carcinoma | Substitution - coding silent |
c.690G>A; p.Q230Q; 20:63698350-63698350 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.765G>A; p.L255L; 20:63698425-63698425 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.874G>A; p.V292I; 20:63698534-63698534 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.357C>A; p.F119L; 20:63697124-63697124 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.889C>T; p.L297F; 20:63698549-63698549 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.156delC; p.P54fs*32; 20:63696923-63696923 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.486C>T; p.S162S; 20:63697389-63697389 |
prostate | adenoma | Substitution - coding silent |
c.486C>T; p.S162S; 20:63697389-63697389 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.459delC; p.P155fs*101; 20:63697362-63697362 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.459delC; p.P155fs*101; 20:63697362-63697362 |
skin; neck | malignant_melanoma | Deletion - Frameshift |
c.333T>C; p.R111R; 20:63697100-63697100 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.333T>C; p.R111R; 20:63697100-63697100 |
pancreas | carcinoma; ductal_carcinoma | Substitution - coding silent |
c.333T>C; p.R111R; 20:63697100-63697100 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.333T>C; p.R111R; 20:63697100-63697100 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.744G>A; p.A248A; 20:63698404-63698404 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.893C>T; p.P298L; 20:63698553-63698553 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.137G>A; p.R46Q; 20:63696904-63696904 |
breast | carcinoma | Substitution - Missense |
c.614T>C; p.V205A; 20:63697517-63697517 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.475T>A; p.S159T; 20:63697378-63697378 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.105C>T; p.T35T; 20:63696872-63696872 |
skin | malignant_melanoma | Substitution - coding silent |
c.118G>A; p.D40N; 20:63696885-63696885 |
skin | malignant_melanoma | Substitution - Missense |
c.772C>T; p.R258C; 20:63698432-63698432 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.255A>G; p.L85L; 20:63697022-63697022 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.255A>G; p.L85L; 20:63697022-63697022 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.143T>G; p.V48G; 20:63696910-63696910 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.143T>G; p.V48G; 20:63696910-63696910 |
thyroid | other; neoplasm | Substitution - Missense |
c.143T>G; p.V48G; 20:63696910-63696910 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.143T>G; p.V48G; 20:63696910-63696910 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.143T>G; p.V48G; 20:63696910-63696910 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.143T>G; p.V48G; 20:63696910-63696910 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.143T>G; p.V48G; 20:63696910-63696910 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.699G>A; p.L233L; 20:63698359-63698359 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.620G>C; p.G207A; 20:63698280-63698280 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.639T>C; p.R213R; 20:63698299-63698299 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |