| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 8741 |
Name | TNFSF13 |
Synonymous | tumor necrosis factor (ligand) superfamily, member 13;TNFSF13;tumor necrosis factor (ligand) superfamily, member 13 |
Definition | TNF- and APOL-related leukocyte expressed ligand 2|a proliferation-inducing ligand|tumor necrosis factor ligand superfamily member 13|tumor necrosis factor-like protein ZTNF2|tumor necrosis factor-related death ligand-1 |
Position | 17p13.1 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.373G>A; p.A125T; 17:7559881-7559881 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.413_414insGCAAA; p.P140fs*37; 17:7560076-7560077 |
liver | carcinoma | Insertion - Frameshift |
c.287A>G; p.N96S; 17:7559652-7559652 |
thyroid | other; neoplasm | Substitution - Missense |
c.93C>T; p.L31L; 17:7559132-7559132 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.83C>G; p.S28*; 17:7559122-7559122 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.744G>A; p.V248V; 17:7560824-7560824 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - coding silent |
c.389A>T; p.D130V; 17:7560052-7560052 |
breast | carcinoma | Substitution - Missense |
c.418C>T; p.P140S; 17:7560081-7560081 |
breast | carcinoma | Substitution - Missense |
c.520G>A; p.V174M; 17:7560365-7560365 |
skin | malignant_melanoma | Substitution - Missense |
c.104delG; p.A37fs*13; 17:7559143-7559143 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.103_104insG; p.A37fs*88; 17:7559142-7559143 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.103_104insG; p.A37fs*88; 17:7559142-7559143 |
large_intestine; caecum | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.103_104insG; p.A37fs*88; 17:7559142-7559143 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.279C>T; p.A93A; 17:7559644-7559644 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.636T>C; p.Y212Y; 17:7560481-7560481 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.362T>C; p.V121A; 17:7559870-7559870 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.509T>A; p.L170Q; 17:7560354-7560354 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.573G>A; p.E191E; 17:7560418-7560418 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - coding silent |
c.534G>T; p.M178I; 17:7560379-7560379 |
kidney | other; neoplasm | Substitution - Missense |
c.75G>A; p.P25P; 17:7559114-7559114 |
upper_aerodigestive_tract; mouth | carcinoma | Substitution - coding silent |
c.744G>T; p.V248V; 17:7560824-7560824 |
breast | carcinoma | Substitution - coding silent |
c.75G>A; p.P25P; 17:7559114-7559114 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.510G>C; p.L170L; 17:7560355-7560355 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.551G>C; p.R184P; 17:7560396-7560396 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.357C>T; p.H119H; 17:7559865-7559865 |
skin | malignant_melanoma | Substitution - coding silent |
c.74C>T; p.P25L; 17:7559113-7559113 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.460G>C; p.G154R; 17:7560123-7560123 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.84A>G; p.S28S; 17:7559123-7559123 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.467G>A; p.R156Q; 17:7560130-7560130 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |