| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 51330 |
Name | TNFRSF12A |
Synonymous | tumor necrosis factor receptor superfamily, member 12A;TNFRSF12A;tumor necrosis factor receptor superfamily, member 12A |
Definition | FGF-inducible 14|fibroblast growth factor-inducible immediate-early response protein 14|tumor necrosis factor receptor superfamily member 12A|tweak-receptor|type I transmembrane protein Fn14 |
Position | 16p13.3 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.48G>A; p.G16G; 16:3020445-3020445 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.301T>A; p.W101R; 16:3021656-3021656 |
pancreas | carcinoma | Substitution - Missense |
c.244C>T; p.L82F; 16:3021599-3021599 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.320G>A; p.R107K; 16:3021675-3021675 |
skin; face | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.221_222CC>TT; p.P74L; 16:3021576-3021577 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.215C>A; p.P72H; 16:3021570-3021570 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.72C>A; p.S24S; 16:3020469-3020469 |
thyroid | other; neoplasm | Substitution - coding silent |
c.274C>T; p.L92L; 16:3021629-3021629 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.71C>T; p.S24F; 16:3020468-3020468 |
skin | malignant_melanoma | Substitution - Missense |