| Gene ID | 3596 |
| Symbol | IL13 |
| Synonymous | IL-13|P600 |
| Full name | interleukin 13 |
| Gene description | interleukin-13 |
| Cytoband | 5q31 |
| Gene type | protein-coding |
| Synonymous | MIM:147683; HGNC:HGNC:5973; Ensembl:ENSG00000169194; HPRD:00981; Vega:OTTHUMG00000059723 |
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.238G>A; p.A80T; 5:132659733-132659733 |
liver | carcinoma | Substitution - Missense |
c.238G>A; p.A80T; 5:132659733-132659733 |
liver | carcinoma | Substitution - Missense |
c.176C>T; p.A59V; 5:132659419-132659419 |
skin; neck | malignant_melanoma | Substitution - Missense |
c.136C>T; p.L46F; 5:132658322-132658322 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; acute_lymphoblastic_leukaemia | Substitution - Missense |
c.153C>A; p.V51V; 5:132658339-132658339 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.248C>A; p.S83Y; 5:132659743-132659743 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.165G>A; p.Q55Q; 5:132658351-132658351 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.421C>T; p.R141C; 5:132660262-132660262 |
skin | malignant_melanoma | Substitution - Missense |
c.421C>T; p.R141C; 5:132660262-132660262 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.430C>T; p.Q144*; 5:132660271-132660271 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.152T>G; p.V51G; 5:132658338-132658338 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.422G>A; p.R141H; 5:132660263-132660263 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.372G>A; p.E124E; 5:132660213-132660213 |
thyroid | carcinoma | Substitution - coding silent |
c.112C>T; p.P38S; 5:132658298-132658298 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.47C>T; p.A16V; 5:132658233-132658233 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.423C>T; p.R141R; 5:132660264-132660264 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.122C>G; p.T41R; 5:132658308-132658308 |
bone; pelvis | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.259G>A; p.V87M; 5:132659754-132659754 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.40C>A; p.L14I; 5:132658226-132658226 |
adrenal_gland; adrenal_gland | adrenal_cortical_carcinoma; functioning | Substitution - Missense |
c.369C>A; p.I123I; 5:132660210-132660210 |
lung; middle_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.152T>C; p.V51A; 5:132658338-132658338 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.96C>T; p.A32A; 5:132658282-132658282 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.96C>T; p.A32A; 5:132658282-132658282 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - coding silent |
c.224G>A; p.G75D; 5:132659467-132659467 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.220G>A; p.A74T; 5:132659463-132659463 |
skin | malignant_melanoma | Substitution - Missense |
c.132G>A; p.R44R; 5:132658318-132658318 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.279C>T; p.I93I; 5:132659774-132659774 |
skin | malignant_melanoma | Substitution - coding silent |
c.100C>T; p.P34S; 5:132658286-132658286 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.383T>G; p.F128C; 5:132660224-132660224 |
skin; leg | malignant_melanoma | Substitution - Missense |
c.383T>G; p.F128C; 5:132660224-132660224 |
skin; leg | malignant_melanoma | Substitution - Missense |
c.8C>T; p.P3L; 5:132658194-132658194 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.8C>T; p.P3L; 5:132658194-132658194 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |