| General information | Literature | Expression | lncRNA |Regulation | Mutation | Homolog | Interaction |
Basic Information | |||
|---|---|---|---|
Gene ID | 6374 | ||
Name | CXCL5 | ||
The somatic mutations from COSMIC database | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.280C>G; p.P94A; 4:73998058-73998058 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.251T>C; p.L84P; 4:73998087-73998087 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.29G>A; p.R10H; 4:73998553-73998553 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.215G>T; p.G72V; 4:73998233-73998233 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.224G>A; p.C75Y; 4:73998224-73998224 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.290_291insT; p.L99fs*>17; 4:73998047-73998048 |
lung | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.253delA; p.K85fs*15; 4:73998085-73998085 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; hairy_cell_leukaemia | Deletion - Frameshift |
c.259G>A; p.G87R; 4:73998079-73998079 |
skin | malignant_melanoma | Substitution - Missense |
c.17G>T; p.S6I; 4:73998565-73998565 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.314A>C; p.K105T; 4:73998024-73998024 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.265G>A; p.E89K; 4:73998073-73998073 |
skin | malignant_melanoma | Substitution - Missense |
c.265G>A; p.E89K; 4:73998073-73998073 |
skin | malignant_melanoma | Substitution - Missense |
c.265G>A; p.E89K; 4:73998073-73998073 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.169G>A; p.G57R; 4:73998279-73998279 |
skin | malignant_melanoma | Substitution - Missense |
c.222G>A; p.Q74Q; 4:73998226-73998226 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.324C>T; p.D108D; 4:73998014-73998014 |
central_nervous_system; brain | glioma | Substitution - coding silent |
c.324C>T; p.D108D; 4:73998014-73998014 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.188T>G; p.I63S; 4:73998260-73998260 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.58G>A; p.A20T; 4:73998524-73998524 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.147C>T; p.C49C; 4:73998301-73998301 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.248C>T; p.S83F; 4:73998090-73998090 |
skin | malignant_melanoma | Substitution - Missense |
c.122C>T; p.A41V; 4:73998326-73998326 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.122C>T; p.A41V; 4:73998326-73998326 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.136G>A; p.E46K; 4:73998312-73998312 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.238G>C; p.V80L; 4:73998210-73998210 |
oesophagus | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.57C>T; p.C19C; 4:73998525-73998525 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.159G>T; p.Q53H; 4:73998289-73998289 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |