| Gene ID | 10663 |
| Symbol | CXCR6 |
| Synonymous | BONZO|CD186|STRL33|TYMSTR |
| Full name | chemokine (C-X-C motif) receptor 6 |
| Gene description | C-X-C chemokine receptor type 6|CDw186|CXC-R6|CXCR-6|G protein-coupled receptor|G-protein coupled receptor STRL33|G-protein coupled receptor bonzo |
| Cytoband | 3p21 |
| Gene type | protein-coding |
| Synonymous | MIM:605163; HGNC:HGNC:16647; Ensembl:ENSG00000172215; HPRD:05520; Vega:OTTHUMG00000133448 |
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.320G>A; p.G107D; 3:45946801-45946801 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.346T>C; p.S116P; 3:45946827-45946827 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.532C>A; p.L178I; 3:45947013-45947013 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.96C>T; p.V32V; 3:45946577-45946577 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.38G>C; p.S13T; 3:45946519-45946519 |
pancreas | carcinoma | Substitution - Missense |
c.250C>T; p.L84L; 3:45946731-45946731 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.378T>C; p.D126D; 3:45946859-45946859 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.574C>T; p.L192F; 3:45947055-45947055 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.675G>A; p.Q225Q; 3:45947156-45947156 |
skin | malignant_melanoma | Substitution - coding silent |
c.411C>T; p.A137A; 3:45946892-45946892 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.36C>G; p.F12L; 3:45946517-45946517 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.887G>A; p.R296Q; 3:45947368-45947368 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.887G>A; p.R296Q; 3:45947368-45947368 |
lung; middle_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.213G>A; p.V71V; 3:45946694-45946694 |
skin | malignant_melanoma | Substitution - coding silent |
c.828C>T; p.I276I; 3:45947309-45947309 |
bone; pelvis | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.74A>G; p.D25G; 3:45946555-45946555 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.829G>A; p.A277T; 3:45947310-45947310 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.829G>A; p.A277T; 3:45947310-45947310 |
ovary | carcinoma | Substitution - Missense |
c.829G>A; p.A277T; 3:45947310-45947310 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.829G>A; p.A277T; 3:45947310-45947310 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.600C>T; p.F200F; 3:45947081-45947081 |
thyroid | other; neoplasm | Substitution - coding silent |
c.198G>A; p.T66T; 3:45946679-45946679 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.443G>C; p.G148A; 3:45946924-45946924 |
liver | carcinoma | Substitution - Missense |
c.255C>T; p.P85P; 3:45946736-45946736 |
skin | malignant_melanoma | Substitution - coding silent |
c.835C>T; p.L279L; 3:45947316-45947316 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.935T>C; p.L312P; 3:45947416-45947416 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.319G>A; p.G107S; 3:45946800-45946800 |
skin | malignant_melanoma | Substitution - Missense |
c.933delC; p.V314fs*>29; 3:45947414-45947414 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.365G>A; p.C122Y; 3:45946846-45946846 |
central_nervous_system; brain | primitive_neuroectodermal_tumour-medulloblastoma | Substitution - Missense |
c.626T>C; p.V209A; 3:45947107-45947107 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.934C>T; p.L312F; 3:45947415-45947415 |
skin | malignant_melanoma | Substitution - Missense |
c.464T>C; p.I155T; 3:45946945-45946945 |
breast | carcinoma | Substitution - Missense |