| Gene ID | 6915 |
| Symbol | TBXA2R |
| Synonymous | BDPLT13|TXA2-R |
| Full name | thromboxane A2 receptor |
| Gene description | prostanoid TP receptor |
| Cytoband | 19p13.3 |
| Gene type | protein-coding |
| Synonymous | MIM:188070; HGNC:HGNC:11608; Ensembl:ENSG00000006638; HPRD:01768; Vega:OTTHUMG00000180806 |
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.666G>T; p.L222L; 19:3599969-3599969 |
thyroid | other; neoplasm | Substitution - coding silent |
c.994C>T; p.L332F; 19:3595726-3595726 |
skin | malignant_melanoma | Substitution - Missense |
c.628C>A; p.L210M; 19:3600007-3600007 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.280G>A; p.E94K; 19:3600355-3600355 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.68G>A; p.R23Q; 19:3600567-3600567 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.473C>T; p.A158V; 19:3600162-3600162 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.567C>T; p.A189A; 19:3600068-3600068 |
skin | malignant_melanoma | Substitution - coding silent |
c.924T>C; p.Y308Y; 19:3595796-3595796 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.924T>C; p.Y308Y; 19:3595796-3595796 |
thyroid | other; neoplasm | Substitution - coding silent |
c.924T>C; p.Y308Y; 19:3595796-3595796 |
central_nervous_system; brain | primitive_neuroectodermal_tumour-medulloblastoma | Substitution - coding silent |
c.906C>T; p.I302I; 19:3595814-3595814 |
skin | malignant_melanoma | Substitution - coding silent |
c.157C>T; p.R53W; 19:3600478-3600478 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1010C>T; p.T337M; 19:3595710-3595710 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.936C>T; p.R312R; 19:3595784-3595784 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.138G>C; p.L46L; 19:3600497-3600497 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.253G>A; p.V85M; 19:3600382-3600382 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.795C>T; p.I265I; 19:3595925-3595925 |
prostate | carcinoma; adenocarcinoma | Substitution - coding silent |
c.977G>A; p.R326Q; 19:3595743-3595743 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.141C>G; p.S47R; 19:3600494-3600494 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.210C>T; p.L70L; 19:3600425-3600425 |
skin | malignant_melanoma | Substitution - coding silent |
c.261C>T; p.S87S; 19:3600374-3600374 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.37C>T; p.R13W; 19:3600598-3600598 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.279C>T; p.F93F; 19:3600356-3600356 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.279C>T; p.F93F; 19:3600356-3600356 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.199C>T; p.L67F; 19:3600436-3600436 |
skin | malignant_melanoma | Substitution - Missense |
c.36C>T; p.F12F; 19:3600599-3600599 |
skin | malignant_melanoma | Substitution - coding silent |
c.90C>T; p.F30F; 19:3600545-3600545 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.423G>A; p.P141P; 19:3600212-3600212 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.21C>T; p.S7S; 19:3600614-3600614 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.29C>T; p.P10L; 19:3600606-3600606 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.171G>A; p.S57S; 19:3600464-3600464 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.787-1G>A; p.?; 19:3595934-3595934 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Unknown |
c.72G>A; p.L24L; 19:3600563-3600563 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.204C>T; p.C68C; 19:3600431-3600431 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.440G>A; p.R147H; 19:3600195-3600195 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.306C>T; p.C102C; 19:3600329-3600329 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.102C>T; p.F34F; 19:3600533-3600533 |
bone; femur | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.636C>T; p.F212F; 19:3599999-3599999 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.564C>T; p.G188G; 19:3600071-3600071 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.112G>A; p.G38S; 19:3600523-3600523 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.176C>T; p.T59M; 19:3600459-3600459 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.330C>T; p.V110V; 19:3600305-3600305 |
skin | malignant_melanoma | Substitution - coding silent |
c.330C>T; p.V110V; 19:3600305-3600305 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.494T>C; p.L165P; 19:3600141-3600141 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.416C>T; p.S139L; 19:3600219-3600219 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.940G>T; p.A314S; 19:3595780-3595780 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.940G>T; p.A314S; 19:3595780-3595780 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.940G>T; p.A314S; 19:3595780-3595780 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.940G>T; p.A314S; 19:3595780-3595780 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.940G>T; p.A314S; 19:3595780-3595780 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.940G>T; p.A314S; 19:3595780-3595780 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.940G>T; p.A314S; 19:3595780-3595780 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.885C>T; p.R295R; 19:3595835-3595835 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.155C>T; p.A52V; 19:3600480-3600480 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.373G>A; p.A125T; 19:3600262-3600262 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.230G>A; p.G77E; 19:3600405-3600405 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.113G>A; p.G38D; 19:3600522-3600522 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.625G>A; p.G209R; 19:3600010-3600010 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.284G>C; p.W95S; 19:3600351-3600351 |
liver | carcinoma | Substitution - Missense |
c.285G>A; p.W95*; 19:3600350-3600350 |
prostate | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.855_856CA>TG; p.T286A; 19:3595864-3595865 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.568G>A; p.E190K; 19:3600067-3600067 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.218C>A; p.T73N; 19:3600417-3600417 |
pancreas | carcinoma | Substitution - Missense |
c.71T>C; p.L24P; 19:3600564-3600564 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.270C>T; p.A90A; 19:3600365-3600365 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.168T>G; p.G56G; 19:3600467-3600467 |
central_nervous_system; brain | glioma | Substitution - coding silent |
c.44C>A; p.T15K; 19:3600591-3600591 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - Missense |
c.91G>A; p.A31T; 19:3600544-3600544 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.553C>T; p.L185L; 19:3600082-3600082 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.673G>A; p.V225I; 19:3599962-3599962 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.862A>T; p.K288*; 19:3595858-3595858 |
ovary | other; neoplasm | Substitution - Nonsense |
c.862A>T; p.K288*; 19:3595858-3595858 |
ovary | other; neoplasm | Substitution - Nonsense |
c.289G>A; p.A97T; 19:3600346-3600346 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.430G>A; p.A144T; 19:3600205-3600205 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.314G>A; p.C105Y; 19:3600321-3600321 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.699G>A; p.Q233Q; 19:3599936-3599936 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.398G>A; p.G133D; 19:3600237-3600237 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.153C>T; p.G51G; 19:3600482-3600482 |
thyroid | carcinoma | Substitution - coding silent |
c.602C>T; p.S201F; 19:3600033-3600033 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.503T>A; p.L168Q; 19:3600132-3600132 |
skin | malignant_melanoma | Substitution - Missense |
c.830G>T; p.S277I; 19:3595890-3595890 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.164G>A; p.G55E; 19:3600471-3600471 |
skin | malignant_melanoma | Substitution - Missense |
c.435G>A; p.S145S; 19:3600200-3600200 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.420C>T; p.R140R; 19:3600215-3600215 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |