| Gene ID | 2150 |
| Symbol | F2RL1 |
| Synonymous | GPR11|PAR2 |
| Full name | coagulation factor II (thrombin) receptor-like 1 |
| Gene description | G-protein coupled receptor 11|coagulation factor II receptor-like 1|protease-activated receptor 2|proteinase-activated receptor 2|thrombin receptor-like 1 |
| Cytoband | 5q13 |
| Gene type | protein-coding |
| Synonymous | MIM:600933; HGNC:HGNC:3538; Ensembl:ENSG00000164251; HPRD:02960; Vega:OTTHUMG00000102118 |
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.992G>A; p.C331Y; 5:76833599-76833599 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.992G>A; p.C331Y; 5:76833599-76833599 |
large_intestine; colon | carcinoma | Substitution - Missense |
c.992G>A; p.C331Y; 5:76833599-76833599 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.549C>T; p.H183H; 5:76833156-76833156 |
thyroid | carcinoma | Substitution - coding silent |
c.491T>A; p.L164H; 5:76833098-76833098 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.290T>A; p.L97Q; 5:76832897-76832897 |
skin | malignant_melanoma | Substitution - Missense |
c.966C>A; p.V322V; 5:76833573-76833573 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1151G>T; p.S384I; 5:76833758-76833758 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.83G>T; p.G28V; 5:76832690-76832690 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.472A>T; p.N158Y; 5:76833079-76833079 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.194C>T; p.S65F; 5:76832801-76832801 |
skin | malignant_melanoma | Substitution - Missense |
c.568A>G; p.I190V; 5:76833175-76833175 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1048G>C; p.D350H; 5:76833655-76833655 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1071C>T; p.N357N; 5:76833678-76833678 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.174C>A; p.V58V; 5:76832781-76832781 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1029C>T; p.V343V; 5:76833636-76833636 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.826G>A; p.E276K; 5:76833433-76833433 |
skin | malignant_melanoma | Substitution - Missense |
c.397G>A; p.A133T; 5:76833004-76833004 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.818C>T; p.A273V; 5:76833425-76833425 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.937C>T; p.L313L; 5:76833544-76833544 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.840G>T; p.K280N; 5:76833447-76833447 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.531C>T; p.I177I; 5:76833138-76833138 |
skin | malignant_melanoma | Substitution - coding silent |
c.345C>T; p.A115A; 5:76832952-76832952 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.750C>A; p.V250V; 5:76833357-76833357 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1083C>T; p.C361C; 5:76833690-76833690 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.519G>A; p.R173R; 5:76833126-76833126 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.678T>C; p.C226C; 5:76833285-76833285 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.677G>T; p.C226F; 5:76833284-76833284 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.676T>C; p.C226R; 5:76833283-76833283 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.676T>C; p.C226R; 5:76833283-76833283 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.676T>C; p.C226R; 5:76833283-76833283 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.676T>C; p.C226R; 5:76833283-76833283 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.676T>C; p.C226R; 5:76833283-76833283 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.676T>C; p.C226R; 5:76833283-76833283 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.676T>C; p.C226R; 5:76833283-76833283 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.367C>T; p.L123F; 5:76832974-76832974 |
skin | malignant_melanoma | Substitution - Missense |
c.308G>A; p.R103Q; 5:76832915-76832915 |
skin | malignant_melanoma | Substitution - Missense |
c.308G>A; p.R103Q; 5:76832915-76832915 |
breast | carcinoma | Substitution - Missense |
c.308G>A; p.R103Q; 5:76832915-76832915 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.633C>G; p.V211V; 5:76833240-76833240 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1081T>A; p.C361S; 5:76833688-76833688 |
skin | malignant_melanoma | Substitution - Missense |
c.603G>T; p.L201L; 5:76833210-76833210 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.427T>A; p.Y143N; 5:76833034-76833034 |
skin | malignant_melanoma | Substitution - Missense |
c.545G>A; p.G182E; 5:76833152-76833152 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1056G>A; p.R352R; 5:76833663-76833663 |
skin | malignant_melanoma | Substitution - coding silent |
c.344C>T; p.A115V; 5:76832951-76832951 |
skin | malignant_melanoma | Substitution - Missense |
c.1143G>A; p.R381R; 5:76833750-76833750 |
skin | malignant_melanoma | Substitution - coding silent |
c.1143G>A; p.R381R; 5:76833750-76833750 |
skin | malignant_melanoma | Substitution - coding silent |
c.301C>A; p.L101I; 5:76832908-76832908 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.677G>C; p.C226S; 5:76833284-76833284 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.426T>A; p.I142I; 5:76833033-76833033 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.231C>T; p.F77F; 5:76832838-76832838 |
skin | malignant_melanoma | Substitution - coding silent |
c.231C>T; p.F77F; 5:76832838-76832838 |
skin | malignant_melanoma | Substitution - coding silent |
c.231C>T; p.F77F; 5:76832838-76832838 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.465C>G; p.F155L; 5:76833072-76833072 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.405C>T; p.H135H; 5:76833012-76833012 |
bone; pelvis | chondrosarcoma | Substitution - coding silent |
c.798C>T; p.I266I; 5:76833405-76833405 |
skin | malignant_melanoma | Substitution - coding silent |
c.835G>C; p.E279Q; 5:76833442-76833442 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.269T>C; p.L90S; 5:76832876-76832876 |
central_nervous_system; brain | primitive_neuroectodermal_tumour-medulloblastoma | Substitution - Missense |
c.769C>A; p.L257I; 5:76833376-76833376 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.280G>T; p.G94C; 5:76832887-76832887 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1018G>A; p.D340N; 5:76833625-76833625 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.930T>C; p.H310H; 5:76833537-76833537 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.279C>T; p.N93N; 5:76832886-76832886 |
breast | carcinoma | Substitution - coding silent |
c.279C>T; p.N93N; 5:76832886-76832886 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.78C>A; p.I26I; 5:76819260-76819260 |
thyroid | other; neoplasm | Substitution - coding silent |
c.463T>A; p.F155I; 5:76833070-76833070 |
skin | malignant_melanoma | Substitution - Missense |
c.675C>A; p.T225T; 5:76833282-76833282 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.634G>T; p.V212L; 5:76833241-76833241 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.808C>T; p.R270*; 5:76833415-76833415 |
stomach | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.808C>T; p.R270*; 5:76833415-76833415 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.808C>T; p.R270*; 5:76833415-76833415 |
skin | malignant_melanoma | Substitution - Nonsense |
c.164T>C; p.V55A; 5:76832771-76832771 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.890T>C; p.L297P; 5:76833497-76833497 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.890T>C; p.L297P; 5:76833497-76833497 |
large_intestine; colon | carcinoma | Substitution - Missense |
c.890T>C; p.L297P; 5:76833497-76833497 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1085G>A; p.R362Q; 5:76833692-76833692 |
skin; trunk | malignant_melanoma | Substitution - Missense |
c.299T>G; p.F100C; 5:76832906-76832906 |
pancreas | carcinoma | Substitution - Missense |
c.546G>A; p.G182G; 5:76833153-76833153 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.754C>T; p.L252L; 5:76833361-76833361 |
skin | malignant_melanoma | Substitution - coding silent |
c.74C>T; p.T25I; 5:76819256-76819256 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.672G>A; p.T224T; 5:76833279-76833279 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.660C>A; p.A220A; 5:76833267-76833267 |
breast | carcinoma; HER-positive_carcinoma | Substitution - coding silent |
c.179C>G; p.S60C; 5:76832786-76832786 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.376A>G; p.I126V; 5:76832983-76832983 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.747G>A; p.G249G; 5:76833354-76833354 |
breast | carcinoma | Substitution - coding silent |
c.1093C>T; p.R365C; 5:76833700-76833700 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.89G>A; p.S30N; 5:76832696-76832696 |
thyroid | other; neoplasm | Substitution - Missense |
c.1111C>T; p.Q371*; 5:76833718-76833718 |
stomach | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1094G>A; p.R365H; 5:76833701-76833701 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1094G>A; p.R365H; 5:76833701-76833701 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.82+5G>A; p.?; 5:76819269-76819269 |
liver | carcinoma | Unknown |
c.809G>A; p.R270Q; 5:76833416-76833416 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |