| Gene ID | 6752 |
| Symbol | SSTR2 |
| Synonymous | - |
| Full name | somatostatin receptor 2 |
| Gene description | SRIF-1|SS2R|somatostatin receptor type 2 |
| Cytoband | 17q24 |
| Gene type | protein-coding |
| Synonymous | MIM:182452; HGNC:HGNC:11331; HPRD:01674 |
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.151T>G; p.F51V; 17:73169470-73169470 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.74T>A; p.V25E; 17:73169393-73169393 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.901A>T; p.T301S; 17:73170220-73170220 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.988G>A; p.V330I; 17:73170307-73170307 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.208C>T; p.R70C; 17:73169527-73169527 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.861C>T; p.T287T; 17:73170180-73170180 |
skin | malignant_melanoma | Substitution - coding silent |
c.345C>T; p.C115C; 17:73169664-73169664 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.425T>A; p.L142Q; 17:73169744-73169744 |
adrenal_gland; adrenal_gland | adrenal_cortical_carcinoma; functioning | Substitution - Missense |
c.147C>A; p.I49I; 17:73169466-73169466 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.541G>A; p.A181T; 17:73169860-73169860 |
autonomic_ganglia | neuroblastoma | Substitution - Missense |
c.327C>G; p.P109P; 17:73169646-73169646 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.979C>A; p.L327I; 17:73170298-73170298 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.838G>A; p.V280I; 17:73170157-73170157 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.672C>G; p.I224M; 17:73169991-73169991 |
stomach | adenocarcinoma | Substitution - Missense |
c.838G>A; p.V280I; 17:73170157-73170157 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.838G>A; p.V280I; 17:73170157-73170157 |
skin | malignant_melanoma | Substitution - Missense |
c.273C>G; p.L91L; 17:73169592-73169592 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1028G>A; p.S343N; 17:73170347-73170347 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.839T>C; p.V280A; 17:73170158-73170158 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.1061C>T; p.T354M; 17:73170380-73170380 |
bone; pelvis | chondrosarcoma | Substitution - Missense |
c.291T>A; p.P97P; 17:73169610-73169610 |
breast | carcinoma | Substitution - coding silent |
c.1062G>A; p.T354T; 17:73170381-73170381 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.470G>T; p.R157L; 17:73169789-73169789 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.265G>A; p.D89N; 17:73169584-73169584 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.1046G>A; p.R349Q; 17:73170365-73170365 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.1046G>A; p.R349Q; 17:73170365-73170365 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.763A>G; p.T255A; 17:73170082-73170082 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.860C>T; p.T287I; 17:73170179-73170179 |
skin | malignant_melanoma | Substitution - Missense |
c.615C>A; p.Y205*; 17:73169934-73169934 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Nonsense |
c.107C>T; p.P36L; 17:73169426-73169426 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.557A>G; p.N186S; 17:73169876-73169876 |
skin | malignant_melanoma | Substitution - Missense |
c.407T>A; p.M136K; 17:73169726-73169726 |
liver | carcinoma | Substitution - Missense |
c.211T>C; p.Y71H; 17:73169530-73169530 |
skin | malignant_melanoma | Substitution - Missense |
c.1018C>T; p.R340W; 17:73170337-73170337 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.407T>A; p.M136K; 17:73169726-73169726 |
liver | carcinoma | Substitution - Missense |
c.661C>T; p.L221F; 17:73169980-73169980 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.376C>G; p.Q126E; 17:73169695-73169695 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.193A>G; p.I65V; 17:73169512-73169512 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.999C>A; p.S333R; 17:73170318-73170318 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.470G>A; p.R157Q; 17:73169789-73169789 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.450G>A; p.S150S; 17:73169769-73169769 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.829G>A; p.V277I; 17:73170148-73170148 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.550C>T; p.R184W; 17:73169869-73169869 |
upper_aerodigestive_tract; mouth | carcinoma | Substitution - Missense |
c.1016A>T; p.E339V; 17:73170335-73170335 |
skin | malignant_melanoma | Substitution - Missense |
c.550C>T; p.R184W; 17:73169869-73169869 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.608C>T; p.A203V; 17:73169927-73169927 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.862C>T; p.P288S; 17:73170181-73170181 |
skin | malignant_melanoma | Substitution - Missense |
c.534G>A; p.M178I; 17:73169853-73169853 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.534G>A; p.M178I; 17:73169853-73169853 |
skin | malignant_melanoma | Substitution - Missense |
c.152T>C; p.F51S; 17:73169471-73169471 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.460A>G; p.R154G; 17:73169779-73169779 |
breast | carcinoma | Substitution - Missense |
c.207C>A; p.L69L; 17:73169526-73169526 |
skin | malignant_melanoma | Substitution - coding silent |
c.509C>T; p.S170F; 17:73169828-73169828 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.262G>T; p.A88S; 17:73169581-73169581 |
prostate | carcinoma | Substitution - Missense |
c.690C>T; p.F230F; 17:73170009-73170009 |
skin | malignant_melanoma | Substitution - coding silent |
c.837C>T; p.S279S; 17:73170156-73170156 |
skin | malignant_melanoma | Substitution - coding silent |
c.286C>A; p.L96M; 17:73169605-73169605 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1058C>G; p.T353S; 17:73170377-73170377 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.732C>T; p.S244S; 17:73170051-73170051 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.474G>A; p.T158T; 17:73169793-73169793 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.414C>T; p.I138I; 17:73169733-73169733 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.268G>C; p.E90Q; 17:73169587-73169587 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.1014G>A; p.G338G; 17:73170333-73170333 |
skin | malignant_melanoma | Substitution - coding silent |
c.674G>T; p.C225F; 17:73169993-73169993 |
thyroid | carcinoma | Substitution - Missense |
c.998G>A; p.S333N; 17:73170317-73170317 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.727G>A; p.G243S; 17:73170046-73170046 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.473C>T; p.T158M; 17:73169792-73169792 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.639C>T; p.F213F; 17:73169958-73169958 |
skin | malignant_melanoma | Substitution - coding silent |