Cancer metastasis database

Annotation category 5

Gene information

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

COSMIC somatic mutation

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.151T>G; p.F51V; 17:73169470-73169470

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.74T>A; p.V25E; 17:73169393-73169393

oesophagus; lower_thirdcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.901A>T; p.T301S; 17:73170220-73170220

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.988G>A; p.V330I; 17:73170307-73170307

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.208C>T; p.R70C; 17:73169527-73169527

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.861C>T; p.T287T; 17:73170180-73170180

skinmalignant_melanomaSubstitution - coding silent

c.345C>T; p.C115C; 17:73169664-73169664

lung; right_lower_lobecarcinoma; adenocarcinomaSubstitution - coding silent

c.425T>A; p.L142Q; 17:73169744-73169744

adrenal_gland; adrenal_glandadrenal_cortical_carcinoma; functioningSubstitution - Missense

c.147C>A; p.I49I; 17:73169466-73169466

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - coding silent

c.541G>A; p.A181T; 17:73169860-73169860

autonomic_ganglianeuroblastomaSubstitution - Missense

c.327C>G; p.P109P; 17:73169646-73169646

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.979C>A; p.L327I; 17:73170298-73170298

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.838G>A; p.V280I; 17:73170157-73170157

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.672C>G; p.I224M; 17:73169991-73169991

stomachadenocarcinomaSubstitution - Missense

c.838G>A; p.V280I; 17:73170157-73170157

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.838G>A; p.V280I; 17:73170157-73170157

skinmalignant_melanomaSubstitution - Missense

c.273C>G; p.L91L; 17:73169592-73169592

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.1028G>A; p.S343N; 17:73170347-73170347

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.839T>C; p.V280A; 17:73170158-73170158

central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.1061C>T; p.T354M; 17:73170380-73170380

bone; pelvischondrosarcomaSubstitution - Missense

c.291T>A; p.P97P; 17:73169610-73169610

breastcarcinomaSubstitution - coding silent

c.1062G>A; p.T354T; 17:73170381-73170381

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.470G>T; p.R157L; 17:73169789-73169789

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.265G>A; p.D89N; 17:73169584-73169584

lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.1046G>A; p.R349Q; 17:73170365-73170365

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - Missense

c.1046G>A; p.R349Q; 17:73170365-73170365

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.763A>G; p.T255A; 17:73170082-73170082

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.860C>T; p.T287I; 17:73170179-73170179

skinmalignant_melanomaSubstitution - Missense

c.615C>A; p.Y205*; 17:73169934-73169934

livercarcinoma; hepatocellular_carcinomaSubstitution - Nonsense

c.107C>T; p.P36L; 17:73169426-73169426

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.557A>G; p.N186S; 17:73169876-73169876

skinmalignant_melanomaSubstitution - Missense

c.407T>A; p.M136K; 17:73169726-73169726

livercarcinomaSubstitution - Missense

c.211T>C; p.Y71H; 17:73169530-73169530

skinmalignant_melanomaSubstitution - Missense

c.1018C>T; p.R340W; 17:73170337-73170337

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.407T>A; p.M136K; 17:73169726-73169726

livercarcinomaSubstitution - Missense

c.661C>T; p.L221F; 17:73169980-73169980

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.376C>G; p.Q126E; 17:73169695-73169695

prostatecarcinoma; adenocarcinomaSubstitution - Missense

c.193A>G; p.I65V; 17:73169512-73169512

oesophaguscarcinoma; adenocarcinomaSubstitution - Missense

c.999C>A; p.S333R; 17:73170318-73170318

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.470G>A; p.R157Q; 17:73169789-73169789

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.450G>A; p.S150S; 17:73169769-73169769

boneEwings_sarcoma-peripheral_primitive_neuroectodermal_tumourSubstitution - coding silent

c.829G>A; p.V277I; 17:73170148-73170148

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.550C>T; p.R184W; 17:73169869-73169869

upper_aerodigestive_tract; mouthcarcinomaSubstitution - Missense

c.1016A>T; p.E339V; 17:73170335-73170335

skinmalignant_melanomaSubstitution - Missense

c.550C>T; p.R184W; 17:73169869-73169869

upper_aerodigestive_tract; mouthcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.608C>T; p.A203V; 17:73169927-73169927

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.862C>T; p.P288S; 17:73170181-73170181

skinmalignant_melanomaSubstitution - Missense

c.534G>A; p.M178I; 17:73169853-73169853

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.534G>A; p.M178I; 17:73169853-73169853

skinmalignant_melanomaSubstitution - Missense

c.152T>C; p.F51S; 17:73169471-73169471

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.460A>G; p.R154G; 17:73169779-73169779

breastcarcinomaSubstitution - Missense

c.207C>A; p.L69L; 17:73169526-73169526

skinmalignant_melanomaSubstitution - coding silent

c.509C>T; p.S170F; 17:73169828-73169828

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.262G>T; p.A88S; 17:73169581-73169581

prostatecarcinomaSubstitution - Missense

c.690C>T; p.F230F; 17:73170009-73170009

skinmalignant_melanomaSubstitution - coding silent

c.837C>T; p.S279S; 17:73170156-73170156

skinmalignant_melanomaSubstitution - coding silent

c.286C>A; p.L96M; 17:73169605-73169605

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1058C>G; p.T353S; 17:73170377-73170377

central_nervous_system; braingliomaSubstitution - Missense

c.732C>T; p.S244S; 17:73170051-73170051

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.474G>A; p.T158T; 17:73169793-73169793

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.414C>T; p.I138I; 17:73169733-73169733

large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.268G>C; p.E90Q; 17:73169587-73169587

stomachcarcinoma; intestinal_adenocarcinomaSubstitution - Missense

c.1014G>A; p.G338G; 17:73170333-73170333

skinmalignant_melanomaSubstitution - coding silent

c.674G>T; p.C225F; 17:73169993-73169993

thyroidcarcinomaSubstitution - Missense

c.998G>A; p.S333N; 17:73170317-73170317

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.727G>A; p.G243S; 17:73170046-73170046

stomachcarcinoma; intestinal_adenocarcinomaSubstitution - Missense

c.473C>T; p.T158M; 17:73169792-73169792

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.639C>T; p.F213F; 17:73169958-73169958

skinmalignant_melanomaSubstitution - coding silent