Epithelial-Mesenchymal Transition gene database (dbEMT) Home
dbEMT
dbEMT 2.0
General information | Literature | Expression | lncRNA |Regulation | Mutation | Homolog | Interaction

Basic Information

Gene ID

8877

Name

SPHK1

The somatic mutations from COSMIC database

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.1160G>C; p.R387P; 17:76387333-76387333

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.1181_1182AG>GA; p.K394R; 17:76387354-76387355

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.556G>A; p.A186T; 17:76386432-76386432

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.1160G>A; p.R387H; 17:76387333-76387333

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.961G>C; p.D321H; 17:76387134-76387134

cervixcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1348G>A; p.G450S; 17:76387521-76387521

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.1216G>A; p.V406I; 17:76387389-76387389

skinmalignant_melanomaSubstitution - Missense

c.676C>T; p.L226L; 17:76386849-76386849

lungcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.451C>T; p.R151W; 17:76386250-76386250

livercarcinoma; hepatocellular_carcinomaSubstitution - Missense

c.451C>T; p.R151W; 17:76386250-76386250

livercarcinomaSubstitution - Missense

c.629C>A; p.A210D; 17:76386505-76386505

upper_aerodigestive_tract; mouthcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.629C>A; p.A210D; 17:76386505-76386505

upper_aerodigestive_tract; mouthcarcinomaSubstitution - Missense

c.1380C>G; p.P460P; 17:76387553-76387553

lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.766G>A; p.A256T; 17:76386939-76386939

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.331G>A; p.G111S; 17:76386047-76386047

central_nervous_system; braingliomaSubstitution - Missense

c.331G>A; p.G111S; 17:76386047-76386047

central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.387T>C; p.A129A; 17:76386103-76386103

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.655G>A; p.D219N; 17:76386828-76386828

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.743G>A; p.R248H; 17:76386916-76386916

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.1218A>G; p.V406V; 17:76387391-76387391

thyroidcarcinomaSubstitution - coding silent

c.693G>A; p.R231R; 17:76386866-76386866

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.1356G>A; p.V452V; 17:76387529-76387529

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.581T>C; p.L194P; 17:76386457-76386457

oesophaguscarcinoma; adenocarcinomaSubstitution - Missense

c.1350T>C; p.G450G; 17:76387523-76387523

large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.1015C>G; p.P339A; 17:76387188-76387188

kidneycarcinoma; papillary_renal_cell_carcinomaSubstitution - Missense

c.1055C>T; p.S352L; 17:76387228-76387228

breastcarcinomaSubstitution - Missense

c.1360delC; p.P455fs*>16; 17:76387533-76387533

large_intestine; caecumcarcinoma; adenocarcinomaDeletion - Frameshift

c.696G>A; p.L232L; 17:76386869-76386869

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.337A>G; p.K113E; 17:76386053-76386053

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.699G>A; p.L233L; 17:76386872-76386872

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.402C>T; p.S134S; 17:76386118-76386118

boneEwings_sarcoma-peripheral_primitive_neuroectodermal_tumourSubstitution - coding silent

c.1160delG; p.R387fs*44; 17:76387333-76387333

large_intestine; caecumcarcinoma; adenocarcinomaDeletion - Frameshift

c.1370G>T; p.S457I; 17:76387543-76387543

livercarcinomaSubstitution - Missense

c.675G>A; p.T225T; 17:76386848-76386848

lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.727A>G; p.T243A; 17:76386900-76386900

ovarycarcinoma; serous_carcinomaSubstitution - Missense

c.1347C>T; p.S449S; 17:76387520-76387520

urinary_tract; bladdercarcinomaSubstitution - coding silent

c.1221T>C; p.Y407Y; 17:76387394-76387394

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.1402G>A; p.E468K; 17:76387575-76387575

skinmalignant_melanomaSubstitution - Missense

c.100G>A; p.A34T; 17:76385486-76385486

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.100G>A; p.A34T; 17:76385486-76385486

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.100G>A; p.A34T; 17:76385486-76385486

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.100G>A; p.A34T; 17:76385486-76385486

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.100G>A; p.A34T; 17:76385486-76385486

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.100G>A; p.A34T; 17:76385486-76385486

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.100G>A; p.A34T; 17:76385486-76385486

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.100G>A; p.A34T; 17:76385486-76385486

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.100G>A; p.A34T; 17:76385486-76385486

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.100G>A; p.A34T; 17:76385486-76385486

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.100G>A; p.A34T; 17:76385486-76385486

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.100G>A; p.A34T; 17:76385486-76385486

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.100G>A; p.A34T; 17:76385486-76385486

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1353C>T; p.C451C; 17:76387526-76387526

kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - coding silent

c.601G>A; p.A201T; 17:76386477-76386477

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.1144C>T; p.R382C; 17:76387317-76387317

kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.1122C>G; p.F374L; 17:76387295-76387295

urinary_tract; bladdercarcinomaSubstitution - Missense

c.1222G>A; p.V408M; 17:76387395-76387395

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.1122C>G; p.F374L; 17:76387295-76387295

urinary_tract; bladdercarcinoma; transitional_cell_carcinomaSubstitution - Missense

c.662T>C; p.L221P; 17:76386835-76386835

lungcarcinoma; small_cell_carcinomaSubstitution - Missense

c.226A>G; p.T76A; 17:76385612-76385612

ovaryother; neoplasmSubstitution - Missense

c.1283G>T; p.G428V; 17:76387456-76387456

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.1283G>T; p.G428V; 17:76387456-76387456

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.1283G>T; p.G428V; 17:76387456-76387456

large_intestine; coloncarcinomaSubstitution - Missense

c.1283G>T; p.G428V; 17:76387456-76387456

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.554C>T; p.T185I; 17:76386430-76386430

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.739C>T; p.L247L; 17:76386912-76386912

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.375G>T; p.Q125H; 17:76386091-76386091

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1328A>G; p.N443S; 17:76387501-76387501

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.1293G>A; p.M431I; 17:76387466-76387466

skinmalignant_melanomaSubstitution - Missense

c.1328A>G; p.N443S; 17:76387501-76387501

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - Missense

c.516+9C>A; p.?; 17:76386324-76386324

livercarcinoma; hepatocellular_carcinomaUnknown

c.516+9C>A; p.?; 17:76386324-76386324

livercarcinomaUnknown

c.88G>A; p.A30T; 17:76385474-76385474

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.88G>A; p.A30T; 17:76385474-76385474

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.88G>A; p.A30T; 17:76385474-76385474

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.88G>A; p.A30T; 17:76385474-76385474

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.88G>A; p.A30T; 17:76385474-76385474

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.88G>A; p.A30T; 17:76385474-76385474

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.88G>A; p.A30T; 17:76385474-76385474

ovarycarcinoma; serous_carcinomaSubstitution - Missense

c.88G>A; p.A30T; 17:76385474-76385474

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.88G>A; p.A30T; 17:76385474-76385474

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.88G>A; p.A30T; 17:76385474-76385474

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.88G>A; p.A30T; 17:76385474-76385474

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.341G>A; p.G114D; 17:76386057-76386057

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.1133C>T; p.A378V; 17:76387306-76387306

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.426G>T; p.R142R; 17:76386225-76386225

thyroidother; neoplasmSubstitution - coding silent


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