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

Basic Information

Gene ID

826

Name

CAPNS1

The somatic mutations from COSMIC database

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.159T>C; p.G53G; 19:36141170-36141170

 thyroidother; neoplasmSubstitution - coding silent

c.159T>C; p.G53G; 19:36141170-36141170

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.484G>T; p.E162*; 19:36145833-36145833

 adrenal_gland; adrenal_glandadrenal_cortical_carcinoma; functioningSubstitution - Nonsense

c.39C>G; p.G13G; 19:36141050-36141050

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.553C>T; p.R185*; 19:36146003-36146003

 large_intestine; colonadenomaSubstitution - Nonsense

c.553C>T; p.R185*; 19:36146003-36146003

 pancreascarcinomaSubstitution - Nonsense

c.150A>C; p.G50G; 19:36141161-36141161

 thyroidother; neoplasmSubstitution - coding silent

c.441G>T; p.M147I; 19:36143113-36143113

 lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.647G>A; p.R216H; 19:36146238-36146238

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.703A>T; p.R235W; 19:36146294-36146294

 livercarcinomaSubstitution - Missense

c.690C>A; p.I230I; 19:36146281-36146281

 thyroidcarcinomaSubstitution - coding silent

c.621G>A; p.E207E; 19:36146212-36146212

 upper_aerodigestive_tract; mouthcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.408T>C; p.T136T; 19:36143080-36143080

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.803C>T; p.S268F; 19:36149835-36149835

 cervixcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.138C>T; p.G46G; 19:36141149-36141149

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.712G>A; p.A238T; 19:36146303-36146303

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.712G>A; p.A238T; 19:36146303-36146303

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.554G>C; p.R185P; 19:36146004-36146004

 kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.554G>C; p.R185P; 19:36146004-36146004

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.213G>T; p.E71D; 19:36142303-36142303

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.45C>G; p.G15G; 19:36141056-36141056

 central_nervous_system; braingliomaSubstitution - coding silent

c.305G>C; p.R102P; 19:36142713-36142713

 lungcarcinoma; non_small_cell_carcinomaSubstitution - Missense

c.433C>T; p.R145C; 19:36143105-36143105

 skinmalignant_melanomaSubstitution - Missense

c.554G>A; p.R185Q; 19:36146004-36146004

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.292G>A; p.V98I; 19:36142700-36142700

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.647_669del23; p.R216fs*4; 19:36146238-36146260

 soft_tissue; striated_musclerhabdomyosarcoma; embryonalDeletion - Frameshift

c.582C>T; p.L194L; 19:36146032-36146032

 skinmalignant_melanomaSubstitution - coding silent

c.643C>T; p.R215*; 19:36146234-36146234

 skinmalignant_melanomaSubstitution - Nonsense

c.759A>C; p.Q253H; 19:36149615-36149615

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.527C>A; p.A176D; 19:36145977-36145977

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.239C>T; p.P80L; 19:36142329-36142329

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.780+10C>G; p.?; 19:36149646-36149646

 skinmalignant_melanomaUnknown

c.434G>A; p.R145H; 19:36143106-36143106

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.111G>C; p.G37G; 19:36141122-36141122

 thyroidother; neoplasmSubstitution - coding silent

c.614T>C; p.L205P; 19:36146205-36146205

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.391C>T; p.H131Y; 19:36142966-36142966

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.426C>T; p.D142D; 19:36143098-36143098

 lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - coding silent

c.721C>T; p.R241C; 19:36146312-36146312

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.426C>T; p.D142D; 19:36143098-36143098

 lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.28_36delGGCGGCGGC; p.G18_G20delGGG; 19:36141039-36141047

 large_intestine; caecumcarcinoma; adenocarcinomaDeletion - In frame

c.144T>C; p.G48G; 19:36141155-36141155

 thyroidother; neoplasmSubstitution - coding silent

c.305G>A; p.R102Q; 19:36142713-36142713

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.292G>T; p.V98F; 19:36142700-36142700

 central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.292G>T; p.V98F; 19:36142700-36142700

 central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.654A>G; p.S218S; 19:36146245-36146245

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.488A>C; p.E163A; 19:36145837-36145837

 prostatecarcinoma; adenocarcinomaSubstitution - Missense

c.278A>G; p.N93S; 19:36142686-36142686

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.433C>A; p.R145S; 19:36143105-36143105

 upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.25A>C; p.K9Q; 19:36141036-36141036

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

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