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

Basic Information

Gene ID

1460

Name

CSNK2B

The somatic mutations from COSMIC database

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.28delA; p.I10fs*41; 6:31666859-31666859

 lungcarcinoma; adenocarcinomaDeletion - Frameshift

c.608C>T; p.A203V; 6:31669886-31669886

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.478G>A; p.G160S; 6:31669429-31669429

 central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.284C>G; p.A95G; 6:31668647-31668647

 oesophaguscarcinoma; adenocarcinomaSubstitution - Missense

c.564C>T; p.Y188Y; 6:31669842-31669842

 pancreascarcinomaSubstitution - coding silent

c.266T>C; p.L89P; 6:31668629-31668629

 central_nervous_system; brainprimitive_neuroectodermal_tumour-medulloblastomaSubstitution - Missense

c.564C>T; p.Y188Y; 6:31669842-31669842

 pancreascarcinomaSubstitution - coding silent

c.138T>C; p.Y46Y; 6:31667933-31667933

 haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - coding silent

c.264C>T; p.I88I; 6:31668627-31668627

 skinmalignant_melanomaSubstitution - coding silent

c.532_533insCCT; p.R178>T*; 6:31669483-31669484

 central_nervous_system; brainprimitive_neuroectodermal_tumour-medulloblastomaComplex - insertion inframe

c.484G>A; p.G162S; 6:31669435-31669435

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.484G>A; p.G162S; 6:31669435-31669435

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.253G>A; p.A85T; 6:31668616-31668616

 livercarcinomaSubstitution - Missense

c.544C>T; p.Q182*; 6:31669495-31669495

 central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Nonsense

c.332G>A; p.R111H; 6:31669137-31669137

 livercarcinomaSubstitution - Missense

c.332G>A; p.R111H; 6:31669137-31669137

 livercarcinomaSubstitution - Missense

c.228C>T; p.A76A; 6:31668591-31668591

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.414C>G; p.P138P; 6:31669365-31669365

 ovarycarcinoma; serous_carcinomaSubstitution - coding silent

c.547T>C; p.F183L; 6:31669498-31669498

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.175+1G>A; p.?; 6:31667971-31667971

 endometriumcarcinoma; endometrioid_carcinomaUnknown

c.463G>T; p.D155Y; 6:31669414-31669414

 central_nervous_system; brainprimitive_neuroectodermal_tumour-medulloblastomaSubstitution - Missense

c.153C>G; p.D51E; 6:31667948-31667948

 urinary_tract; bladdercarcinomaSubstitution - Missense

c.532A>ACCT; p.R178>?; 6:31669483-31669483

 central_nervous_system; brainprimitive_neuroectodermal_tumour-medulloblastomaComplex

c.532A>T; p.R178*; 6:31669483-31669483

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Nonsense

c.317T>G; p.F106C; 6:31669122-31669122

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.265C>T; p.L89F; 6:31668628-31668628

 skinmalignant_melanomaSubstitution - Missense

c.523C>T; p.R175W; 6:31669474-31669474

 central_nervous_system; brainprimitive_neuroectodermal_tumour-medulloblastoma; medullomyoblastomaSubstitution - Missense

c.523C>T; p.R175W; 6:31669474-31669474

 central_nervous_system; brainstemprimitive_neuroectodermal_tumour-medulloblastoma; WNT_subtypeSubstitution - Missense

c.296A>G; p.E99G; 6:31669101-31669101

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.156G>T; p.M52I; 6:31667951-31667951

 urinary_tract; bladdercarcinomaSubstitution - Missense

c.329C>G; p.P110R; 6:31669134-31669134

 ovaryother; neoplasmSubstitution - Missense

c.625A>T; p.S209C; 6:31669903-31669903

 livercarcinoma; hepatocellular_carcinomaSubstitution - Missense

c.625A>T; p.S209C; 6:31669903-31669903

 livercarcinoma; hepatocellular_carcinomaSubstitution - Missense

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