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

Basic Information

Gene ID

51741

Name

WWOX

The somatic mutations from COSMIC database

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.452T>C; p.V151A; 16:78164225-78164225

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.211G>A; p.G71R; 16:78109816-78109816

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.448C>G; p.H150D; 16:78164221-78164221

haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; follicular_lymphomaSubstitution - Missense

c.537G>A; p.P179P; 16:78278623-78278623

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.415G>A; p.E139K; 16:78164188-78164188

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.511G>T; p.E171*; 16:78164284-78164284

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.451G>C; p.V151L; 16:78164224-78164224

haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; follicular_lymphomaSubstitution - Missense

c.160C>T; p.R54*; 16:78108475-78108475

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.119A>T; p.E40V; 16:78108434-78108434

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.374A>G; p.K125R; 16:78115119-78115119

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.517-3C>A; p.?; 16:78278600-78278600

central_nervous_system; brainstemglioma; astrocytoma_Grade_IIUnknown

c.410G>T; p.G137V; 16:78164183-78164183

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.544A>G; p.K182E; 16:78278630-78278630

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - Missense

c.556A>C; p.K186Q; 16:78278642-78278642

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.177G>A; p.L59L; 16:78109782-78109782

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.500G>A; p.R167H; 16:78164273-78164273

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.500G>A; p.R167H; 16:78164273-78164273

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.500G>A; p.R167H; 16:78164273-78164273

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.517-1G>A; p.?; 16:78278602-78278602

endometriumcarcinoma; serous_carcinomaUnknown

c.479G>T; p.R160M; 16:78164252-78164252

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.411G>A; p.G137G; 16:78164184-78164184

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.414C>T; p.F138F; 16:78164187-78164187

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.482C>T; p.A161V; 16:78164255-78164255

urinary_tract; bladdercarcinomaSubstitution - Missense

c.425A>T; p.K142M; 16:78164198-78164198

upper_aerodigestive_tract; mouthcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.454A>T; p.I152F; 16:78164227-78164227

haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; follicular_lymphomaSubstitution - Missense


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