Entrez Gene

Basic Information
Gene ID	8838
Name	WISP3

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.460C>T; p.Q154*; 6:112064814-112064814	skin	malignant_melanoma	Substitution - Nonsense
c.1070G>T; p.R357I; 6:112069571-112069571	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.1070G>T; p.R357I; 6:112069571-112069571	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.474G>T; p.L158F; 6:112064828-112064828	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.14G>A; p.R5Q; 6:112054317-112054317	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.29C>T; p.S10L; 6:112054332-112054332	oesophagus; middle_third	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.316G>T; p.E106*; 6:112061204-112061204	large_intestine	carcinoma; adenocarcinoma	Substitution - Nonsense
c.316G>T; p.E106*; 6:112061204-112061204	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Nonsense
c.564T>G; p.G188G; 6:112064918-112064918	breast	carcinoma	Substitution - coding silent
c.698A>C; p.K233T; 6:112068259-112068259	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.698A>C; p.K233T; 6:112068259-112068259	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.781G>C; p.E261Q; 6:112068342-112068342	breast	carcinoma	Substitution - Missense
c.909C>T; p.C303C; 6:112069410-112069410	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.122G>A; p.G41D; 6:112061010-112061010	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.861A>G; p.Q287Q; 6:112069362-112069362	thyroid	other; neoplasm	Substitution - coding silent
c.861A>G; p.Q287Q; 6:112069362-112069362	liver	carcinoma; hepatocellular_carcinoma	Substitution - coding silent
c.256G>A; p.V86M; 6:112061144-112061144	breast	carcinoma	Substitution - Missense
c.811G>A; p.D271N; 6:112068372-112068372	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.811G>A; p.D271N; 6:112068372-112068372	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.631A>G; p.K211E; 6:112064985-112064985	lung	carcinoma; small_cell_carcinoma	Substitution - Missense
c.151G>A; p.G51R; 6:112061039-112061039	skin	malignant_melanoma	Substitution - Missense
c.345G>T; p.G115G; 6:112061233-112061233	lung; right_upper_lobe	carcinoma; adenocarcinoma	Substitution - coding silent
c.570G>A; p.K190K; 6:112064924-112064924	skin	malignant_melanoma	Substitution - coding silent
c.414T>C; p.V138V; 6:112064768-112064768	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.577G>T; p.D193Y; 6:112064931-112064931	liver	carcinoma; hepatocellular_carcinoma	Substitution - Missense
c.1064G>A; p.C355Y; 6:112069565-112069565	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.422A>G; p.E141G; 6:112064776-112064776	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Missense
c.422A>G; p.E141G; 6:112064776-112064776	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Missense
c.933C>T; p.P311P; 6:112069434-112069434	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.919C>G; p.Q307E; 6:112069420-112069420	urinary_tract; bladder	carcinoma; transitional_cell_carcinoma	Substitution - Missense
c.919C>G; p.Q307E; 6:112069420-112069420	urinary_tract; bladder	carcinoma	Substitution - Missense
c.572A>C; p.K191T; 6:112064926-112064926	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.88G>T; p.A30S; 6:112054391-112054391	lung	carcinoma; small_cell_carcinoma	Substitution - Missense
c.590G>A; p.C197Y; 6:112064944-112064944	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.272G>T; p.G91V; 6:112061160-112061160	upper_aerodigestive_tract; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.600A>G; p.E200E; 6:112064954-112064954	bone	Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour	Substitution - coding silent
c.874C>G; p.L292V; 6:112069375-112069375	central_nervous_system; brain	primitive_neuroectodermal_tumour-medulloblastoma	Substitution - Missense
c.535G>T; p.A179S; 6:112064889-112064889	prostate	carcinoma	Substitution - Missense
c.669_670insA; p.C227fs*21; 6:112068230-112068231	large_intestine	carcinoma; adenocarcinoma	Insertion - Frameshift
c.669_670insA; p.C227fs*21; 6:112068230-112068231	large_intestine; caecum	carcinoma; adenocarcinoma	Insertion - Frameshift
c.294G>T; p.K98N; 6:112061182-112061182	urinary_tract; bladder	carcinoma	Substitution - Missense
c.294G>T; p.K98N; 6:112061182-112061182	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.788G>A; p.R263K; 6:112068349-112068349	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.237C>A; p.C79*; 6:112061125-112061125	lung	carcinoma; squamous_cell_carcinoma	Substitution - Nonsense
c.40C>T; p.H14Y; 6:112054343-112054343	skin	malignant_melanoma	Substitution - Missense
c.791T>C; p.L264P; 6:112068352-112068352	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.570G>T; p.K190N; 6:112064924-112064924	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.722G>A; p.C241Y; 6:112068283-112068283	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.163G>T; p.E55*; 6:112061051-112061051	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Nonsense
c.163G>T; p.E55*; 6:112061051-112061051	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Nonsense
c.163G>T; p.E55*; 6:112061051-112061051	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Nonsense
c.670delA; p.K226fs*24; 6:112068231-112068231	large_intestine; colon	carcinoma; adenocarcinoma	Deletion - Frameshift
c.670delA; p.K226fs*24; 6:112068231-112068231	large_intestine; caecum	carcinoma; adenocarcinoma	Deletion - Frameshift
c.102+1G>T; p.?; 6:112054406-112054406	liver	carcinoma; hepatocellular_carcinoma	Unknown
c.670delA; p.K226fs*24; 6:112068231-112068231	large_intestine; colon	carcinoma; adenocarcinoma	Deletion - Frameshift
c.670delA; p.K226fs*24; 6:112068231-112068231	large_intestine; caecum	carcinoma; adenocarcinoma	Deletion - Frameshift
c.670delA; p.K226fs*24; 6:112068231-112068231	skin	malignant_melanoma	Deletion - Frameshift
c.670delA; p.K226fs*24; 6:112068231-112068231	large_intestine; colon	carcinoma; adenocarcinoma	Deletion - Frameshift
c.670delA; p.K226fs*24; 6:112068231-112068231	oesophagus; lower_third	carcinoma; adenocarcinoma	Deletion - Frameshift
c.539G>A; p.G180D; 6:112064893-112064893	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.306A>C; p.E102D; 6:112061194-112061194	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.449G>A; p.G150D; 6:112064803-112064803	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.513A>C; p.T171T; 6:112064867-112064867	breast	carcinoma	Substitution - coding silent
c.253C>T; p.L85L; 6:112061141-112061141	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.679T>A; p.C227S; 6:112068240-112068240	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.260G>A; p.R87K; 6:112061148-112061148	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.548G>T; p.C183F; 6:112064902-112064902	skin	malignant_melanoma	Substitution - Missense

The somatic mutations from COSMIC database