Entrez Gene

Basic Information
Gene ID	9686
Name	VGLL4

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.20T>C; p.V7A; 3:11703015-11703015	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.855C>T; p.S285S; 3:11558574-11558574	skin	malignant_melanoma	Substitution - coding silent
c.355C>T; p.H119Y; 3:11564919-11564919	skin	malignant_melanoma	Substitution - Missense
c.193G>T; p.E65*; 3:11601894-11601894	ovary	carcinoma; serous_carcinoma	Substitution - Nonsense
c.139G>A; p.G47S; 3:11601948-11601948	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.621C>T; p.P207P; 3:11558808-11558808	prostate	carcinoma	Substitution - coding silent
c.213C>G; p.N71K; 3:11601874-11601874	urinary_tract; bladder	carcinoma	Substitution - Missense
c.854C>T; p.S285F; 3:11558575-11558575	kidney	carcinoma; papillary_renal_cell_carcinoma	Substitution - Missense
c.281G>A; p.R94H; 3:11564993-11564993	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.141C>G; p.G47G; 3:11601946-11601946	liver	carcinoma	Substitution - coding silent
c.141C>G; p.G47G; 3:11601946-11601946	liver	carcinoma	Substitution - coding silent
c.282C>A; p.R94R; 3:11564992-11564992	thyroid	other; neoplasm	Substitution - coding silent
c.4G>A; p.E2K; 3:11703031-11703031	skin	malignant_melanoma	Substitution - Missense
c.516C>A; p.A172A; 3:11559417-11559417	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - coding silent
c.236G>A; p.R79H; 3:11601851-11601851	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.494T>G; p.I165S; 3:11559439-11559439	NS	malignant_melanoma	Substitution - Missense
c.295G>A; p.E99K; 3:11564979-11564979	skin; trunk	malignant_melanoma	Substitution - Missense
c.287A>C; p.D96A; 3:11564987-11564987	thyroid	other; neoplasm	Substitution - Missense
c.38C>T; p.S13F; 3:11702997-11702997	upper_aerodigestive_tract; pharynx	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.74C>A; p.A25D; 3:11602013-11602013	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.491T>C; p.V164A; 3:11559442-11559442	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.817G>A; p.A273T; 3:11558612-11558612	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.622G>A; p.V208M; 3:11558807-11558807	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.297G>T; p.E99D; 3:11564977-11564977	upper_aerodigestive_tract; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.517C>T; p.R173C; 3:11559416-11559416	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.867C>A; p.V289V; 3:11558562-11558562	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.867C>A; p.V289V; 3:11558562-11558562	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.867C>A; p.V289V; 3:11558562-11558562	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.38C>A; p.S13Y; 3:11702997-11702997	prostate	carcinoma; adenocarcinoma	Substitution - Missense
c.197A>G; p.D66G; 3:11601890-11601890	oesophagus	carcinoma; adenocarcinoma	Substitution - Missense
c.838G>A; p.V280I; 3:11558591-11558591	central_nervous_system; brain	glioma	Substitution - Missense
c.134G>A; p.R45H; 3:11601953-11601953	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.250_251insC; p.H84fs*123; 3:11601836-11601837	large_intestine; caecum	carcinoma; adenocarcinoma	Insertion - Frameshift
c.715G>C; p.D239H; 3:11558714-11558714	urinary_tract; bladder	carcinoma	Substitution - Missense
c.138C>T; p.T46T; 3:11601949-11601949	lung; right_upper_lobe	carcinoma; adenocarcinoma	Substitution - coding silent
c.220G>A; p.V74I; 3:11601867-11601867	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.220G>C; p.V74L; 3:11601867-11601867	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.417C>T; p.S139S; 3:11564857-11564857	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - coding silent
c.292C>T; p.R98W; 3:11564982-11564982	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.368C>T; p.S123F; 3:11564906-11564906	skin	malignant_melanoma	Substitution - Missense
c.64C>T; p.R22C; 3:11702971-11702971	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.320G>A; p.R107H; 3:11564954-11564954	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.320G>A; p.R107H; 3:11564954-11564954	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.193G>A; p.E65K; 3:11601894-11601894	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.8C>T; p.T3M; 3:11703027-11703027	oesophagus	carcinoma; adenocarcinoma	Substitution - Missense
c.8C>T; p.T3M; 3:11703027-11703027	prostate	carcinoma; adenocarcinoma	Substitution - Missense
c.329C>T; p.A110V; 3:11564945-11564945	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.651G>A; p.L217L; 3:11558778-11558778	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.194A>G; p.E65G; 3:11601893-11601893	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.247C>G; p.P83A; 3:11601840-11601840	haematopoietic_and_lymphoid_tissue; central_nervous_system	lymphoid_neoplasm; primary_central_nervous_system_lymphoma	Substitution - Missense
c.691G>C; p.V231L; 3:11558738-11558738	lung; right_upper_lobe	carcinoma; adenocarcinoma	Substitution - Missense
c.744G>C; p.T248T; 3:11558685-11558685	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.707C>T; p.S236F; 3:11558722-11558722	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.260A>G; p.K87R; 3:11565014-11565014	prostate	carcinoma	Substitution - Missense
c.694T>C; p.S232P; 3:11558735-11558735	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.133C>T; p.R45C; 3:11601954-11601954	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.744G>A; p.T248T; 3:11558685-11558685	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.146C>T; p.P49L; 3:11601941-11601941	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.373C>T; p.P125S; 3:11564901-11564901	skin	malignant_melanoma	Substitution - Missense
c.733C>T; p.L245L; 3:11558696-11558696	biliary_tract; gallbladder	carcinoma; adenocarcinoma	Substitution - coding silent

The somatic mutations from COSMIC database