Entrez Gene

Basic Information
Gene ID	5228
Name	PGF

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.201C>T; p.S67S; 14:74949471-74949471	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - coding silent
c.129C>T; p.F43F; 14:74949543-74949543	skin	malignant_melanoma	Substitution - coding silent
c.73_74insC; p.Q25fs*66; 14:74955169-74955170	large_intestine; colon	carcinoma; adenocarcinoma	Insertion - Frameshift
c.73_74insC; p.Q25fs*66; 14:74955169-74955170	large_intestine; caecum	carcinoma; adenocarcinoma	Insertion - Frameshift
c.327C>A; p.I109I; 14:74948572-74948572	stomach	carcinoma; diffuse_adenocarcinoma	Substitution - coding silent
c.162G>A; p.A54A; 14:74949510-74949510	liver	carcinoma	Substitution - coding silent
c.162G>A; p.A54A; 14:74949510-74949510	liver	carcinoma	Substitution - coding silent
c.162G>A; p.A54A; 14:74949510-74949510	liver	carcinoma	Substitution - coding silent
c.363G>A; p.T121T; 14:74948536-74948536	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.315+1G>A; p.?; 14:74949356-74949356	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Unknown
c.109G>A; p.E37K; 14:74953913-74953913	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.188C>G; p.S63C; 14:74949484-74949484	lung	carcinoma; small_cell_carcinoma	Substitution - Missense
c.286C>T; p.P96S; 14:74949386-74949386	breast	carcinoma	Substitution - Missense
c.89C>A; p.S30Y; 14:74953933-74953933	pancreas	carcinoma	Substitution - Missense
c.490G>A; p.G164S; 14:74942729-74942729	ovary	carcinoma; serous_carcinoma	Substitution - Missense
c.450G>A; p.R150R; 14:74946248-74946248	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.113T>G; p.V38G; 14:74953909-74953909	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.451A>G; p.R151G; 14:74946247-74946247	pancreas	carcinoma	Substitution - Missense
c.158G>A; p.R53Q; 14:74949514-74949514	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.386A>G; p.E129G; 14:74948513-74948513	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.190G>A; p.E64K; 14:74949482-74949482	liver	carcinoma	Substitution - Missense
c.190G>A; p.E64K; 14:74949482-74949482	liver	carcinoma	Substitution - Missense
c.493G>A; p.D165N; 14:74942726-74942726	breast	carcinoma	Substitution - Missense
c.118+8G>A; p.?; 14:74953896-74953896	liver	carcinoma	Unknown
c.118+8G>A; p.?; 14:74953896-74953896	liver	carcinoma	Unknown
c.380G>A; p.R127H; 14:74948519-74948519	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.380G>A; p.R127H; 14:74948519-74948519	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.380G>A; p.R127H; 14:74948519-74948519	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.253G>A; p.G85S; 14:74949419-74949419	central_nervous_system; brain	glioma	Substitution - Missense
c.169A>G; p.R57G; 14:74949503-74949503	liver	carcinoma	Substitution - Missense
c.169A>G; p.R57G; 14:74949503-74949503	liver	carcinoma	Substitution - Missense
c.179A>G; p.D60G; 14:74949493-74949493	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.405G>T; p.E135D; 14:74946396-74946396	breast	carcinoma	Substitution - Missense
c.261C>T; p.C87C; 14:74949411-74949411	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - coding silent
c.202G>A; p.E68K; 14:74949470-74949470	skin	malignant_melanoma	Substitution - Missense
c.73delC; p.Q25fs*83; 14:74955170-74955170	large_intestine; colon	carcinoma; adenocarcinoma	Deletion - Frameshift
c.176T>G; p.V59G; 14:74949496-74949496	upper_aerodigestive_tract; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.176T>G; p.V59G; 14:74949496-74949496	upper_aerodigestive_tract; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.176T>G; p.V59G; 14:74949496-74949496	thyroid	other; neoplasm	Substitution - Missense
c.176T>G; p.V59G; 14:74949496-74949496	upper_aerodigestive_tract; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.176T>G; p.V59G; 14:74949496-74949496	upper_aerodigestive_tract; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.176T>G; p.V59G; 14:74949496-74949496	upper_aerodigestive_tract; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.176T>G; p.V59G; 14:74949496-74949496	upper_aerodigestive_tract; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.176T>G; p.V59G; 14:74949496-74949496	upper_aerodigestive_tract; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.176T>G; p.V59G; 14:74949496-74949496	upper_aerodigestive_tract; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.176T>G; p.V59G; 14:74949496-74949496	upper_aerodigestive_tract; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.176T>G; p.V59G; 14:74949496-74949496	thyroid	other; neoplasm	Substitution - Missense
c.176T>G; p.V59G; 14:74949496-74949496	thyroid	other; neoplasm	Substitution - Missense
c.176T>G; p.V59G; 14:74949496-74949496	upper_aerodigestive_tract; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.176T>G; p.V59G; 14:74949496-74949496	upper_aerodigestive_tract; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.100G>A; p.G34S; 14:74953922-74953922	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - Missense
c.385G>A; p.E129K; 14:74948514-74948514	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.385G>A; p.E129K; 14:74948514-74948514	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.511T>C; p.*171Q; 14:74942708-74942708	large_intestine	carcinoma; adenocarcinoma	Nonstop extension
c.511T>C; p.*171Q; 14:74942708-74942708	large_intestine	carcinoma; adenocarcinoma	Nonstop extension

The somatic mutations from COSMIC database