Entrez Gene

Basic Information
Gene ID	9965
Name	FGF19

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.508C>T; p.P170S; 11:69699405-69699405	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.635C>T; p.P212L; 11:69699278-69699278	skin	malignant_melanoma	Substitution - Missense
c.506T>C; p.L169P; 11:69699407-69699407	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.495C>T; p.F165F; 11:69699418-69699418	skin	malignant_melanoma	Substitution - coding silent
c.499C>T; p.P167S; 11:69699414-69699414	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.267C>T; p.T89T; 11:69703330-69703330	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.373G>A; p.E125K; 11:69699540-69699540	skin; extremity	malignant_melanoma	Substitution - Missense
c.128G>A; p.R43H; 11:69703749-69703749	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.562T>C; p.F188L; 11:69699351-69699351	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.367G>A; p.E123K; 11:69699546-69699546	kidney	carcinoma; papillary_renal_cell_carcinoma	Substitution - Missense
c.291C>T; p.S97S; 11:69703306-69703306	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.564C>A; p.F188L; 11:69699349-69699349	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.408C>T; p.S136S; 11:69699505-69699505	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - coding silent
c.360T>A; p.C120*; 11:69699553-69699553	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - Nonsense
c.33G>T; p.W11C; 11:69703844-69703844	oesophagus	carcinoma	Substitution - Missense
c.527C>T; p.P176L; 11:69699386-69699386	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.167C>A; p.S56Y; 11:69703710-69703710	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.295C>T; p.R99W; 11:69703302-69703302	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.452G>T; p.R151L; 11:69699461-69699461	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.351G>A; p.E117E; 11:69699562-69699562	lung	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.407_408CC>TT; p.S136>F; 11:69699505-69699506	skin	malignant_melanoma	Complex - compound substitution
c.566C>T; p.S189F; 11:69699347-69699347	skin	malignant_melanoma	Substitution - Missense
c.581C>T; p.T194I; 11:69699332-69699332	skin	malignant_melanoma	Substitution - Missense
c.451C>T; p.R151W; 11:69699462-69699462	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.528T>C; p.P176P; 11:69699385-69699385	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - coding silent
c.613G>A; p.G205R; 11:69699300-69699300	bone	Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour	Substitution - Missense
c.485T>A; p.L162H; 11:69699428-69699428	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.527C>A; p.P176H; 11:69699386-69699386	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.527C>A; p.P176H; 11:69699386-69699386	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.549G>A; p.L183L; 11:69699364-69699364	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.28G>A; p.V10I; 11:69703849-69703849	oesophagus	carcinoma; adenocarcinoma	Substitution - Missense
c.522G>A; p.E174E; 11:69699391-69699391	oesophagus	carcinoma	Substitution - coding silent
c.555T>G; p.S185S; 11:69699358-69699358	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent

The somatic mutations from COSMIC database