Entrez Gene

Basic Information
Gene ID	2254
Name	FGF9

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.41A>G; p.Q14R; 13:21671953-21671953	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.562T>A; p.L188I; 13:21701370-21701370	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.481C>T; p.R161*; 13:21701289-21701289	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - Nonsense
c.481C>T; p.R161*; 13:21701289-21701289	stomach	carcinoma; adenocarcinoma	Substitution - Nonsense
c.302C>A; p.A101E; 13:21681066-21681066	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.424G>T; p.E142*; 13:21701232-21701232	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Nonsense
c.603T>C; p.Y201Y; 13:21701411-21701411	ovary	carcinoma; serous_carcinoma	Substitution - coding silent
c.603T>C; p.Y201Y; 13:21701411-21701411	ovary	carcinoma; serous_carcinoma	Substitution - coding silent
c.603T>C; p.Y201Y; 13:21701411-21701411	ovary	carcinoma; serous_carcinoma	Substitution - coding silent
c.603T>C; p.Y201Y; 13:21701411-21701411	ovary	carcinoma; serous_carcinoma	Substitution - coding silent
c.376G>A; p.G126R; 13:21681140-21681140	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.558delT; p.L188fs*18; 13:21701366-21701366	large_intestine	carcinoma; adenocarcinoma	Deletion - Frameshift
c.552C>T; p.F184F; 13:21701360-21701360	skin	malignant_melanoma	Substitution - coding silent
c.552C>T; p.F184F; 13:21701360-21701360	skin	malignant_melanoma	Substitution - coding silent
c.481C>A; p.R161R; 13:21701289-21701289	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.552C>T; p.F184F; 13:21701360-21701360	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.349G>T; p.G117W; 13:21681113-21681113	skin	malignant_melanoma	Substitution - Missense
c.538C>T; p.R180W; 13:21701346-21701346	breast	carcinoma; basal_(triple-negative)_carcinoma	Substitution - Missense
c.20T>C; p.V7A; 13:21671932-21671932	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.323G>A; p.R108Q; 13:21681087-21681087	skin; trunk	malignant_melanoma	Substitution - Missense
c.323G>A; p.R108Q; 13:21681087-21681087	breast	carcinoma	Substitution - Missense
c.121G>A; p.E41K; 13:21672033-21672033	prostate	carcinoma; adenocarcinoma	Substitution - Missense
c.100A>G; p.S34G; 13:21672012-21672012	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.524G>A; p.G175E; 13:21701332-21701332	skin	malignant_melanoma	Substitution - Missense
c.524G>A; p.G175E; 13:21701332-21701332	skin; scalp	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.177G>A; p.G59G; 13:21672089-21672089	biliary_tract; bile_duct	carcinoma; adenocarcinoma	Substitution - coding silent
c.410G>T; p.R137I; 13:21701218-21701218	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.292A>T; p.I98F; 13:21681056-21681056	liver	carcinoma	Substitution - Missense
c.540G>A; p.R180R; 13:21701348-21701348	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.33C>A; p.F11L; 13:21671945-21671945	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.515C>A; p.P172Q; 13:21701323-21701323	pancreas	carcinoma; ductal_carcinoma	Substitution - Missense
c.560T>G; p.F187C; 13:21701368-21701368	prostate	carcinoma; adenocarcinoma	Substitution - Missense
c.560T>G; p.F187C; 13:21701368-21701368	prostate	carcinoma; adenocarcinoma	Substitution - Missense
c.156G>A; p.T52T; 13:21672068-21672068	skin	malignant_melanoma	Substitution - coding silent
c.449C>A; p.S150*; 13:21701257-21701257	ovary	carcinoma; serous_carcinoma	Substitution - Nonsense
c.322C>T; p.R108*; 13:21681086-21681086	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Nonsense
c.244A>G; p.I82V; 13:21672156-21672156	lung; right_upper_lobe	carcinoma; adenocarcinoma	Substitution - Missense
c.246C>A; p.I82I; 13:21672158-21672158	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.328G>T; p.V110L; 13:21681092-21681092	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.520G>A; p.E174K; 13:21701328-21701328	skin	malignant_melanoma	Substitution - Missense
c.208A>G; p.T70A; 13:21672120-21672120	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.518G>A; p.R173K; 13:21701326-21701326	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.518G>A; p.R173K; 13:21701326-21701326	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.520G>A; p.E174K; 13:21701328-21701328	skin	malignant_melanoma	Substitution - Missense
c.441G>A; p.T147T; 13:21701249-21701249	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.441G>A; p.T147T; 13:21701249-21701249	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.338G>A; p.G113E; 13:21681102-21681102	skin	malignant_melanoma	Substitution - Missense
c.420C>T; p.F140F; 13:21701228-21701228	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.420C>T; p.F140F; 13:21701228-21701228	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.420C>T; p.F140F; 13:21701228-21701228	skin	malignant_melanoma	Substitution - coding silent
c.420C>T; p.F140F; 13:21701228-21701228	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.420C>T; p.F140F; 13:21701228-21701228	skin	malignant_melanoma	Substitution - coding silent
c.420C>T; p.F140F; 13:21701228-21701228	oesophagus	carcinoma; adenocarcinoma	Substitution - coding silent
c.420C>T; p.F140F; 13:21701228-21701228	skin	malignant_melanoma	Substitution - coding silent
c.239G>A; p.G80D; 13:21672151-21672151	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.307G>A; p.G103S; 13:21681071-21681071	skin	malignant_melanoma	Substitution - Missense
c.382G>A; p.E128K; 13:21701190-21701190	skin	malignant_melanoma	Substitution - Missense
c.382G>A; p.E128K; 13:21701190-21701190	skin; mucosal	malignant_melanoma	Substitution - Missense

The somatic mutations from COSMIC database