Entrez Gene

Basic Information
Gene ID	3976
Name	LIF

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.213G>A; p.G71G; 22:30244047-30244047	skin	malignant_melanoma	Substitution - coding silent
c.518C>T; p.S173L; 22:30243742-30243742	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.518C>T; p.S173L; 22:30243742-30243742	skin	malignant_melanoma	Substitution - Missense
c.290C>T; p.T97M; 22:30243970-30243970	skin	malignant_melanoma	Substitution - Missense
c.290C>T; p.T97M; 22:30243970-30243970	kidney	carcinoma; renal_cell_carcinoma	Substitution - Missense
c.579G>A; p.Q193Q; 22:30243681-30243681	skin	malignant_melanoma	Substitution - coding silent
c.376C>T; p.L126F; 22:30243884-30243884	skin; face	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.543G>A; p.K181K; 22:30243717-30243717	skin	malignant_melanoma	Substitution - coding silent
c.20-1G>A; p.?; 22:30244934-30244934	skin; scalp	carcinoma; squamous_cell_carcinoma	Unknown
c.291G>A; p.T97T; 22:30243969-30243969	skin	malignant_melanoma	Substitution - coding silent
c.225C>A; p.P75P; 22:30244035-30244035	lung	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.503A>G; p.Y168C; 22:30243757-30243757	liver	carcinoma	Substitution - Missense
c.503A>G; p.Y168C; 22:30243757-30243757	liver	carcinoma	Substitution - Missense
c.321C>T; p.R107R; 22:30243939-30243939	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - coding silent
c.214G>A; p.E72K; 22:30244046-30244046	lung	carcinoma; small_cell_carcinoma	Substitution - Missense
c.588C>T; p.A196A; 22:30243672-30243672	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.194T>G; p.L65R; 22:30244759-30244759	upper_aerodigestive_tract; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.271C>T; p.P91S; 22:30243989-30243989	skin	malignant_melanoma	Substitution - Missense
c.169_171GGC>TGT; p.G57C; 22:30244782-30244784	biliary_tract; bile_duct	carcinoma; adenocarcinoma	Substitution - Missense
c.64G>A; p.G22R; 22:30244889-30244889	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.567G>A; p.G189G; 22:30243693-30243693	skin	malignant_melanoma	Substitution - coding silent
c.567G>A; p.G189G; 22:30243693-30243693	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.423C>T; p.A141A; 22:30243837-30243837	breast	carcinoma	Substitution - coding silent
c.421G>A; p.A141T; 22:30243839-30243839	oesophagus	carcinoma; adenocarcinoma	Substitution - Missense
c.421G>A; p.A141T; 22:30243839-30243839	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.102T>G; p.C34W; 22:30244851-30244851	breast	carcinoma	Substitution - Missense
c.565G>T; p.G189W; 22:30243695-30243695	prostate	carcinoma; adenocarcinoma	Substitution - Missense
c.434G>A; p.R145Q; 22:30243826-30243826	skin; extremity	malignant_melanoma	Substitution - Missense
c.75C>T; p.L25L; 22:30244878-30244878	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.451G>A; p.V151M; 22:30243809-30243809	breast	carcinoma	Substitution - Missense
c.54A>G; p.K18K; 22:30244899-30244899	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.269C>T; p.P90L; 22:30243991-30243991	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.601G>A; p.A201T; 22:30243659-30243659	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.506G>A; p.G169D; 22:30243754-30243754	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.514A>T; p.T172S; 22:30243746-30243746	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense

The somatic mutations from COSMIC database