Entrez Gene

Basic Information
Gene ID	3927
Name	LASP1

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.484C>T; p.H162Y; 17:38914451-38914451	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.357C>T; p.N119N; 17:38898519-38898519	thyroid	other; neoplasm	Substitution - coding silent
c.357C>T; p.N119N; 17:38898519-38898519	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.711C>T; p.D237D; 17:38918703-38918703	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.711C>T; p.D237D; 17:38918703-38918703	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - coding silent
c.728C>T; p.T243M; 17:38918720-38918720	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.247C>T; p.Q83*; 17:38890502-38890502	urinary_tract; bladder	carcinoma	Substitution - Nonsense
c.717G>C; p.W239C; 17:38918709-38918709	oesophagus	carcinoma; adenocarcinoma	Substitution - Missense
c.719T>A; p.M240K; 17:38918711-38918711	liver	carcinoma	Substitution - Missense
c.539C>T; p.A180V; 17:38915073-38915073	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.188C>G; p.T63S; 17:38890443-38890443	thyroid	other; neoplasm	Substitution - Missense
c.756G>T; p.M252I; 17:38918748-38918748	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.469G>A; p.E157K; 17:38914436-38914436	pancreas	carcinoma	Substitution - Missense
c.191T>C; p.M64T; 17:38890446-38890446	thyroid	other; neoplasm	Substitution - Missense
c.649G>A; p.D217N; 17:38918641-38918641	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.438A>G; p.S146S; 17:38914405-38914405	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.438A>G; p.S146S; 17:38914405-38914405	breast	carcinoma	Substitution - coding silent
c.438A>G; p.S146S; 17:38914405-38914405	breast	carcinoma	Substitution - coding silent
c.438A>G; p.S146S; 17:38914405-38914405	thyroid	other; neoplasm	Substitution - coding silent
c.438A>G; p.S146S; 17:38914405-38914405	thyroid	other; neoplasm	Substitution - coding silent
c.626C>T; p.A209V; 17:38918618-38918618	lung	carcinoma; small_cell_carcinoma	Substitution - Missense
c.34G>A; p.V12M; 17:38870223-38870223	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.493C>T; p.P165S; 17:38914460-38914460	skin	malignant_melanoma	Substitution - Missense
c.326G>A; p.R109K; 17:38898488-38898488	breast	carcinoma	Substitution - Missense
c.616C>T; p.R206W; 17:38918608-38918608	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.189C>A; p.T63T; 17:38890444-38890444	thyroid	other; neoplasm	Substitution - coding silent
c.296G>T; p.S99I; 17:38898458-38898458	upper_aerodigestive_tract; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.658G>T; p.E220*; 17:38918650-38918650	prostate	carcinoma; adenocarcinoma	Substitution - Nonsense
c.694G>A; p.V232M; 17:38918686-38918686	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.190A>T; p.M64L; 17:38890445-38890445	thyroid	other; neoplasm	Substitution - Missense
c.418G>C; p.E140Q; 17:38914385-38914385	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.262G>C; p.E88Q; 17:38898424-38898424	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.621C>T; p.Y207Y; 17:38918613-38918613	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.675C>T; p.D225D; 17:38918667-38918667	liver	carcinoma	Substitution - coding silent
c.675C>T; p.D225D; 17:38918667-38918667	liver	carcinoma	Substitution - coding silent
c.622C>T; p.R208C; 17:38918614-38918614	ovary	other; neoplasm	Substitution - Missense
c.762G>A; p.P254P; 17:38918754-38918754	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.402C>G; p.S134R; 17:38914369-38914369	lung; right_upper_lobe	carcinoma; adenocarcinoma	Substitution - Missense
c.239T>C; p.L80P; 17:38890494-38890494	ovary	other; neoplasm	Substitution - Missense
c.239T>C; p.L80P; 17:38890494-38890494	ovary	other; neoplasm	Substitution - Missense
c.164C>T; p.A55V; 17:38878180-38878180	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.164C>T; p.A55V; 17:38878180-38878180	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.650A>C; p.D217A; 17:38918642-38918642	breast	carcinoma	Substitution - Missense
c.19C>G; p.R7G; 17:38870208-38870208	urinary_tract; bladder	carcinoma	Substitution - Missense
c.609C>T; p.G203G; 17:38915143-38915143	urinary_tract; bladder	carcinoma; transitional_cell_carcinoma	Substitution - coding silent
c.508G>A; p.V170I; 17:38914475-38914475	kidney	carcinoma; papillary_renal_cell_carcinoma	Substitution - Missense
c.609C>T; p.G203G; 17:38915143-38915143	urinary_tract; bladder	carcinoma	Substitution - coding silent
c.394G>T; p.G132C; 17:38914361-38914361	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.771C>T; p.Y257Y; 17:38918763-38918763	bone; femur	Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour	Substitution - coding silent
c.114A>G; p.T38T; 17:38878130-38878130	lung	carcinoma; adenocarcinoma	Substitution - coding silent
c.538G>T; p.A180S; 17:38915072-38915072	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.687C>T; p.I229I; 17:38918679-38918679	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm; acute_myeloid_leukaemia	Substitution - coding silent
c.19C>T; p.R7W; 17:38870208-38870208	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.60T>A; p.C20*; 17:38870249-38870249	liver	carcinoma	Substitution - Nonsense
c.60T>A; p.C20*; 17:38870249-38870249	liver	carcinoma	Substitution - Nonsense
c.693C>T; p.N231N; 17:38918685-38918685	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent

The somatic mutations from COSMIC database