Entrez Gene

Basic Information
Gene ID	977
Name	CD151

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.389T>C; p.M130T; 11:837287-837287	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.520G>T; p.E174*; 11:837523-837523	haematopoietic_and_lymphoid_tissue	lymphoid_neoplasm; acute_lymphoblastic_leukaemia	Substitution - Nonsense
c.497A>G; p.D166G; 11:837500-837500	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - Missense
c.277T>C; p.Y93H; 11:836769-836769	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.636G>T; p.L212F; 11:837962-837962	thyroid	other; neoplasm	Substitution - Missense
c.603C>G; p.I201M; 11:837606-837606	central_nervous_system; brain	glioma	Substitution - Missense
c.331G>A; p.A111T; 11:836823-836823	skin	malignant_melanoma	Substitution - Missense
c.627C>T; p.I209I; 11:837953-837953	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.551G>A; p.C184Y; 11:837554-837554	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.596C>T; p.S199F; 11:837599-837599	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.349C>G; p.Q117E; 11:836841-836841	pancreas	carcinoma	Substitution - Missense
c.699_702+6delGCAGGTGAGG; p.?; 11:838025-838034	large_intestine	carcinoma; adenocarcinoma	Unknown
c.757T>C; p.Y253H; 11:838187-838187	breast	carcinoma	Substitution - Missense
c.533delG; p.R178fs*43; 11:837536-837536	large_intestine; colon	carcinoma; adenocarcinoma	Deletion - Frameshift
c.285C>T; p.I95I; 11:836777-836777	upper_aerodigestive_tract; pharynx	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.122C>T; p.T41M; 11:836288-836288	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.510C>T; p.I170I; 11:837513-837513	skin	malignant_melanoma	Substitution - coding silent
c.634T>C; p.L212L; 11:837960-837960	thyroid	other; neoplasm	Substitution - coding silent
c.717C>A; p.I239I; 11:838147-838147	breast	carcinoma	Substitution - coding silent
c.575_576GT>AA; p.C192*; 11:837578-837579	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Nonsense
c.744C>G; p.L248L; 11:838174-838174	urinary_tract; bladder	carcinoma	Substitution - coding silent
c.744C>G; p.L248L; 11:838174-838174	urinary_tract; bladder	carcinoma; transitional_cell_carcinoma	Substitution - coding silent
c.540delC; p.P181fs*40; 11:837543-837543	large_intestine; colon	carcinoma; adenocarcinoma	Deletion - Frameshift
c.695G>T; p.C232F; 11:838021-838021	lung; left_upper_lobe	carcinoma; adenocarcinoma	Substitution - Missense
c.399C>T; p.R133R; 11:837297-837297	bone; extraskeletal	Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour	Substitution - coding silent
c.479A>G; p.N160S; 11:837482-837482	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.645C>A; p.F215L; 11:837971-837971	breast	carcinoma	Substitution - Missense
c.684C>T; p.I228I; 11:838010-838010	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - coding silent
c.703-3C>T; p.?; 11:838130-838130	oesophagus; lower_third	carcinoma; adenocarcinoma	Unknown
c.526G>A; p.G176S; 11:837529-837529	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.561G>A; p.T187T; 11:837564-837564	upper_aerodigestive_tract; mouth	carcinoma	Substitution - coding silent
c.561G>A; p.T187T; 11:837564-837564	upper_aerodigestive_tract; mouth	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.377T>C; p.L126P; 11:837275-837275	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.94C>A; p.L32M; 11:836260-836260	adrenal_gland; adrenal_gland	adrenal_cortical_carcinoma; functioning	Substitution - Missense

The somatic mutations from COSMIC database