Entrez Gene

Basic Information
Gene ID	1020
Name	CDK5

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.726C>T; p.Y242Y; 7:151054278-151054278	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.510G>A; p.P170P; 7:151055347-151055347	oesophagus; lower_third	carcinoma; adenocarcinoma	Substitution - coding silent
c.543G>A; p.T181T; 7:151055314-151055314	oesophagus	carcinoma; adenocarcinoma	Substitution - coding silent
c.91G>A; p.A31T; 7:151057107-151057107	urinary_tract; bladder	carcinoma	Substitution - Missense
c.217G>A; p.D73N; 7:151056774-151056774	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.875C>T; p.P292L; 7:151054013-151054013	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.68delA; p.N23fs*10; 7:151057130-151057130	skin	malignant_melanoma	Deletion - Frameshift
c.550G>A; p.D184N; 7:151055307-151055307	oesophagus	carcinoma; adenocarcinoma	Substitution - Missense
c.500A>G; p.Y167C; 7:151055357-151055357	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.508C>T; p.P170S; 7:151055349-151055349	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.640A>G; p.R214G; 7:151055037-151055037	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.45C>T; p.Y15Y; 7:151057153-151057153	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.168G>T; p.K56N; 7:151056934-151056934	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.168G>T; p.K56N; 7:151056934-151056934	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.168G>T; p.K56N; 7:151056934-151056934	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.587C>G; p.A196G; 7:151055090-151055090	skin	malignant_melanoma	Substitution - Missense
c.201T>C; p.H67H; 7:151056790-151056790	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.484G>T; p.V162L; 7:151055373-151055373	breast	carcinoma	Substitution - Missense
c.48A>G; p.G16G; 7:151057150-151057150	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.46G>A; p.G16R; 7:151057152-151057152	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Missense
c.599G>A; p.R200Q; 7:151055078-151055078	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.142G>A; p.A48T; 7:151056960-151056960	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.301G>C; p.E101Q; 7:151056591-151056591	breast	carcinoma	Substitution - Missense
c.519C>T; p.L173L; 7:151055338-151055338	skin	malignant_melanoma	Substitution - coding silent
c.719C>T; p.P240L; 7:151054285-151054285	skin	malignant_melanoma	Substitution - Missense
c.149G>A; p.R50Q; 7:151056953-151056953	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.680G>T; p.W227L; 7:151054436-151054436	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.711+9G>T; p.?; 7:151054396-151054396	liver	carcinoma	Unknown
c.611C>T; p.P204L; 7:151055066-151055066	skin	malignant_melanoma	Substitution - Missense
c.404A>G; p.N135S; 7:151055757-151055757	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.547A>T; p.I183F; 7:151055310-151055310	lung; right_upper_lobe	carcinoma; adenocarcinoma	Substitution - Missense
c.669C>T; p.T223T; 7:151054447-151054447	pancreas	carcinoma	Substitution - coding silent
c.669C>T; p.T223T; 7:151054447-151054447	pancreas	carcinoma	Substitution - coding silent
c.867C>T; p.F289F; 7:151054021-151054021	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.31G>T; p.G11W; 7:151057818-151057818	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.148C>T; p.R50W; 7:151056954-151056954	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.358C>T; p.R120C; 7:151055803-151055803	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.662C>T; p.T221M; 7:151054454-151054454	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.294C>T; p.L98L; 7:151056598-151056598	thyroid	carcinoma	Substitution - coding silent
c.413G>A; p.G138E; 7:151055602-151055602	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.413G>A; p.G138E; 7:151055602-151055602	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.413G>A; p.G138E; 7:151055602-151055602	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.615C>T; p.G205G; 7:151055062-151055062	lung	carcinoma; adenocarcinoma	Substitution - coding silent
c.103_104insG; p.V35fs*5; 7:151057094-151057095	large_intestine; colon	carcinoma; adenocarcinoma	Insertion - Frameshift
c.803A>G; p.K268R; 7:151054085-151054085	ovary	other; neoplasm	Substitution - Missense

The somatic mutations from COSMIC database