Entrez Gene

Basic Information
Gene ID	94241
Name	TP53INP1

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.150A>G; p.E50E; 8:94940183-94940183	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.150A>G; p.E50E; 8:94940183-94940183	breast	carcinoma	Substitution - coding silent
c.681C>A; p.G227G; 8:94930521-94930521	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.681C>A; p.G227G; 8:94930521-94930521	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.416C>A; p.P139H; 8:94939917-94939917	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - Missense
c.196T>C; p.F66L; 8:94940137-94940137	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Missense
c.181G>A; p.E61K; 8:94940152-94940152	urinary_tract; bladder	carcinoma	Substitution - Missense
c.276G>T; p.M92I; 8:94940057-94940057	oesophagus	carcinoma; adenocarcinoma	Substitution - Missense
c.189T>C; p.P63P; 8:94940144-94940144	skin	malignant_melanoma	Substitution - coding silent
c.621T>G; p.N207K; 8:94930581-94930581	haematopoietic_and_lymphoid_tissue	lymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma	Substitution - Missense
c.257A>G; p.Q86R; 8:94940076-94940076	liver	carcinoma	Substitution - Missense
c.257A>G; p.Q86R; 8:94940076-94940076	liver	carcinoma; hepatocellular_carcinoma	Substitution - Missense
c.150_152delAGA; p.E52delE; 8:94940181-94940183	skin	malignant_melanoma	Deletion - In frame
c.150_152delAGA; p.E52delE; 8:94940181-94940183	urinary_tract; bladder	carcinoma; transitional_cell_carcinoma	Deletion - In frame
c.150_152delAGA; p.E52delE; 8:94940181-94940183	endometrium	carcinoma; endometrioid_carcinoma	Deletion - In frame
c.150_152delAGA; p.E52delE; 8:94940181-94940183	stomach	carcinoma; intestinal_adenocarcinoma	Deletion - In frame
c.718T>A; p.Y240N; 8:94930484-94930484	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.606G>T; p.Q202H; 8:94930596-94930596	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.137A>C; p.E46A; 8:94940196-94940196	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.605A>G; p.Q202R; 8:94930597-94930597	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.490G>A; p.E164K; 8:94930712-94930712	skin; trunk	malignant_melanoma; nodular	Substitution - Missense
c.211G>A; p.A71T; 8:94940122-94940122	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.73G>C; p.E25Q; 8:94940869-94940869	urinary_tract; bladder	carcinoma	Substitution - Missense
c.139G>A; p.E47K; 8:94940194-94940194	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.628C>T; p.R210C; 8:94930574-94930574	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.654C>T; p.C218C; 8:94930548-94930548	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - coding silent
c.654C>T; p.C218C; 8:94930548-94930548	prostate	carcinoma	Substitution - coding silent
c.461C>A; p.P154Q; 8:94939872-94939872	skin	malignant_melanoma	Substitution - Missense
c.649G>A; p.D217N; 8:94930553-94930553	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.301C>T; p.P101S; 8:94940032-94940032	thyroid	carcinoma	Substitution - Missense
c.389C>G; p.S130C; 8:94939944-94939944	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm; acute_myeloid_leukaemia	Substitution - Missense
c.256C>T; p.Q86*; 8:94940077-94940077	haematopoietic_and_lymphoid_tissue	lymphoid_neoplasm; acute_lymphoblastic_leukaemia	Substitution - Nonsense
c.589G>T; p.E197*; 8:94930613-94930613	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Nonsense
c.69C>A; p.F23L; 8:94940873-94940873	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.256C>G; p.Q86E; 8:94940077-94940077	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.629G>A; p.R210H; 8:94930573-94930573	lung	carcinoma; adenocarcinoma	Substitution - Missense

The somatic mutations from COSMIC database