Entrez Gene

Basic Information
Gene ID	5074
Name	PAWR

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.419C>T; p.S140L; 12:79689826-79689826	kidney	carcinoma; papillary_renal_cell_carcinoma	Substitution - Missense
c.139A>G; p.S47G; 12:79690106-79690106	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.489C>T; p.T163T; 12:79689756-79689756	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.71A>G; p.K24R; 12:79690174-79690174	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.863G>A; p.R288K; 12:79594402-79594402	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.913G>A; p.E305K; 12:79594352-79594352	skin; trunk	malignant_melanoma	Substitution - Missense
c.439G>A; p.G147S; 12:79689806-79689806	ovary	other; neoplasm	Substitution - Missense
c.597T>G; p.I199M; 12:79621127-79621127	thyroid	other; neoplasm	Substitution - Missense
c.809delA; p.K270fs*10; 12:79596533-79596533	large_intestine; colon	carcinoma; adenocarcinoma	Deletion - Frameshift
c.937-2A>G; p.?; 12:79592695-79592695	oesophagus; lower_third	carcinoma; squamous_cell_carcinoma	Unknown
c.798C>T; p.S266S; 12:79596544-79596544	breast	carcinoma	Substitution - coding silent
c.728G>A; p.R243Q; 12:79596614-79596614	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.728G>A; p.R243Q; 12:79596614-79596614	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.728G>A; p.R243Q; 12:79596614-79596614	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.728G>A; p.R243Q; 12:79596614-79596614	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.635C>T; p.S212F; 12:79621089-79621089	NS	malignant_melanoma	Substitution - Missense
c.472G>A; p.E158K; 12:79689773-79689773	skin	malignant_melanoma	Substitution - Missense
c.860T>C; p.L287P; 12:79594405-79594405	lung	carcinoma; small_cell_carcinoma	Substitution - Missense
c.940C>T; p.L314L; 12:79592690-79592690	urinary_tract; bladder	carcinoma	Substitution - coding silent
c.410G>C; p.G137A; 12:79689835-79689835	breast	carcinoma	Substitution - Missense
c.916G>T; p.E306*; 12:79594349-79594349	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Nonsense
c.559C>T; p.R187W; 12:79621165-79621165	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.517-1G>A; p.?; 12:79621208-79621208	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Unknown
c.909C>G; p.L303L; 12:79594356-79594356	oesophagus; middle_third	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.561G>A; p.R187R; 12:79621163-79621163	skin	malignant_melanoma	Substitution - coding silent
c.425C>A; p.P142H; 12:79689820-79689820	ovary	carcinoma; serous_carcinoma	Substitution - Missense
c.33C>T; p.G11G; 12:79690212-79690212	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.597T>A; p.I199I; 12:79621127-79621127	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.597T>A; p.I199I; 12:79621127-79621127	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm; acute_myeloid_leukaemia	Substitution - coding silent
c.550C>T; p.Q184*; 12:79621174-79621174	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Nonsense
c.550C>T; p.Q184*; 12:79621174-79621174	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Nonsense
c.460A>T; p.R154W; 12:79689785-79689785	prostate	carcinoma; adenocarcinoma	Substitution - Missense
c.994T>C; p.L332L; 12:79592636-79592636	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.711C>T; p.V237V; 12:79596631-79596631	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.526G>A; p.E176K; 12:79621198-79621198	urinary_tract; bladder	carcinoma	Substitution - Missense
c.526G>A; p.E176K; 12:79621198-79621198	urinary_tract; bladder	carcinoma; transitional_cell_carcinoma	Substitution - Missense
c.403G>C; p.E135Q; 12:79689842-79689842	oesophagus; middle_third	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.722A>G; p.Y241C; 12:79596620-79596620	thyroid	carcinoma	Substitution - Missense

The somatic mutations from COSMIC database