Entrez Gene

Basic Information
Gene ID	5652
Name	PRSS8

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.957C>A; p.G319G; 16:31132084-31132084	upper_aerodigestive_tract; mouth	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.957C>A; p.G319G; 16:31132084-31132084	upper_aerodigestive_tract; mouth	carcinoma	Substitution - coding silent
c.841A>G; p.I281V; 16:31132200-31132200	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.944C>T; p.A315V; 16:31132097-31132097	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.793C>T; p.R265C; 16:31132248-31132248	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.659_660insATG; p.D220>EC; 16:31132474-31132475	breast	carcinoma	Complex - insertion inframe
c.609C>T; p.C203C; 16:31132525-31132525	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.395A>C; p.Q132P; 16:31132825-31132825	upper_aerodigestive_tract; mouth	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.363C>T; p.I121I; 16:31132857-31132857	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.628A>G; p.K210E; 16:31132506-31132506	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.362T>C; p.I121T; 16:31132858-31132858	kidney	carcinoma; papillary_renal_cell_carcinoma	Substitution - Missense
c.741G>A; p.E247E; 16:31132300-31132300	lung	carcinoma; adenocarcinoma	Substitution - coding silent
c.467C>T; p.P156L; 16:31132753-31132753	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.111C>T; p.C37C; 16:31133381-31133381	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - coding silent
c.696C>T; p.D232D; 16:31132438-31132438	breast	carcinoma	Substitution - coding silent
c.886A>C; p.T296P; 16:31132155-31132155	oesophagus	carcinoma; adenocarcinoma	Substitution - Missense
c.697G>A; p.A233T; 16:31132437-31132437	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.236G>T; p.W79L; 16:31133256-31133256	skin; extremity	malignant_melanoma	Substitution - Missense
c.268G>A; p.E90K; 16:31132952-31132952	skin	malignant_melanoma	Substitution - Missense
c.625G>A; p.A209T; 16:31132509-31132509	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.719delG; p.G240fs*13; 16:31132322-31132322	large_intestine; colon	carcinoma; adenocarcinoma	Deletion - Frameshift
c.216C>A; p.G72G; 16:31133276-31133276	breast	carcinoma	Substitution - coding silent
c.665T>G; p.V222G; 16:31132469-31132469	breast	carcinoma	Substitution - Missense
c.929T>C; p.L310P; 16:31132112-31132112	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.420C>T; p.L140L; 16:31132800-31132800	urinary_tract; bladder	carcinoma	Substitution - coding silent
c.245C>T; p.S82L; 16:31133247-31133247	lung; right_upper_lobe	carcinoma; adenocarcinoma	Substitution - Missense
c.199G>A; p.V67I; 16:31133293-31133293	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.324C>G; p.Y108*; 16:31132896-31132896	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Nonsense
c.156C>T; p.V52V; 16:31133336-31133336	skin	malignant_melanoma	Substitution - coding silent
c.478G>A; p.A160T; 16:31132742-31132742	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.478G>A; p.A160T; 16:31132742-31132742	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.592C>T; p.R198C; 16:31132542-31132542	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.551C>T; p.T184M; 16:31132583-31132583	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.621C>T; p.I207I; 16:31132513-31132513	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.124delC; p.Q42fs*64; 16:31133368-31133368	large_intestine; colon	carcinoma; adenocarcinoma	Deletion - Frameshift
c.124delC; p.Q42fs*64; 16:31133368-31133368	large_intestine	carcinoma; adenocarcinoma	Deletion - Frameshift
c.124delC; p.Q42fs*64; 16:31133368-31133368	large_intestine	carcinoma; adenocarcinoma	Deletion - Frameshift
c.819G>A; p.L273L; 16:31132222-31132222	skin	malignant_melanoma	Substitution - coding silent
c.330G>A; p.E110E; 16:31132890-31132890	skin	malignant_melanoma	Substitution - coding silent
c.73C>T; p.R25W; 16:31135426-31135426	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.871C>T; p.R291C; 16:31132170-31132170	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.335C>T; p.A112V; 16:31132885-31132885	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.883delC; p.Q295fs*27; 16:31132158-31132158	large_intestine; colon	carcinoma; adenocarcinoma	Deletion - Frameshift
c.1016G>A; p.W339*; 16:31132025-31132025	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Nonsense
c.333C>T; p.D111D; 16:31132887-31132887	central_nervous_system; brain	primitive_neuroectodermal_tumour-medulloblastoma	Substitution - coding silent
c.333C>T; p.D111D; 16:31132887-31132887	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.802C>T; p.P268S; 16:31132239-31132239	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense

The somatic mutations from COSMIC database