Entrez Gene

Basic Information
Gene ID	51280
Name	GOLM1

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.8G>T; p.G3V; 9:86079313-86079313	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.331A>T; p.T111S; 9:86052570-86052570	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.393C>T; p.Y131Y; 9:86046544-86046544	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.164G>A; p.R55K; 9:86077557-86077557	skin	malignant_melanoma	Substitution - Missense
c.26G>A; p.R9H; 9:86079295-86079295	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.26G>A; p.R9H; 9:86079295-86079295	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.26G>A; p.R9H; 9:86079295-86079295	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.26G>A; p.R9H; 9:86079295-86079295	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.141G>A; p.M47I; 9:86077580-86077580	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.113G>A; p.R38Q; 9:86079208-86079208	breast	carcinoma	Substitution - Missense
c.1199C>A; p.T400K; 9:86027824-86027824	liver	carcinoma; hepatocellular_carcinoma	Substitution - Missense
c.634G>A; p.A212T; 9:86036471-86036471	oesophagus	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.395G>C; p.G132A; 9:86046542-86046542	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.815A>G; p.Q272R; 9:86035568-86035568	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.352C>T; p.R118*; 9:86052549-86052549	skin	malignant_melanoma	Substitution - Nonsense
c.300G>A; p.Q100Q; 9:86077421-86077421	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.456C>A; p.F152L; 9:86046481-86046481	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.740A>C; p.K247T; 9:86036365-86036365	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.1183G>A; p.E395K; 9:86027840-86027840	upper_aerodigestive_tract; mouth	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.1183G>A; p.E395K; 9:86027840-86027840	upper_aerodigestive_tract; mouth	carcinoma	Substitution - Missense
c.813G>A; p.P271P; 9:86035570-86035570	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.1180C>T; p.R394C; 9:86027843-86027843	haematopoietic_and_lymphoid_tissue	lymphoid_neoplasm; hairy_cell_leukaemia	Substitution - Missense
c.909G>A; p.Q303Q; 9:86035474-86035474	breast	carcinoma	Substitution - coding silent
c.177G>A; p.E59E; 9:86077544-86077544	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - coding silent
c.978C>T; p.P326P; 9:86035405-86035405	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.590_591delGA; p.R197fs*8; 9:86040745-86040746	large_intestine; caecum	carcinoma; adenocarcinoma	Deletion - Frameshift
c.1040_1042delGAG; p.G347delG; 9:86033369-86033371	large_intestine; colon	carcinoma; adenocarcinoma	Deletion - In frame
c.1040_1042delGAG; p.G347delG; 9:86033369-86033371	large_intestine; rectum	carcinoma; adenocarcinoma	Deletion - In frame
c.741G>T; p.K247N; 9:86036364-86036364	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.141G>T; p.M47I; 9:86077580-86077580	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.68C>T; p.A23V; 9:86079253-86079253	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.906G>A; p.V302V; 9:86035477-86035477	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.582C>T; p.N194N; 9:86040754-86040754	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.364+10G>A; p.?; 9:86052527-86052527	stomach	adenocarcinoma	Unknown
c.46C>T; p.L16F; 9:86079275-86079275	skin	malignant_melanoma	Substitution - Missense
c.378C>T; p.T126T; 9:86046559-86046559	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.650A>G; p.H217R; 9:86036455-86036455	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.871_872GG>AA; p.G291K; 9:86035511-86035512	skin; face	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.650A>G; p.H217R; 9:86036455-86036455	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm; acute_myeloid_leukaemia	Substitution - Missense
c.124C>G; p.L42V; 9:86079197-86079197	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm; acute_myeloid_leukaemia	Substitution - Missense
c.995A>T; p.E332V; 9:86035388-86035388	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.702G>A; p.Q234Q; 9:86036403-86036403	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.630G>A; p.L210L; 9:86036475-86036475	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - coding silent
c.982G>A; p.G328R; 9:86035401-86035401	skin	malignant_melanoma	Substitution - Missense
c.539_540insT; p.K180fs*4; 9:86040796-86040797	large_intestine; colon	carcinoma; adenocarcinoma	Insertion - Frameshift
c.57C>A; p.A19A; 9:86079264-86079264	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.252C>G; p.I84M; 9:86077469-86077469	liver	carcinoma; hepatocellular_carcinoma	Substitution - Missense
c.944_962del19; p.M315fs*25; 9:86035421-86035439	large_intestine; colon	carcinoma; adenocarcinoma	Deletion - Frameshift
c.389A>T; p.N130I; 9:86046548-86046548	skin	malignant_melanoma	Substitution - Missense
c.1082A>G; p.E361G; 9:86033329-86033329	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.42G>A; p.P14P; 9:86079279-86079279	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.942G>T; p.E314D; 9:86035441-86035441	adrenal_gland; adrenal_gland	adrenal_cortical_carcinoma; functioning	Substitution - Missense
c.304G>A; p.E102K; 9:86077417-86077417	skin	malignant_melanoma	Substitution - Missense
c.252C>T; p.I84I; 9:86077469-86077469	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.875G>C; p.G292A; 9:86035508-86035508	pancreas	carcinoma; adenocarcinoma	Substitution - Missense
c.1189C>T; p.R397W; 9:86027834-86027834	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.1033C>T; p.L345L; 9:86033378-86033378	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - coding silent
c.517C>A; p.R173R; 9:86040819-86040819	lung	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.328A>C; p.I110L; 9:86052573-86052573	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.827G>T; p.R276L; 9:86035556-86035556	upper_aerodigestive_tract; mouth	carcinoma	Substitution - Missense
c.827G>T; p.R276L; 9:86035556-86035556	upper_aerodigestive_tract; mouth	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.256T>C; p.S86P; 9:86077465-86077465	thyroid	other; neoplasm	Substitution - Missense
c.1005T>C; p.A335A; 9:86035378-86035378	prostate	carcinoma; adenocarcinoma	Substitution - coding silent
c.161G>A; p.R54H; 9:86077560-86077560	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.311C>T; p.A104V; 9:86052590-86052590	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.1185A>C; p.E395D; 9:86027838-86027838	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.186C>T; p.A62A; 9:86077535-86077535	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.668G>A; p.G223E; 9:86036437-86036437	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.668G>A; p.G223E; 9:86036437-86036437	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.211C>T; p.Q71*; 9:86077510-86077510	skin	malignant_melanoma	Substitution - Nonsense
c.630G>T; p.L210L; 9:86036475-86036475	lung	carcinoma; adenocarcinoma	Substitution - coding silent
c.994G>T; p.E332*; 9:86035389-86035389	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Nonsense
c.342G>C; p.E114D; 9:86052559-86052559	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - Missense

The somatic mutations from COSMIC database