Entrez Gene

Basic Information
Gene ID	10399
Name	GNB2L1

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.170G>T; p.R57L; 5:181242285-181242285	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.470C>T; p.S157L; 5:181239542-181239542	skin; scalp	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.340T>G; p.S114A; 5:181241581-181241581	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - Missense
c.327G>A; p.L109L; 5:181241594-181241594	skin	malignant_melanoma	Substitution - coding silent
c.107G>C; p.R36P; 5:181243694-181243694	oesophagus	carcinoma; adenocarcinoma	Substitution - Missense
c.74_75insC; p.Q26fs*13; 5:181243726-181243727	large_intestine; colon	carcinoma; adenocarcinoma	Insertion - Frameshift
c.240A>G; p.S80S; 5:181242215-181242215	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.240A>G; p.S80S; 5:181242215-181242215	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.348C>T; p.D116D; 5:181241573-181241573	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.712G>A; p.A238T; 5:181238164-181238164	ovary	other; neoplasm	Substitution - Missense
c.712G>A; p.A238T; 5:181238164-181238164	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.342_344delCTC; p.S115delS; 5:181241577-181241579	large_intestine; colon	carcinoma; adenocarcinoma	Deletion - In frame
c.342_344delCTC; p.S115delS; 5:181241577-181241579	large_intestine	carcinoma; adenocarcinoma	Deletion - In frame
c.908C>T; p.T303M; 5:181237023-181237023	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.600C>T; p.V200V; 5:181239103-181239103	skin	malignant_melanoma	Substitution - coding silent
c.357G>T; p.Q119H; 5:181241564-181241564	breast	carcinoma	Substitution - Missense
c.224G>A; p.G75D; 5:181242231-181242231	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.637-4C>T; p.?; 5:181238243-181238243	skin	malignant_melanoma	Unknown
c.637-4C>T; p.?; 5:181238243-181238243	skin	malignant_melanoma	Unknown
c.495C>T; p.I165I; 5:181239517-181239517	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.299G>T; p.R100L; 5:181241622-181241622	skin	malignant_melanoma	Substitution - Missense
c.22C>T; p.R8C; 5:181243779-181243779	central_nervous_system; brainstem	glioma; astrocytoma_Grade_II	Substitution - Missense
c.373C>T; p.R125*; 5:181241548-181241548	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Nonsense
c.373C>T; p.R125*; 5:181241548-181241548	skin; scalp	carcinoma; squamous_cell_carcinoma	Substitution - Nonsense
c.749C>T; p.A250V; 5:181238127-181238127	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.616C>T; p.L206F; 5:181239087-181239087	upper_aerodigestive_tract; mouth	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.260T>G; p.L87R; 5:181242195-181242195	breast	carcinoma	Substitution - Missense
c.396G>A; p.W132*; 5:181241525-181241525	skin	malignant_melanoma	Substitution - Nonsense
c.462C>G; p.V154V; 5:181239550-181239550	lung	carcinoma; adenocarcinoma	Substitution - coding silent
c.283G>A; p.G95S; 5:181241638-181241638	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.594G>A; p.V198V; 5:181239109-181239109	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.784G>C; p.E262Q; 5:181237713-181237713	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.838A>G; p.K280E; 5:181237659-181237659	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.352C>T; p.R118W; 5:181241569-181241569	oesophagus; middle_third	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.733C>T; p.R245C; 5:181238143-181238143	skin	malignant_melanoma	Substitution - Missense
c.889-2A>C; p.?; 5:181237044-181237044	pancreas	carcinoma; acinar_carcinoma	Unknown
c.821T>G; p.V274G; 5:181237676-181237676	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.327G>C; p.L109L; 5:181241594-181241594	urinary_tract; bladder	carcinoma	Substitution - coding silent
c.435G>A; p.E145E; 5:181239577-181239577	breast	carcinoma	Substitution - coding silent
c.281C>T; p.T94M; 5:181242174-181242174	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.438C>A; p.S146R; 5:181239574-181239574	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.635A>G; p.K212R; 5:181239068-181239068	oesophagus	carcinoma; adenocarcinoma	Substitution - Missense
c.425T>C; p.V142A; 5:181241496-181241496	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.425T>C; p.V142A; 5:181241496-181241496	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.774C>A; p.I258I; 5:181238102-181238102	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.735C>G; p.R245R; 5:181238141-181238141	breast	carcinoma	Substitution - coding silent

The somatic mutations from COSMIC database