Entrez Gene

Basic Information
Gene ID	8742
Name	TNFSF12

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.268C>T; p.R90W; 17:7550180-7550180	breast	carcinoma	Substitution - Missense
c.414C>G; p.I138M; 17:7556818-7556818	breast	carcinoma	Substitution - Missense
c.269G>A; p.R90Q; 17:7550181-7550181	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.234C>A; p.S78R; 17:7550146-7550146	autonomic_ganglia	neuroblastoma	Substitution - Missense
c.569G>C; p.R190P; 17:7557169-7557169	prostate	carcinoma; adenocarcinoma	Substitution - Missense
c.568C>T; p.R190C; 17:7557168-7557168	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.374-5T>C; p.?; 17:7556773-7556773	ovary	other; neoplasm	Unknown
c.392G>A; p.S131N; 17:7556796-7556796	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - Missense
c.720C>A; p.L240L; 17:7557320-7557320	urinary_tract; bladder	carcinoma	Substitution - coding silent
c.674G>A; p.R225Q; 17:7557274-7557274	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.438C>T; p.Y146Y; 17:7556842-7556842	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.401A>G; p.E134G; 17:7556805-7556805	breast	carcinoma	Substitution - Missense
c.707C>T; p.A236V; 17:7557307-7557307	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.425G>A; p.S142N; 17:7556829-7556829	skin	malignant_melanoma	Substitution - Missense
c.289A>T; p.K97*; 17:7550804-7550804	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Nonsense
c.743T>C; p.V248A; 17:7557343-7557343	prostate	carcinoma	Substitution - Missense
c.347G>A; p.R116Q; 17:7550952-7550952	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.219C>T; p.P73P; 17:7550131-7550131	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.488T>C; p.L163P; 17:7556892-7556892	large_intestine; colon	carcinoma	Substitution - Missense
c.640G>A; p.G214S; 17:7557240-7557240	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.730G>A; p.G244R; 17:7557330-7557330	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.516G>A; p.G172G; 17:7557116-7557116	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - coding silent
c.600G>C; p.A200A; 17:7557200-7557200	liver	carcinoma; hepatocellular_carcinoma	Substitution - coding silent
c.600G>C; p.A200A; 17:7557200-7557200	upper_aerodigestive_tract; mouth	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.600G>C; p.A200A; 17:7557200-7557200	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.600G>C; p.A200A; 17:7557200-7557200	liver	carcinoma; hepatocellular_carcinoma	Substitution - coding silent
c.600G>C; p.A200A; 17:7557200-7557200	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.600G>C; p.A200A; 17:7557200-7557200	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm; acute_myeloid_leukaemia	Substitution - coding silent
c.600G>C; p.A200A; 17:7557200-7557200	liver	carcinoma; hepatocellular_carcinoma	Substitution - coding silent
c.600G>C; p.A200A; 17:7557200-7557200	thyroid	other; neoplasm	Substitution - coding silent
c.569G>A; p.R190H; 17:7557169-7557169	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.623G>A; p.R208H; 17:7557223-7557223	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.697C>A; p.H233N; 17:7557297-7557297	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.514G>A; p.G172R; 17:7557114-7557114	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.276C>A; p.R92R; 17:7550188-7550188	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.276C>A; p.R92R; 17:7550188-7550188	thyroid	other; neoplasm	Substitution - coding silent
c.202C>G; p.P68A; 17:7549516-7549516	central_nervous_system; brain	primitive_neuroectodermal_tumour-medulloblastoma	Substitution - Missense

The somatic mutations from COSMIC database