Entrez Gene

Basic Information
Gene ID	7039
Name	TGFA

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.56C>T; p.A19V; 2:70514897-70514897	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Missense
c.56C>T; p.A19V; 2:70514897-70514897	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.56C>T; p.A19V; 2:70514897-70514897	kidney	carcinoma; papillary_renal_cell_carcinoma	Substitution - Missense
c.480C>T; p.V160V; 2:70450862-70450862	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.480C>T; p.V160V; 2:70450862-70450862	haematopoietic_and_lymphoid_tissue	lymphoid_neoplasm; plasma_cell_myeloma	Substitution - coding silent
c.266C>T; p.A89V; 2:70456438-70456438	skin	malignant_melanoma	Substitution - Missense
c.47T>C; p.V16A; 2:70514906-70514906	autonomic_ganglia	neuroblastoma	Substitution - Missense
c.47T>C; p.V16A; 2:70514906-70514906	autonomic_ganglia	neuroblastoma	Substitution - Missense
c.268G>A; p.V90M; 2:70456436-70456436	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Missense
c.268G>A; p.V90M; 2:70456436-70456436	prostate	carcinoma	Substitution - Missense
c.149C>T; p.S50F; 2:70465682-70465682	skin	malignant_melanoma	Substitution - Missense
c.366-1_376delGCTGCTGCCAGG; p.?; 2:70453317-70453328	skin	malignant_melanoma	Unknown
c.57G>A; p.A19A; 2:70514896-70514896	upper_aerodigestive_tract; mouth	carcinoma	Substitution - coding silent
c.57G>A; p.A19A; 2:70514896-70514896	upper_aerodigestive_tract; mouth	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.247G>A; p.E83K; 2:70456457-70456457	skin	malignant_melanoma	Substitution - Missense
c.208G>T; p.A70S; 2:70465623-70465623	ovary	other; neoplasm	Substitution - Missense
c.320C>T; p.S107F; 2:70456384-70456384	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.320C>T; p.S107F; 2:70456384-70456384	skin	malignant_melanoma	Substitution - Missense
c.4G>T; p.V2F; 2:70553764-70553764	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.398G>C; p.C133S; 2:70453295-70453295	urinary_tract; bladder	carcinoma	Substitution - Missense
c.398G>C; p.C133S; 2:70453295-70453295	urinary_tract; bladder	carcinoma; transitional_cell_carcinoma	Substitution - Missense
c.351A>G; p.T117T; 2:70456353-70456353	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.351A>G; p.T117T; 2:70456353-70456353	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.425A>C; p.K142T; 2:70453268-70453268	oesophagus; lower_third	carcinoma; adenocarcinoma	Substitution - Missense
c.379C>T; p.R127*; 2:70453314-70453314	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Nonsense
c.379C>T; p.R127*; 2:70453314-70453314	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Nonsense
c.73A>G; p.N25D; 2:70514880-70514880	breast	carcinoma	Substitution - Missense
c.236G>A; p.G79D; 2:70456468-70456468	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.14C>T; p.A5V; 2:70553754-70553754	thyroid	other; neoplasm	Substitution - Missense
c.85C>T; p.P29S; 2:70514868-70514868	skin	malignant_melanoma	Substitution - Missense
c.86C>T; p.P29L; 2:70514867-70514867	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.335C>T; p.A112V; 2:70456369-70456369	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.468A>G; p.S156S; 2:70453225-70453225	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.436C>T; p.L146F; 2:70453257-70453257	skin	malignant_melanoma	Substitution - Missense
c.429C>T; p.P143P; 2:70453264-70453264	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.106G>A; p.V36M; 2:70465725-70465725	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.309G>A; p.L103L; 2:70456395-70456395	liver	carcinoma	Substitution - coding silent
c.309G>A; p.L103L; 2:70456395-70456395	liver	carcinoma	Substitution - coding silent
c.401G>A; p.R134Q; 2:70453292-70453292	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.401G>A; p.R134Q; 2:70453292-70453292	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.459C>T; p.C153C; 2:70453234-70453234	prostate	carcinoma; adenocarcinoma	Substitution - coding silent
c.84C>T; p.S28S; 2:70514869-70514869	skin	malignant_melanoma	Substitution - coding silent
c.453C>T; p.T151T; 2:70453240-70453240	lung	carcinoma; adenocarcinoma	Substitution - coding silent
c.261C>T; p.L87L; 2:70456443-70456443	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.62A>G; p.Q21R; 2:70514891-70514891	central_nervous_system; brain	glioma; astrocytoma_Grade_IV	Substitution - Missense

The somatic mutations from COSMIC database