Entrez Gene

Basic Information
Gene ID	6997
Name	TDGF1

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.162G>A; p.Q54Q; 3:46579305-46579305	skin	malignant_melanoma	Substitution - coding silent
c.292C>A; p.P98T; 3:46579807-46579807	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.321G>A; p.E107E; 3:46579836-46579836	bone; extraskeletal	Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour	Substitution - coding silent
c.77G>C; p.G26A; 3:46579136-46579136	cervix	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.75G>A; p.L25L; 3:46579134-46579134	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - coding silent
c.75G>A; p.L25L; 3:46579134-46579134	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - coding silent
c.77G>A; p.G26E; 3:46579136-46579136	breast	carcinoma	Substitution - Missense
c.355C>T; p.P119S; 3:46579967-46579967	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.66C>A; p.V22V; 3:46579125-46579125	endometrium	carcinoma; endometrioid_carcinoma	Substitution - coding silent
c.496C>T; p.L166L; 3:46581179-46581179	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.122G>A; p.R41Q; 3:46579265-46579265	bone	Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour	Substitution - Missense
c.291C>A; p.C97*; 3:46579806-46579806	ovary	carcinoma; serous_carcinoma	Substitution - Nonsense
c.263C>A; p.T88N; 3:46579778-46579778	prostate	adenoma	Substitution - Missense
c.260G>A; p.G87E; 3:46579775-46579775	cervix	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.256G>T; p.G86W; 3:46579771-46579771	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.39G>A; p.V13V; 3:46579098-46579098	skin	malignant_melanoma	Substitution - coding silent
c.406G>A; p.G136S; 3:46580018-46580018	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.560A>G; p.Y187C; 3:46581243-46581243	skin	malignant_melanoma	Substitution - Missense
c.442G>A; p.G148S; 3:46580054-46580054	urinary_tract; bladder	carcinoma	Substitution - Missense
c.274G>A; p.G92R; 3:46579789-46579789	skin	malignant_melanoma	Substitution - Missense
c.125G>A; p.G42E; 3:46579268-46579268	skin	malignant_melanoma	Substitution - Missense
c.89-1G>A; p.?; 3:46579231-46579231	skin	malignant_melanoma	Unknown
c.191C>T; p.S64F; 3:46579334-46579334	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.312G>A; p.R104R; 3:46579827-46579827	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.312G>A; p.R104R; 3:46579827-46579827	skin	malignant_melanoma	Substitution - coding silent
c.361G>C; p.D121H; 3:46579973-46579973	urinary_tract; bladder	carcinoma	Substitution - Missense
c.49A>G; p.M17V; 3:46579108-46579108	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.259G>A; p.G87R; 3:46579774-46579774	skin	malignant_melanoma	Substitution - Missense
c.278C>T; p.S93F; 3:46579793-46579793	skin	malignant_melanoma	Substitution - Missense
c.528G>T; p.M176I; 3:46581211-46581211	ovary	carcinoma; serous_carcinoma	Substitution - Missense
c.350C>A; p.S117Y; 3:46579962-46579962	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.52G>A; p.A18T; 3:46579111-46579111	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.70G>A; p.E24K; 3:46579129-46579129	skin	malignant_melanoma	Substitution - Missense
c.65T>C; p.V22A; 3:46579124-46579124	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.36-1G>C; p.?; 3:46579094-46579094	lung	carcinoma; adenocarcinoma	Unknown

The somatic mutations from COSMIC database