Entrez Gene

Basic Information
Gene ID	6477
Name	SIAH1

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.714G>A; p.A238A; 16:48361715-48361715	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.231C>T; p.G77G; 16:48362198-48362198	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.231C>T; p.G77G; 16:48362198-48362198	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.718C>T; p.P240S; 16:48361711-48361711	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.361T>A; p.C121S; 16:48362068-48362068	skin	malignant_melanoma	Substitution - Missense
c.242C>A; p.S81Y; 16:48362187-48362187	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.370A>C; p.R124R; 16:48362059-48362059	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.600T>C; p.D200D; 16:48361829-48361829	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.451C>G; p.Q151E; 16:48361978-48361978	lung	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.741T>G; p.I247M; 16:48361688-48361688	liver	carcinoma; hepatocellular_carcinoma	Substitution - Missense
c.226C>T; p.R76W; 16:48362203-48362203	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.713C>T; p.A238V; 16:48361716-48361716	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.443T>A; p.L148Q; 16:48361986-48361986	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.9T>C; p.R3R; 16:48362420-48362420	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.693G>A; p.R231R; 16:48361736-48361736	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.494T>C; p.F165S; 16:48361935-48361935	autonomic_ganglia	neuroblastoma	Substitution - Missense
c.39C>G; p.T13T; 16:48362390-48362390	ovary	carcinoma; serous_carcinoma	Substitution - coding silent
c.10C>T; p.Q4*; 16:48362419-48362419	breast	carcinoma	Substitution - Nonsense
c.472C>A; p.L158I; 16:48361957-48361957	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.221C>T; p.T74I; 16:48362208-48362208	oesophagus	carcinoma; adenocarcinoma	Substitution - Missense
c.664G>A; p.A222T; 16:48361765-48361765	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.85A>G; p.T29A; 16:48362344-48362344	breast	carcinoma	Substitution - Missense
c.435G>A; p.M145I; 16:48361994-48361994	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.570G>A; p.M190I; 16:48361859-48361859	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.42G>A; p.S14S; 16:48362387-48362387	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - coding silent
c.690T>C; p.H230H; 16:48361739-48361739	thyroid	carcinoma	Substitution - coding silent
c.571T>G; p.L191V; 16:48361858-48361858	biliary_tract; gallbladder	carcinoma; adenocarcinoma	Substitution - Missense
c.722G>A; p.R241Q; 16:48361707-48361707	breast	carcinoma	Substitution - Missense
c.514C>G; p.L172V; 16:48361915-48361915	oesophagus; lower_third	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.282A>T; p.V94V; 16:48362147-48362147	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - coding silent
c.282A>T; p.V94V; 16:48362147-48362147	kidney	carcinoma; clear_cell_renal_cell_carcinoma	Substitution - coding silent
c.328C>A; p.P110T; 16:48362101-48362101	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense

The somatic mutations from COSMIC database