Entrez Gene

Basic Information
Gene ID	3090
Name	HIC1

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.189C>A; p.L63L; 17:2056879-2056879	kidney	other; neoplasm	Substitution - coding silent
c.303G>A; p.P101P; 17:2056993-2056993	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.1597C>T; p.R533C; 17:2058287-2058287	liver	carcinoma	Substitution - Missense
c.1597C>T; p.R533C; 17:2058287-2058287	liver	carcinoma	Substitution - Missense
c.1732G>A; p.G578S; 17:2058422-2058422	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.277G>A; p.A93T; 17:2056967-2056967	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.274G>A; p.E92K; 17:2056964-2056964	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.1176G>A; p.P392P; 17:2057866-2057866	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.1591A>G; p.M531V; 17:2058281-2058281	liver	carcinoma	Substitution - Missense
c.1681G>A; p.E561K; 17:2058371-2058371	oesophagus	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.990C>T; p.R330R; 17:2057680-2057680	liver	carcinoma; hepatocellular_carcinoma	Substitution - coding silent
c.894_895insC; p.G301fs*7; 17:2057584-2057585	large_intestine; rectum	carcinoma; adenocarcinoma	Insertion - Frameshift
c.1754G>A; p.R585H; 17:2058444-2058444	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.1299G>A; p.L433L; 17:2057989-2057989	lung	carcinoma; adenocarcinoma	Substitution - coding silent
c.1413G>A; p.G471G; 17:2058103-2058103	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.1155T>C; p.G385G; 17:2057845-2057845	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - coding silent
c.84C>T; p.C28C; 17:2056774-2056774	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - coding silent
c.122C>T; p.A41V; 17:2056812-2056812	prostate	carcinoma	Substitution - Missense
c.1175C>T; p.P392L; 17:2057865-2057865	prostate	carcinoma; adenocarcinoma	Substitution - Missense
c.1175C>T; p.P392L; 17:2057865-2057865	prostate	carcinoma; adenocarcinoma	Substitution - Missense
c.1380C>T; p.A460A; 17:2058070-2058070	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - coding silent
c.1380C>T; p.A460A; 17:2058070-2058070	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.1814C>T; p.A605V; 17:2058504-2058504	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.1471G>A; p.A491T; 17:2058161-2058161	liver	carcinoma	Substitution - Missense
c.1471G>A; p.A491T; 17:2058161-2058161	liver	carcinoma	Substitution - Missense
c.1471G>A; p.A491T; 17:2058161-2058161	liver	carcinoma	Substitution - Missense
c.1122C>T; p.G374G; 17:2057812-2057812	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.1122C>T; p.G374G; 17:2057812-2057812	lung	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.1305G>A; p.A435A; 17:2057995-2057995	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.1373C>A; p.A458D; 17:2058063-2058063	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.1373C>A; p.A458D; 17:2058063-2058063	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.278C>T; p.A93V; 17:2056968-2056968	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.1265C>T; p.P422L; 17:2057955-2057955	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.1782C>T; p.H594H; 17:2058472-2058472	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.1309G>A; p.V437M; 17:2057999-2057999	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.1952C>T; p.A651V; 17:2058642-2058642	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.1448A>T; p.E483V; 17:2058138-2058138	pancreas	carcinoma	Substitution - Missense
c.142G>A; p.A48T; 17:2056832-2056832	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.1444G>A; p.G482R; 17:2058134-2058134	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.1672C>T; p.R558C; 17:2058362-2058362	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.1255G>A; p.V419M; 17:2057945-2057945	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.1680G>A; p.T560T; 17:2058370-2058370	skin	malignant_melanoma	Substitution - coding silent
c.1680G>A; p.T560T; 17:2058370-2058370	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.256C>T; p.R86C; 17:2056946-2056946	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.1329delG; p.E444fs*20; 17:2058019-2058019	large_intestine	carcinoma; adenocarcinoma	Deletion - Frameshift
c.1735G>A; p.G579S; 17:2058425-2058425	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.1562G>A; p.C521Y; 17:2058252-2058252	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.2001G>A; p.V667V; 17:2058691-2058691	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - coding silent
c.1705G>A; p.E569K; 17:2058395-2058395	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.1346G>A; p.G449D; 17:2058036-2058036	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.146G>A; p.S49N; 17:2056836-2056836	endometrium	carcinoma; serous_carcinoma	Substitution - Missense
c.1121G>A; p.G374D; 17:2057811-2057811	stomach	carcinoma; adenocarcinoma	Substitution - Missense
c.147C>T; p.S49S; 17:2056837-2056837	large_intestine	carcinoma; adenocarcinoma	Substitution - coding silent
c.1051C>G; p.P351A; 17:2057741-2057741	thyroid	other; neoplasm	Substitution - Missense
c.1564G>A; p.G522R; 17:2058254-2058254	prostate	carcinoma; adenocarcinoma	Substitution - Missense
c.1195G>A; p.G399S; 17:2057885-2057885	skin; head_neck	carcinoma; squamous_cell_carcinoma	Substitution - Missense

The somatic mutations from COSMIC database