Entrez Gene

Epithelial-Mesenchymal Transition gene database (dbEMT) Home

General information | Literature | Expression | lncRNA |Regulation | Mutation | Homolog | Interaction

Basic Information
Gene ID	6717
Name	SRI

Mutation (CDS; AA; Chr)	Site	Histology	Mutation Type
The somatic mutations from COSMIC database
c.29G>T; p.G10V; 7:88219998-88219998	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.28G>T; p.G10C; 7:88219999-88219999	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - Missense
c.480C>A; p.I160I; 7:88209370-88209370	bone	Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour	Substitution - coding silent
c.356C>T; p.T119I; 7:88210024-88210024	lung	carcinoma; adenocarcinoma	Substitution - Missense
c.567T>C; p.D189D; 7:88208510-88208510	lung	carcinoma; adenocarcinoma	Substitution - coding silent
c.317G>T; p.R106I; 7:88210063-88210063	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.191C>T; p.A64V; 7:88217136-88217136	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.392C>T; p.T131I; 7:88209988-88209988	liver	carcinoma	Substitution - Missense
c.392C>T; p.T131I; 7:88209988-88209988	liver	carcinoma	Substitution - Missense
c.440G>A; p.R147Q; 7:88209410-88209410	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense
c.327_328insT; p.I110fs*4; 7:88210052-88210053	lung	carcinoma; adenocarcinoma	Insertion - Frameshift
c.226C>T; p.R76W; 7:88210905-88210905	lung	carcinoma; small_cell_carcinoma	Substitution - Missense
c.282A>T; p.E94D; 7:88210098-88210098	large_intestine	carcinoma; adenocarcinoma	Substitution - Missense
c.531T>C; p.D177D; 7:88208546-88208546	pancreas	carcinoma	Substitution - coding silent
c.531T>C; p.D177D; 7:88208546-88208546	pancreas	carcinoma	Substitution - coding silent
c.471C>T; p.D157D; 7:88209379-88209379	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.240A>G; p.S80S; 7:88210891-88210891	stomach	carcinoma; adenocarcinoma	Substitution - coding silent
c.450C>A; p.T150T; 7:88209400-88209400	oesophagus; lower_third	carcinoma; adenocarcinoma	Substitution - coding silent
c.511+1G>T; p.?; 7:88209338-88209338	lung; right_upper_lobe	carcinoma; adenocarcinoma	Unknown
c.389C>A; p.T130K; 7:88209991-88209991	upper_aerodigestive_tract; larynx	carcinoma; squamous_cell_carcinoma	Substitution - Missense
c.111T>C; p.G37G; 7:88218883-88218883	large_intestine; caecum	carcinoma; adenocarcinoma	Substitution - coding silent
c.590G>A; p.S197N; 7:88206485-88206485	ovary	carcinoma; serous_carcinoma	Substitution - Missense
c.279T>C; p.N93N; 7:88210101-88210101	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.271G>A; p.G91S; 7:88210109-88210109	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.18_19ins19; p.P7fs*52; 7:88220008-88220009	stomach	carcinoma; mixed_intestinal_and_diffuse_adenocarcinoma-unclassifiable	Insertion - Frameshift
c.432T>C; p.I144I; 7:88209418-88209418	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - coding silent
c.273T>G; p.G91G; 7:88210107-88210107	breast	carcinoma	Substitution - coding silent
c.8A>G; p.Y3C; 7:88220019-88220019	large_intestine; colon	carcinoma; adenocarcinoma	Substitution - Missense
c.481G>A; p.A161T; 7:88209369-88209369	skin	malignant_melanoma	Substitution - Missense
c.481G>A; p.A161T; 7:88209369-88209369	endometrium	carcinoma; endometrioid_carcinoma	Substitution - Missense
c.469G>A; p.D157N; 7:88209381-88209381	large_intestine; rectum	carcinoma; adenocarcinoma	Substitution - Missense

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