| General information | Literature | Expression | lncRNA |Regulation | Mutation | Homolog | Interaction |
Basic Information | |||
|---|---|---|---|
Gene ID | 6591 | ||
Name | SNAI2 | ||
The somatic mutations from COSMIC database | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.213T>C; p.N71N; 8:48920308-48920308 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.453C>G; p.C151W; 8:48920068-48920068 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.61G>A; p.E21K; 8:48921205-48921205 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.8G>A; p.R3H; 8:48921258-48921258 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.8G>A; p.R3H; 8:48921258-48921258 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.292G>T; p.D98Y; 8:48920229-48920229 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.682C>A; p.L228M; 8:48918932-48918932 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.421delT; p.S141fs*29; 8:48920100-48920100 |
stomach | adenocarcinoma | Deletion - Frameshift |
c.627G>T; p.G209G; 8:48918987-48918987 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.627G>T; p.G209G; 8:48918987-48918987 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.116T>C; p.M39T; 8:48920405-48920405 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.57C>T; p.Y19Y; 8:48921209-48921209 |
skin | malignant_melanoma | Substitution - coding silent |
c.657C>A; p.N219K; 8:48918957-48918957 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.747C>T; p.T249T; 8:48918867-48918867 |
skin | malignant_melanoma | Substitution - coding silent |
c.128C>A; p.P43Q; 8:48920393-48920393 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.26A>G; p.K9R; 8:48921240-48921240 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.516C>T; p.G172G; 8:48920005-48920005 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.135A>C; p.P45P; 8:48920386-48920386 |
prostate | carcinoma | Substitution - coding silent |
c.614G>T; p.R205I; 8:48919907-48919907 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.614G>T; p.R205I; 8:48919907-48919907 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.6G>A; p.P2P; 8:48921260-48921260 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.91C>T; p.P31S; 8:48920430-48920430 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.12C>T; p.S4S; 8:48921254-48921254 |
skin | malignant_melanoma | Substitution - coding silent |
c.523A>G; p.K175E; 8:48919998-48919998 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.231C>T; p.S77S; 8:48920290-48920290 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.536G>A; p.R179Q; 8:48919985-48919985 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.53A>C; p.N18T; 8:48921213-48921213 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.424_425GG>TT; p.G142L; 8:48920096-48920097 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.329A>T; p.E110V; 8:48920192-48920192 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.216C>T; p.G72G; 8:48920305-48920305 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.540C>T; p.T180T; 8:48919981-48919981 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.24G>T; p.K8N; 8:48921242-48921242 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.517G>A; p.A173T; 8:48920004-48920004 |
thyroid | carcinoma | Substitution - Missense |
c.716A>G; p.K239R; 8:48918898-48918898 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.803A>G; p.H268R; 8:48918811-48918811 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.401A>G; p.N134S; 8:48920120-48920120 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.401A>G; p.N134S; 8:48920120-48920120 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.764T>C; p.L255P; 8:48918850-48918850 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.795T>A; p.C265*; 8:48918819-48918819 |
liver | carcinoma | Substitution - Nonsense |
c.795T>A; p.C265*; 8:48918819-48918819 |
liver | carcinoma | Substitution - Nonsense |
c.682C>T; p.L228L; 8:48918932-48918932 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.73C>A; p.H25N; 8:48921193-48921193 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.626G>T; p.G209V; 8:48918988-48918988 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.626G>T; p.G209V; 8:48918988-48918988 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.626G>T; p.G209V; 8:48918988-48918988 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.626G>T; p.G209V; 8:48918988-48918988 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.60C>T; p.S20S; 8:48921206-48921206 |
large_intestine; colon | NS | Substitution - coding silent |
c.103G>A; p.E35K; 8:48920418-48920418 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.614G>A; p.R205K; 8:48919907-48919907 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.349C>A; p.L117I; 8:48920172-48920172 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.422C>T; p.S141F; 8:48920099-48920099 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.155C>A; p.A52E; 8:48920366-48920366 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.122T>C; p.V41A; 8:48920399-48920399 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.8G>C; p.R3P; 8:48921258-48921258 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.89C>T; p.S30F; 8:48920432-48920432 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.89C>T; p.S30F; 8:48920432-48920432 |
skin | malignant_melanoma | Substitution - Missense |
c.232G>A; p.G78R; 8:48920289-48920289 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.232G>A; p.G78R; 8:48920289-48920289 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.151G>T; p.G51*; 8:48920370-48920370 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.783A>T; p.E261D; 8:48918831-48918831 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.626-1G>T; p.?; 8:48918989-48918989 |
large_intestine; colon | carcinoma; adenocarcinoma | Unknown |
c.626-1G>T; p.?; 8:48918989-48918989 |
large_intestine; colon | carcinoma; adenocarcinoma | Unknown |
c.626-1G>T; p.?; 8:48918989-48918989 |
large_intestine; colon | carcinoma; adenocarcinoma | Unknown |
c.745A>C; p.T249P; 8:48918869-48918869 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.163C>T; p.P55S; 8:48920358-48920358 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.390C>T; p.C130C; 8:48920131-48920131 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.733A>G; p.N245D; 8:48918881-48918881 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.453C>T; p.C151C; 8:48920068-48920068 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.453C>T; p.C151C; 8:48920068-48920068 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.380A>C; p.K127T; 8:48920141-48920141 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.453C>T; p.C151C; 8:48920068-48920068 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.404A>G; p.K135R; 8:48920117-48920117 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.426G>A; p.G142G; 8:48920095-48920095 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.603A>T; p.Q201H; 8:48919918-48919918 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; chronic_myeloid_leukaemia | Substitution - Missense |
c.714A>G; p.V238V; 8:48918900-48918900 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.11C>T; p.S4F; 8:48921255-48921255 |
skin; upper_leg | malignant_melanoma | Substitution - Missense |
c.627G>A; p.G209G; 8:48918987-48918987 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.83T>G; p.I28S; 8:48920438-48920438 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.782A>T; p.E261V; 8:48918832-48918832 |
pancreas | carcinoma | Substitution - Missense |
c.400A>G; p.N134D; 8:48920121-48920121 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.50C>A; p.P17Q; 8:48921216-48921216 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.715A>G; p.K239E; 8:48918899-48918899 |
skin | malignant_melanoma | Substitution - Missense |
c.715A>G; p.K239E; 8:48918899-48918899 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.715A>G; p.K239E; 8:48918899-48918899 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.200C>A; p.A67D; 8:48920321-48920321 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.36C>T; p.N12N; 8:48921230-48921230 |
endometrium | carcinoma; serous_carcinoma | Substitution - coding silent |
c.208C>T; p.P70S; 8:48920313-48920313 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.237C>T; p.Y79Y; 8:48920284-48920284 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |