| General information | Literature | Expression | lncRNA |Regulation | Mutation | Homolog | Interaction |
Basic Information | |||
|---|---|---|---|
Gene ID | 51162 | ||
Name | EGFL7 | ||
The somatic mutations from COSMIC database | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.428C>T; p.A143V; 9:136670187-136670187 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.113A>T; p.D38V; 9:136668589-136668589 |
prostate | carcinoma | Substitution - Missense |
c.151C>A; p.P51T; 9:136668627-136668627 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.122C>G; p.S41C; 9:136668598-136668598 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.802T>A; p.S268T; 9:136672266-136672266 |
liver | carcinoma | Substitution - Missense |
c.802T>A; p.S268T; 9:136672266-136672266 |
liver | carcinoma | Substitution - Missense |
c.451C>T; p.R151C; 9:136670210-136670210 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.466G>A; p.A156T; 9:136670225-136670225 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.457G>A; p.V153I; 9:136670216-136670216 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.327G>A; p.P109P; 9:136669927-136669927 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.214G>A; p.A72T; 9:136669622-136669622 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.516C>T; p.D172D; 9:136670275-136670275 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.786G>A; p.E262E; 9:136672075-136672075 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.318_319insT; p.C107fs*26; 9:136669918-136669919 |
liver | carcinoma | Insertion - Frameshift |
c.603G>A; p.Q201Q; 9:136670981-136670981 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.106C>T; p.H36Y; 9:136668582-136668582 |
bone; extraskeletal | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.492G>C; p.W164C; 9:136670251-136670251 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.116C>G; p.P39R; 9:136668592-136668592 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.810G>A; p.K270K; 9:136672274-136672274 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.240C>A; p.A80A; 9:136669648-136669648 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - coding silent |
c.578A>G; p.D193G; 9:136670956-136670956 |
kidney | other; neoplasm | Substitution - Missense |
c.578A>G; p.D193G; 9:136670956-136670956 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.345G>A; p.G115G; 9:136669945-136669945 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.388C>T; p.R130W; 9:136669988-136669988 |
prostate | carcinoma | Substitution - Missense |
c.407C>T; p.S136L; 9:136670007-136670007 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.760A>C; p.S254R; 9:136672049-136672049 |
liver | carcinoma | Substitution - Missense |