| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 7448 |
Name | VTN |
Synonymous | vitronectin;VTN;vitronectin |
Definition | S-protein|complement S-protein|epibolin|serum spreading factor|serum-spreading factor|somatomedin B |
Position | 17q11 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.590G>A; p.R197Q; 17:28369368-28369368 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.607G>A; p.E203K; 17:28369351-28369351 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - Missense |
c.615C>T; p.P205P; 17:28369343-28369343 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.607G>A; p.E203K; 17:28369351-28369351 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.590G>A; p.R197Q; 17:28369368-28369368 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.553G>A; p.E185K; 17:28369405-28369405 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.553G>A; p.E185K; 17:28369405-28369405 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.686G>A; p.R229H; 17:28369012-28369012 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.371C>T; p.A124V; 17:28369665-28369665 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.504G>A; p.K168K; 17:28369532-28369532 |
skin | malignant_melanoma | Substitution - coding silent |
c.643T>A; p.C215S; 17:28369315-28369315 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.632C>T; p.T211I; 17:28369326-28369326 |
skin | malignant_melanoma | Substitution - Missense |
c.1085G>A; p.R362H; 17:28367954-28367954 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1192C>A; p.R398S; 17:28367847-28367847 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.56C>A; p.A19D; 17:28370148-28370148 |
breast | carcinoma | Substitution - Missense |
c.685C>T; p.R229C; 17:28369013-28369013 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.487G>A; p.A163T; 17:28369549-28369549 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.18C>A; p.P6P; 17:28370186-28370186 |
liver | carcinoma | Substitution - coding silent |
c.530-10T>G; p.?; 17:28369438-28369438 |
liver | carcinoma | Unknown |
c.124G>A; p.E42K; 17:28369987-28369987 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.530-10T>G; p.?; 17:28369438-28369438 |
liver | carcinoma | Unknown |
c.1411G>C; p.G471R; 17:28367395-28367395 |
pancreas | carcinoma; acinar_carcinoma | Substitution - Missense |
c.759C>T; p.N253N; 17:28368939-28368939 |
large_intestine; rectum | NS | Substitution - coding silent |
c.759C>T; p.N253N; 17:28368939-28368939 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.661C>G; p.L221V; 17:28369297-28369297 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.277_278insG; p.V93fs*9; 17:28369758-28369759 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Insertion - Frameshift |
c.855G>A; p.Q285Q; 17:28368645-28368645 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1184G>A; p.R395Q; 17:28367855-28367855 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1129A>G; p.K377E; 17:28367910-28367910 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.742G>A; p.D248N; 17:28368956-28368956 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.759C>A; p.N253K; 17:28368939-28368939 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.287C>T; p.P96L; 17:28369749-28369749 |
oesophagus; middle_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.305T>C; p.L102P; 17:28369731-28369731 |
liver | carcinoma | Substitution - Missense |
c.305T>C; p.L102P; 17:28369731-28369731 |
liver | carcinoma | Substitution - Missense |
c.967G>A; p.G323S; 17:28368533-28368533 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1042G>A; p.A348T; 17:28367997-28367997 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1166G>A; p.R389H; 17:28367873-28367873 |
pancreas | carcinoma | Substitution - Missense |
c.1166G>A; p.R389H; 17:28367873-28367873 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1319C>G; p.S440C; 17:28367720-28367720 |
lung | carcinoma; non_small_cell_carcinoma | Substitution - Missense |
c.1319C>G; p.S440C; 17:28367720-28367720 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.193G>A; p.G65R; 17:28369843-28369843 |
bone; extraskeletal | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.1182C>T; p.R394R; 17:28367857-28367857 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.808C>A; p.R270R; 17:28368890-28368890 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.919A>G; p.M307V; 17:28368581-28368581 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.430C>T; p.P144S; 17:28369606-28369606 |
breast | carcinoma | Substitution - Missense |
c.24C>A; p.L8L; 17:28370180-28370180 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.1337G>A; p.R446Q; 17:28367469-28367469 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.808C>T; p.R270W; 17:28368890-28368890 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.874_876delGAG; p.E292delE; 17:28368624-28368626 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - In frame |
c.808C>T; p.R270W; 17:28368890-28368890 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.789T>C; p.H263H; 17:28368909-28368909 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.79C>T; p.R27C; 17:28370032-28370032 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.508G>C; p.G170R; 17:28369528-28369528 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.634C>T; p.R212C; 17:28369324-28369324 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.708C>A; p.D236E; 17:28368990-28368990 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.819C>G; p.F273L; 17:28368879-28368879 |
breast | carcinoma | Substitution - Missense |
c.606C>T; p.I202I; 17:28369352-28369352 |
bone; extraskeletal | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.1348C>T; p.R450C; 17:28367458-28367458 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1229G>A; p.S410N; 17:28367810-28367810 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.10C>A; p.L4M; 17:28370194-28370194 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.430C>G; p.P144A; 17:28369606-28369606 |
liver | carcinoma | Substitution - Missense |
c.1148G>A; p.R383Q; 17:28367891-28367891 |
skin | malignant_melanoma | Substitution - Missense |
c.746G>A; p.G249D; 17:28368952-28368952 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.705G>A; p.L235L; 17:28368993-28368993 |
skin | malignant_melanoma | Substitution - coding silent |
c.430C>G; p.P144A; 17:28369606-28369606 |
liver | carcinoma | Substitution - Missense |
c.27A>G; p.I9M; 17:28370177-28370177 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.383G>C; p.G128A; 17:28369653-28369653 |
thyroid | carcinoma | Substitution - Missense |
c.1016G>A; p.W339*; 17:28368023-28368023 |
skin | malignant_melanoma | Substitution - Nonsense |
c.483C>T; p.F161F; 17:28369553-28369553 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.714T>G; p.D238E; 17:28368984-28368984 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.793T>C; p.Y265H; 17:28368905-28368905 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.714T>G; p.D238E; 17:28368984-28368984 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.718C>T; p.P240S; 17:28368980-28368980 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.120T>C; p.C40C; 17:28369991-28369991 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.376G>A; p.E126K; 17:28369660-28369660 |
skin | malignant_melanoma | Substitution - Missense |
c.238G>A; p.D80N; 17:28369798-28369798 |
skin | malignant_melanoma | Substitution - Missense |
c.722G>A; p.R241Q; 17:28368976-28368976 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.315G>C; p.Q105H; 17:28369721-28369721 |
ovary | other; neoplasm | Substitution - Missense |
c.484G>A; p.D162N; 17:28369552-28369552 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1393A>C; p.I465L; 17:28367413-28367413 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.372G>A; p.A124A; 17:28369664-28369664 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1320T>A; p.S440S; 17:28367719-28367719 |
pancreas | carcinoma | Substitution - coding silent |
c.372G>A; p.A124A; 17:28369664-28369664 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1320T>A; p.S440S; 17:28367719-28367719 |
pancreas | carcinoid-endocrine_tumour | Substitution - coding silent |
c.1199C>T; p.T400M; 17:28367840-28367840 |
thyroid | other; neoplasm | Substitution - Missense |
c.720C>G; p.P240P; 17:28368978-28368978 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.1387C>T; p.R463C; 17:28367419-28367419 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1180C>T; p.R394C; 17:28367859-28367859 |
oesophagus | carcinoma | Substitution - Missense |
c.752C>T; p.P251L; 17:28368946-28368946 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.527G>A; p.R176Q; 17:28369509-28369509 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1349G>A; p.R450H; 17:28367457-28367457 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1349G>A; p.R450H; 17:28367457-28367457 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.384C>T; p.G128G; 17:28369652-28369652 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.410C>G; p.S137*; 17:28369626-28369626 |
urinary_tract; bladder | carcinoma | Substitution - Nonsense |