| General information | Literature | Expression | lncRNA |Regulation | Mutation | Homolog | Interaction |
Basic Information | |||
|---|---|---|---|
Gene ID | 6624 | ||
Name | FSCN1 | ||
The somatic mutations from COSMIC database | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.1462G>A; p.A488T; 7:5605454-5605454 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.570C>T; p.T190T; 7:5593506-5593506 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1223G>C; p.R408P; 7:5603974-5603974 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.392A>C; p.K131T; 7:5593328-5593328 |
pancreas | carcinoma | Substitution - Missense |
c.1059G>C; p.K353N; 7:5603565-5603565 |
skin | malignant_melanoma | Substitution - Missense |
c.1022G>A; p.R341H; 7:5603528-5603528 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.905C>T; p.T302I; 7:5603329-5603329 |
skin | malignant_melanoma | Substitution - Missense |
c.1167C>T; p.R389R; 7:5603918-5603918 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1159G>A; p.V387M; 7:5603910-5603910 |
bone; calcaneus | chondrosarcoma | Substitution - Missense |
c.326G>A; p.R109Q; 7:5593262-5593262 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.967G>A; p.V323M; 7:5603391-5603391 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.710G>A; p.S237N; 7:5593646-5593646 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.859G>A; p.E287K; 7:5603283-5603283 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.528C>T; p.L176L; 7:5593464-5593464 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - coding silent |
c.528C>T; p.L176L; 7:5593464-5593464 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.1128C>T; p.F376F; 7:5603879-5603879 |
skin | malignant_melanoma | Substitution - coding silent |
c.649C>T; p.R217C; 7:5593585-5593585 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.1350_1352delCTT; p.F453delF; 7:5605342-5605344 |
liver | carcinoma; hepatocellular_carcinoma | Deletion - In frame |
c.853C>T; p.Q285*; 7:5603277-5603277 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.1350_1352delCTT; p.F453delF; 7:5605342-5605344 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - In frame |
c.1398C>T; p.G466G; 7:5605390-5605390 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1365C>T; p.F455F; 7:5605357-5605357 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1147C>T; p.R383C; 7:5603898-5603898 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.537C>T; p.L179L; 7:5593473-5593473 |
skin | malignant_melanoma | Substitution - coding silent |
c.1385C>T; p.A462V; 7:5605377-5605377 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.901G>A; p.D301N; 7:5603325-5603325 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1353C>G; p.F451L; 7:5605345-5605345 |
oesophagus; middle_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.484G>A; p.E162K; 7:5593420-5593420 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1122G>T; p.E374D; 7:5603873-5603873 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.539C>T; p.A180V; 7:5593475-5593475 |
skin | malignant_melanoma | Substitution - Missense |
c.517G>A; p.V173I; 7:5593453-5593453 |
biliary_tract; gallbladder | carcinoma; adenocarcinoma | Substitution - Missense |
c.353G>A; p.R118H; 7:5593289-5593289 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.202C>T; p.R68C; 7:5593138-5593138 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1368C>T; p.C456C; 7:5605360-5605360 |
pancreas | carcinoma | Substitution - coding silent |
c.1368C>T; p.C456C; 7:5605360-5605360 |
breast | carcinoma | Substitution - coding silent |
c.991A>T; p.N331Y; 7:5603497-5603497 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.979G>A; p.A327T; 7:5603403-5603403 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1280-1G>A; p.?; 7:5605271-5605271 |
large_intestine; colon | carcinoma; adenocarcinoma | Unknown |
c.105G>A; p.A35A; 7:5593041-5593041 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.104C>T; p.A35V; 7:5593040-5593040 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.591C>T; p.R197R; 7:5593527-5593527 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.614G>A; p.R205H; 7:5593550-5593550 |
haematopoietic_and_lymphoid_tissue; central_nervous_system | lymphoid_neoplasm; primary_central_nervous_system_lymphoma | Substitution - Missense |
c.418C>T; p.P140S; 7:5593354-5593354 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.894C>T; p.I298I; 7:5603318-5603318 |
skin | malignant_melanoma | Substitution - coding silent |
c.894C>T; p.I298I; 7:5603318-5603318 |
central_nervous_system; brain | primitive_neuroectodermal_tumour-medulloblastoma | Substitution - coding silent |
c.1343C>A; p.P448H; 7:5605335-5605335 |
skin | malignant_melanoma | Substitution - Missense |
c.1023T>C; p.R341R; 7:5603529-5603529 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.769G>C; p.E257Q; 7:5593705-5593705 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.541T>C; p.F181L; 7:5593477-5593477 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.926C>T; p.T309I; 7:5603350-5603350 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1192C>T; p.R398C; 7:5603943-5603943 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.947C>T; p.T316M; 7:5603371-5603371 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1456G>T; p.D486Y; 7:5605448-5605448 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.175G>C; p.A59P; 7:5593111-5593111 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.279C>T; p.I93I; 7:5593215-5593215 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1114G>A; p.D372N; 7:5603865-5603865 |
prostate | adenoma | Substitution - Missense |
c.1165C>A; p.R389S; 7:5603916-5603916 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1031G>A; p.R344H; 7:5603537-5603537 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.320C>A; p.A107E; 7:5593256-5593256 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1074G>C; p.K358N; 7:5603580-5603580 |
liver | carcinoma | Substitution - Missense |
c.1045G>T; p.A349S; 7:5603551-5603551 |
breast | carcinoma | Substitution - Missense |
c.1074G>C; p.K358N; 7:5603580-5603580 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.1182C>T; p.F394F; 7:5603933-5603933 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.1056C>T; p.G352G; 7:5603562-5603562 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1320G>A; p.A440A; 7:5605312-5605312 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.567G>C; p.Q189H; 7:5593503-5593503 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.938A>G; p.K313R; 7:5603362-5603362 |
skin | malignant_melanoma | Substitution - Missense |
c.247G>C; p.E83Q; 7:5593183-5593183 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |