| Gene information | Literature | Expression | lncRNA | Mutation | Homolog |
Basic Information | |
|---|---|
Gene ID | 2251 |
Name | FGF6 |
Synonymous | fibroblast growth factor 6;FGF6;fibroblast growth factor 6 |
Definition | FGF-6|HST-2|HSTF-2|heparin secretory-transforming protein 2|heparin-binding growth factor 6 |
Position | 12p13 |
Gene Type | protein-coding |
COSMIC confirmed somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.565G>C; p.V189L; 12:4434277-4434277 |
biliary_tract; gallbladder | carcinoma; adenocarcinoma | Substitution - Missense |
c.211G>A; p.G71R; 12:4445360-4445360 |
bone; fibula | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.562C>T; p.R188W; 12:4434280-4434280 |
breast | carcinoma | Substitution - Missense |
c.367G>A; p.V123M; 12:4444216-4444216 |
breast | carcinoma | Substitution - Missense |
c.128G>A; p.R43H; 12:4445443-4445443 |
breast | carcinoma; basal_(triple-negative)_carcinoma | Substitution - Missense |
c.321C>T; p.S107S; 12:4445250-4445250 |
breast | carcinoma | Substitution - coding silent |
c.184C>T; p.R62C; 12:4445387-4445387 |
breast | carcinoma | Substitution - Missense |
c.306C>G; p.P102P; 12:4445265-4445265 |
breast | carcinoma | Substitution - coding silent |
c.377G>A; p.G126D; 12:4444206-4444206 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.559G>A; p.G187R; 12:4434283-4434283 |
central_nervous_system; brain | primitive_neuroectodermal_tumour-medulloblastoma | Substitution - Missense |
c.379G>A; p.V127M; 12:4444204-4444204 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.481G>T; p.E161*; 12:4434361-4434361 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.450G>A; p.T150T; 12:4444133-4444133 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.450+1G>A; p.?; 12:4444132-4444132 |
endometrium | carcinoma; endometrioid_carcinoma | Unknown |
c.367G>A; p.V123M; 12:4444216-4444216 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; myelofibrosis | Substitution - Missense |
c.107T>C; p.V36A; 12:4445464-4445464 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.328C>A; p.H110N; 12:4445243-4445243 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.192G>A; p.G64G; 12:4445379-4445379 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.238G>T; p.V80L; 12:4445333-4445333 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.351G>C; p.L117L; 12:4444232-4444232 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.237G>C; p.L79F; 12:4445334-4445334 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.562C>T; p.R188W; 12:4434280-4434280 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.307G>A; p.D103N; 12:4445264-4445264 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.63G>A; p.T21T; 12:4445508-4445508 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.508G>A; p.A170T; 12:4434334-4434334 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.49C>T; p.R17C; 12:4445522-4445522 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.187G>A; p.A63T; 12:4445384-4445384 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.128G>A; p.R43H; 12:4445443-4445443 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.38G>A; p.R13Q; 12:4445533-4445533 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.373C>T; p.R125*; 12:4444210-4444210 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.366T>C; p.T122T; 12:4444217-4444217 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.188C>T; p.A63V; 12:4445383-4445383 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.186C>T; p.R62R; 12:4445385-4445385 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.186C>T; p.R62R; 12:4445385-4445385 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.185G>A; p.R62H; 12:4445386-4445386 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.607C>A; p.H203N; 12:4434235-4434235 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.37C>T; p.R13W; 12:4445534-4445534 |
large_intestine; colon | adenoma | Substitution - Missense |
c.414C>T; p.F138F; 12:4444169-4444169 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.414C>T; p.F138F; 12:4444169-4444169 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.563G>A; p.R188Q; 12:4434279-4434279 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.228T>C; p.S76S; 12:4445343-4445343 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.594C>G; p.I198M; 12:4434248-4434248 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.452C>A; p.P151H; 12:4434390-4434390 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.127C>A; p.R43S; 12:4445444-4445444 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.223delG; p.E75fs*54; 12:4445348-4445348 |
lung | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.176_177CC>AA; p.S59*; 12:4445394-4445395 |
lung | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.161G>T; p.W54L; 12:4445410-4445410 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.190G>T; p.G64W; 12:4445381-4445381 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.342C>T; p.P114P; 12:4445229-4445229 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.58G>T; p.G20C; 12:4445513-4445513 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.11G>T; p.G4V; 12:4445560-4445560 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.530A>T; p.Q177L; 12:4434312-4434312 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.374G>A; p.R125Q; 12:4444209-4444209 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.307G>T; p.D103Y; 12:4445264-4445264 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.32T>C; p.M11T; 12:4445539-4445539 |
NS | NS | Substitution - Missense |
c.389T>A; p.L130H; 12:4444194-4444194 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - Missense |
c.571C>T; p.R191W; 12:4434271-4434271 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.572G>A; p.R191Q; 12:4434270-4434270 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - Missense |
c.227G>T; p.S76I; 12:4445344-4445344 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.367G>A; p.V123M; 12:4444216-4444216 |
pancreas | carcinoma | Substitution - Missense |
c.395G>C; p.G132A; 12:4444188-4444188 |
pancreas | carcinoma | Substitution - Missense |
c.561A>G; p.G187G; 12:4434281-4434281 |
pancreas | carcinoma | Substitution - coding silent |
c.242G>C; p.G81A; 12:4445329-4445329 |
peritoneum; appendix | other; pseudomyxoma_peritonei | Substitution - Missense |
c.415G>A; p.V139I; 12:4444168-4444168 |
prostate | carcinoma | Substitution - Missense |
c.250C>T; p.R84W; 12:4445321-4445321 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.612C>T; p.F204F; 12:4434230-4434230 |
skin | malignant_melanoma | Substitution - coding silent |
c.2T>G; p.M1R; 12:4445569-4445569 |
skin | malignant_melanoma | Substitution - Missense |
c.434G>A; p.G145E; 12:4444149-4444149 |
skin | malignant_melanoma | Substitution - Missense |
c.434G>A; p.G145E; 12:4444149-4444149 |
skin | malignant_melanoma | Substitution - Missense |
c.460C>T; p.Q154*; 12:4434382-4434382 |
skin | malignant_melanoma | Substitution - Nonsense |
c.506A>T; p.N169I; 12:4434336-4434336 |
skin | malignant_melanoma | Substitution - Missense |
c.223G>A; p.E75K; 12:4445348-4445348 |
skin | malignant_melanoma | Substitution - Missense |
c.355G>A; p.E119K; 12:4444228-4444228 |
skin; trunk | malignant_melanoma; nodular | Substitution - Missense |
c.258G>A; p.R86R; 12:4445313-4445313 |
skin | malignant_melanoma | Substitution - coding silent |
c.437G>A; p.R146K; 12:4444146-4444146 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.204G>A; p.E68E; 12:4445367-4445367 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.27C>T; p.I9I; 12:4445544-4445544 |
skin | malignant_melanoma | Substitution - coding silent |
c.414C>T; p.F138F; 12:4444169-4444169 |
skin | malignant_melanoma | Substitution - coding silent |
c.414C>T; p.F138F; 12:4444169-4444169 |
skin | malignant_melanoma | Substitution - coding silent |
c.415G>A; p.V139I; 12:4444168-4444168 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.321C>T; p.S107S; 12:4445250-4445250 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.449C>T; p.T150M; 12:4444134-4444134 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.256C>T; p.R86W; 12:4445315-4445315 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.250C>T; p.R84W; 12:4445321-4445321 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.104T>C; p.V35A; 12:4445467-4445467 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.572G>A; p.R191Q; 12:4434270-4434270 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.141G>A; p.T47T; 12:4445430-4445430 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.521A>T; p.D174V; 12:4434321-4434321 |
thyroid | other; neoplasm | Substitution - Missense |
c.189C>G; p.A63A; 12:4445382-4445382 |
thyroid | other; neoplasm | Substitution - coding silent |
c.128G>A; p.R43H; 12:4445443-4445443 |
upper_aerodigestive_tract; larynx | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.477C>T; p.F159F; 12:4434365-4434365 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.373C>T; p.R125*; 12:4444210-4444210 |
urinary_tract; bladder | carcinoma | Substitution - Nonsense |
c.373C>T; p.R125*; 12:4444210-4444210 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - Nonsense |
c.374G>A; p.R125Q; 12:4444209-4444209 |
urinary_tract; bladder | carcinoma | Substitution - Missense |