| Gene information | Literature | Expression | lncRNA | Mutation | Homolog |
Basic Information | |
|---|---|
Gene ID | 2249 |
Name | FGF4 |
Synonymous | fibroblast growth factor 4;FGF4;fibroblast growth factor 4 |
Definition | FGF-4|HSTF-1|fibroblast growth factor 4 splice isoform|heparin secretory transforming protein 1|heparin secretory-transforming protein 1|heparin-binding growth factor 4|human stomach cancer, transforming factor from FGF-related oncogene|kaposi sarcoma onc |
Position | 11q13.3 |
Gene Type | protein-coding |
COSMIC confirmed somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.585C>A; p.P195P; 11:69773345-69773345 |
breast | carcinoma | Substitution - coding silent |
c.506A>C; p.Y169S; 11:69773424-69773424 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.519G>A; p.K173K; 11:69773411-69773411 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.581C>T; p.S194L; 11:69773349-69773349 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; hairy_cell_leukaemia | Substitution - Missense |
c.507C>T; p.Y169Y; 11:69773423-69773423 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.502G>A; p.A168T; 11:69773428-69773428 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.334C>T; p.R112C; 11:69774751-69774751 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.426G>A; p.K142K; 11:69774042-69774042 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.424A>C; p.K142Q; 11:69774044-69774044 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.401G>A; p.R134Q; 11:69774067-69774067 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.498C>A; p.Y166*; 11:69773432-69773432 |
large_intestine; colon | carcinoma | Substitution - Nonsense |
c.498C>A; p.Y166*; 11:69773432-69773432 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.205G>A; p.V69I; 11:69774880-69774880 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.474G>A; p.K158K; 11:69773456-69773456 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.582G>A; p.S194S; 11:69773348-69773348 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.394G>C; p.A132P; 11:69774074-69774074 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.343C>A; p.L115M; 11:69774125-69774125 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.304G>T; p.G102C; 11:69774781-69774781 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.574C>T; p.R192*; 11:69773356-69773356 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.504C>T; p.A168A; 11:69773426-69773426 |
ovary | other; neoplasm | Substitution - coding silent |
c.610C>A; p.P204T; 11:69773320-69773320 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.195G>A; p.K65K; 11:69774890-69774890 |
ovary | other; neoplasm | Substitution - coding silent |
c.277G>C; p.G93R; 11:69774808-69774808 |
ovary | other; neoplasm | Substitution - Missense |
c.361G>A; p.V121M; 11:69774107-69774107 |
pancreas | carcinoma | Substitution - Missense |
c.569G>A; p.G190E; 11:69773361-69773361 |
skin | malignant_melanoma | Substitution - Missense |
c.569G>A; p.G190E; 11:69773361-69773361 |
skin | malignant_melanoma | Substitution - Missense |
c.570G>A; p.G190G; 11:69773360-69773360 |
skin | malignant_melanoma | Substitution - coding silent |
c.443C>T; p.S148L; 11:69774025-69774025 |
skin | malignant_melanoma | Substitution - Missense |
c.481C>G; p.L161V; 11:69773449-69773449 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.582G>A; p.S194S; 11:69773348-69773348 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.297C>T; p.L99L; 11:69774788-69774788 |
thyroid | other; neoplasm | Substitution - coding silent |