| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 3171 |
Name | FOXA3 |
Synonymous | forkhead box A3;FOXA3;forkhead box A3 |
Definition | HNF-3-gamma|HNF-3G|TCF-3G|fork head-related protein FKH H3|forkhead box protein A3|hepatocyte nuclear factor 3, gamma|hepatocyte nuclear factor 3-gamma|transcription factor 3G |
Position | 19q13.32 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.335C>T; p.P112L; 19:45872340-45872340 |
skin | malignant_melanoma | Substitution - Missense |
c.838A>G; p.T280A; 19:45872843-45872843 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.152C>A; p.P51H; 19:45872157-45872157 |
ovary | other; neoplasm | Substitution - Missense |
c.912C>T; p.F304F; 19:45872917-45872917 |
breast | carcinoma | Substitution - coding silent |
c.106C>A; p.P36T; 19:45872111-45872111 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.426A>T; p.E142D; 19:45872431-45872431 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.130A>G; p.N44D; 19:45872135-45872135 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1043A>G; p.N348S; 19:45873048-45873048 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.963C>T; p.D321D; 19:45872968-45872968 |
upper_aerodigestive_tract; mouth | carcinoma | Substitution - coding silent |
c.963C>T; p.D321D; 19:45872968-45872968 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.448C>T; p.L150F; 19:45872453-45872453 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.634C>T; p.R212C; 19:45872639-45872639 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.697G>A; p.G233R; 19:45872702-45872702 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.566C>T; p.S189F; 19:45872571-45872571 |
liver | carcinoma | Substitution - Missense |
c.147C>A; p.P49P; 19:45872152-45872152 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.109C>A; p.L37I; 19:45872114-45872114 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.356C>T; p.P119L; 19:45872361-45872361 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.567C>T; p.S189S; 19:45872572-45872572 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.224G>A; p.G75E; 19:45872229-45872229 |
skin | malignant_melanoma | Substitution - Missense |
c.887C>T; p.A296V; 19:45872892-45872892 |
breast | carcinoma | Substitution - Missense |
c.978C>T; p.G326G; 19:45872983-45872983 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.173C>T; p.S58F; 19:45872178-45872178 |
autonomic_ganglia | neuroblastoma | Substitution - Missense |
c.908C>A; p.P303H; 19:45872913-45872913 |
skin | malignant_melanoma | Substitution - Missense |
c.870G>A; p.G290G; 19:45872875-45872875 |
skin | malignant_melanoma | Substitution - coding silent |
c.625C>T; p.R209C; 19:45872630-45872630 |
autonomic_ganglia | neuroblastoma | Substitution - Missense |
c.625C>T; p.R209C; 19:45872630-45872630 |
peritoneum; appendix | other; pseudomyxoma_peritonei | Substitution - Missense |
c.665G>A; p.G222E; 19:45872670-45872670 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.214delG; p.A72fs*67; 19:45872219-45872219 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; peripheral_T_cell_lymphoma_unspecified | Deletion - Frameshift |
c.867A>T; p.P289P; 19:45872872-45872872 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.513C>G; p.F171L; 19:45872518-45872518 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.954C>A; p.P318P; 19:45872959-45872959 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.152C>T; p.P51L; 19:45872157-45872157 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.811C>G; p.L271V; 19:45872816-45872816 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.131A>G; p.N44S; 19:45872136-45872136 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.849C>A; p.F283L; 19:45872854-45872854 |
breast | carcinoma | Substitution - Missense |
c.456T>G; p.P152P; 19:45872461-45872461 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.792C>T; p.G264G; 19:45872797-45872797 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.792C>T; p.G264G; 19:45872797-45872797 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.503C>T; p.S168L; 19:45872508-45872508 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.305G>A; p.G102E; 19:45872310-45872310 |
skin | malignant_melanoma | Substitution - Missense |
c.259A>G; p.S87G; 19:45872264-45872264 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.946G>A; p.A316T; 19:45872951-45872951 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.542C>T; p.S181F; 19:45872547-45872547 |
skin | malignant_melanoma | Substitution - Missense |
c.542C>T; p.S181F; 19:45872547-45872547 |
skin | malignant_melanoma | Substitution - Missense |
c.512T>C; p.F171S; 19:45872517-45872517 |
pancreas | other; adenoma | Substitution - Missense |
c.1041T>C; p.L347L; 19:45873046-45873046 |
breast | carcinoma; ductal_carcinoma | Substitution - coding silent |
c.306G>A; p.G102G; 19:45872311-45872311 |
skin | malignant_melanoma | Substitution - coding silent |
c.306G>A; p.G102G; 19:45872311-45872311 |
skin | malignant_melanoma | Substitution - coding silent |
c.328C>T; p.R110W; 19:45872333-45872333 |
pancreas | carcinoma | Substitution - Missense |
c.240C>T; p.G80G; 19:45872245-45872245 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.726C>T; p.T242T; 19:45872731-45872731 |
skin | malignant_melanoma | Substitution - coding silent |
c.77C>T; p.S26L; 19:45872082-45872082 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.215C>A; p.A72D; 19:45872220-45872220 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; peripheral_T_cell_lymphoma_unspecified | Substitution - Missense |
c.27C>T; p.A9A; 19:45864483-45864483 |
large_intestine; colon | NS | Substitution - coding silent |
c.298G>A; p.V100M; 19:45872303-45872303 |
skin; mucosal | malignant_melanoma | Substitution - Missense |
c.864C>T; p.L288L; 19:45872869-45872869 |
skin | malignant_melanoma | Substitution - coding silent |
c.516C>T; p.N172N; 19:45872521-45872521 |
thyroid | other; neoplasm | Substitution - coding silent |
c.666_667GG>AA; p.G223S; 19:45872671-45872672 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.961G>T; p.D321Y; 19:45872966-45872966 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.284C>T; p.P95L; 19:45872289-45872289 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.187G>A; p.G63R; 19:45872192-45872192 |
skin | malignant_melanoma | Substitution - Missense |
c.180_181GC>TG; p.P61A; 19:45872185-45872186 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |