| Gene information | Literature | Expression | lncRNA | Mutation | Homolog |
Basic Information | |
|---|---|
Gene ID | 2268 |
Name | FGR |
Synonymous | FGR proto-oncogene, Src family tyrosine kinase;FGR;FGR proto-oncogene, Src family tyrosine kinase |
Definition | Gardner-Rasheed feline sarcoma viral (v-fgr) oncogene homolog|c-fgr protooncogene|c-src-2 proto-oncogene|feline Gardner-Rasheed sarcoma viral oncogene homolog|p55-c-fgr protein|proto-oncogene c-Fgr|proto-oncogene tyrosine-protein kinase FGR|tyrosine-prote |
Position | 1p36.2-p36.1 |
Gene Type | protein-coding |
COSMIC confirmed somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.711C>T; p.L237L; 1:27615816-27615816 |
bone; tibia | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.1348G>A; p.E450K; 1:27613252-27613252 |
breast | carcinoma | Substitution - Missense |
c.1412T>G; p.V471G; 1:27613092-27613092 |
breast | carcinoma | Substitution - Missense |
c.511C>T; p.R171W; 1:27617214-27617214 |
breast | carcinoma; HER-positive_carcinoma | Substitution - Missense |
c.781A>G; p.S261G; 1:27615746-27615746 |
breast | carcinoma | Substitution - Missense |
c.648C>T; p.F216F; 1:27616891-27616891 |
central_nervous_system; brain | glioma | Substitution - coding silent |
c.737C>T; p.P246L; 1:27615790-27615790 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1497G>A; p.P499P; 1:27613007-27613007 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.268G>A; p.A90T; 1:27623103-27623103 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.619G>A; p.G207S; 1:27616920-27616920 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1130A>G; p.N377S; 1:27614549-27614549 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.417C>T; p.I139I; 1:27621570-27621570 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1448G>A; p.C483Y; 1:27613056-27613056 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; acute_lymphoblastic_leukaemia | Substitution - Missense |
c.894G>C; p.M298I; 1:27615558-27615558 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm | Substitution - Missense |
c.1481C>T; p.T494I; 1:27613023-27613023 |
kidney | other; neoplasm | Substitution - Missense |
c.1481C>T; p.T494I; 1:27613023-27613023 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.605A>T; p.K202I; 1:27616934-27616934 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.1098A>G; p.V366V; 1:27614581-27614581 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.1487G>A; p.R496H; 1:27613017-27613017 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.33G>A; p.P11P; 1:27623884-27623884 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1512C>A; p.T504T; 1:27612992-27612992 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.970G>A; p.V324M; 1:27615482-27615482 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.800G>A; p.R267H; 1:27615727-27615727 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.263A>G; p.Y88C; 1:27623108-27623108 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.31C>T; p.P11S; 1:27623886-27623886 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.576C>T; p.G192G; 1:27616963-27616963 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1486C>T; p.R496C; 1:27613018-27613018 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.333A>C; p.E111D; 1:27621654-27621654 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.805C>A; p.L269M; 1:27615722-27615722 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.890C>T; p.T297I; 1:27615562-27615562 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1273A>G; p.T425A; 1:27613327-27613327 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.51G>A; p.E17E; 1:27623866-27623866 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.76A>G; p.R26G; 1:27623841-27623841 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.1561C>A; p.P521T; 1:27612943-27612943 |
liver | carcinoma | Substitution - Missense |
c.228G>T; p.G76G; 1:27623143-27623143 |
liver | carcinoma | Substitution - coding silent |
c.228G>T; p.G76G; 1:27623143-27623143 |
liver | carcinoma | Substitution - coding silent |
c.1152G>A; p.R384R; 1:27614527-27614527 |
liver | carcinoma | Substitution - coding silent |
c.846G>A; p.W282*; 1:27615606-27615606 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.979G>C; p.E327Q; 1:27615473-27615473 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.532G>T; p.G178C; 1:27617193-27617193 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.945C>T; p.H315H; 1:27615507-27615507 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.967G>A; p.A323T; 1:27615485-27615485 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.1383C>T; p.G461G; 1:27613121-27613121 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.228G>A; p.G76G; 1:27623143-27623143 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1396G>A; p.E466K; 1:27613108-27613108 |
NS | malignant_melanoma | Substitution - Missense |
c.867G>A; p.A289A; 1:27615585-27615585 |
oesophagus | carcinoma | Substitution - coding silent |
c.791C>T; p.T264M; 1:27615736-27615736 |
oesophagus | carcinoma | Substitution - Missense |
c.941G>A; p.R314Q; 1:27615511-27615511 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.924G>A; p.Q308Q; 1:27615528-27615528 |
pancreas | carcinoma | Substitution - coding silent |
c.1141C>T; p.R381C; 1:27614538-27614538 |
pancreas | carcinoma | Substitution - Missense |
c.898C>A; p.P300T; 1:27615554-27615554 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.1017C>T; p.H339H; 1:27615435-27615435 |
prostate | carcinoma | Substitution - coding silent |
c.1425C>T; p.Y475Y; 1:27613079-27613079 |
skin | malignant_melanoma | Substitution - coding silent |
c.1425C>T; p.Y475Y; 1:27613079-27613079 |
skin | malignant_melanoma | Substitution - coding silent |
c.49G>A; p.E17K; 1:27623868-27623868 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.846G>A; p.W282*; 1:27615606-27615606 |
skin | malignant_melanoma | Substitution - Nonsense |
c.440G>A; p.G147E; 1:27617285-27617285 |
skin | malignant_melanoma | Substitution - Missense |
c.577G>A; p.D193N; 1:27616962-27616962 |
skin | malignant_melanoma | Substitution - Missense |
c.891C>T; p.T297T; 1:27615561-27615561 |
skin; arm | malignant_melanoma | Substitution - coding silent |
c.1579G>A; p.D527N; 1:27612925-27612925 |
skin | malignant_melanoma | Substitution - Missense |
c.824G>A; p.G275E; 1:27615703-27615703 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.237G>A; p.V79V; 1:27623134-27623134 |
skin | malignant_melanoma | Substitution - coding silent |
c.272G>A; p.R91Q; 1:27623099-27623099 |
skin | malignant_melanoma | Substitution - Missense |
c.107C>T; p.P36L; 1:27623810-27623810 |
skin | malignant_melanoma | Substitution - Missense |
c.1262C>T; p.P421L; 1:27613338-27613338 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.496G>A; p.G166R; 1:27617229-27617229 |
skin | malignant_melanoma | Substitution - Missense |
c.885G>A; p.P295P; 1:27615567-27615567 |
skin | malignant_melanoma | Substitution - coding silent |
c.1357A>C; p.T453P; 1:27613243-27613243 |
skin | malignant_melanoma | Substitution - Missense |
c.1357A>C; p.T453P; 1:27613243-27613243 |
skin | malignant_melanoma | Substitution - Missense |
c.514G>A; p.E172K; 1:27617211-27617211 |
skin | malignant_melanoma | Substitution - Missense |
c.1469C>T; p.A490V; 1:27613035-27613035 |
skin | malignant_melanoma | Substitution - Missense |
c.252C>T; p.A84A; 1:27623119-27623119 |
skin | malignant_melanoma | Substitution - coding silent |
c.916G>A; p.E306K; 1:27615536-27615536 |
skin | malignant_melanoma | Substitution - Missense |
c.417C>T; p.I139I; 1:27621570-27621570 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.346G>A; p.E116K; 1:27621641-27621641 |
skin | malignant_melanoma | Substitution - Missense |
c.1554C>T; p.S518S; 1:27612950-27612950 |
skin | malignant_melanoma | Substitution - coding silent |
c.1285G>A; p.A429T; 1:27613315-27613315 |
skin | malignant_melanoma | Substitution - Missense |
c.228G>A; p.G76G; 1:27623143-27623143 |
skin | malignant_melanoma | Substitution - coding silent |
c.667G>A; p.V223M; 1:27616872-27616872 |
skin; extremity | malignant_melanoma | Substitution - Missense |
c.242T>G; p.L81R; 1:27623129-27623129 |
skin | malignant_melanoma | Substitution - Missense |
c.1146C>T; p.D382D; 1:27614533-27614533 |
skin | malignant_melanoma | Substitution - coding silent |
c.1362G>A; p.K454K; 1:27613238-27613238 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.305A>T; p.E102V; 1:27623066-27623066 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1539G>T; p.E513D; 1:27612965-27612965 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1487G>A; p.R496H; 1:27613017-27613017 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.653C>T; p.S218L; 1:27616886-27616886 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1575C>T; p.P525P; 1:27612929-27612929 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.329+1G>A; p.?; 1:27623041-27623041 |
stomach | carcinoma; adenocarcinoma | Unknown |
c.601C>T; p.R201C; 1:27616938-27616938 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.300G>A; p.K100K; 1:27623071-27623071 |
thyroid | carcinoma | Substitution - coding silent |
c.49G>T; p.E17*; 1:27623868-27623868 |
urinary_tract; bladder | carcinoma | Substitution - Nonsense |
c.358C>G; p.L120V; 1:27621629-27621629 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - Missense |
c.358C>G; p.L120V; 1:27621629-27621629 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.314A>G; p.H105R; 1:27623057-27623057 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.572G>C; p.R191T; 1:27616967-27616967 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1062G>C; p.L354F; 1:27614883-27614883 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.85G>A; p.G29R; 1:27623832-27623832 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1515C>G; p.F505L; 1:27612989-27612989 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.346G>A; p.E116K; 1:27621641-27621641 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.77G>T; p.R26I; 1:27623840-27623840 |
urinary_tract; bladder | carcinoma | Substitution - Missense |