| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 2212 |
Name | FCGR2A |
Synonymous | Fc fragment of IgG, low affinity IIa, receptor (CD32);FCGR2A;Fc fragment of IgG, low affinity IIa, receptor (CD32) |
Definition | Immunoglobulin G Fc receptor II|fc-gamma RII-a|fc-gamma-RIIa|fcRII-a|igG Fc receptor II-a|low affinity immunoglobulin gamma Fc region receptor II-a |
Position | 1q23 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.899A>T; p.K300I; 1:161518096-161518096 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.501G>A; p.L167L; 1:161509959-161509959 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.573C>A; p.G191G; 1:161510031-161510031 |
prostate | carcinoma; adenocarcinoma | Substitution - coding silent |
c.876C>T; p.P292P; 1:161518073-161518073 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.876C>T; p.P292P; 1:161518073-161518073 |
thyroid | other; neoplasm | Substitution - coding silent |
c.876C>T; p.P292P; 1:161518073-161518073 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.579G>A; p.T193T; 1:161510037-161510037 |
oesophagus | carcinoma | Substitution - coding silent |
c.579G>A; p.T193T; 1:161510037-161510037 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.250C>T; p.H84Y; 1:161506480-161506480 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.672G>A; p.A224A; 1:161510889-161510889 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.482C>T; p.S161F; 1:161509940-161509940 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.8T>C; p.M3T; 1:161505475-161505475 |
autonomic_ganglia | neuroblastoma | Substitution - Missense |
c.38C>T; p.P13L; 1:161505505-161505505 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.721A>G; p.R241G; 1:161510938-161510938 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.193C>T; p.R65C; 1:161506423-161506423 |
skin | malignant_melanoma | Substitution - Missense |
c.193C>T; p.R65C; 1:161506423-161506423 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.547G>T; p.D183Y; 1:161510005-161510005 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.475G>A; p.G159R; 1:161509933-161509933 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.827C>T; p.T276I; 1:161518024-161518024 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.497A>G; p.H166R; 1:161509955-161509955 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.497A>G; p.H166R; 1:161509955-161509955 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.860A>T; p.Y287F; 1:161518057-161518057 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.531C>G; p.N177K; 1:161509989-161509989 |
breast | carcinoma; ductal_carcinoma | Substitution - Missense |
c.168T>G; p.S56S; 1:161506398-161506398 |
stomach | adenocarcinoma | Substitution - coding silent |
c.928G>C; p.D310H; 1:161518125-161518125 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.856G>A; p.G286S; 1:161518053-161518053 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.805_808delAGAA; p.K270fs*18; 1:161518002-161518005 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Deletion - Frameshift |
c.842A>C; p.E281A; 1:161518039-161518039 |
breast | carcinoma | Substitution - Missense |
c.578C>T; p.T193M; 1:161510036-161510036 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.545G>T; p.G182V; 1:161510003-161510003 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.39C>T; p.P13P; 1:161505506-161505506 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.837C>A; p.D279E; 1:161518034-161518034 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.884C>A; p.P295H; 1:161518081-161518081 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.777+1G>A; p.?; 1:161513933-161513933 |
stomach | carcinoma; diffuse_adenocarcinoma | Unknown |
c.777+1G>A; p.?; 1:161513933-161513933 |
liver | carcinoma | Unknown |
c.777+1G>A; p.?; 1:161513933-161513933 |
stomach | carcinoma; diffuse_adenocarcinoma | Unknown |
c.334G>A; p.D112N; 1:161506564-161506564 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.725A>C; p.K242T; 1:161510942-161510942 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.140C>T; p.P47L; 1:161506370-161506370 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.927C>T; p.N309N; 1:161518124-161518124 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.927C>T; p.N309N; 1:161518124-161518124 |
thyroid | other; neoplasm | Substitution - coding silent |
c.67A>C; p.T23P; 1:161505534-161505534 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.67A>C; p.T23P; 1:161505534-161505534 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.138C>T; p.P46P; 1:161506368-161506368 |
skin | malignant_melanoma | Substitution - coding silent |
c.560C>A; p.T187K; 1:161510018-161510018 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.788G>T; p.R263L; 1:161517985-161517985 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.27G>A; p.Q9Q; 1:161505494-161505494 |
breast | carcinoma | Substitution - coding silent |
c.629G>T; p.G210V; 1:161510846-161510846 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.208G>A; p.D70N; 1:161506438-161506438 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.844A>G; p.T282A; 1:161518041-161518041 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.492C>A; p.F164L; 1:161509950-161509950 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.327C>T; p.S109S; 1:161506557-161506557 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.207C>T; p.S69S; 1:161506437-161506437 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.403G>A; p.G135R; 1:161509861-161509861 |
skin | malignant_melanoma | Substitution - Missense |
c.194G>A; p.R65H; 1:161506424-161506424 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.6T>C; p.T2T; 1:161505473-161505473 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.217C>T; p.Q73*; 1:161506447-161506447 |
skin | malignant_melanoma | Substitution - Nonsense |
c.777+5G>T; p.?; 1:161513937-161513937 |
liver | carcinoma | Unknown |
c.777+5G>T; p.?; 1:161513937-161513937 |
liver | carcinoma | Unknown |
c.578C>A; p.T193K; 1:161510036-161510036 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.802A>C; p.I268L; 1:161517999-161517999 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.384T>C; p.P128P; 1:161509842-161509842 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.730C>T; p.R244W; 1:161510947-161510947 |
liver | carcinoma | Substitution - Missense |
c.730C>T; p.R244W; 1:161510947-161510947 |
liver | carcinoma | Substitution - Missense |
c.658G>A; p.A220T; 1:161510875-161510875 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.365G>A; p.W122*; 1:161509823-161509823 |
lung | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.882A>T; p.A294A; 1:161518079-161518079 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.167C>G; p.S56C; 1:161506397-161506397 |
breast | carcinoma | Substitution - Missense |
c.501G>C; p.L167F; 1:161509959-161509959 |
skin | malignant_melanoma | Substitution - Missense |
c.919C>T; p.P307S; 1:161518116-161518116 |
skin | malignant_melanoma | Substitution - Missense |
c.723G>A; p.R241R; 1:161510940-161510940 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.570A>G; p.I190M; 1:161510028-161510028 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.757G>A; p.V253M; 1:161513912-161513912 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.699T>A; p.A233A; 1:161510916-161510916 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.91G>A; p.A31T; 1:161505992-161505992 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.91G>A; p.A31T; 1:161505992-161505992 |
pancreas | carcinoma | Substitution - Missense |
c.892G>A; p.D298N; 1:161518089-161518089 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.812G>C; p.R271T; 1:161518009-161518009 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.892G>A; p.D298N; 1:161518089-161518089 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.126G>A; p.L42L; 1:161506356-161506356 |
skin | malignant_melanoma | Substitution - coding silent |