| Gene information | Literature | Expression | lncRNA | Mutation | Homolog |
Basic Information | |
|---|---|
Gene ID | 5983 |
Name | RFC3 |
Synonymous | replication factor C (activator 1) 3, 38kDa;RFC3;replication factor C (activator 1) 3, 38kDa |
Definition | A1 38 kDa subunit|RF-C 38 kDa subunit|RFC, 38 kD subunit|activator 1 38 kDa subunit|activator 1 subunit 3|replication factor C 38 kDa subunit|replication factor C subunit 3 |
Position | 13q13.2 |
Gene Type | protein-coding |
COSMIC confirmed somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.526_553del28; p.R176fs*21; 13:33829970-33829997 |
endometrium | carcinoma; endometrioid_carcinoma | Deletion - Frameshift |
c.824G>A; p.R275H; 13:33835162-33835162 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.152G>T; p.R51I; 13:33821196-33821196 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.203G>A; p.R68K; 13:33821247-33821247 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.43C>T; p.R15W; 13:33818221-33818221 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm | Substitution - Missense |
c.544G>A; p.V182I; 13:33829988-33829988 |
haematopoietic_and_lymphoid_tissue; central_nervous_system | lymphoid_neoplasm; primary_central_nervous_system_lymphoma | Substitution - Missense |
c.502A>C; p.T168P; 13:33829946-33829946 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.810G>A; p.R270R; 13:33835148-33835148 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.601A>G; p.K201E; 13:33830746-33830746 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.512T>A; p.V171E; 13:33829956-33829956 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.423C>A; p.T141T; 13:33829867-33829867 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.147G>T; p.K49N; 13:33821191-33821191 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.801T>C; p.T267T; 13:33831346-33831346 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.471T>C; p.S157S; 13:33829915-33829915 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.234_235insA; p.I82fs*2; 13:33823925-33823926 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.235delA; p.I82fs*25; 13:33823926-33823926 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.235delA; p.I82fs*25; 13:33823926-33823926 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.235delA; p.I82fs*25; 13:33823926-33823926 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.235delA; p.I82fs*25; 13:33823926-33823926 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.235delA; p.I82fs*25; 13:33823926-33823926 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.235delA; p.I82fs*25; 13:33823926-33823926 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.235delA; p.I82fs*25; 13:33823926-33823926 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.235delA; p.I82fs*25; 13:33823926-33823926 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.235delA; p.I82fs*25; 13:33823926-33823926 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.235delA; p.I82fs*25; 13:33823926-33823926 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.235delA; p.I82fs*25; 13:33823926-33823926 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.235delA; p.I82fs*25; 13:33823926-33823926 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.235delA; p.I82fs*25; 13:33823926-33823926 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.235delA; p.I82fs*25; 13:33823926-33823926 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.235delA; p.I82fs*25; 13:33823926-33823926 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.763C>A; p.L255M; 13:33831308-33831308 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.243A>C; p.K81N; 13:33823934-33823934 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.835T>C; p.Y279H; 13:33835173-33835173 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.515delT; p.I172fs*34; 13:33829959-33829959 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.943G>T; p.A315S; 13:33836167-33836167 |
liver | carcinoma | Substitution - Missense |
c.943G>T; p.A315S; 13:33836167-33836167 |
liver | carcinoma | Substitution - Missense |
c.943G>T; p.A315S; 13:33836167-33836167 |
liver | carcinoma | Substitution - Missense |
c.124G>C; p.G42R; 13:33821168-33821168 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.325C>G; p.Q109E; 13:33825820-33825820 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.659G>T; p.C220F; 13:33830804-33830804 |
lung; middle_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.661A>T; p.R221*; 13:33830806-33830806 |
lung | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.634G>C; p.A212P; 13:33830779-33830779 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.506C>T; p.S169F; 13:33829950-33829950 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.425A>G; p.K142R; 13:33829869-33829869 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.396A>G; p.V132V; 13:33829840-33829840 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.876G>A; p.M292I; 13:33835214-33835214 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.99T>C; p.G33G; 13:33821143-33821143 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.827G>A; p.G276E; 13:33835165-33835165 |
skin; extremity | malignant_melanoma | Substitution - Missense |
c.880-1G>A; p.?; 13:33836103-33836103 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Unknown |
c.961C>T; p.R321C; 13:33836185-33836185 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.823C>T; p.R275C; 13:33835161-33835161 |
skin | malignant_melanoma | Substitution - Missense |
c.934G>A; p.A312T; 13:33836158-33836158 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.855T>C; p.C285C; 13:33835193-33835193 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.235delA; p.I82fs*25; 13:33823926-33823926 |
stomach | carcinoma; intestinal_adenocarcinoma | Deletion - Frameshift |
c.1003T>C; p.F335L; 13:33836227-33836227 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.449G>A; p.R150K; 13:33829893-33829893 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.549T>G; p.R183R; 13:33829993-33829993 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.823C>T; p.R275C; 13:33835161-33835161 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.823C>T; p.R275C; 13:33835161-33835161 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |