| Gene information | Literature | Expression | lncRNA | Mutation | Homolog |
Basic Information | |
|---|---|
Gene ID | 51773 |
Name | RSF1 |
Synonymous | remodeling and spacing factor 1;RSF1;remodeling and spacing factor 1 |
Definition | HBV pX associated protein-8|HBV pX-associated protein 8|hepatitis B virus x associated protein|hepatitis B virus x-associated protein|p325 subunit of RSF chromatin-remodeling complex |
Position | 11q14.1 |
Gene Type | protein-coding |
COSMIC confirmed somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.222G>A; p.L74L; 11:77764655-77764655 |
biliary_tract; gallbladder | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1039G>A; p.E347K; 11:77702190-77702190 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.2537C>T; p.T846I; 11:77698665-77698665 |
bone; extraskeletal | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.3005A>T; p.K1002I; 11:77683770-77683770 |
bone; femur | chondrosarcoma | Substitution - Missense |
c.3695G>A; p.R1232H; 11:77672098-77672098 |
breast | carcinoma; ductal_carcinoma | Substitution - Missense |
c.2775G>C; p.L925L; 11:77693552-77693552 |
breast | carcinoma | Substitution - coding silent |
c.3947G>C; p.G1316A; 11:77667296-77667296 |
breast | carcinoma | Substitution - Missense |
c.2908C>T; p.R970C; 11:77685152-77685152 |
breast | carcinoma; basal_(triple-negative)_carcinoma | Substitution - Missense |
c.3925_3927delGAG; p.E1309delE; 11:77667316-77667318 |
breast | carcinoma | Deletion - In frame |
c.1989A>C; p.K663N; 11:77701240-77701240 |
breast | carcinoma | Substitution - Missense |
c.806A>G; p.N269S; 11:77702423-77702423 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.3519T>C; p.D1173D; 11:77675079-77675079 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.3347A>G; p.Q1116R; 11:77675251-77675251 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.749G>A; p.S250N; 11:77702480-77702480 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.3820C>T; p.R1274W; 11:77667423-77667423 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.4143G>A; p.E1381E; 11:77667100-77667100 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.3835G>T; p.D1279Y; 11:77667408-77667408 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.3263G>A; p.R1088H; 11:77676870-77676870 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2585G>A; p.S862N; 11:77698617-77698617 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.3805C>T; p.R1269W; 11:77667438-77667438 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1608A>C; p.E536D; 11:77701621-77701621 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2552G>A; p.R851H; 11:77698650-77698650 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.550G>T; p.D184Y; 11:77740759-77740759 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.3156C>T; p.I1052I; 11:77676977-77676977 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.3488G>A; p.R1163Q; 11:77675110-77675110 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2829C>T; p.L943L; 11:77691230-77691230 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.479G>A; p.G160D; 11:77740830-77740830 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.3692G>A; p.R1231Q; 11:77672101-77672101 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1645G>T; p.D549Y; 11:77701584-77701584 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.627T>C; p.I209I; 11:77725651-77725651 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1451G>A; p.G484E; 11:77701778-77701778 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.3900A>G; p.L1300L; 11:77667343-77667343 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.2679A>G; p.P893P; 11:77698523-77698523 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.3783T>C; p.D1261D; 11:77667460-77667460 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.2320A>G; p.T774A; 11:77700909-77700909 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.3658G>A; p.D1220N; 11:77672135-77672135 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1111A>G; p.T371A; 11:77702118-77702118 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.3984G>A; p.R1328R; 11:77667259-77667259 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.1614A>C; p.E538D; 11:77701615-77701615 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1914T>A; p.C638*; 11:77701315-77701315 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Nonsense |
c.3919G>A; p.E1307K; 11:77667324-77667324 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1733G>A; p.R578H; 11:77701496-77701496 |
large_intestine; colon | NS | Substitution - Missense |
c.2004C>A; p.T668T; 11:77701225-77701225 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.216G>T; p.L72F; 11:77764661-77764661 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.2584A>T; p.S862C; 11:77698618-77698618 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.2584A>T; p.S862C; 11:77698618-77698618 |
large_intestine; colon | carcinoma | Substitution - Missense |
c.2584A>T; p.S862C; 11:77698618-77698618 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1628C>T; p.S543F; 11:77701601-77701601 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3519T>C; p.D1173D; 11:77675079-77675079 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.10G>A; p.A4T; 11:77820705-77820705 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.2849A>G; p.Q950R; 11:77691210-77691210 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2199C>T; p.I733I; 11:77701030-77701030 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3124G>A; p.D1042N; 11:77678095-77678095 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1760A>G; p.K587R; 11:77701469-77701469 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1786C>A; p.L596I; 11:77701443-77701443 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3805C>T; p.R1269W; 11:77667438-77667438 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3805C>T; p.R1269W; 11:77667438-77667438 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.3805C>T; p.R1269W; 11:77667438-77667438 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2312T>C; p.V771A; 11:77700917-77700917 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.262G>A; p.E88K; 11:77764615-77764615 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1446G>A; p.T482T; 11:77701783-77701783 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.4019C>T; p.P1340L; 11:77667224-77667224 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3782A>G; p.D1261G; 11:77667461-77667461 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.2988G>T; p.K996N; 11:77683787-77683787 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.3250C>T; p.R1084*; 11:77676883-77676883 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.2424A>C; p.E808D; 11:77700805-77700805 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.3517G>A; p.D1173N; 11:77675081-77675081 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1083C>T; p.H361H; 11:77702146-77702146 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1158delA; p.K386fs*6; 11:77702071-77702071 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1158delA; p.K386fs*6; 11:77702071-77702071 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1158delA; p.K386fs*6; 11:77702071-77702071 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.3175C>T; p.R1059C; 11:77676958-77676958 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.267delA; p.K89fs*3; 11:77764610-77764610 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.3448C>T; p.R1150*; 11:77675150-77675150 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.439G>A; p.D147N; 11:77740870-77740870 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1989_1990insA; p.V664fs*11; 11:77701239-77701240 |
large_intestine; caecum | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.53G>A; p.G18D; 11:77820662-77820662 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2536A>G; p.T846A; 11:77698666-77698666 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.603T>C; p.T201T; 11:77725675-77725675 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.748A>G; p.S250G; 11:77702481-77702481 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.748A>G; p.S250G; 11:77702481-77702481 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.748A>G; p.S250G; 11:77702481-77702481 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.748A>G; p.S250G; 11:77702481-77702481 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3691C>T; p.R1231*; 11:77672102-77672102 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.768G>T; p.E256D; 11:77702461-77702461 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.768G>T; p.E256D; 11:77702461-77702461 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.768G>T; p.E256D; 11:77702461-77702461 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.2506A>G; p.K836E; 11:77700723-77700723 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1705A>C; p.K569Q; 11:77701524-77701524 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1652C>G; p.S551C; 11:77701577-77701577 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.2530C>T; p.R844*; 11:77698672-77698672 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.2530C>T; p.R844*; 11:77698672-77698672 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.2887C>T; p.R963C; 11:77691172-77691172 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3268C>T; p.R1090*; 11:77676865-77676865 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.3814C>T; p.R1272*; 11:77667429-77667429 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.3814C>T; p.R1272*; 11:77667429-77667429 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1930delG; p.E644fs*5; 11:77701299-77701299 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.2827C>T; p.L943F; 11:77691232-77691232 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.3624G>A; p.R1208R; 11:77672169-77672169 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1053C>T; p.I351I; 11:77702176-77702176 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1648C>A; p.L550I; 11:77701581-77701581 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.3016A>G; p.N1006D; 11:77683759-77683759 |
liver | carcinoma | Substitution - Missense |
c.3016A>G; p.N1006D; 11:77683759-77683759 |
liver | carcinoma | Substitution - Missense |
c.1415A>G; p.Y472C; 11:77701814-77701814 |
liver | carcinoma | Substitution - Missense |
c.1415A>G; p.Y472C; 11:77701814-77701814 |
liver | carcinoma | Substitution - Missense |
c.3471G>T; p.R1157S; 11:77675127-77675127 |
liver | carcinoma | Substitution - Missense |
c.3021G>T; p.L1007F; 11:77683754-77683754 |
liver | carcinoma | Substitution - Missense |
c.2334T>G; p.S778S; 11:77700895-77700895 |
liver | carcinoma | Substitution - coding silent |
c.2334T>G; p.S778S; 11:77700895-77700895 |
liver | carcinoma | Substitution - coding silent |
c.677A>G; p.E226G; 11:77725601-77725601 |
liver | carcinoma | Substitution - Missense |
c.3656A>G; p.E1219G; 11:77672137-77672137 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.3435C>T; p.S1145S; 11:77675163-77675163 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1061G>C; p.G354A; 11:77702168-77702168 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.3425A>G; p.D1142G; 11:77675173-77675173 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.632C>A; p.P211H; 11:77725646-77725646 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.4079C>A; p.P1360Q; 11:77667164-77667164 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2813G>T; p.C938F; 11:77693514-77693514 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3143G>A; p.R1048Q; 11:77676990-77676990 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1992A>G; p.V664V; 11:77701237-77701237 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.2558G>T; p.R853I; 11:77698644-77698644 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1821A>G; p.P607P; 11:77701408-77701408 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.822T>C; p.T274T; 11:77702407-77702407 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2587G>T; p.E863*; 11:77698615-77698615 |
lung | carcinoma; small_cell_carcinoma | Substitution - Nonsense |
c.1039G>T; p.E347*; 11:77702190-77702190 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.3826C>T; p.R1276*; 11:77667417-77667417 |
lung | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1138G>T; p.A380S; 11:77702091-77702091 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3827G>A; p.R1276Q; 11:77667416-77667416 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3303T>A; p.D1101E; 11:77676830-77676830 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1783T>C; p.F595L; 11:77701446-77701446 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2252A>T; p.K751I; 11:77700977-77700977 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.3458C>T; p.S1153F; 11:77675140-77675140 |
NS | malignant_melanoma | Substitution - Missense |
c.2968delT; p.S990fs*30; 11:77683807-77683807 |
oesophagus | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.948G>T; p.K316N; 11:77702281-77702281 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - Missense |
c.2398delA; p.R800fs*24; 11:77700831-77700831 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.2209A>T; p.I737F; 11:77701020-77701020 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.378C>T; p.L126L; 11:77740931-77740931 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.3251G>A; p.R1084Q; 11:77676882-77676882 |
ovary | other; neoplasm | Substitution - Missense |
c.4100A>G; p.D1367G; 11:77667143-77667143 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.112G>T; p.D38Y; 11:77820603-77820603 |
pancreas | carcinoma | Substitution - Missense |
c.1392T>C; p.F464F; 11:77701837-77701837 |
pancreas | carcinoma; ductal_carcinoma | Substitution - coding silent |
c.1084G>A; p.E362K; 11:77702145-77702145 |
pancreas | carcinoma | Substitution - Missense |
c.1084G>A; p.E362K; 11:77702145-77702145 |
pancreas | carcinoma | Substitution - Missense |
c.1084G>A; p.E362K; 11:77702145-77702145 |
pancreas | carcinoma | Substitution - Missense |
c.3155T>A; p.I1052N; 11:77676978-77676978 |
pancreas | carcinoma; ductal_carcinoma | Substitution - Missense |
c.2398delA; p.R800fs*24; 11:77700831-77700831 |
pancreas | carcinoma; acinar_carcinoma | Deletion - Frameshift |
c.3607_3608insGGCGAA; p.R1206_S1207insRR; 11:77672185-77672186 |
prostate | carcinoma | Insertion - In frame |
c.2598C>A; p.G866G; 11:77698604-77698604 |
prostate | adenoma | Substitution - coding silent |
c.3967C>T; p.R1323C; 11:77667276-77667276 |
prostate | carcinoma | Substitution - Missense |
c.1606G>A; p.E536K; 11:77701623-77701623 |
skin; mucosal | malignant_melanoma | Substitution - Missense |
c.847G>A; p.E283K; 11:77702382-77702382 |
skin; trunk | malignant_melanoma | Substitution - Missense |
c.306G>A; p.W102*; 11:77747102-77747102 |
skin | malignant_melanoma | Substitution - Nonsense |
c.481C>T; p.L161F; 11:77740828-77740828 |
skin | malignant_melanoma | Substitution - Missense |
c.1364T>A; p.F455Y; 11:77701865-77701865 |
skin | malignant_melanoma | Substitution - Missense |
c.2612C>T; p.S871F; 11:77698590-77698590 |
skin | malignant_melanoma | Substitution - Missense |
c.1612G>A; p.E538K; 11:77701617-77701617 |
skin | malignant_melanoma | Substitution - Missense |
c.1612G>A; p.E538K; 11:77701617-77701617 |
skin | malignant_melanoma | Substitution - Missense |
c.2003C>T; p.T668I; 11:77701226-77701226 |
skin | malignant_melanoma | Substitution - Missense |
c.1404G>A; p.K468K; 11:77701825-77701825 |
skin | malignant_melanoma | Substitution - coding silent |
c.3884C>T; p.P1295L; 11:77667359-77667359 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3643A>G; p.I1215V; 11:77672150-77672150 |
skin; upper_leg | malignant_melanoma | Substitution - Missense |
c.1249G>A; p.E417K; 11:77701980-77701980 |
skin | malignant_melanoma | Substitution - Missense |
c.3158C>T; p.S1053F; 11:77676975-77676975 |
skin | malignant_melanoma | Substitution - Missense |
c.2398A>T; p.R800*; 11:77700831-77700831 |
skin | malignant_melanoma | Substitution - Nonsense |
c.483C>A; p.L161L; 11:77740826-77740826 |
skin | malignant_melanoma | Substitution - coding silent |
c.2646T>A; p.S882R; 11:77698556-77698556 |
skin | malignant_melanoma | Substitution - Missense |
c.1202G>A; p.G401E; 11:77702027-77702027 |
skin | malignant_melanoma | Substitution - Missense |
c.1743C>T; p.I581I; 11:77701486-77701486 |
skin | malignant_melanoma | Substitution - coding silent |
c.1467C>T; p.S489S; 11:77701762-77701762 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.2074G>A; p.E692K; 11:77701155-77701155 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2158G>A; p.E720K; 11:77701071-77701071 |
skin | malignant_melanoma | Substitution - Missense |
c.1673C>T; p.S558F; 11:77701556-77701556 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2892C>T; p.A964A; 11:77691167-77691167 |
skin | malignant_melanoma | Substitution - coding silent |
c.1902C>T; p.I634I; 11:77701327-77701327 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.3827G>A; p.R1276Q; 11:77667416-77667416 |
skin | malignant_melanoma | Substitution - Missense |
c.506A>G; p.Q169R; 11:77740803-77740803 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3889C>T; p.R1297C; 11:77667354-77667354 |
skin | malignant_melanoma | Substitution - Missense |
c.2621C>T; p.S874L; 11:77698581-77698581 |
skin | malignant_melanoma | Substitution - Missense |
c.583C>T; p.R195*; 11:77725695-77725695 |
skin | malignant_melanoma | Substitution - Nonsense |
c.3678C>T; p.S1226S; 11:77672115-77672115 |
skin | malignant_melanoma | Substitution - coding silent |
c.2530C>T; p.R844*; 11:77698672-77698672 |
skin | malignant_melanoma | Substitution - Nonsense |
c.2530C>T; p.R844*; 11:77698672-77698672 |
skin | malignant_melanoma | Substitution - Nonsense |
c.2530C>T; p.R844*; 11:77698672-77698672 |
skin | malignant_melanoma | Substitution - Nonsense |
c.3192T>A; p.S1064S; 11:77676941-77676941 |
skin | malignant_melanoma | Substitution - coding silent |
c.1832C>T; p.P611L; 11:77701397-77701397 |
skin | malignant_melanoma | Substitution - Missense |
c.2598C>T; p.G866G; 11:77698604-77698604 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1980T>C; p.S660S; 11:77701249-77701249 |
stomach | adenocarcinoma | Substitution - coding silent |
c.3900A>G; p.L1300L; 11:77667343-77667343 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3398C>T; p.P1133L; 11:77675200-77675200 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2410G>A; p.E804K; 11:77700819-77700819 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.3940G>A; p.A1314T; 11:77667303-77667303 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.3437G>A; p.R1146H; 11:77675161-77675161 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.4205C>A; p.A1402E; 11:77667038-77667038 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.3129A>G; p.G1043G; 11:77678090-77678090 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1475C>A; p.S492Y; 11:77701754-77701754 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1444A>C; p.T482P; 11:77701785-77701785 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2702A>C; p.N901T; 11:77698500-77698500 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1158delA; p.K386fs*6; 11:77702071-77702071 |
stomach | carcinoma; intestinal_adenocarcinoma | Deletion - Frameshift |
c.1158delA; p.K386fs*6; 11:77702071-77702071 |
stomach | adenocarcinoma | Deletion - Frameshift |
c.2105A>G; p.Q702R; 11:77701124-77701124 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.3610C>T; p.R1204*; 11:77672183-77672183 |
stomach | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1955G>A; p.S652N; 11:77701274-77701274 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2994A>G; p.K998K; 11:77683781-77683781 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3436C>T; p.R1146C; 11:77675162-77675162 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.578+2T>C; p.?; 11:77740729-77740729 |
stomach | carcinoma; mixed_intestinal_and_diffuse_adenocarcinoma-unclassifiable | Unknown |
c.2143G>T; p.E715*; 11:77701086-77701086 |
stomach | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.3141C>T; p.G1047G; 11:77676992-77676992 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.3223A>G; p.K1075E; 11:77676910-77676910 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1430A>G; p.D477G; 11:77701799-77701799 |
thyroid | carcinoma | Substitution - Missense |
c.3269G>T; p.R1090L; 11:77676864-77676864 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3862G>A; p.E1288K; 11:77667381-77667381 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.3474G>A; p.Q1158Q; 11:77675124-77675124 |
upper_aerodigestive_tract; pharynx | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1773C>T; p.S591S; 11:77701456-77701456 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1773C>T; p.S591S; 11:77701456-77701456 |
upper_aerodigestive_tract; mouth | carcinoma | Substitution - coding silent |
c.2837A>G; p.K946R; 11:77691222-77691222 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1509G>C; p.E503D; 11:77701720-77701720 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - Missense |
c.1509G>C; p.E503D; 11:77701720-77701720 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.2069G>A; p.G690D; 11:77701160-77701160 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - Missense |
c.2069G>A; p.G690D; 11:77701160-77701160 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.2377G>A; p.D793N; 11:77700852-77700852 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1377A>C; p.P459P; 11:77701852-77701852 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.4250C>G; p.A1417G; 11:77666993-77666993 |
urinary_tract; bladder | carcinoma | Substitution - Missense |