| Gene information | Literature | Expression | lncRNA | Mutation | Homolog |
Basic Information | |
|---|---|
Gene ID | 2534 |
Name | FYN |
Synonymous | FYN proto-oncogene, Src family tyrosine kinase;FYN;FYN proto-oncogene, Src family tyrosine kinase |
Definition | FYN oncogene related to SRC, FGR, YES|OKT3-induced calcium influx regulator|c-syn protooncogene|proto-oncogene Syn|proto-oncogene c-Fyn|src-like kinase|src/yes-related novel|tyrosine kinase p59fyn(T)|tyrosine-protein kinase Fyn |
Position | 6q21 |
Gene Type | protein-coding |
COSMIC confirmed somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.1483C>T; p.L495L; 6:111661870-111661870 |
bone; pelvis | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.1050A>G; p.L350L; 6:111694697-111694697 |
breast | carcinoma | Substitution - coding silent |
c.980T>C; p.V327A; 6:111696339-111696339 |
breast | carcinoma | Substitution - Missense |
c.870G>A; p.W290*; 6:111696449-111696449 |
central_nervous_system; brain | glioma | Substitution - Nonsense |
c.870G>A; p.W290*; 6:111696449-111696449 |
central_nervous_system; brain | glioma | Substitution - Nonsense |
c.1087A>G; p.K363E; 6:111694660-111694660 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.530A>G; p.E177G; 6:111704016-111704016 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1059C>A; p.F353L; 6:111694688-111694688 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.944C>T; p.A315V; 6:111696375-111696375 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.247G>T; p.G83*; 6:111719805-111719805 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.805G>T; p.E269*; 6:111700161-111700161 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.1189C>A; p.L397I; 6:111694459-111694459 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1227C>T; p.F409F; 6:111694421-111694421 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.521T>G; p.L174R; 6:111704025-111704025 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; peripheral_T_cell_lymphoma_unspecified | Substitution - Missense |
c.1591T>C; p.Y531H; 6:111661762-111661762 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; peripheral_T_cell_lymphoma_unspecified | Substitution - Missense |
c.526C>T; p.R176C; 6:111704020-111704020 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; peripheral_T_cell_lymphoma_unspecified | Substitution - Missense |
c.526C>T; p.R176C; 6:111704020-111704020 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; peripheral_T_cell_lymphoma_unspecified | Substitution - Missense |
c.1002T>A; p.S334S; 6:111696317-111696317 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.1535C>A; p.T512N; 6:111661818-111661818 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1220C>T; p.A407V; 6:111694428-111694428 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1042+1G>A; p.?; 6:111696276-111696276 |
large_intestine; caecum | carcinoma; adenocarcinoma | Unknown |
c.1042+1G>A; p.?; 6:111696276-111696276 |
large_intestine; colon | carcinoma; adenocarcinoma | Unknown |
c.60C>T; p.G20G; 6:111719992-111719992 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.328C>A; p.Q110K; 6:111714363-111714363 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.569G>A; p.R190H; 6:111703013-111703013 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.569G>A; p.R190H; 6:111703013-111703013 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.869G>T; p.W290L; 6:111696450-111696450 |
large_intestine; rectum | NS | Substitution - Missense |
c.1514delA; p.K505fs*>33; 6:111661839-111661839 |
large_intestine; rectum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.870G>A; p.W290*; 6:111696449-111696449 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1561G>A; p.E521K; 6:111661792-111661792 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1561G>A; p.E521K; 6:111661792-111661792 |
large_intestine; colon | carcinoma | Substitution - Missense |
c.1561G>A; p.E521K; 6:111661792-111661792 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.87C>A; p.R29R; 6:111719965-111719965 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1544A>G; p.Y515C; 6:111661809-111661809 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.727G>A; p.V243I; 6:111700239-111700239 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.210G>A; p.S70S; 6:111719842-111719842 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.481C>T; p.R161*; 6:111704065-111704065 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.481C>T; p.R161*; 6:111704065-111704065 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.481C>T; p.R161*; 6:111704065-111704065 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.296A>T; p.D99V; 6:111714395-111714395 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1488T>C; p.H496H; 6:111661865-111661865 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.156C>A; p.N52K; 6:111719896-111719896 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.327T>G; p.F109L; 6:111714364-111714364 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.28G>T; p.E10*; 6:111720024-111720024 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1344C>T; p.D448D; 6:111674560-111674560 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.229C>T; p.R77C; 6:111719823-111719823 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1372G>A; p.E458K; 6:111674532-111674532 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1230A>G; p.G410G; 6:111694418-111694418 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.127G>A; p.G43S; 6:111719925-111719925 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.868T>C; p.W290R; 6:111696451-111696451 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.616C>T; p.R206C; 6:111702966-111702966 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.616C>T; p.R206C; 6:111702966-111702966 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.616C>T; p.R206C; 6:111702966-111702966 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.616C>T; p.R206C; 6:111702966-111702966 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1216A>G; p.I406V; 6:111694432-111694432 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.230G>A; p.R77H; 6:111719822-111719822 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.44C>T; p.T15M; 6:111720008-111720008 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.85C>G; p.R29G; 6:111719967-111719967 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1509G>T; p.W503C; 6:111661844-111661844 |
lung; middle_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.1042+1G>A; p.?; 6:111696276-111696276 |
lung | carcinoma; squamous_cell_carcinoma | Unknown |
c.1042+1G>A; p.?; 6:111696276-111696276 |
lung | carcinoma; adenocarcinoma | Unknown |
c.503A>T; p.N168I; 6:111704043-111704043 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.831G>C; p.L277L; 6:111700135-111700135 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.315A>T; p.K105N; 6:111714376-111714376 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.287G>A; p.R96Q; 6:111714404-111714404 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.684A>T; p.V228V; 6:111702898-111702898 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1286C>T; p.P429L; 6:111674618-111674618 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1377G>T; p.L459L; 6:111674527-111674527 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1003G>C; p.E335Q; 6:111696316-111696316 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.355_356insA; p.W119fs*1; 6:111708009-111708010 |
lung | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.1324A>G; p.R442G; 6:111674580-111674580 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1081G>T; p.A361S; 6:111694666-111694666 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1376T>C; p.L459P; 6:111674528-111674528 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.169G>A; p.G57R; 6:111719883-111719883 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1420G>T; p.E474*; 6:111661933-111661933 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1503C>G; p.H501Q; 6:111661850-111661850 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.727G>C; p.V243L; 6:111700239-111700239 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.727G>C; p.V243L; 6:111700239-111700239 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.727G>C; p.V243L; 6:111700239-111700239 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.727G>C; p.V243L; 6:111700239-111700239 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.233C>T; p.T78M; 6:111719819-111719819 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.45G>A; p.T15T; 6:111720007-111720007 |
pancreas | carcinoma | Substitution - coding silent |
c.45G>A; p.T15T; 6:111720007-111720007 |
pancreas | carcinoma; ductal_carcinoma | Substitution - coding silent |
c.100C>G; p.P34A; 6:111719952-111719952 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.962T>G; p.L321R; 6:111696357-111696357 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1162C>T; p.H388Y; 6:111694486-111694486 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.328C>A; p.Q110K; 6:111714363-111714363 |
skin | malignant_melanoma | Substitution - Missense |
c.1352C>T; p.S451F; 6:111674552-111674552 |
skin | malignant_melanoma | Substitution - Missense |
c.1228G>A; p.G410R; 6:111694420-111694420 |
skin | malignant_melanoma | Substitution - Missense |
c.1228G>A; p.G410R; 6:111694420-111694420 |
skin | malignant_melanoma | Substitution - Missense |
c.375G>A; p.L125L; 6:111707990-111707990 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1298C>T; p.T433M; 6:111674606-111674606 |
skin | malignant_melanoma | Substitution - Missense |
c.939G>A; p.E313E; 6:111696380-111696380 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.861G>A; p.M287I; 6:111700105-111700105 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1532C>T; p.P511L; 6:111661821-111661821 |
skin | malignant_melanoma | Substitution - Missense |
c.292G>A; p.E98K; 6:111714399-111714399 |
skin | malignant_melanoma | Substitution - Missense |
c.466C>T; p.R156*; 6:111704080-111704080 |
skin | malignant_melanoma | Substitution - Nonsense |
c.509G>A; p.R170K; 6:111704037-111704037 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.45G>A; p.T15T; 6:111720007-111720007 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.328C>T; p.Q110*; 6:111714363-111714363 |
skin | malignant_melanoma | Substitution - Nonsense |
c.799C>T; p.P267S; 6:111700167-111700167 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1229G>A; p.G410E; 6:111694419-111694419 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.616C>T; p.R206C; 6:111702966-111702966 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.770C>T; p.S257F; 6:111700196-111700196 |
skin | malignant_melanoma | Substitution - Missense |
c.46G>A; p.E16K; 6:111720006-111720006 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.652C>T; p.R218W; 6:111702930-111702930 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.388_404del17; p.T130fs*7; 6:111707961-111707977 |
stomach | carcinoma; intestinal_adenocarcinoma | Deletion - Frameshift |
c.1175G>A; p.R392Q; 6:111694473-111694473 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.514A>G; p.T172A; 6:111704032-111704032 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.252G>A; p.V84V; 6:111714439-111714439 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1283T>G; p.F428C; 6:111674621-111674621 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1394T>C; p.V465A; 6:111674510-111674510 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1156T>C; p.Y386H; 6:111694492-111694492 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1315C>A; p.L439M; 6:111674589-111674589 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1451G>T; p.R484M; 6:111661902-111661902 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.118C>T; p.P40S; 6:111719934-111719934 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.616C>T; p.R206C; 6:111702966-111702966 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.354T>C; p.D118D; 6:111708011-111708011 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1606A>C; p.N536H; 6:111661747-111661747 |
thyroid | other; neoplasm | Substitution - Missense |
c.16T>C; p.C6R; 6:111720036-111720036 |
upper_aerodigestive_tract; larynx | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.258C>G; p.L86L; 6:111714433-111714433 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.258C>G; p.L86L; 6:111714433-111714433 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - coding silent |
c.328C>G; p.Q110E; 6:111714363-111714363 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1479C>T; p.I493I; 6:111661874-111661874 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |