ClinVar Miner

List of variants in gene EGFR reported as likely benign for not provided

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 87
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HGVS dbSNP gnomAD frequency
NM_005228.5(EGFR):c.1881-891T>C rs17336974 0.02080
NM_005228.5(EGFR):c.1919+174G>A rs17290260 0.02080
NM_005228.5(EGFR):c.1299-197G>A rs17289991 0.02037
NM_005228.5(EGFR):c.2061+65G>A rs17290301 0.01996
NM_005228.5(EGFR):c.2283+69G>A rs17337135 0.01932
NM_005228.5(EGFR):c.560-184T>A rs17289760 0.01459
NM_005228.5(EGFR):c.425-126T>C rs17172450 0.01416
NM_005228.5(EGFR):c.1881-2611A>C rs140321332 0.01394
NM_005228.5(EGFR):c.88+63G>C rs17335724 0.01268
NM_005228.5(EGFR):c.88+61C>A rs17335717 0.01265
NM_005228.5(EGFR):c.1881-721G>A rs17336988 0.01263
NM_005228.5(EGFR):c.3115-180G>T rs17337486 0.01194
NM_005228.5(EGFR):c.1631+133G>A rs75985451 0.01073
NM_005228.5(EGFR):c.747+295T>C rs17336584 0.01059
NM_005228.5(EGFR):c.1881-2410T>C rs75040104 0.01054
NM_005228.5(EGFR):c.2849-165C>T rs17337444 0.01044
NM_005228.5(EGFR):c.2184+154A>G rs17172452 0.00969
NM_005228.5(EGFR):c.*78C>T rs17290762 0.00926
NM_005228.5(EGFR):c.1723-64T>G rs17336933 0.00890
NM_005228.5(EGFR):c.1880+34C>T rs17290176 0.00884
NM_005228.5(EGFR):c.1880+294A>T rs572751534 0.00881
NM_005228.5(EGFR):c.1722+68T>C rs17290117 0.00880
NM_005228.5(EGFR):c.1509C>T (p.Gly503=) rs17336800 0.00859
NM_005228.5(EGFR):c.2047C>T (p.Leu683=) rs55669340 0.00851
NM_005228.5(EGFR):c.1723-88C>T rs17336926 0.00850
NM_005228.5(EGFR):c.1723-294C>T rs17336912 0.00838
NM_005228.5(EGFR):c.1881-2372T>A rs184292880 0.00788
NM_005228.5(EGFR):c.2946+241G>A rs41466248 0.00758
NM_005228.5(EGFR):c.2849-188C>T rs41499254 0.00742
NM_005228.5(EGFR):c.*35C>T rs17290755 0.00720
NM_005228.5(EGFR):c.747+169C>T rs78896241 0.00686
NM_005228.5(EGFR):c.2963A>C (p.His988Pro) rs17290699 0.00672
NM_005228.5(EGFR):c.425-84C>T rs115102360 0.00610
NM_005228.5(EGFR):c.1919+183C>T rs17290267 0.00530
NM_005228.5(EGFR):c.2284-56C>T rs41323247 0.00491
NM_005228.5(EGFR):c.3163-304G>A rs17337500 0.00489
NM_005228.5(EGFR):c.1919+136A>G rs41491049 0.00445
NM_005228.5(EGFR):c.3114+90C>T rs17337479 0.00379
NM_005228.5(EGFR):c.3272-52A>G rs145306310 0.00257
NM_005228.5(EGFR):c.3015A>G (p.Glu1005=) rs55737335 0.00247
NM_005228.5(EGFR):c.2748C>T (p.Asp916=) rs41396448 0.00046
NM_005228.5(EGFR):c.2355C>T (p.Thr785=) rs148188503 0.00033
NM_005228.5(EGFR):c.3225C>T (p.Gly1075=) rs140117937 0.00032
NM_005228.5(EGFR):c.241-8C>G rs138872748 0.00031
NM_005228.5(EGFR):c.1851C>T (p.Cys617=) rs143422127 0.00010
NM_005228.5(EGFR):c.2457G>A (p.Val819=) rs56183713 0.00010
NM_005228.5(EGFR):c.3087G>A (p.Thr1029=) rs141489713 0.00009
NM_005228.5(EGFR):c.1774G>A (p.Val592Ile) rs144943614 0.00007
NM_005228.5(EGFR):c.2019C>T (p.Ile673=) rs763193362 0.00005
NM_005228.5(EGFR):c.768C>T (p.Asp256=) rs146098757 0.00004
NM_005228.5(EGFR):c.2259G>A (p.Pro753=) rs764064214 0.00003
NM_005228.5(EGFR):c.339C>T (p.Tyr113=) rs374582814 0.00003
NM_005228.5(EGFR):c.21C>T (p.Ala7=) rs369581368 0.00002
NM_005228.5(EGFR):c.30G>T (p.Ala10=) rs757936561 0.00001
NC_000007.14:g.55018796C>A rs17335710
NM_005228.5(EGFR):c.*294del
NM_005228.5(EGFR):c.1446G>A (p.Gly482=) rs1351950283
NM_005228.5(EGFR):c.1722+136G>T rs17290124
NM_005228.5(EGFR):c.1722+26G>A rs17290110
NM_005228.5(EGFR):c.1880+77C>A rs41421952
NM_005228.5(EGFR):c.1881-226C>T rs17337009
NM_005228.5(EGFR):c.1881-2340A>T rs189248205
NM_005228.5(EGFR):c.1881-409G>A
NM_005228.5(EGFR):c.1881-615G>A rs17290225
NM_005228.5(EGFR):c.1881-658G>A
NM_005228.5(EGFR):c.1881-670T>G
NM_005228.5(EGFR):c.1919+134T>G rs17290253
NM_005228.5(EGFR):c.1995C>T (p.Gly665=) rs1383165136
NM_005228.5(EGFR):c.2062-293G>A rs6952904
NM_005228.5(EGFR):c.2185-214A>T rs17337128
NM_005228.5(EGFR):c.2223C>T (p.Pro741=) rs372772241
NM_005228.5(EGFR):c.2470-128A>G
NM_005228.5(EGFR):c.2496C>T (p.Arg832=)
NM_005228.5(EGFR):c.2946+240C>G rs150947992
NM_005228.5(EGFR):c.2946+371G>A
NM_005228.5(EGFR):c.2947-128G>A rs17290692
NM_005228.5(EGFR):c.2976T>C (p.Pro992=)
NM_005228.5(EGFR):c.3057A>C (p.Pro1019=)
NM_005228.5(EGFR):c.3271+26C>T
NM_005228.5(EGFR):c.425-113G>T rs17289665
NM_005228.5(EGFR):c.425-326A>G
NM_005228.5(EGFR):c.438C>T (p.Gly146=) rs199637112
NM_005228.5(EGFR):c.629-329del rs17289809
NM_005228.5(EGFR):c.629-330G>T rs41364648
NM_005228.5(EGFR):c.748-193G>T
NM_005228.5(EGFR):c.748-253C>G rs17289851
NM_005228.5(EGFR):c.828G>A (p.Gln276=) rs2128935031

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