ClinVar Miner

List of variants reported as benign for EGFR-related lung cancer

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Total variants: 60
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HGVS dbSNP gnomAD frequency
NM_005228.5(EGFR):c.2709T>C (p.Thr903=) rs1140475 0.89501
NM_005228.5(EGFR):c.2361G>A (p.Gln787=) rs1050171 0.51617
NM_005228.5(EGFR):c.474C>T (p.Asn158=) rs2072454 0.50662
NM_005228.5(EGFR):c.89-17723A>C rs13244925 0.49781
NM_005228.5(EGFR):c.1887T>A (p.Thr629=) rs2227984 0.33239
NM_005228.5(EGFR):c.1562G>A (p.Arg521Lys) rs2227983 0.22212
NM_005228.5(EGFR):c.2709= (p.Thr903=) rs1140475 0.10499
NM_005228.5(EGFR):c.2982C>T (p.Asp994=) rs2293347 0.09191
NM_005228.5(EGFR):c.559+10G>A rs7801956 0.06316
NM_005228.5(EGFR):c.1839C>T (p.Ala613=) rs17290169 0.05521
NM_005228.5(EGFR):c.2626-19C>T rs17337360 0.03371
NM_005228.5(EGFR):c.2184+19G>A rs17337107 0.02954
NM_005228.5(EGFR):c.531G>A (p.Ser177=) rs17336437 0.01924
NM_005228.5(EGFR):c.1632T>C (p.Gly544=) rs17290103 0.00901
NM_005228.5(EGFR):c.1317A>G (p.Ala439=) rs17290005 0.00886
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.1788G>A (p.Pro596=) rs17290162 0.00841
NM_005228.5(EGFR):c.1299-7A>G rs75911944 0.00690
NM_005228.5(EGFR):c.2963A>C (p.His988Pro) rs17290699 0.00672
NM_005228.5(EGFR):c.1830C>T (p.Tyr610=) rs115350205 0.00515
NM_005228.5(EGFR):c.3485G>A (p.Ser1162Asn) rs41321844 0.00362
NM_005228.5(EGFR):c.3210C>T (p.Ser1070=) rs41494749 0.00327
NM_005228.5(EGFR):c.921C>T (p.Cys307=) rs17289893 0.00302
NM_005228.5(EGFR):c.1119G>A (p.Pro373=) rs2302536 0.00289
NM_005228.5(EGFR):c.3015A>G (p.Glu1005=) rs55737335 0.00247
NM_005228.5(EGFR):c.2487G>A (p.Glu829=) rs41420046 0.00198
NM_005228.5(EGFR):c.3592C>T (p.Leu1198=) rs142188270 0.00165
NM_005228.5(EGFR):c.889+18G>T rs41323746 0.00126
NM_005228.5(EGFR):c.3114+12C>T rs199997298 0.00060
NM_005228.5(EGFR):c.2061+17G>A rs376276646 0.00053
NM_005228.5(EGFR):c.2289C>G (p.Ala763=) rs117420095 0.00046
NM_005228.5(EGFR):c.2748C>T (p.Asp916=) rs41396448 0.00046
NM_005228.5(EGFR):c.513C>T (p.Asp171=) rs17289686 0.00036
NM_005228.5(EGFR):c.241-8C>G rs138872748 0.00031
NM_005228.5(EGFR):c.1749C>T (p.Ala583=) rs141232284 0.00028
NM_005228.5(EGFR):c.633C>T (p.Thr211=) rs373970245 0.00024
NM_005228.5(EGFR):c.844G>A (p.Glu282Lys) rs199796955 0.00022
NM_005228.5(EGFR):c.2469+19T>C rs199585163 0.00021
NM_005228.5(EGFR):c.2175G>A (p.Thr725=) rs55959834 0.00014
NM_005228.5(EGFR):c.2700C>T (p.Tyr900=) rs530256683 0.00011
NM_005228.5(EGFR):c.2457G>A (p.Val819=) rs56183713 0.00010
NM_005228.5(EGFR):c.1554G>A (p.Pro518=) rs142429250 0.00009
NM_005228.5(EGFR):c.3139G>A (p.Val1047Met) rs142442994 0.00008
NM_005228.5(EGFR):c.1878C>T (p.Tyr626=) rs533525993 0.00006
NM_005228.5(EGFR):c.1047C>G (p.Leu349=) rs759932677 0.00005
NM_005228.5(EGFR):c.1499-15A>G rs17336793 0.00004
NM_005228.5(EGFR):c.222T>C (p.Tyr74=) rs200383389 0.00004
NM_005228.5(EGFR):c.912C>T (p.His304=) rs182002674 0.00004
NM_005228.5(EGFR):c.758A>G (p.Lys253Arg) rs374084791 0.00003
NM_005228.5(EGFR):c.1029T>C (p.Gly343=) rs774905136 0.00001
NM_005228.5(EGFR):c.2427T>C (p.Ile809=) rs571225968 0.00001
NM_005228.5(EGFR):c.3566G>C (p.Gly1189Ala) rs747600559 0.00001
NM_005228.5(EGFR):c.1438C>T (p.Leu480=) rs147732025
NM_005228.5(EGFR):c.2062-3dup rs770889681
NM_005228.5(EGFR):c.2508C>T (p.Arg836=) rs2229066
NM_005228.5(EGFR):c.3114+15TC[7] rs753534663
NM_005228.5(EGFR):c.3114+15TC[9] rs753534663
NM_005228.5(EGFR):c.89-8del
NM_005228.5(EGFR):c.915C>A (p.Gly305=) rs566001525

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