ClinVar Miner

List of variants in gene EGFR reported as uncertain significance for Inflammatory skin and bowel disease, neonatal, 2; Lung cancer

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Total variants: 45
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HGVS dbSNP gnomAD frequency
NM_005228.5(EGFR):c.769G>A (p.Glu257Lys) rs138847501 0.00035
NM_005228.5(EGFR):c.3629C>T (p.Ala1210Val) rs35918369 0.00034
NM_005228.5(EGFR):c.2024G>A (p.Arg675Gln) rs150423237 0.00025
NM_005228.5(EGFR):c.1557G>T (p.Glu519Asp) rs116057045 0.00019
NM_005228.5(EGFR):c.2996G>A (p.Arg999His) rs149248025 0.00015
NM_005228.5(EGFR):c.2491C>T (p.Arg831Cys) rs371228501 0.00012
NM_005228.5(EGFR):c.1739T>C (p.Ile580Thr) rs761585117 0.00011
NM_005228.5(EGFR):c.2885G>A (p.Arg962His) rs144496976 0.00009
NM_005228.5(EGFR):c.493C>T (p.Arg165Trp) rs587778252 0.00008
NM_005228.5(EGFR):c.2180A>G (p.Tyr727Cys) rs138240620 0.00007
NM_005228.5(EGFR):c.2518G>A (p.Ala840Thr) rs143884981 0.00007
NM_005228.5(EGFR):c.38C>T (p.Ala13Val) rs567894670 0.00006
NM_005228.5(EGFR):c.938C>T (p.Ala313Val) rs149321481 0.00006
NM_005228.5(EGFR):c.3572C>T (p.Thr1191Ile) rs372948989 0.00005
NM_005228.5(EGFR):c.434A>G (p.His145Arg) rs780476417 0.00005
NM_005228.5(EGFR):c.1900G>A (p.Glu634Lys) rs765068810 0.00004
NM_005228.5(EGFR):c.1936A>C (p.Ile646Leu) rs140516819 0.00004
NM_005228.5(EGFR):c.3405C>A (p.Asn1135Lys) rs765499904 0.00004
NM_005228.5(EGFR):c.1931C>T (p.Pro644Leu) rs770443325 0.00003
NM_005228.5(EGFR):c.1913C>T (p.Thr638Met) rs571064657 0.00002
NM_005228.5(EGFR):c.1333A>G (p.Ile445Val) rs372990493 0.00001
NM_005228.5(EGFR):c.1437A>C (p.Lys479Asn) rs768208443 0.00001
NM_005228.5(EGFR):c.2386G>A (p.Gly796Ser) rs754426793 0.00001
NM_005228.5(EGFR):c.2749G>A (p.Gly917Arg) rs775695605 0.00001
NM_005228.5(EGFR):c.3017A>C (p.Asp1006Ala) rs752859687 0.00001
NM_005228.5(EGFR):c.3034G>C (p.Asp1012His) rs1420841957 0.00001
NM_005228.5(EGFR):c.3409G>A (p.Glu1137Lys) rs780967013 0.00001
NM_005228.5(EGFR):c.3476A>G (p.Gln1159Arg) rs1179392671 0.00001
NM_005228.5(EGFR):c.534G>A (p.Met178Ile) rs745755245 0.00001
NM_005228.5(EGFR):c.8C>T (p.Pro3Leu) rs749433287 0.00001
NM_005228.5(EGFR):c.1270G>A (p.Glu424Lys)
NM_005228.5(EGFR):c.1288A>T (p.Thr430Ser) rs1785501999
NM_005228.5(EGFR):c.1513G>T (p.Val505Phe) rs2128942714
NM_005228.5(EGFR):c.1881-774G>A
NM_005228.5(EGFR):c.1881-778G>C
NM_005228.5(EGFR):c.1925A>G (p.Lys642Arg)
NM_005228.5(EGFR):c.2012G>A (p.Arg671His) rs1266662784
NM_005228.5(EGFR):c.2618G>A (p.Gly873Glu)
NM_005228.5(EGFR):c.286G>A (p.Val96Met) rs1260357262
NM_005228.5(EGFR):c.3381C>G (p.Asp1127Glu)
NM_005228.5(EGFR):c.424+5G>A
NM_005228.5(EGFR):c.474C>A (p.Asn158Lys)
NM_005228.5(EGFR):c.676A>C (p.Lys226Gln) rs2128933753
NM_005228.5(EGFR):c.74T>C (p.Leu25Pro)
NM_005228.5(EGFR):c.818C>G (p.Thr273Ser) rs1785289358

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