ClinVar Miner

List of variants in gene NFE2L2 reported as benign for not provided

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Total variants: 43
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HGVS dbSNP gnomAD frequency
NM_006164.5(NFE2L2):c.312+11C>T rs114377436 0.00594
NM_006164.5(NFE2L2):c.128G>A (p.Arg43Gln) rs35248500 0.00449
NM_006164.5(NFE2L2):c.802G>A (p.Val268Met) rs34154613 0.00263
NM_006164.5(NFE2L2):c.529T>G (p.Leu177Val) rs35577826 0.00197
NM_006164.5(NFE2L2):c.925C>T (p.Leu309Phe) rs141363120 0.00166
NM_006164.5(NFE2L2):c.313-19T>C rs569372603 0.00062
NM_006164.5(NFE2L2):c.1032C>T (p.Ser344=) rs35007548 0.00061
NM_006164.5(NFE2L2):c.46-4A>G rs201921480 0.00047
NM_006164.5(NFE2L2):c.1346G>A (p.Arg449His) rs181294188 0.00016
NM_006164.5(NFE2L2):c.454G>A (p.Glu152Lys) rs201992337 0.00015
NM_006164.5(NFE2L2):c.127C>T (p.Arg43Trp) rs182428269 0.00013
NM_006164.5(NFE2L2):c.402+13A>G rs191231706 0.00011
NM_006164.5(NFE2L2):c.372G>A (p.Ala124=) rs183034165 0.00007
NM_006164.5(NFE2L2):c.798G>C (p.Leu266Phe) rs770882525 0.00005
NM_006164.5(NFE2L2):c.1163T>C (p.Val388Ala) rs772306849 0.00004
NM_006164.5(NFE2L2):c.171A>G (p.Glu57=) rs377620960 0.00004
NM_006164.5(NFE2L2):c.1769A>G (p.Asn590Ser) rs747640258 0.00002
NM_006164.5(NFE2L2):c.416C>T (p.Thr139Met) rs376926526 0.00001
NM_006164.5(NFE2L2):c.595-19A>G rs529192853 0.00001
NM_006164.5(NFE2L2):c.1170G>C (p.Gln390His) rs757703926
NM_006164.5(NFE2L2):c.1172A>G (p.Asn391Ser)
NM_006164.5(NFE2L2):c.1189G>A (p.Val397Ile) rs2105452499
NM_006164.5(NFE2L2):c.1195T>C (p.Ser399Pro)
NM_006164.5(NFE2L2):c.1202G>A (p.Gly401Glu)
NM_006164.5(NFE2L2):c.1228T>C (p.Ser410Pro) rs2105452360
NM_006164.5(NFE2L2):c.1263A>T (p.Gln421His) rs953784008
NM_006164.5(NFE2L2):c.1290G>C (p.Leu430Phe) rs1321023832
NM_006164.5(NFE2L2):c.1294G>A (p.Val432Ile) rs748491229
NM_006164.5(NFE2L2):c.1338T>G (p.His446Gln)
NM_006164.5(NFE2L2):c.1487C>T (p.Ala496Val)
NM_006164.5(NFE2L2):c.1497G>A (p.Arg499=)
NM_006164.5(NFE2L2):c.1696A>G (p.Ser566Gly)
NM_006164.5(NFE2L2):c.1798C>G (p.Pro600Ala)
NM_006164.5(NFE2L2):c.425C>T (p.Ser142Leu)
NM_006164.5(NFE2L2):c.440T>C (p.Ile147Thr)
NM_006164.5(NFE2L2):c.470T>C (p.Ile157Thr)
NM_006164.5(NFE2L2):c.548A>C (p.Asp183Ala) rs2105455133
NM_006164.5(NFE2L2):c.677A>G (p.Tyr226Cys)
NM_006164.5(NFE2L2):c.692C>G (p.Ser231Cys)
NM_006164.5(NFE2L2):c.697C>A (p.Pro233Thr)
NM_006164.5(NFE2L2):c.703A>G (p.Met235Val)
NM_006164.5(NFE2L2):c.778A>C (p.Thr260Pro)
NM_006164.5(NFE2L2):c.965T>C (p.Leu322Pro)

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