ClinVar Miner

List of variants in gene WWOX reported as benign for Epileptic encephalopathy, early infantile, 1; Spinocerebellar ataxia, autosomal recessive 12

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Total variants: 20
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HGVS dbSNP
NM_016373.4(WWOX):c.1056+191744T>G rs2548861
NM_016373.4(WWOX):c.293C>T (p.Pro98Leu) rs144601717
NM_016373.4(WWOX):c.332C>G (p.Thr111Ser) rs114755364
NM_016373.4(WWOX):c.351C>G (p.Leu117=) rs34944716
NM_016373.4(WWOX):c.358C>T (p.Arg120Trp) rs141361080
NM_016373.4(WWOX):c.410-4A>T rs183410581
NM_016373.4(WWOX):c.421G>A (p.Ala141Thr) rs369907002
NM_016373.4(WWOX):c.547G>A (p.Asp183Asn) rs74944733
NM_016373.4(WWOX):c.613C>A (p.His205Asn) rs74860463
NM_016373.4(WWOX):c.618G>A (p.Val206=) rs376279847
NM_016373.4(WWOX):c.646C>G (p.Leu216Val) rs7201683
NM_016373.4(WWOX):c.754C>G (p.Pro252Ala) rs75559202
NM_016373.4(WWOX):c.807C>T (p.Asn269=) rs62034095
NM_016373.4(WWOX):c.816G>T (p.Leu272Phe) rs186745328
NM_016373.4(WWOX):c.835C>T (p.Arg279Cys) rs77314072
NM_016373.4(WWOX):c.876T>C (p.Ala292=) rs74030232
NM_016373.4(WWOX):c.876T>G (p.Ala292=) rs74030232
NM_016373.4(WWOX):c.885G>A (p.Arg295=) rs79771882
NM_016373.4(WWOX):c.888C>G (p.Ser296=) rs3764341
NM_016373.4(WWOX):c.941G>A (p.Arg314His) rs73572838

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