ClinVar Miner

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

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Total variants: 88
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HGVS dbSNP
NC_000016.9:g.(?_78133656)_(78133806_?)dup
NC_000016.9:g.(?_78133656)_(78149071_?)dup
NC_000016.9:g.(?_78133656)_(78198206_?)dup
NC_000016.9:g.(?_78133656)_(78466669_?)dup
NM_016373.4(WWOX):c.101A>G (p.Tyr34Cys) rs766309882
NM_016373.4(WWOX):c.1021C>A (p.Leu341Met)
NM_016373.4(WWOX):c.1038G>T (p.Arg346Ser)
NM_016373.4(WWOX):c.1039C>A (p.Pro347Thr)
NM_016373.4(WWOX):c.1039C>G (p.Pro347Ala)
NM_016373.4(WWOX):c.128A>G (p.Gln43Arg)
NM_016373.4(WWOX):c.167C>T (p.Ala56Val)
NM_016373.4(WWOX):c.173-6T>G
NM_016373.4(WWOX):c.177G>C (p.Leu59Phe)
NM_016373.4(WWOX):c.203A>G (p.Asp68Gly) rs1567575033
NM_016373.4(WWOX):c.248C>T (p.Thr83Ile)
NM_016373.4(WWOX):c.251C>G (p.Thr84Ser) rs757145186
NM_016373.4(WWOX):c.301C>G (p.Pro101Ala)
NM_016373.4(WWOX):c.310C>T (p.Arg104Trp) rs750226191
NM_016373.4(WWOX):c.32A>T (p.Asp11Val)
NM_016373.4(WWOX):c.340A>G (p.Met114Val)
NM_016373.4(WWOX):c.341T>C (p.Met114Thr) rs761906386
NM_016373.4(WWOX):c.349C>A (p.Leu117Ile)
NM_016373.4(WWOX):c.35C>G (p.Thr12Arg) rs1567567249
NM_016373.4(WWOX):c.362A>G (p.Asp121Gly)
NM_016373.4(WWOX):c.385G>C (p.Val129Leu) rs781732002
NM_016373.4(WWOX):c.406A>G (p.Ile136Val) rs193027041
NM_016373.4(WWOX):c.410-3T>C rs201178351
NM_016373.4(WWOX):c.410G>A (p.Gly137Glu) rs761879076
NM_016373.4(WWOX):c.440A>G (p.His147Arg) rs188859796
NM_016373.4(WWOX):c.443G>C (p.Gly148Ala)
NM_016373.4(WWOX):c.445G>A (p.Ala149Thr)
NM_016373.4(WWOX):c.481G>A (p.Ala161Thr)
NM_016373.4(WWOX):c.482C>T (p.Ala161Val)
NM_016373.4(WWOX):c.499C>T (p.Arg167Cys) rs201228765
NM_016373.4(WWOX):c.513A>G (p.Glu171=) rs1060502728
NM_016373.4(WWOX):c.517-10C>G rs199820033
NM_016373.4(WWOX):c.51G>T (p.Glu17Asp) rs991773402
NM_016373.4(WWOX):c.52C>A (p.Leu18Met)
NM_016373.4(WWOX):c.535G>T (p.Ala179Ser) rs11545029
NM_016373.4(WWOX):c.562C>A (p.Arg188Ser) rs199511589
NM_016373.4(WWOX):c.562C>T (p.Arg188Cys) rs199511589
NM_016373.4(WWOX):c.568G>A (p.Val190Met) rs769400934
NM_016373.4(WWOX):c.586G>A (p.Ala196Thr) rs370367979
NM_016373.4(WWOX):c.587C>T (p.Ala196Val)
NM_016373.4(WWOX):c.596C>G (p.Ala199Gly)
NM_016373.4(WWOX):c.599A>G (p.Lys200Arg)
NM_016373.4(WWOX):c.605+5G>A rs1039151413
NM_016373.4(WWOX):c.605T>G (p.Val202Gly)
NM_016373.4(WWOX):c.635C>T (p.Ala212Val) rs202006159
NM_016373.4(WWOX):c.638C>A (p.Thr213Asn)
NM_016373.4(WWOX):c.667G>A (p.Asp223Asn)
NM_016373.4(WWOX):c.673C>G (p.Leu225Val) rs376040091
NM_016373.4(WWOX):c.682A>C (p.Thr228Pro) rs1567565338
NM_016373.4(WWOX):c.708C>G (p.His236Gln) rs745681407
NM_016373.4(WWOX):c.713A>G (p.Tyr238Cys) rs142806268
NM_016373.4(WWOX):c.715C>G (p.Leu239Val) rs575080327
NM_016373.4(WWOX):c.745C>T (p.Arg249Cys)
NM_016373.4(WWOX):c.746G>A (p.Arg249His)
NM_016373.4(WWOX):c.757G>T (p.Ala253Ser)
NM_016373.4(WWOX):c.791+4G>T
NM_016373.4(WWOX):c.791+5G>C rs756074406
NM_016373.4(WWOX):c.7G>A (p.Ala3Thr) rs1336300148
NM_016373.4(WWOX):c.828C>G (p.Asp276Glu)
NM_016373.4(WWOX):c.842C>T (p.Ser281Phe) rs1567570252
NM_016373.4(WWOX):c.848C>A (p.Thr283Lys) rs1186552961
NM_016373.4(WWOX):c.851A>G (p.Lys284Arg) rs897453553
NM_016373.4(WWOX):c.856G>T (p.Asp286Tyr) rs374658336
NM_016373.4(WWOX):c.869T>C (p.Met290Thr) rs1035627222
NM_016373.4(WWOX):c.887C>G (p.Ser296Cys)
NM_016373.4(WWOX):c.898A>G (p.Asn300Asp) rs374541202
NM_016373.4(WWOX):c.8C>T (p.Ala3Val)
NM_016373.4(WWOX):c.90C>T (p.Gly30=) rs772839022
NM_016373.4(WWOX):c.925C>T (p.Arg309Cys) rs761545702
NM_016373.4(WWOX):c.928C>T (p.Arg310Cys)
NM_016373.4(WWOX):c.935C>A (p.Ser312Tyr)
NM_016373.4(WWOX):c.937C>G (p.Pro313Ala) rs370345936
NM_016373.4(WWOX):c.943G>A (p.Gly315Arg) rs768172617
NM_016373.4(WWOX):c.943G>C (p.Gly315Arg)
NM_016373.4(WWOX):c.946G>C (p.Val316Leu) rs201941494
NM_016373.4(WWOX):c.953C>T (p.Ser318Leu)
NM_016373.4(WWOX):c.958G>A (p.Ala320Thr) rs368670215
NM_016373.4(WWOX):c.965A>G (p.His322Arg) rs878855022
NM_016373.4(WWOX):c.977T>C (p.Met326Thr)
NM_016373.4(WWOX):c.978G>C (p.Met326Ile) rs748074874
NM_016373.4(WWOX):c.990C>G (p.Asn330Lys) rs117209694
NM_016373.4(WWOX):c.994C>T (p.His332Tyr) rs923399366
NM_016373.4(WWOX):c.995A>C (p.His332Pro) rs775584864
NM_016373.4(WWOX):c.998G>A (p.Arg333His)

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