ClinVar Miner

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

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Total variants: 115
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HGVS dbSNP
NC_000016.10:g.(?_78099759)_(78099909_?)dup
NC_000016.10:g.(?_78099759)_(78164309_?)dup
NC_000016.10:g.(?_78164163)_(78164309_?)del
NC_000016.10:g.(?_78318746)_(78386940_?)dup
NC_000016.10:g.(?_78386840)_(78386968_?)del
NC_000016.10:g.(?_78424850)_(78425075_?)del
NC_000016.10:g.(?_78432468)_(78432772_?)del
NC_000016.9:g.(?_78133656)_(78466669_?)dup
NM_016373.3(WWOX):c.101A>G (p.Tyr34Cys) rs766309882
NM_016373.3(WWOX):c.1021C>A (p.Leu341Met)
NM_016373.3(WWOX):c.1029C>G (p.Thr343=) rs752273047
NM_016373.3(WWOX):c.1035G>A (p.Ala345=) rs189695070
NM_016373.3(WWOX):c.1039C>A (p.Pro347Thr)
NM_016373.3(WWOX):c.1056+191744T>G rs2548861
NM_016373.3(WWOX):c.128A>G (p.Gln43Arg)
NM_016373.3(WWOX):c.172+9G>A rs1220647416
NM_016373.3(WWOX):c.173-6T>G
NM_016373.3(WWOX):c.177G>C (p.Leu59Phe)
NM_016373.3(WWOX):c.203A>G (p.Asp68Gly)
NM_016373.3(WWOX):c.210C>T (p.Asn70=) rs762102064
NM_016373.3(WWOX):c.228T>C (p.Val76=) rs370579498
NM_016373.3(WWOX):c.251C>G (p.Thr84Ser) rs757145186
NM_016373.3(WWOX):c.293C>T (p.Pro98Leu) rs144601717
NM_016373.3(WWOX):c.294G>C (p.Pro98=) rs200208343
NM_016373.3(WWOX):c.310C>T (p.Arg104Trp) rs750226191
NM_016373.3(WWOX):c.321C>T (p.Tyr107=) rs373306276
NM_016373.3(WWOX):c.324C>T (p.Asp108=) rs377442022
NM_016373.3(WWOX):c.332C>G (p.Thr111Ser) rs114755364
NM_016373.3(WWOX):c.341T>C (p.Met114Thr) rs761906386
NM_016373.3(WWOX):c.351C>G (p.Leu117=) rs34944716
NM_016373.3(WWOX):c.358C>T (p.Arg120Trp) rs141361080
NM_016373.3(WWOX):c.35C>G (p.Thr12Arg)
NM_016373.3(WWOX):c.362A>G (p.Asp121Gly)
NM_016373.3(WWOX):c.36G>C (p.Thr12=) rs1438602210
NM_016373.3(WWOX):c.385G>C (p.Val129Leu) rs781732002
NM_016373.3(WWOX):c.406A>G (p.Ile136Val) rs193027041
NM_016373.3(WWOX):c.409+1G>C rs1060502727
NM_016373.3(WWOX):c.410-4A>T rs183410581
NM_016373.3(WWOX):c.410-6C>T rs1488901499
NM_016373.3(WWOX):c.410G>A (p.Gly137Glu) rs761879076
NM_016373.3(WWOX):c.421G>A (p.Ala141Thr) rs369907002
NM_016373.3(WWOX):c.440A>G (p.His147Arg) rs188859796
NM_016373.3(WWOX):c.443G>C (p.Gly148Ala)
NM_016373.3(WWOX):c.445G>A (p.Ala149Thr)
NM_016373.3(WWOX):c.468G>T (p.Arg156Ser) rs140817689
NM_016373.3(WWOX):c.481G>A (p.Ala161Thr)
NM_016373.3(WWOX):c.482C>T (p.Ala161Val)
NM_016373.3(WWOX):c.499C>T (p.Arg167Cys) rs201228765
NM_016373.3(WWOX):c.513A>G (p.Glu171=) rs1060502728
NM_016373.3(WWOX):c.517-10C>G rs199820033
NM_016373.3(WWOX):c.51G>T (p.Glu17Asp) rs991773402
NM_016373.3(WWOX):c.52C>A (p.Leu18Met)
NM_016373.3(WWOX):c.535G>T (p.Ala179Ser) rs11545029
NM_016373.3(WWOX):c.547G>A (p.Asp183Asn) rs74944733
NM_016373.3(WWOX):c.552C>T (p.Leu184=) rs199715254
NM_016373.3(WWOX):c.562C>A (p.Arg188Ser) rs199511589
NM_016373.3(WWOX):c.562C>T (p.Arg188Cys) rs199511589
NM_016373.3(WWOX):c.568G>A (p.Val190Met) rs769400934
NM_016373.3(WWOX):c.586G>A (p.Ala196Thr) rs370367979
NM_016373.3(WWOX):c.599A>G (p.Lys200Arg)
NM_016373.3(WWOX):c.605+5G>A rs1039151413
NM_016373.3(WWOX):c.605+9T>A rs368853054
NM_016373.3(WWOX):c.613C>A (p.His205Asn) rs74860463
NM_016373.3(WWOX):c.618G>A (p.Val206=) rs376279847
NM_016373.3(WWOX):c.635C>T (p.Ala212Val) rs202006159
NM_016373.3(WWOX):c.638C>A (p.Thr213Asn)
NM_016373.3(WWOX):c.646C>G (p.Leu216Val) rs7201683
NM_016373.3(WWOX):c.667G>A (p.Asp223Asn)
NM_016373.3(WWOX):c.678G>A (p.Glu226=) rs750905852
NM_016373.3(WWOX):c.682A>C (p.Thr228Pro)
NM_016373.3(WWOX):c.708C>G (p.His236Gln) rs745681407
NM_016373.3(WWOX):c.713A>G (p.Tyr238Cys) rs142806268
NM_016373.3(WWOX):c.715C>G (p.Leu239Val) rs575080327
NM_016373.3(WWOX):c.745C>T (p.Arg249Cys)
NM_016373.3(WWOX):c.754C>G (p.Pro252Ala) rs75559202
NM_016373.3(WWOX):c.779C>G (p.Ser260Ter) rs878855021
NM_016373.3(WWOX):c.790C>T (p.Arg264Ter) rs756762196
NM_016373.3(WWOX):c.791+5G>C rs756074406
NM_016373.3(WWOX):c.7G>A (p.Ala3Thr) rs1336300148
NM_016373.3(WWOX):c.807C>T (p.Asn269=) rs62034095
NM_016373.3(WWOX):c.816G>T (p.Leu272Phe) rs186745328
NM_016373.3(WWOX):c.823C>T (p.Leu275=) rs1272996029
NM_016373.3(WWOX):c.828C>G (p.Asp276Glu)
NM_016373.3(WWOX):c.835C>T (p.Arg279Cys) rs77314072
NM_016373.3(WWOX):c.842C>T (p.Ser281Phe)
NM_016373.3(WWOX):c.848C>A (p.Thr283Lys) rs1186552961
NM_016373.3(WWOX):c.851A>G (p.Lys284Arg) rs897453553
NM_016373.3(WWOX):c.856G>T (p.Asp286Tyr) rs374658336
NM_016373.3(WWOX):c.867G>C (p.Ala289=) rs755002954
NM_016373.3(WWOX):c.869T>C (p.Met290Thr) rs1035627222
NM_016373.3(WWOX):c.876T>C (p.Ala292=) rs74030232
NM_016373.3(WWOX):c.876T>G (p.Ala292=) rs74030232
NM_016373.3(WWOX):c.885G>A (p.Arg295=) rs79771882
NM_016373.3(WWOX):c.888C>G (p.Ser296=) rs3764341
NM_016373.3(WWOX):c.898A>G (p.Asn300Asp) rs374541202
NM_016373.3(WWOX):c.90C>T (p.Gly30=) rs772839022
NM_016373.3(WWOX):c.925C>T (p.Arg309Cys) rs761545702
NM_016373.3(WWOX):c.935C>A (p.Ser312Tyr)
NM_016373.3(WWOX):c.937C>G (p.Pro313Ala) rs370345936
NM_016373.3(WWOX):c.941G>A (p.Arg314His) rs73572838
NM_016373.3(WWOX):c.943G>A (p.Gly315Arg) rs768172617
NM_016373.3(WWOX):c.946G>C (p.Val316Leu) rs201941494
NM_016373.3(WWOX):c.948C>G (p.Val316=) rs201986739
NM_016373.3(WWOX):c.953C>T (p.Ser318Leu)
NM_016373.3(WWOX):c.957C>T (p.Asn319=) rs144417100
NM_016373.3(WWOX):c.958G>A (p.Ala320Thr) rs368670215
NM_016373.3(WWOX):c.965A>G (p.His322Arg) rs878855022
NM_016373.3(WWOX):c.978G>C (p.Met326Ile) rs748074874
NM_016373.3(WWOX):c.990C>G (p.Asn330Lys) rs117209694
NM_016373.3(WWOX):c.990C>T (p.Asn330=) rs117209694
NM_016373.3(WWOX):c.994C>T (p.His332Tyr) rs923399366
NM_016373.3(WWOX):c.995A>C (p.His332Pro) rs775584864
NM_016373.3(WWOX):c.998G>A (p.Arg333His)
NM_016373.3(WWOX):c.99C>T (p.Tyr33=) rs760762887
NM_016373.4(WWOX):c.583G>T (p.Glu195Ter)

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