ClinVar Miner

List of variants in gene WWOX reported by GeneDx

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Gene type:
ClinVar version:
Total variants: 143
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HGVS dbSNP
GRCh38/hg38 16q23.1(chr16:78624328-78711823)x1
NC_000016.10:g.78108410dup
NM_016373.3(WWOX):c.108-6dupT rs754221329
NM_016373.4(WWOX):c.-23_-22delinsT rs1555532919
NM_016373.4(WWOX):c.-25G>A rs773772350
NM_016373.4(WWOX):c.-27G>A rs570978891
NM_016373.4(WWOX):c.-27G>C rs570978891
NM_016373.4(WWOX):c.-34G>A rs544250661
NM_016373.4(WWOX):c.-39A>T rs377066400
NM_016373.4(WWOX):c.-5C>T rs11545028
NM_016373.4(WWOX):c.1019T>C (p.Leu340Pro) rs761125565
NM_016373.4(WWOX):c.1029C>G (p.Thr343=) rs752273047
NM_016373.4(WWOX):c.1035G>A (p.Ala345=) rs189695070
NM_016373.4(WWOX):c.1043del (p.Phe348fs) rs1064795117
NM_016373.4(WWOX):c.1044C>A (p.Phe348Leu) rs1057524658
NM_016373.4(WWOX):c.1056+109A>C
NM_016373.4(WWOX):c.1056+16C>A rs1045551368
NM_016373.4(WWOX):c.1056+6A>G rs772213220
NM_016373.4(WWOX):c.1056+6A>T rs772213220
NM_016373.4(WWOX):c.107+18G>A rs146301453
NM_016373.4(WWOX):c.108-12G>T rs67493355
NM_016373.4(WWOX):c.108-12del rs149533117
NM_016373.4(WWOX):c.108-13dup
NM_016373.4(WWOX):c.108-171C>G
NM_016373.4(WWOX):c.108-42T>A
NM_016373.4(WWOX):c.131G>A (p.Trp44Ter) rs1057517846
NM_016373.4(WWOX):c.132G>A (p.Trp44Ter) rs1555535072
NM_016373.4(WWOX):c.172+103C>G
NM_016373.4(WWOX):c.172G>A (p.Asp58Asn) rs1131691285
NM_016373.4(WWOX):c.173-11T>C rs370729028
NM_016373.4(WWOX):c.173-91G>T
NM_016373.4(WWOX):c.214C>T (p.Gln72Ter) rs201008667
NM_016373.4(WWOX):c.222T>C (p.Phe74=) rs748079925
NM_016373.4(WWOX):c.230+104C>T
NM_016373.4(WWOX):c.231-11C>G rs372011945
NM_016373.4(WWOX):c.231-129T>A
NM_016373.4(WWOX):c.231-17C>A rs372361154
NM_016373.4(WWOX):c.231-20C>G rs768620458
NM_016373.4(WWOX):c.231-233G>A
NM_016373.4(WWOX):c.231-41G>C
NM_016373.4(WWOX):c.231-43C>T
NM_016373.4(WWOX):c.251C>G (p.Thr84Ser) rs757145186
NM_016373.4(WWOX):c.255C>G (p.Tyr85Ter) rs990150249
NM_016373.4(WWOX):c.293C>T (p.Pro98Leu) rs144601717
NM_016373.4(WWOX):c.315A>G (p.Gln105=) rs752822745
NM_016373.4(WWOX):c.322G>A (p.Asp108Asn) rs747575799
NM_016373.4(WWOX):c.324C>T (p.Asp108=) rs377442022
NM_016373.4(WWOX):c.332C>G (p.Thr111Ser) rs114755364
NM_016373.4(WWOX):c.341T>C (p.Met114Thr) rs761906386
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.409+122A>C
NM_016373.4(WWOX):c.409+16A>C rs12934985
NM_016373.4(WWOX):c.409+16A>T rs12934985
NM_016373.4(WWOX):c.409+17G>A rs771445250
NM_016373.4(WWOX):c.410-169T>C
NM_016373.4(WWOX):c.410-1G>A rs886039653
NM_016373.4(WWOX):c.410-249G>A
NM_016373.4(WWOX):c.410-270C>T
NM_016373.4(WWOX):c.410-296A>T
NM_016373.4(WWOX):c.410-3T>C rs201178351
NM_016373.4(WWOX):c.410-56A>T
NM_016373.4(WWOX):c.414C>T (p.Phe138=) rs767693780
NM_016373.4(WWOX):c.421G>A (p.Ala141Thr) rs369907002
NM_016373.4(WWOX):c.468G>T (p.Arg156Ser) rs140817689
NM_016373.4(WWOX):c.499C>T (p.Arg167Cys) rs201228765
NM_016373.4(WWOX):c.516+316T>C
NM_016373.4(WWOX):c.516+50G>A
NM_016373.4(WWOX):c.516+6T>C rs2303191
NM_016373.4(WWOX):c.516+7G>T rs769717758
NM_016373.4(WWOX):c.517-10C>G rs199820033
NM_016373.4(WWOX):c.517-115G>A
NM_016373.4(WWOX):c.517-12C>A
NM_016373.4(WWOX):c.517-12C>T rs373188700
NM_016373.4(WWOX):c.517-17A>G rs79423401
NM_016373.4(WWOX):c.517-19T>C rs1057518552
NM_016373.4(WWOX):c.517-296A>G
NM_016373.4(WWOX):c.517-74C>G
NM_016373.4(WWOX):c.524C>T (p.Ala175Val) rs1131691324
NM_016373.4(WWOX):c.535G>A (p.Ala179Thr) rs11545029
NM_016373.4(WWOX):c.547G>A (p.Asp183Asn) rs74944733
NM_016373.4(WWOX):c.552C>T (p.Leu184=) rs199715254
NM_016373.4(WWOX):c.566G>A (p.Ser189Asn) rs776354746
NM_016373.4(WWOX):c.579T>C (p.Phe193=) rs554077107
NM_016373.4(WWOX):c.583G>T (p.Glu195Ter) rs1567542020
NM_016373.4(WWOX):c.591C>G (p.Phe197Leu) rs200847456
NM_016373.4(WWOX):c.605+138G>A
NM_016373.4(WWOX):c.605+17A>C rs757657426
NM_016373.4(WWOX):c.605+17A>T rs757657426
NM_016373.4(WWOX):c.605+283G>C
NM_016373.4(WWOX):c.605+37C>T
NM_016373.4(WWOX):c.605+5G>A rs1039151413
NM_016373.4(WWOX):c.605+9T>A rs368853054
NM_016373.4(WWOX):c.606-150G>A
NM_016373.4(WWOX):c.606-17G>A rs4130513
NM_016373.4(WWOX):c.606-17G>C rs4130513
NM_016373.4(WWOX):c.606-183G>A
NM_016373.4(WWOX):c.606-254C>T
NM_016373.4(WWOX):c.606-283T>C
NM_016373.4(WWOX):c.606-296G>C
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.618G>C (p.Val206=) rs376279847
NM_016373.4(WWOX):c.646C>G (p.Leu216Val) rs7201683
NM_016373.4(WWOX):c.669T>C (p.Asp223=) rs72549408
NM_016373.4(WWOX):c.673C>G (p.Leu225Val) rs376040091
NM_016373.4(WWOX):c.688C>G (p.Gln230Glu) rs1057524749
NM_016373.4(WWOX):c.713A>G (p.Tyr238Cys) rs142806268
NM_016373.4(WWOX):c.718G>T (p.Val240Phe) rs1057517847
NM_016373.4(WWOX):c.723G>A (p.Gln241=) rs191029309
NM_016373.4(WWOX):c.739T>C (p.Leu247=) rs1195368309
NM_016373.4(WWOX):c.745C>A (p.Arg249Ser) rs749277249
NM_016373.4(WWOX):c.747C>G (p.Arg249=) rs375934868
NM_016373.4(WWOX):c.749C>G (p.Ser250Ter) rs368928190
NM_016373.4(WWOX):c.754C>G (p.Pro252Ala) rs75559202
NM_016373.4(WWOX):c.766A>T (p.Ile256Phe) rs1023419687
NM_016373.4(WWOX):c.767T>C (p.Ile256Thr) rs775895501
NM_016373.4(WWOX):c.790C>T (p.Arg264Ter) rs756762196
NM_016373.4(WWOX):c.791+203G>C
NM_016373.4(WWOX):c.791+228T>A
NM_016373.4(WWOX):c.792-135G>A
NM_016373.4(WWOX):c.792-15T>C rs769065057
NM_016373.4(WWOX):c.792-182A>G
NM_016373.4(WWOX):c.792-222T>G
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.844C>G (p.Pro282Ala) rs3764340
NM_016373.4(WWOX):c.851A>G (p.Lys284Arg) rs897453553
NM_016373.4(WWOX):c.856G>A (p.Asp286Asn) rs374658336
NM_016373.4(WWOX):c.856G>T (p.Asp286Tyr) rs374658336
NM_016373.4(WWOX):c.867G>A (p.Ala289=) rs755002954
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.933C>G (p.Leu311=) rs757508300
NM_016373.4(WWOX):c.941G>A (p.Arg314His) rs73572838
NM_016373.4(WWOX):c.942C>T (p.Arg314=)
NM_016373.4(WWOX):c.951G>A (p.Thr317=) rs759801417
NM_016373.4(WWOX):c.954G>A (p.Ser318=) rs971458936
NM_016373.4(WWOX):c.957C>T (p.Asn319=) rs144417100
NM_016373.4(WWOX):c.9G>C (p.Ala3=) rs778036247

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