ClinVar Miner

List of variants in gene WWOX reported as uncertain significance for not provided

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Gene type:
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Total variants: 105
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HGVS dbSNP gnomAD frequency
NM_016373.4(WWOX):c.816G>T (p.Leu272Phe) rs186745328 0.00280
NM_016373.4(WWOX):c.935C>A (p.Ser312Tyr) rs79399971 0.00038
NM_016373.4(WWOX):c.998G>A (p.Arg333His) rs184773837 0.00036
NM_016373.4(WWOX):c.713A>G (p.Tyr238Cys) rs142806268 0.00026
NM_016373.4(WWOX):c.928C>T (p.Arg310Cys) rs193001955 0.00024
NM_016373.4(WWOX):c.301C>G (p.Pro101Ala) rs574637594 0.00016
NM_016373.4(WWOX):c.990C>G (p.Asn330Lys) rs117209694 0.00016
NM_016373.4(WWOX):c.499C>T (p.Arg167Cys) rs201228765 0.00014
NM_016373.4(WWOX):c.898A>G (p.Asn300Asp) rs374541202 0.00012
NM_016373.4(WWOX):c.591C>G (p.Phe197Leu) rs200847456 0.00011
NM_016373.4(WWOX):c.851A>G (p.Lys284Arg) rs897453553 0.00010
NM_016373.4(WWOX):c.406A>G (p.Ile136Val) rs193027041 0.00009
NM_016373.4(WWOX):c.482C>T (p.Ala161Val) rs369055872 0.00009
NM_016373.4(WWOX):c.981G>A (p.Met327Ile) rs758307666 0.00007
NM_016373.4(WWOX):c.421G>A (p.Ala141Thr) rs369907002 0.00006
NM_016373.4(WWOX):c.958G>A (p.Ala320Thr) rs368670215 0.00006
NM_016373.4(WWOX):c.214C>G (p.Gln72Glu) rs201008667 0.00004
NM_016373.4(WWOX):c.322G>A (p.Asp108Asn) rs747575799 0.00004
NM_016373.4(WWOX):c.410G>A (p.Gly137Glu) rs761879076 0.00004
NM_016373.4(WWOX):c.605T>G (p.Val202Gly) rs112636835 0.00004
NM_016373.4(WWOX):c.673C>G (p.Leu225Val) rs376040091 0.00004
NM_016373.4(WWOX):c.760C>T (p.Arg254Cys) rs369715848 0.00004
NM_016373.4(WWOX):c.926G>A (p.Arg309His) rs370792938 0.00004
NM_016373.4(WWOX):c.251C>G (p.Thr84Ser) rs757145186 0.00003
NM_016373.4(WWOX):c.563G>A (p.Arg188His) rs771163284 0.00003
NM_016373.4(WWOX):c.746G>A (p.Arg249His) rs756703833 0.00003
NM_016373.4(WWOX):c.439C>T (p.His147Tyr) rs746480783 0.00002
NM_016373.4(WWOX):c.658C>G (p.Leu220Val) rs770774574 0.00002
NM_016373.4(WWOX):c.697C>A (p.His233Asn) rs757863128 0.00002
NM_016373.4(WWOX):c.997C>T (p.Arg333Cys) rs369281766 0.00002
NM_016373.4(WWOX):c.1019T>C (p.Leu340Pro) rs761125565 0.00001
NM_016373.4(WWOX):c.1026T>G (p.Phe342Leu) rs1322358404 0.00001
NM_016373.4(WWOX):c.119A>G (p.Glu40Gly) rs778346490 0.00001
NM_016373.4(WWOX):c.193C>A (p.Gln65Lys) rs558101281 0.00001
NM_016373.4(WWOX):c.287A>G (p.Asp96Gly) rs776969977 0.00001
NM_016373.4(WWOX):c.51G>T (p.Glu17Asp) rs991773402 0.00001
NM_016373.4(WWOX):c.524C>T (p.Ala175Val) rs1131691324 0.00001
NM_016373.4(WWOX):c.538A>G (p.Met180Val) rs569297468 0.00001
NM_016373.4(WWOX):c.566G>A (p.Ser189Asn) rs776354746 0.00001
NM_016373.4(WWOX):c.59C>T (p.Pro20Leu) rs761638116 0.00001
NM_016373.4(WWOX):c.605+5G>A rs1039151413 0.00001
NM_016373.4(WWOX):c.631G>A (p.Ala211Thr) rs370737224 0.00001
NM_016373.4(WWOX):c.647T>C (p.Leu216Pro) rs1385370021 0.00001
NM_016373.4(WWOX):c.691G>C (p.Val231Leu) rs755974419 0.00001
NM_016373.4(WWOX):c.708C>G (p.His236Gln) rs745681407 0.00001
NM_016373.4(WWOX):c.737T>C (p.Val246Ala) rs200966505 0.00001
NM_016373.4(WWOX):c.818G>A (p.Gly273Glu) rs756228469 0.00001
NM_016373.4(WWOX):c.82A>C (p.Lys28Gln) rs771726317 0.00001
NM_016373.4(WWOX):c.940C>T (p.Arg314Cys) rs781683643 0.00001
GRCh37/hg19 16q23.1(chr16:78080329-78325545)x3
GRCh37/hg19 16q23.1(chr16:78103821-78334723)x3
GRCh37/hg19 16q23.1(chr16:78112284-78183613)x3
GRCh37/hg19 16q23.1(chr16:78180603-78236617)x1
GRCh37/hg19 16q23.1(chr16:78205565-78344587)x1
GRCh37/hg19 16q23.1(chr16:78229572-78687523)x1
GRCh37/hg19 16q23.1(chr16:78296293-78426119)x1
GRCh37/hg19 16q23.1(chr16:78298421-78473829)x3
GRCh37/hg19 16q23.1(chr16:78308767-78367613)x1
GRCh37/hg19 16q23.1(chr16:78308940-78367613)x1
GRCh37/hg19 16q23.1(chr16:78372426-78426119)x1
GRCh37/hg19 16q23.1(chr16:78372597-78504169)x1
GRCh37/hg19 16q23.1(chr16:78372847-78466128)x1
GRCh37/hg19 16q23.1(chr16:78384725-78508065)x1
GRCh37/hg19 16q23.1(chr16:78420576-78519780)x1
GRCh37/hg19 16q23.1(chr16:78454450-78466097)x1
GRCh37/hg19 16q23.1(chr16:78469169-78739257)x1
GRCh37/hg19 16q23.1(chr16:78520848-78630819)x1
GRCh37/hg19 16q23.1-23.2(chr16:79031223-79456467)x3
GRCh37/hg19 16q23.1-23.2(chr16:79031223-79456816)x3
NM_016373.4(WWOX):c.-460C>T
NM_016373.4(WWOX):c.1039C>G (p.Pro347Ala) rs200699154
NM_016373.4(WWOX):c.1039C>T (p.Pro347Ser)
NM_016373.4(WWOX):c.1044C>A (p.Phe348Leu) rs1057524658
NM_016373.4(WWOX):c.1047C>G (p.Thr349=)
NM_016373.4(WWOX):c.11T>G (p.Leu4Arg)
NM_016373.4(WWOX):c.161G>A (p.Arg54Gln) rs543154053
NM_016373.4(WWOX):c.189G>C (p.Trp63Cys) rs1265607632
NM_016373.4(WWOX):c.253T>G (p.Tyr85Asp) rs781063964
NM_016373.4(WWOX):c.28G>T (p.Asp10Tyr) rs781180473
NM_016373.4(WWOX):c.310C>T (p.Arg104Trp) rs750226191
NM_016373.4(WWOX):c.341T>C (p.Met114Thr) rs761906386
NM_016373.4(WWOX):c.416A>C (p.Glu139Ala) rs2151735391
NM_016373.4(WWOX):c.454A>G (p.Ile152Val) rs961514796
NM_016373.4(WWOX):c.476C>G (p.Ala159Gly) rs2034894480
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.641T>C (p.Phe214Ser) rs1474238209
NM_016373.4(WWOX):c.688C>G (p.Gln230Glu) rs1057524749
NM_016373.4(WWOX):c.700C>A (p.Leu234Met)
NM_016373.4(WWOX):c.711C>G (p.Phe237Leu) rs769589145
NM_016373.4(WWOX):c.733G>A (p.Asp245Asn)
NM_016373.4(WWOX):c.745C>A (p.Arg249Ser) rs749277249
NM_016373.4(WWOX):c.745C>T (p.Arg249Cys) rs749277249
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.782A>G (p.Glu261Gly) rs1464495960
NM_016373.4(WWOX):c.7G>A (p.Ala3Thr) rs1336300148
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.935C>T (p.Ser312Phe) rs79399971
NM_016373.4(WWOX):c.965A>G (p.His322Arg) rs878855022
NM_016373.4(WWOX):c.968C>G (p.Pro323Arg) rs1567570468
NM_016373.4(WWOX):c.978G>C (p.Met326Ile) rs748074874
NM_016373.4(WWOX):c.981G>C (p.Met327Ile) rs758307666

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