ClinVar Miner

List of variants in gene WWOX studied for not specified

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Gene type:
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Total variants: 74
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HGVS dbSNP gnomAD frequency
NM_016373.4(WWOX):c.516+6T>C rs2303191 0.75307
NM_016373.4(WWOX):c.108-12G>T rs67493355 0.34450
NM_016373.4(WWOX):c.-5C>T rs11545028 0.27934
NM_016373.4(WWOX):c.606-17G>A rs4130513 0.24208
NM_016373.4(WWOX):c.844C>G (p.Pro282Ala) rs3764340 0.07330
NM_016373.4(WWOX):c.646C>G (p.Leu216Val) rs7201683 0.03724
NM_016373.4(WWOX):c.941G>A (p.Arg314His) rs73572838 0.03269
NM_016373.4(WWOX):c.547G>A (p.Asp183Asn) rs74944733 0.02435
NM_016373.4(WWOX):c.108-12del rs149533117 0.01497
NM_016373.4(WWOX):c.293C>T (p.Pro98Leu) rs144601717 0.01477
NM_016373.4(WWOX):c.351C>G (p.Leu117=) rs34944716 0.01231
NM_016373.4(WWOX):c.885G>A (p.Arg295=) rs79771882 0.00946
NM_016373.4(WWOX):c.754C>G (p.Pro252Ala) rs75559202 0.00684
NM_016373.4(WWOX):c.613C>A (p.His205Asn) rs74860463 0.00674
NM_016373.4(WWOX):c.358C>T (p.Arg120Trp) rs141361080 0.00523
NM_016373.4(WWOX):c.835C>T (p.Arg279Cys) rs77314072 0.00444
NM_016373.4(WWOX):c.816G>T (p.Leu272Phe) rs186745328 0.00280
NM_016373.4(WWOX):c.669T>C (p.Asp223=) rs72549408 0.00103
NM_016373.4(WWOX):c.888C>G (p.Ser296=) rs3764341 0.00102
NM_016373.4(WWOX):c.107+18G>A rs146301453 0.00078
NM_016373.4(WWOX):c.605+9T>A rs368853054 0.00069
NM_016373.4(WWOX):c.807C>T (p.Asn269=) rs62034095 0.00067
NM_016373.4(WWOX):c.60G>C (p.Pro20=) rs376165565 0.00051
NM_016373.4(WWOX):c.552C>T (p.Leu184=) rs199715254 0.00029
NM_016373.4(WWOX):c.517-17A>G rs79423401 0.00014
NM_016373.4(WWOX):c.898A>G (p.Asn300Asp) rs374541202 0.00012
NM_016373.4(WWOX):c.851A>G (p.Lys284Arg) rs897453553 0.00010
NM_016373.4(WWOX):c.-34G>A rs544250661 0.00009
NM_016373.4(WWOX):c.635C>T (p.Ala212Val) rs202006159 0.00008
NM_016373.4(WWOX):c.867G>A (p.Ala289=) rs755002954 0.00005
NM_016373.4(WWOX):c.114C>T (p.Thr38=) rs372635270 0.00004
NM_016373.4(WWOX):c.231-11C>G rs372011945 0.00004
NM_016373.4(WWOX):c.517-10C>G rs199820033 0.00004
NM_016373.4(WWOX):c.605T>G (p.Val202Gly) rs112636835 0.00004
NM_016373.4(WWOX):c.1029C>G (p.Thr343=) rs752273047 0.00003
NM_016373.4(WWOX):c.409+17G>A rs771445250 0.00003
NM_016373.4(WWOX):c.718G>T (p.Val240Phe) rs1057517847 0.00003
NM_016373.4(WWOX):c.-25G>A rs773772350 0.00002
NM_016373.4(WWOX):c.410-3T>C rs201178351 0.00002
NM_016373.4(WWOX):c.414C>T (p.Phe138=) rs767693780 0.00002
NM_016373.4(WWOX):c.919C>G (p.Leu307Val) rs200320711 0.00002
NM_016373.4(WWOX):c.933C>G (p.Leu311=) rs757508300 0.00002
NM_016373.4(WWOX):c.1056+6A>G rs772213220 0.00001
NM_016373.4(WWOX):c.222T>C (p.Phe74=) rs748079925 0.00001
NM_016373.4(WWOX):c.231-20C>G rs768620458 0.00001
NM_016373.4(WWOX):c.579T>C (p.Phe193=) rs554077107 0.00001
NM_016373.4(WWOX):c.605+17A>T rs757657426 0.00001
NM_016373.4(WWOX):c.948C>G (p.Val316=) rs201986739 0.00001
NM_016373.4(WWOX):c.954G>A (p.Ser318=) rs971458936 0.00001
NM_016373.4(WWOX):c.9G>C (p.Ala3=) rs778036247 0.00001
GRCh37/hg19 16q23.1(chr16:78384987-78487387)
NM_016373.4(WWOX):c.-23_-22delinsT rs1555532919
NM_016373.4(WWOX):c.-27G>A rs570978891
NM_016373.4(WWOX):c.-27G>C rs570978891
NM_016373.4(WWOX):c.-39A>T rs377066400
NM_016373.4(WWOX):c.1056+16C>A rs1045551368
NM_016373.4(WWOX):c.1056+6A>T rs772213220
NM_016373.4(WWOX):c.152A>G (p.Lys51Arg) rs2032292763
NM_016373.4(WWOX):c.231-17C>A rs372361154
NM_016373.4(WWOX):c.409+16A>C rs12934985
NM_016373.4(WWOX):c.409+16A>T rs12934985
NM_016373.4(WWOX):c.516+7G>T rs769717758
NM_016373.4(WWOX):c.517-19T>C rs1057518552
NM_016373.4(WWOX):c.526A>G (p.Lys176Glu) rs2151934098
NM_016373.4(WWOX):c.535G>A (p.Ala179Thr) rs11545029
NM_016373.4(WWOX):c.605+17A>C rs757657426
NM_016373.4(WWOX):c.606-17G>C rs4130513
NM_016373.4(WWOX):c.608C>G (p.Pro203Arg) rs1405481740
NM_016373.4(WWOX):c.656G>C (p.Ser219Thr) rs367599412
NM_016373.4(WWOX):c.766A>T (p.Ile256Phe) rs1023419687
NM_016373.4(WWOX):c.792-15T>C rs769065057
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.935C>T (p.Ser312Phe) rs79399971

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