ClinVar Miner

List of variants in gene WWOX reported as likely benign

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Gene type:
ClinVar version:
Total variants: 82
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HGVS dbSNP
GRCh37/hg19 16q23.1(chr16:78080345-78712074)x3
GRCh37/hg19 16q23.1(chr16:78098478-78206297)x3
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.1029C>G (p.Thr343=) rs752273047
NM_016373.4(WWOX):c.1035G>A (p.Ala345=) rs189695070
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.108-42T>A
NM_016373.4(WWOX):c.108-6dup rs754221329
NM_016373.4(WWOX):c.114C>T (p.Thr38=) rs372635270
NM_016373.4(WWOX):c.172+9G>A rs1220647416
NM_016373.4(WWOX):c.173-11T>C rs370729028
NM_016373.4(WWOX):c.173-91G>T
NM_016373.4(WWOX):c.210C>T (p.Asn70=) rs762102064
NM_016373.4(WWOX):c.222T>C (p.Phe74=) rs748079925
NM_016373.4(WWOX):c.228T>C (p.Val76=) rs370579498
NM_016373.4(WWOX):c.231-11C>G rs372011945
NM_016373.4(WWOX):c.231-17C>A rs372361154
NM_016373.4(WWOX):c.231-20C>G rs768620458
NM_016373.4(WWOX):c.231-41G>C
NM_016373.4(WWOX):c.294G>C (p.Pro98=) rs200208343
NM_016373.4(WWOX):c.315A>G (p.Gln105=) rs752822745
NM_016373.4(WWOX):c.321C>T (p.Tyr107=) rs373306276
NM_016373.4(WWOX):c.324C>T (p.Asp108=) rs377442022
NM_016373.4(WWOX):c.358C>T (p.Arg120Trp) rs141361080
NM_016373.4(WWOX):c.36G>C (p.Thr12=) rs1438602210
NM_016373.4(WWOX):c.409+16A>T rs12934985
NM_016373.4(WWOX):c.409+17G>A rs771445250
NM_016373.4(WWOX):c.410-3T>C rs201178351
NM_016373.4(WWOX):c.410-6C>T rs1488901499
NM_016373.4(WWOX):c.414C>T (p.Phe138=) rs767693780
NM_016373.4(WWOX):c.468G>T (p.Arg156Ser) rs140817689
NM_016373.4(WWOX):c.516+7G>T rs769717758
NM_016373.4(WWOX):c.517-108230A>G rs77067228
NM_016373.4(WWOX):c.517-10C>G rs199820033
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.517-74C>G
NM_016373.4(WWOX):c.552C>T (p.Leu184=) rs199715254
NM_016373.4(WWOX):c.579T>C (p.Phe193=) rs554077107
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+9T>A rs368853054
NM_016373.4(WWOX):c.606-17G>C rs4130513
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.669T>C (p.Asp223=) rs72549408
NM_016373.4(WWOX):c.678G>A (p.Glu226=) rs750905852
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.747C>G (p.Arg249=) rs375934868
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.823C>T (p.Leu275=) rs1272996029
NM_016373.4(WWOX):c.835C>T (p.Arg279Cys) rs77314072
NM_016373.4(WWOX):c.867G>A (p.Ala289=) rs755002954
NM_016373.4(WWOX):c.867G>C (p.Ala289=) rs755002954
NM_016373.4(WWOX):c.876T>G (p.Ala292=) rs74030232
NM_016373.4(WWOX):c.933C>G (p.Leu311=) rs757508300
NM_016373.4(WWOX):c.942C>T (p.Arg314=)
NM_016373.4(WWOX):c.948C>G (p.Val316=) rs201986739
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.990C>T (p.Asn330=) rs117209694
NM_016373.4(WWOX):c.99C>T (p.Tyr33=) rs760762887
NM_016373.4(WWOX):c.9G>C (p.Ala3=) rs778036247

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