List of variants in gene WWOX reported as benign for infancy electroclinical syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 45

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_016373.4(WWOX):c.516+6T>C	rs2303191	0.75307
NM_016373.4(WWOX):c.1056+191744T>G	rs2548861	0.51877
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.517-108230A>G	rs77067228	0.05744
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.332C>G (p.Thr111Ser)	rs114755364	0.00326
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.410-4A>T	rs183410581	0.00076
NM_016373.4(WWOX):c.807C>T (p.Asn269=)	rs62034095	0.00067
NM_016373.4(WWOX):c.517-17A>G	rs79423401	0.00014
NM_016373.4(WWOX):c.851A>G (p.Lys284Arg)	rs897453553	0.00010
NM_016373.4(WWOX):c.421G>A (p.Ala141Thr)	rs369907002	0.00006
NM_016373.4(WWOX):c.533A>G (p.Glu178Gly)	rs764588235	0.00006
NM_016373.4(WWOX):c.542C>T (p.Thr181Ile)	rs756339242	0.00004
NM_016373.4(WWOX):c.538A>G (p.Met180Val)	rs569297468	0.00001
NM_016373.4(WWOX):c.107+9del	rs2151651994
NM_016373.4(WWOX):c.108-13dup	rs146697931
NM_016373.4(WWOX):c.108-14_108-13dup	rs146697931
NM_016373.4(WWOX):c.108-6dup	rs754221329
NM_016373.4(WWOX):c.409+16A>C	rs12934985
NM_016373.4(WWOX):c.525C>G (p.Ala175=)
NM_016373.4(WWOX):c.535G>A (p.Ala179Thr)	rs11545029
NM_016373.4(WWOX):c.535G>C (p.Ala179Pro)	rs11545029
NM_016373.4(WWOX):c.535G>T (p.Ala179Ser)	rs11545029
NM_016373.4(WWOX):c.544C>G (p.Leu182Val)
NM_016373.4(WWOX):c.618G>A (p.Val206=)	rs376279847
NM_016373.4(WWOX):c.747C>G (p.Arg249=)	rs375934868
NM_016373.4(WWOX):c.876T>C (p.Ala292=)	rs74030232
NM_016373.4(WWOX):c.876T>G (p.Ala292=)	rs74030232

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.