List of variants reported as benign for autosomal recessive spinocerebellar ataxia 12 by Genome-Nilou Lab

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Total variants: 38

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HGVS	dbSNP	gnomAD frequency
NM_016373.4(WWOX):c.516+6T>C	rs2303191	0.75307
NM_016373.4(WWOX):c.1057-40T>C	rs384216	0.49671
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.1238C>A (p.Ser413Tyr)	rs117065412	0.01316
NM_016373.4(WWOX):c.351C>G (p.Leu117=)	rs34944716	0.01231
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.*3G>T	rs140060332	0.00275
NM_016373.4(WWOX):c.1134C>T (p.Asn378=)	rs201088847	0.00274
NM_016373.4(WWOX):c.1197G>A (p.Ala399=)	rs376935572	0.00203
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.1141C>T (p.Arg381Cys)	rs200461412	0.00083
NM_016373.4(WWOX):c.107+18G>A	rs146301453	0.00078
NM_016373.4(WWOX):c.807C>T (p.Asn269=)	rs62034095	0.00067
NM_016373.4(WWOX):c.468G>T (p.Arg156Ser)	rs140817689	0.00063
NM_016373.4(WWOX):c.517-17A>G	rs79423401	0.00014
NM_016373.4(WWOX):c.1057-14T>C	rs66481974
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.1239C>T (p.Ser413=)	rs199576434
NM_016373.4(WWOX):c.409+16A>C	rs12934985
NM_016373.4(WWOX):c.535G>A (p.Ala179Thr)	rs11545029
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

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