ClinVar Miner

List of variants in gene WWOX reported as likely benign for Epileptic encephalopathy, early infantile, 1; Spinocerebellar ataxia, autosomal recessive 12

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Total variants: 20
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HGVS dbSNP
NM_016373.3(WWOX):c.1029C>G (p.Thr343=) rs752273047
NM_016373.3(WWOX):c.1035G>A (p.Ala345=) rs189695070
NM_016373.3(WWOX):c.172+9G>A rs1220647416
NM_016373.3(WWOX):c.210C>T (p.Asn70=) rs762102064
NM_016373.3(WWOX):c.228T>C (p.Val76=) rs370579498
NM_016373.3(WWOX):c.294G>C (p.Pro98=) rs200208343
NM_016373.3(WWOX):c.321C>T (p.Tyr107=) rs373306276
NM_016373.3(WWOX):c.324C>T (p.Asp108=) rs377442022
NM_016373.3(WWOX):c.36G>C (p.Thr12=) rs1438602210
NM_016373.3(WWOX):c.410-6C>T rs1488901499
NM_016373.3(WWOX):c.468G>T (p.Arg156Ser) rs140817689
NM_016373.3(WWOX):c.552C>T (p.Leu184=) rs199715254
NM_016373.3(WWOX):c.605+9T>A rs368853054
NM_016373.3(WWOX):c.678G>A (p.Glu226=) rs750905852
NM_016373.3(WWOX):c.823C>T (p.Leu275=) rs1272996029
NM_016373.3(WWOX):c.867G>C (p.Ala289=) rs755002954
NM_016373.3(WWOX):c.948C>G (p.Val316=) rs201986739
NM_016373.3(WWOX):c.957C>T (p.Asn319=) rs144417100
NM_016373.3(WWOX):c.990C>T (p.Asn330=) rs117209694
NM_016373.3(WWOX):c.99C>T (p.Tyr33=) rs760762887

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