List of variants reported as uncertain significance for Spinocerebellar ataxia type 40

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_001080414.4(CCDC88C):c.5251G>A (p.Val1751Ile)	rs142295786	0.00150
NM_001080414.4(CCDC88C):c.6026C>T (p.Pro2009Leu)	rs201940261	0.00078
NM_001080414.4(CCDC88C):c.3170A>G (p.Asp1057Gly)	rs548699524	0.00006
NM_001080414.4(CCDC88C):c.786G>T (p.Arg262Ser)	rs368545314	0.00004
NM_001080414.4(CCDC88C):c.1888G>A (p.Ala630Thr)	rs773899627	0.00001
NM_001080414.4(CCDC88C):c.3020G>A (p.Cys1007Tyr)	rs917595672	0.00001
NM_001080414.4(CCDC88C):c.932A>G (p.Tyr311Cys)	rs751049970	0.00001
NM_001080414.4(CCDC88C):c.2687T>G (p.Leu896Arg)	rs1891910013
NM_001080414.4(CCDC88C):c.2845G>A (p.Asp949Asn)
NM_001080414.4(CCDC88C):c.3320ACA[1] (p.Asn1108del)
NM_001080414.4(CCDC88C):c.3554A>C (p.Tyr1185Ser)
NM_001080414.4(CCDC88C):c.5440C>T (p.Arg1814Trp)
NM_001080414.4(CCDC88C):c.5668C>G (p.Pro1890Ala)
NM_001080414.4(CCDC88C):c.6035C>T (p.Pro2012Leu)	rs771028975
NM_001080414.4(CCDC88C):c.739G>A (p.Glu247Lys)

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