List of variants reported as uncertain significance for Spinocerebellar ataxia type 28 by Illumina Laboratory Services, Illumina

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Total variants: 24

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HGVS	dbSNP	gnomAD frequency
NM_006796.3(AFG3L2):c.114+12C>T	rs758470020	0.00124
NM_006796.3(AFG3L2):c.-92T>C	rs574201536	0.00087
NM_006796.3(AFG3L2):c.*379T>A	rs150224434	0.00073
NM_006796.3(AFG3L2):c.*221A>G	rs886053613	0.00048
NM_006796.3(AFG3L2):c.2167G>A (p.Val723Met)	rs139469785	0.00024
NM_006796.3(AFG3L2):c.*484A>G	rs565352114	0.00019
NM_006796.2(AFG3L2):c.-179C>T	rs576218520	0.00016
NM_006796.3(AFG3L2):c.*326G>A	rs180917336	0.00015
NM_006796.3(AFG3L2):c.-139T>C	rs542643055	0.00010
NM_006796.3(AFG3L2):c.*373G>A	rs886053612	0.00004
NM_006796.3(AFG3L2):c.1706A>C (p.Lys569Thr)	rs758811358	0.00004
NM_006796.3(AFG3L2):c.*585A>C	rs886053611	0.00001
NM_006796.3(AFG3L2):c.1796G>A (p.Arg599His)	rs1263405472	0.00001
NM_006796.3(AFG3L2):c.2346G>T (p.Glu782Asp)	rs886053614	0.00001
NM_006796.3(AFG3L2):c.267T>G (p.Pro89=)	rs1308467906	0.00001
NM_006796.3(AFG3L2):c.365A>T (p.Lys122Ile)	rs915684170	0.00001
NM_006796.3(AFG3L2):c.-18A>G	rs886053618
NM_006796.3(AFG3L2):c.-78C>A	rs1909190689
NM_006796.3(AFG3L2):c.1397C>T (p.Pro466Leu)	rs375098002
NM_006796.3(AFG3L2):c.1516G>T (p.Ala506Ser)	rs1908301962
NM_006796.3(AFG3L2):c.1664-5G>C	rs886053615
NM_006796.3(AFG3L2):c.268A>G (p.Lys90Glu)	rs886053616
NM_006796.3(AFG3L2):c.891G>A (p.Lys297=)	rs1908570292
NM_006796.3(AFG3L2):c.89C>T (p.Pro30Leu)	rs886053617

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