List of variants reported as uncertain significance for Charlevoix-Saguenay spastic ataxia by Fulgent Genetics, Fulgent Genetics

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Total variants: 28

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HGVS	dbSNP	gnomAD frequency
NM_014363.6(SACS):c.4076T>C (p.Met1359Thr)	rs146451611	0.00197
NM_014363.6(SACS):c.8972G>A (p.Arg2991His)	rs192610957	0.00084
NM_014363.6(SACS):c.2580A>G (p.Gln860=)	rs41283958	0.00031
NM_014363.6(SACS):c.9562T>C (p.Phe3188Leu)	rs137905181	0.00029
NM_014363.6(SACS):c.6640C>T (p.Arg2214Cys)	rs138379074	0.00017
NM_014363.6(SACS):c.8245A>G (p.Ile2749Val)	rs186436335	0.00013
NM_014363.6(SACS):c.13036G>A (p.Asp4346Asn)	rs372359781	0.00011
NM_014363.6(SACS):c.4900G>C (p.Glu1634Gln)	rs143961484	0.00011
NM_014363.6(SACS):c.4936C>A (p.Leu1646Met)	rs200810800	0.00011
NM_014363.6(SACS):c.2996T>C (p.Ile999Thr)	rs371869943	0.00009
NM_014363.6(SACS):c.5744A>G (p.His1915Arg)	rs144822691	0.00009
NM_014363.6(SACS):c.9791C>G (p.Thr3264Arg)	rs758563983	0.00007
NM_014363.6(SACS):c.11327T>C (p.Ile3776Thr)	rs145188410	0.00004
NM_014363.6(SACS):c.1640C>T (p.Pro547Leu)	rs140507581	0.00004
NM_014363.6(SACS):c.6409C>G (p.Gln2137Glu)	rs201690040	0.00004
NM_014363.6(SACS):c.8315G>C (p.Gly2772Ala)	rs763504656	0.00004
NM_014363.6(SACS):c.11942A>G (p.Gln3981Arg)	rs747314113	0.00002
NM_014363.6(SACS):c.9805G>A (p.Asp3269Asn)	rs754144089	0.00002
NM_014363.6(SACS):c.10819A>G (p.Ile3607Val)	rs372494676	0.00001
NM_014363.6(SACS):c.2564T>C (p.Leu855Ser)	rs142037771	0.00001
NM_014363.6(SACS):c.2585C>T (p.Pro862Leu)	rs776290829	0.00001
NM_014363.6(SACS):c.818T>A (p.Phe273Tyr)	rs182864646	0.00001
NM_014363.6(SACS):c.944A>G (p.Asp315Gly)	rs771115225	0.00001
NM_014363.6(SACS):c.13738_13739del (p.Ter4580LysextTer?)	rs776682685
NM_014363.6(SACS):c.2225G>A (p.Arg742Gln)	rs2137645971
NM_014363.6(SACS):c.2726G>T (p.Ser909Ile)	rs2137641417
NM_014363.6(SACS):c.5639C>T (p.Thr1880Ile)	rs1555252070
NM_014363.6(SACS):c.9356GTC[1] (p.Arg3120del)	rs1388341388

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