List of variants reported as benign for Charlevoix-Saguenay spastic ataxia by Genome-Nilou Lab

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Total variants: 24

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HGVS	dbSNP	gnomAD frequency
NM_014363.6(SACS):c.10338G>A (p.Gln3446=)	rs2737701	0.98600
NM_014363.6(SACS):c.9981T>C (p.Ala3327=)	rs2737700	0.36123
NM_014363.6(SACS):c.-13A>G	rs17078720	0.27905
NM_014363.6(SACS):c.6195T>C (p.Ile2065=)	rs4143768	0.21785
NM_014363.6(SACS):c.8853T>C (p.Val2951=)	rs9552929	0.21755
NM_014363.6(SACS):c.10106T>C (p.Val3369Ala)	rs17078605	0.21747
NM_014363.6(SACS):c.12304T>C (p.Leu4102=)	rs2737699	0.21736
NM_014363.6(SACS):c.171+6C>T	rs3751368	0.13441
NM_014363.6(SACS):c.696T>A (p.Asn232Lys)	rs2031640	0.08558
NM_014363.6(SACS):c.1656A>G (p.Leu552=)	rs1536365	0.08543
NM_014363.6(SACS):c.11032C>G (p.Pro3678Ala)	rs17078601	0.02418
NM_014363.6(SACS):c.4117G>C (p.Ala1373Pro)	rs61326562	0.00706
NM_014363.6(SACS):c.6069C>T (p.Asn2023=)	rs35369023	0.00706
NM_014363.6(SACS):c.4118C>T (p.Ala1373Val)	rs61548169	0.00705
NM_014363.6(SACS):c.5502G>C (p.Leu1834=)	rs34389000	0.00705
NM_014363.6(SACS):c.10896A>G (p.Ile3632Met)	rs35256065	0.00558
NM_014363.6(SACS):c.6781C>A (p.Leu2261Ile)	rs146722795	0.00506
NM_014363.6(SACS):c.10821C>A (p.Ile3607=)	rs113595574	0.00447
NM_014363.6(SACS):c.6336A>C (p.Arg2112Ser)	rs80132141	0.00343
NM_014363.6(SACS):c.3129A>G (p.Ser1043=)	rs148878361	0.00292
NM_014363.6(SACS):c.1917A>G (p.Ala639=)	rs138457742	0.00084
NM_014363.6(SACS):c.2146C>T (p.His716Tyr)	rs146852400	0.00075
NM_014363.6(SACS):c.1224C>T (p.Asp408=)	rs2274386	0.00004
NM_014363.6(SACS):c.5461T>C (p.Cys1821Arg)	rs376680832	0.00004

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