ClinVar Miner

List of variants in gene SACS reported as likely benign for Spastic paraplegia

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Total variants: 22
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HGVS dbSNP
NM_014363.6(SACS):c.10572A>G (p.Leu3524=) rs878854976
NM_014363.6(SACS):c.10982C>T (p.Ala3661Val) rs36061856
NM_014363.6(SACS):c.11703T>C (p.Asn3901=) rs146154135
NM_014363.6(SACS):c.12813T>G (p.Pro4271=) rs146376949
NM_014363.6(SACS):c.13443C>G (p.Thr4481=) rs201439638
NM_014363.6(SACS):c.13717A>C (p.Asn4573His) rs34382952
NM_014363.6(SACS):c.1373C>T (p.Thr458Ile) rs61729954
NM_014363.6(SACS):c.2040C>T (p.Ser680=) rs142115704
NM_014363.6(SACS):c.2427G>A (p.Glu809=) rs878854978
NM_014363.6(SACS):c.260-9G>A rs376676263
NM_014363.6(SACS):c.2643G>C (p.Glu881Asp) rs200517685
NM_014363.6(SACS):c.2682G>A (p.Ser894=) rs369958174
NM_014363.6(SACS):c.279G>A (p.Thr93=) rs373415912
NM_014363.6(SACS):c.3282C>T (p.Asn1094=) rs145499245
NM_014363.6(SACS):c.3414T>C (p.Asn1138=) rs146431793
NM_014363.6(SACS):c.3427C>A (p.Gln1143Lys) rs144267558
NM_014363.6(SACS):c.591C>T (p.Val197=) rs750923640
NM_014363.6(SACS):c.6576C>T (p.Ile2192=) rs145327845
NM_014363.6(SACS):c.7569G>A (p.Gly2523=) rs749462494
NM_014363.6(SACS):c.8339T>G (p.Phe2780Cys) rs111540787
NM_014363.6(SACS):c.9399A>G (p.Lys3133=) rs762665640
NM_014363.6(SACS):c.972C>A (p.Asp324Glu) rs546652936

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