ClinVar Miner

List of variants in gene SACS reported as likely benign by Athena Diagnostics Inc

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Total variants: 24
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HGVS dbSNP
NM_014363.6(SACS):c.11781G>A (p.Ala3927=)
NM_014363.6(SACS):c.12216T>A (p.Thr4072=) rs574182225
NM_014363.6(SACS):c.12585A>G (p.Gly4195=) rs200305087
NM_014363.6(SACS):c.12813T>G (p.Pro4271=) rs146376949
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.1662C>T (p.Ser554=)
NM_014363.6(SACS):c.1815A>G (p.Pro605=) rs377649927
NM_014363.6(SACS):c.1885G>A (p.Ala629Thr) rs149638449
NM_014363.6(SACS):c.1917A>G (p.Ala639=) rs138457742
NM_014363.6(SACS):c.260-9G>A rs376676263
NM_014363.6(SACS):c.4117_4118delinsCT (p.Ala1373Leu) rs797045938
NM_014363.6(SACS):c.4302A>G (p.Leu1434=) rs34559250
NM_014363.6(SACS):c.5946A>G (p.Gly1982=) rs746358078
NM_014363.6(SACS):c.6051G>C (p.Lys2017Asn) rs35865691
NM_014363.6(SACS):c.6336A>C (p.Arg2112Ser) rs80132141
NM_014363.6(SACS):c.6456T>C (p.Gly2152=)
NM_014363.6(SACS):c.6781C>A (p.Leu2261Ile) rs146722795
NM_014363.6(SACS):c.7384C>T (p.Pro2462Ser) rs78239814
NM_014363.6(SACS):c.7527T>C (p.Tyr2509=) rs140034972
NM_014363.6(SACS):c.7737G>A (p.Lys2579=) rs139279302
NM_014363.6(SACS):c.789C>T (p.Asn263=) rs771920263
NM_014363.6(SACS):c.8339T>G (p.Phe2780Cys) rs111540787
NM_014363.6(SACS):c.8344_8345delinsAT (p.Ala2782Ile) rs386768924

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