ClinVar Miner

List of variants in gene SACS reported as likely benign

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Gene type:
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Total variants: 81
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HGVS dbSNP
NM_014363.5(SACS):c.*20del rs143617437
NM_014363.5(SACS):c.10106T>C (p.Val3369Ala) rs17078605
NM_014363.5(SACS):c.10274A>G (p.Lys3425Arg) rs147317123
NM_014363.5(SACS):c.10338G>A (p.Gln3446=) rs2737701
NM_014363.5(SACS):c.10572A>G (p.Leu3524=) rs878854976
NM_014363.5(SACS):c.10611A>G (p.Ala3537=) rs137856939
NM_014363.5(SACS):c.10668G>A (p.Leu3556=) rs139517699
NM_014363.5(SACS):c.1066A>C (p.Ile356Leu) rs148286091
NM_014363.5(SACS):c.10972C>T (p.Arg3658Trp) rs115155117
NM_014363.5(SACS):c.10982C>T (p.Ala3661Val) rs36061856
NM_014363.5(SACS):c.11032C>G (p.Pro3678Ala) rs17078601
NM_014363.5(SACS):c.11703T>C (p.Asn3901=) rs146154135
NM_014363.5(SACS):c.1173T>A (p.Ser391=) rs150683286
NM_014363.5(SACS):c.11781G>A (p.Ala3927=)
NM_014363.5(SACS):c.12216T>A (p.Thr4072=) rs574182225
NM_014363.5(SACS):c.12304T>C (p.Leu4102=) rs2737699
NM_014363.5(SACS):c.12585A>G (p.Gly4195=) rs200305087
NM_014363.5(SACS):c.12649A>G (p.Asn4217Asp) rs35799469
NM_014363.5(SACS):c.12813T>G (p.Pro4271=) rs146376949
NM_014363.5(SACS):c.13443C>G (p.Thr4481=) rs201439638
NM_014363.5(SACS):c.13717A>C (p.Asn4573His) rs34382952
NM_014363.5(SACS):c.1373C>T (p.Thr458Ile) rs61729954
NM_014363.5(SACS):c.1656A>G (p.Leu552=) rs1536365
NM_014363.5(SACS):c.1662C>T (p.Ser554=)
NM_014363.5(SACS):c.171+13C>T rs374672041
NM_014363.5(SACS):c.171+6C>T rs3751368
NM_014363.5(SACS):c.1815A>G (p.Pro605=) rs377649927
NM_014363.5(SACS):c.1839G>A (p.Gln613=) rs35840595
NM_014363.5(SACS):c.1885G>A (p.Ala629Thr) rs149638449
NM_014363.5(SACS):c.1917A>G (p.Ala639=) rs138457742
NM_014363.5(SACS):c.2040C>T (p.Ser680=) rs142115704
NM_014363.5(SACS):c.2080G>A (p.Ala694Thr) rs17325713
NM_014363.5(SACS):c.2094-14C>T rs886038601
NM_014363.5(SACS):c.2427G>A (p.Glu809=) rs878854978
NM_014363.5(SACS):c.260-9G>A rs376676263
NM_014363.5(SACS):c.2643G>C (p.Glu881Asp) rs200517685
NM_014363.5(SACS):c.2682G>A (p.Ser894=) rs369958174
NM_014363.5(SACS):c.2721G>A (p.Leu907=) rs140118958
NM_014363.5(SACS):c.279G>A (p.Thr93=) rs373415912
NM_014363.5(SACS):c.2983G>T (p.Val995Phe) rs142967124
NM_014363.5(SACS):c.2988A>G (p.Leu996=) rs111846884
NM_014363.5(SACS):c.3129A>G (p.Ser1043=) rs148878361
NM_014363.5(SACS):c.3282C>T (p.Asn1094=) rs145499245
NM_014363.5(SACS):c.3414T>C (p.Asn1138=) rs146431793
NM_014363.5(SACS):c.3427C>A (p.Gln1143Lys) rs144267558
NM_014363.5(SACS):c.345+35T>C rs886038602
NM_014363.5(SACS):c.3752T>C (p.Ile1251Thr) rs76872266
NM_014363.5(SACS):c.4117_4118delGCinsCT (p.Ala1373Leu) rs797045938
NM_014363.5(SACS):c.4118C>T (p.Ala1373Val) rs61548169
NM_014363.5(SACS):c.4188C>T (p.His1396=) rs61754477
NM_014363.5(SACS):c.4302A>G (p.Leu1434=) rs34559250
NM_014363.5(SACS):c.591C>T (p.Val197=) rs750923640
NM_014363.5(SACS):c.5946A>G (p.Gly1982=) rs746358078
NM_014363.5(SACS):c.6051G>C (p.Lys2017Asn) rs35865691
NM_014363.5(SACS):c.6195T>C (p.Ile2065=) rs4143768
NM_014363.5(SACS):c.6240T>C (p.Val2080=) rs550680855
NM_014363.5(SACS):c.6267G>A (p.Ser2089=) rs9550956
NM_014363.5(SACS):c.6336A>C (p.Arg2112Ser) rs80132141
NM_014363.5(SACS):c.6456T>C (p.Gly2152=)
NM_014363.5(SACS):c.6576C>T (p.Ile2192=) rs145327845
NM_014363.5(SACS):c.6781C>A (p.Leu2261Ile) rs146722795
NM_014363.5(SACS):c.696T>A (p.Asn232Lys) rs2031640
NM_014363.5(SACS):c.7384C>T (p.Pro2462Ser) rs78239814
NM_014363.5(SACS):c.7527T>C (p.Tyr2509=) rs140034972
NM_014363.5(SACS):c.7528G>A (p.Ala2510Thr) rs111920492
NM_014363.5(SACS):c.7569G>A (p.Gly2523=) rs749462494
NM_014363.5(SACS):c.7713A>T (p.Pro2571=) rs557113294
NM_014363.5(SACS):c.7737G>A (p.Lys2579=) rs139279302
NM_014363.5(SACS):c.789C>T (p.Asn263=) rs771920263
NM_014363.5(SACS):c.8022T>C (p.Phe2674=) rs34928783
NM_014363.5(SACS):c.8339T>G (p.Phe2780Cys) rs111540787
NM_014363.5(SACS):c.8344G>A (p.Ala2782Thr) rs61742502
NM_014363.5(SACS):c.8344_8345delGCinsAT (p.Ala2782Ile) rs386768924
NM_014363.5(SACS):c.8345C>T (p.Ala2782Val) rs61742500
NM_014363.5(SACS):c.8577C>T (p.His2859=) rs140016265
NM_014363.5(SACS):c.8853T>C (p.Val2951=) rs9552929
NM_014363.5(SACS):c.909A>G (p.Ala303=) rs41315020
NM_014363.5(SACS):c.9399A>G (p.Lys3133=) rs762665640
NM_014363.5(SACS):c.972C>A (p.Asp324Glu) rs546652936
NM_014363.5(SACS):c.9981T>C (p.Ala3327=) rs2737700
NM_014363.6(SACS):c.-13A>G rs17078720

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