ClinVar Miner

List of variants in gene SACS reported as uncertain significance by Natera, Inc.

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 102
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HGVS dbSNP
NM_014363.6(SACS):c.10047A>G (p.Ser3349=) rs138909482
NM_014363.6(SACS):c.10181A>G (p.Asn3394Ser) rs375898103
NM_014363.6(SACS):c.10205A>G (p.Asp3402Gly) rs543563990
NM_014363.6(SACS):c.10274A>G (p.Lys3425Arg) rs147317123
NM_014363.6(SACS):c.1033C>T (p.Arg345Trp) rs776156836
NM_014363.6(SACS):c.10443C>G (p.Leu3481=) rs144087359
NM_014363.6(SACS):c.10482A>G (p.Leu3494=) rs149643158
NM_014363.6(SACS):c.10737G>A (p.Met3579Ile) rs199970621
NM_014363.6(SACS):c.10819A>G (p.Ile3607Val)
NM_014363.6(SACS):c.10983G>A (p.Ala3661=)
NM_014363.6(SACS):c.11003C>G (p.Pro3668Arg)
NM_014363.6(SACS):c.11066C>A (p.Pro3689Gln) rs148925505
NM_014363.6(SACS):c.11215G>A (p.Val3739Ile) rs1027336196
NM_014363.6(SACS):c.11301A>T (p.Lys3767Asn) rs762041995
NM_014363.6(SACS):c.11327T>C (p.Ile3776Thr) rs145188410
NM_014363.6(SACS):c.11884A>T (p.Ile3962Leu) rs746953932
NM_014363.6(SACS):c.11927G>A (p.Ser3976Asn)
NM_014363.6(SACS):c.11928T>C (p.Ser3976=) rs145680118
NM_014363.6(SACS):c.12075T>G (p.Asn4025Lys)
NM_014363.6(SACS):c.12148T>C (p.Phe4050Leu) rs147013767
NM_014363.6(SACS):c.12232C>A (p.Arg4078=) rs141315518
NM_014363.6(SACS):c.12260A>G (p.Tyr4087Cys) rs373478772
NM_014363.6(SACS):c.12635G>A (p.Arg4212Lys)
NM_014363.6(SACS):c.1278A>T (p.Leu426Phe) rs138413501
NM_014363.6(SACS):c.12829C>T (p.Pro4277Ser) rs370655945
NM_014363.6(SACS):c.12905C>A (p.Ser4302Tyr) rs778808568
NM_014363.6(SACS):c.1297G>C (p.Ala433Pro)
NM_014363.6(SACS):c.13272C>T (p.Ala4424=) rs567495567
NM_014363.6(SACS):c.13284C>T (p.Tyr4428=) rs753277514
NM_014363.6(SACS):c.1331C>G (p.Ala444Gly)
NM_014363.6(SACS):c.13320G>A (p.Ser4440=)
NM_014363.6(SACS):c.13506A>G (p.Pro4502=) rs1593119067
NM_014363.6(SACS):c.13509T>G (p.Thr4503=)
NM_014363.6(SACS):c.13538G>A (p.Ser4513Asn) rs138328181
NM_014363.6(SACS):c.13738_13739del (p.Ter4580LysextTer?) rs776682685
NM_014363.6(SACS):c.1378C>T (p.Leu460Phe) rs145213666
NM_014363.6(SACS):c.1463C>T (p.Pro488Leu) rs375875022
NM_014363.6(SACS):c.1519A>G (p.Thr507Ala) rs372022664
NM_014363.6(SACS):c.1562G>C (p.Ser521Thr) rs190617851
NM_014363.6(SACS):c.1884C>T (p.Pro628=) rs144468379
NM_014363.6(SACS):c.2096C>T (p.Ser699Phe) rs374680967
NM_014363.6(SACS):c.2182C>G (p.Arg728Gly) rs752059006
NM_014363.6(SACS):c.2322A>G (p.Pro774=)
NM_014363.6(SACS):c.2403A>G (p.Pro801=) rs758503842
NM_014363.6(SACS):c.2451C>T (p.Leu817=) rs756595744
NM_014363.6(SACS):c.2492A>G (p.Glu831Gly) rs375968367
NM_014363.6(SACS):c.2494T>C (p.Ser832Pro) rs549957998
NM_014363.6(SACS):c.2776A>G (p.Ile926Val) rs144362131
NM_014363.6(SACS):c.3017A>G (p.His1006Arg) rs368149368
NM_014363.6(SACS):c.3070A>G (p.Lys1024Glu)
NM_014363.6(SACS):c.3729A>G (p.Glu1243=) rs756663705
NM_014363.6(SACS):c.3768C>T (p.Tyr1256=) rs200350631
NM_014363.6(SACS):c.396A>G (p.Leu132=) rs1256540997
NM_014363.6(SACS):c.3992A>G (p.His1331Arg)
NM_014363.6(SACS):c.4149T>C (p.His1383=) rs749219225
NM_014363.6(SACS):c.432G>T (p.Trp144Cys) rs368570790
NM_014363.6(SACS):c.4522A>C (p.Asn1508His) rs144653411
NM_014363.6(SACS):c.4612A>G (p.Ile1538Val) rs544249449
NM_014363.6(SACS):c.4757A>G (p.Asn1586Ser) rs201558584
NM_014363.6(SACS):c.4936C>A (p.Leu1646Met) rs200810800
NM_014363.6(SACS):c.4963A>G (p.Lys1655Glu)
NM_014363.6(SACS):c.5060C>T (p.Thr1687Ile)
NM_014363.6(SACS):c.5064G>A (p.Gln1688=) rs760628805
NM_014363.6(SACS):c.51C>T (p.Cys17=) rs763979020
NM_014363.6(SACS):c.5356G>A (p.Asp1786Asn) rs763496360
NM_014363.6(SACS):c.5368G>A (p.Ala1790Thr) rs147517201
NM_014363.6(SACS):c.5583G>C (p.Trp1861Cys) rs140678034
NM_014363.6(SACS):c.5732C>T (p.Thr1911Met) rs368494148
NM_014363.6(SACS):c.5785C>T (p.Arg1929Trp)
NM_014363.6(SACS):c.5858A>T (p.His1953Leu) rs1428265468
NM_014363.6(SACS):c.598A>G (p.Ile200Val)
NM_014363.6(SACS):c.6059G>A (p.Gly2020Glu) rs747566710
NM_014363.6(SACS):c.6084A>T (p.Glu2028Asp) rs149018756
NM_014363.6(SACS):c.6119C>G (p.Ala2040Gly)
NM_014363.6(SACS):c.6266C>T (p.Ser2089Leu) rs370095300
NM_014363.6(SACS):c.6349G>A (p.Glu2117Lys) rs754033201
NM_014363.6(SACS):c.6518T>C (p.Ile2173Thr) rs368624188
NM_014363.6(SACS):c.6634A>G (p.Thr2212Ala) rs556248979
NM_014363.6(SACS):c.6640C>T (p.Arg2214Cys) rs138379074
NM_014363.6(SACS):c.6776C>T (p.Pro2259Leu) rs150098233
NM_014363.6(SACS):c.6844T>C (p.Leu2282=)
NM_014363.6(SACS):c.6857A>G (p.Lys2286Arg) rs754381972
NM_014363.6(SACS):c.6952G>A (p.Ala2318Thr) rs147949881
NM_014363.6(SACS):c.7100C>T (p.Ala2367Val) rs752273313
NM_014363.6(SACS):c.7200T>C (p.Phe2400=) rs148544893
NM_014363.6(SACS):c.7262T>A (p.Phe2421Tyr) rs1213144547
NM_014363.6(SACS):c.7497C>T (p.Val2499=) rs774558627
NM_014363.6(SACS):c.7528G>A (p.Ala2510Thr) rs111920492
NM_014363.6(SACS):c.7833G>A (p.Thr2611=) rs1237743096
NM_014363.6(SACS):c.8022T>G (p.Phe2674Leu) rs34928783
NM_014363.6(SACS):c.8414C>T (p.Thr2805Ile) rs772742353
NM_014363.6(SACS):c.8482A>G (p.Ser2828Gly) rs9552930
NM_014363.6(SACS):c.8539C>G (p.Leu2847Val) rs760976439
NM_014363.6(SACS):c.8693G>A (p.Arg2898His) rs201977288
NM_014363.6(SACS):c.8768T>C (p.Val2923Ala)
NM_014363.6(SACS):c.8799T>C (p.Tyr2933=) rs779302353
NM_014363.6(SACS):c.8802C>T (p.Phe2934=)
NM_014363.6(SACS):c.8948A>G (p.Asn2983Ser) rs200106708
NM_014363.6(SACS):c.9232A>G (p.Asn3078Asp)
NM_014363.6(SACS):c.9359G>T (p.Arg3120Leu) rs569955570
NM_014363.6(SACS):c.9550C>T (p.Arg3184Cys) rs143557803
NM_014363.6(SACS):c.9677A>G (p.Tyr3226Cys) rs776143384

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