ClinVar Miner

List of variants in gene SYNE1 reported as uncertain significance for not specified

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Gene type:
ClinVar version:
Total variants: 144
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HGVS dbSNP
NC_000006.12:g.152442228G>A
NC_000006.12:g.152463343_152463355del
NM_033071.3(SYNE1):c.10246G>A (p.Glu3416Lys) rs1554541299
NM_033071.3(SYNE1):c.10381G>T (p.Ala3461Ser) rs797046022
NM_033071.3(SYNE1):c.10531T>C (p.Phe3511Leu) rs1161158102
NM_033071.3(SYNE1):c.10771C>T (p.His3591Tyr) rs752209637
NM_033071.3(SYNE1):c.10839G>T (p.Lys3613Asn) rs752187409
NM_033071.3(SYNE1):c.10936A>G (p.Arg3646Gly) rs767172575
NM_033071.3(SYNE1):c.1118A>C (p.Glu373Ala) rs372327585
NM_033071.3(SYNE1):c.11451A>G (p.Ile3817Met) rs1554518035
NM_033071.3(SYNE1):c.11580A>G (p.Ser3860=) rs1057518265
NM_033071.3(SYNE1):c.12142G>A (p.Glu4048Lys) rs148935596
NM_033071.3(SYNE1):c.12158A>C (p.Gln4053Pro) rs911413208
NM_033071.3(SYNE1):c.1234A>G (p.Lys412Glu) rs1554785680
NM_033071.3(SYNE1):c.13160T>G (p.Phe4387Cys) rs764410604
NM_033071.3(SYNE1):c.13223G>A (p.Arg4408His) rs768085752
NM_033071.3(SYNE1):c.1343C>T (p.Thr448Met) rs772375574
NM_033071.3(SYNE1):c.13615G>C (p.Glu4539Gln)
NM_033071.3(SYNE1):c.14122G>T (p.Ala4708Ser) rs368490158
NM_033071.3(SYNE1):c.14352G>C (p.Arg4784Ser) rs1237053788
NM_033071.3(SYNE1):c.15662C>T (p.Pro5221Leu) rs200626370
NM_033071.3(SYNE1):c.15706A>T (p.Met5236Leu) rs1554441847
NM_033071.3(SYNE1):c.16655G>A (p.Arg5552His) rs753544584
NM_033071.3(SYNE1):c.16994-9C>A rs886044642
NM_033071.3(SYNE1):c.17270C>G (p.Thr5757Arg) rs150376715
NM_033071.3(SYNE1):c.17545G>T (p.Ala5849Ser) rs765300968
NM_033071.3(SYNE1):c.17612G>A (p.Arg5871His) rs746220387
NM_033071.3(SYNE1):c.17635G>C (p.Val5879Leu) rs200589166
NM_033071.3(SYNE1):c.1795G>T (p.Ala599Ser) rs747150703
NM_033071.3(SYNE1):c.18421G>A (p.Val6141Ile) rs138258566
NM_033071.3(SYNE1):c.18445C>A (p.Arg6149Ser) rs201685248
NM_033071.3(SYNE1):c.18449C>T (p.Thr6150Ile) rs150335599
NM_033071.3(SYNE1):c.19321G>T (p.Ala6441Ser) rs149272010
NM_033071.3(SYNE1):c.19522A>T (p.Ser6508Cys) rs1554264075
NM_033071.3(SYNE1):c.1972C>T (p.Pro658Ser) rs1455678689
NM_033071.3(SYNE1):c.19969C>T (p.Arg6657Cys) rs150063353
NM_033071.3(SYNE1):c.20432C>T (p.Ser6811Leu) rs373012438
NM_033071.3(SYNE1):c.21058A>C (p.Asn7020His) rs777618601
NM_033071.3(SYNE1):c.21109G>A (p.Gly7037Ser) rs777227521
NM_033071.3(SYNE1):c.21318A>T (p.Gln7106His) rs1554227607
NM_033071.3(SYNE1):c.21690T>G (p.Phe7230Leu) rs1415687146
NM_033071.3(SYNE1):c.21690_21691delinsGG (p.Phe7230_Phe7231delinsLeuVal) rs1554223069
NM_033071.3(SYNE1):c.21694C>T (p.Leu7232Phe) rs753138419
NM_033071.3(SYNE1):c.22090C>T (p.Arg7364Cys) rs371642308
NM_033071.3(SYNE1):c.22091G>A (p.Arg7364His) rs748260996
NM_033071.3(SYNE1):c.22346G>A (p.Arg7449His) rs752057121
NM_033071.3(SYNE1):c.22450C>T (p.Arg7484Trp) rs755302191
NM_033071.3(SYNE1):c.22773A>C (p.Glu7591Asp) rs763100950
NM_033071.3(SYNE1):c.23027T>A (p.Ile7676Asn) rs1435183530
NM_033071.3(SYNE1):c.23432A>G (p.Glu7811Gly) rs1057518415
NM_033071.3(SYNE1):c.23491G>A (p.Ala7831Thr) rs372990463
NM_033071.3(SYNE1):c.23578-6del rs757124573
NM_033071.3(SYNE1):c.23578-7C>T rs375558499
NM_033071.3(SYNE1):c.23756G>A (p.Arg7919Lys) rs777371816
NM_033071.3(SYNE1):c.24342C>G (p.Ile8114Met) rs201799566
NM_033071.3(SYNE1):c.245G>T (p.Arg82Leu) rs143900928
NM_033071.3(SYNE1):c.24652T>C (p.Tyr8218His) rs1016679896
NM_033071.3(SYNE1):c.25424G>A (p.Arg8475His) rs759577495
NM_033071.3(SYNE1):c.25439A>G (p.Asn8480Ser) rs1554393115
NM_033071.3(SYNE1):c.25562T>C (p.Ile8521Thr) rs760698113
NM_033071.3(SYNE1):c.25900G>C (p.Gly8634Arg) rs201664645
NM_033071.3(SYNE1):c.2749A>T (p.Ser917Cys) rs141214076
NM_033071.3(SYNE1):c.2910C>T (p.His970=) rs747231741
NM_033071.3(SYNE1):c.3494C>T (p.Ala1165Val) rs746060505
NM_033071.3(SYNE1):c.382A>G (p.Ile128Val) rs1554830234
NM_033071.3(SYNE1):c.3970C>G (p.Leu1324Val) rs1554709399
NM_033071.3(SYNE1):c.4319C>T (p.Thr1440Met) rs139798419
NM_033071.3(SYNE1):c.4545G>T (p.Gln1515His) rs1378400021
NM_033071.3(SYNE1):c.5091C>G (p.Val1697=) rs146789107
NM_033071.3(SYNE1):c.5390C>T (p.Thr1797Ile) rs1554666956
NM_033071.3(SYNE1):c.6115G>A (p.Glu2039Lys) rs367594476
NM_033071.3(SYNE1):c.757G>A (p.Ala253Thr) rs1251834592
NM_033071.3(SYNE1):c.7613T>C (p.Ile2538Thr) rs138766629
NM_033071.3(SYNE1):c.7678A>G (p.Lys2560Glu) rs777368779
NM_033071.3(SYNE1):c.8475A>T (p.Lys2825Asn) rs764853272
NM_033071.3(SYNE1):c.8860C>G (p.Leu2954Val) rs756300560
NM_033071.3(SYNE1):c.9530A>G (p.Asn3177Ser) rs1554563052
NM_033071.3(SYNE1):c.9736C>G (p.Gln3246Glu) rs149901087
NM_033071.3(SYNE1):c.9820T>A (p.Leu3274Ile) rs1554560113
NM_033071.3(SYNE1):c.9868A>C (p.Asn3290His) rs745707616
NM_182961.4(SYNE1):c.11521G>A (p.Val3841Ile) rs1323758453
NM_182961.4(SYNE1):c.11627T>C (p.Val3876Ala) rs372944688
NM_182961.4(SYNE1):c.11702G>C (p.Ser3901Thr) rs376327805
NM_182961.4(SYNE1):c.11861_11875del (p.Ser3954_Thr3958del) rs1200141982
NM_182961.4(SYNE1):c.12272A>G (p.Asp4091Gly) rs767294741
NM_182961.4(SYNE1):c.12391G>T (p.Gly4131Cys) rs139139296
NM_182961.4(SYNE1):c.1330C>T (p.Arg444Trp) rs75153800
NM_182961.4(SYNE1):c.13331G>A (p.Arg4444Gln) rs139075013
NM_182961.4(SYNE1):c.13724G>T (p.Cys4575Phe) rs199701902
NM_182961.4(SYNE1):c.13768A>G (p.Asn4590Asp) rs199761238
NM_182961.4(SYNE1):c.14452T>A (p.Tyr4818Asn) rs142422990
NM_182961.4(SYNE1):c.15202A>G (p.Lys5068Glu) rs139805184
NM_182961.4(SYNE1):c.15337G>A (p.Val5113Ile) rs139170018
NM_182961.4(SYNE1):c.15377A>C (p.Glu5126Ala) rs773536890
NM_182961.4(SYNE1):c.15451G>A (p.Val5151Met) rs199996504
NM_182961.4(SYNE1):c.15489G>A (p.Glu5163=) rs750155092
NM_182961.4(SYNE1):c.15863G>C (p.Gly5288Ala) rs201313856
NM_182961.4(SYNE1):c.15907C>T (p.Arg5303Trp) rs149215868
NM_182961.4(SYNE1):c.16295G>A (p.Arg5432Gln) rs200812806
NM_182961.4(SYNE1):c.16901T>C (p.Met5634Thr) rs138509817
NM_182961.4(SYNE1):c.17531C>G (p.Ser5844Cys) rs144244988
NM_182961.4(SYNE1):c.17930C>T (p.Thr5977Met) rs767144952
NM_182961.4(SYNE1):c.19255C>G (p.Gln6419Glu) rs150700669
NM_182961.4(SYNE1):c.20027G>A (p.Arg6676Gln) rs190673256
NM_182961.4(SYNE1):c.20417A>C (p.Asp6806Ala) rs753654674
NM_182961.4(SYNE1):c.2066G>A (p.Arg689Gln) rs769628070
NM_182961.4(SYNE1):c.21377A>G (p.Lys7126Arg) rs145882956
NM_182961.4(SYNE1):c.21782G>A (p.Arg7261Gln) rs61742716
NM_182961.4(SYNE1):c.21815A>G (p.Lys7272Arg) rs764715827
NM_182961.4(SYNE1):c.21952G>A (p.Ala7318Thr) rs145494541
NM_182961.4(SYNE1):c.21995A>C (p.His7332Pro) rs151247098
NM_182961.4(SYNE1):c.22346+6G>T rs368678916
NM_182961.4(SYNE1):c.22495-9A>T rs762256509
NM_182961.4(SYNE1):c.22783A>G (p.Ile7595Val) rs146320179
NM_182961.4(SYNE1):c.23315G>A (p.Arg7772Gln) rs138787771
NM_182961.4(SYNE1):c.23403C>G (p.Ser7801Arg) rs886043281
NM_182961.4(SYNE1):c.23480C>G (p.Ala7827Gly) rs141315921
NM_182961.4(SYNE1):c.24349C>T (p.Arg8117Trp) rs144056525
NM_182961.4(SYNE1):c.24717C>G (p.His8239Gln) rs201548223
NM_182961.4(SYNE1):c.24815G>A (p.Arg8272Gln) rs201029723
NM_182961.4(SYNE1):c.25246+3G>A rs765849365
NM_182961.4(SYNE1):c.2569-8C>T rs376033376
NM_182961.4(SYNE1):c.25C>T (p.Arg9Trp) rs200346529
NM_182961.4(SYNE1):c.3404A>C (p.Glu1135Ala) rs764928878
NM_182961.4(SYNE1):c.3436C>G (p.Gln1146Glu) rs760256766
NM_182961.4(SYNE1):c.3916C>A (p.Leu1306Met) rs1454797342
NM_182961.4(SYNE1):c.3934G>A (p.Glu1312Lys) rs200276242
NM_182961.4(SYNE1):c.4031G>A (p.Arg1344Gln) rs144566713
NM_182961.4(SYNE1):c.4107T>A (p.Phe1369Leu) rs149109801
NM_182961.4(SYNE1):c.5101G>T (p.Ala1701Ser) rs149758808
NM_182961.4(SYNE1):c.5282A>G (p.Gln1761Arg) rs146244669
NM_182961.4(SYNE1):c.5421+9G>T rs376218204
NM_182961.4(SYNE1):c.6154T>C (p.Phe2052Leu) rs147511500
NM_182961.4(SYNE1):c.6521C>T (p.Thr2174Ile) rs141858284
NM_182961.4(SYNE1):c.6826-6A>G rs183683592
NM_182961.4(SYNE1):c.7052G>A (p.Ser2351Asn) rs151039167
NM_182961.4(SYNE1):c.7156A>G (p.Ile2386Val) rs147947903
NM_182961.4(SYNE1):c.7976C>A (p.Thr2659Asn) rs117480635
NM_182961.4(SYNE1):c.8005-3C>T rs117084693
NM_182961.4(SYNE1):c.8015T>C (p.Leu2672Pro) rs147870520
NM_182961.4(SYNE1):c.8557A>G (p.Thr2853Ala) rs77853132
NM_182961.4(SYNE1):c.9091A>G (p.Arg3031Gly) rs144643941
NM_182961.4(SYNE1):c.9377C>G (p.Ser3126Cys) rs139089832
NM_182961.4(SYNE1):c.9857C>T (p.Ser3286Phe) rs770774159

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