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: 134
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HGVS dbSNP
NM_182961.4(SYNE1):c.10225G>A (p.Glu3409Lys) rs1554541299
NM_182961.4(SYNE1):c.10360G>T (p.Ala3454Ser) rs797046022
NM_182961.4(SYNE1):c.10510T>C (p.Phe3504Leu) rs1161158102
NM_182961.4(SYNE1):c.10750C>T (p.His3584Tyr) rs752209637
NM_182961.4(SYNE1):c.10818G>T (p.Lys3606Asn) rs752187409
NM_182961.4(SYNE1):c.1097A>C (p.Glu366Ala) rs372327585
NM_182961.4(SYNE1):c.10981A>G (p.Arg3661Gly) rs767172575
NM_182961.4(SYNE1):c.11496A>G (p.Ile3832Met) rs1554518035
NM_182961.4(SYNE1):c.11521G>A (p.Val3841Ile) rs1323758453
NM_182961.4(SYNE1):c.11625A>G (p.Ser3875=) rs1057518265
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.1213A>G (p.Lys405Glu) rs1554785680
NM_182961.4(SYNE1):c.12272A>G (p.Asp4091Gly) rs767294741
NM_182961.4(SYNE1):c.12355G>A (p.Glu4119Lys) rs148935596
NM_182961.4(SYNE1):c.12371A>C (p.Gln4124Pro) rs911413208
NM_182961.4(SYNE1):c.12391G>T (p.Gly4131Cys) rs139139296
NM_182961.4(SYNE1):c.1322C>T (p.Thr441Met) rs772375574
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.13373T>G (p.Phe4458Cys) rs764410604
NM_182961.4(SYNE1):c.13436G>A (p.Arg4479His) rs768085752
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.13828G>C (p.Glu4610Gln) rs1590224228
NM_182961.4(SYNE1):c.14335G>T (p.Ala4779Ser) rs368490158
NM_182961.4(SYNE1):c.14565G>C (p.Arg4855Ser) rs1237053788
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.15875C>T (p.Pro5292Leu) rs200626370
NM_182961.4(SYNE1):c.15919A>T (p.Met5307Leu) rs1554441847
NM_182961.4(SYNE1):c.16868G>A (p.Arg5623His) rs753544584
NM_182961.4(SYNE1):c.16901T>C (p.Met5634Thr) rs138509817
NM_182961.4(SYNE1):c.17203-5C>A rs886044642
NM_182961.4(SYNE1):c.17332A>G (p.Ile5778Val) rs762422242
NM_182961.4(SYNE1):c.17483C>G (p.Thr5828Arg) rs150376715
NM_182961.4(SYNE1):c.17531C>G (p.Ser5844Cys) rs144244988
NM_182961.4(SYNE1):c.17545A>G (p.Thr5849Ala)
NM_182961.4(SYNE1):c.1774G>T (p.Ala592Ser) rs747150703
NM_182961.4(SYNE1):c.17758G>T (p.Ala5920Ser) rs765300968
NM_182961.4(SYNE1):c.17825G>A (p.Arg5942His) rs746220387
NM_182961.4(SYNE1):c.17827T>C (p.Ser5943Pro) rs147998933
NM_182961.4(SYNE1):c.17848G>C (p.Val5950Leu) rs200589166
NM_182961.4(SYNE1):c.17930C>T (p.Thr5977Met) rs767144952
NM_182961.4(SYNE1):c.18634G>A (p.Val6212Ile) rs138258566
NM_182961.4(SYNE1):c.18658C>A (p.Arg6220Ser) rs201685248
NM_182961.4(SYNE1):c.18662C>T (p.Thr6221Ile) rs150335599
NM_182961.4(SYNE1):c.19255C>G (p.Gln6419Glu) rs150700669
NM_182961.4(SYNE1):c.1951C>T (p.Pro651Ser) rs1455678689
NM_182961.4(SYNE1):c.19534G>T (p.Ala6512Ser) rs149272010
NM_182961.4(SYNE1):c.19735A>T (p.Ser6579Cys) rs1554264075
NM_182961.4(SYNE1):c.20027G>A (p.Arg6676Gln) rs190673256
NM_182961.4(SYNE1):c.20182C>T (p.Arg6728Cys) rs150063353
NM_182961.4(SYNE1):c.20417A>C (p.Asp6806Ala) rs753654674
NM_182961.4(SYNE1):c.20645C>T (p.Ser6882Leu) rs373012438
NM_182961.4(SYNE1):c.2066G>A (p.Arg689Gln) rs769628070
NM_182961.4(SYNE1):c.2097+3_2097+15del rs1593220945
NM_182961.4(SYNE1):c.21271A>C (p.Asn7091His) rs777618601
NM_182961.4(SYNE1):c.21322G>A (p.Gly7108Ser) rs777227521
NM_182961.4(SYNE1):c.21377A>G (p.Lys7126Arg) rs145882956
NM_182961.4(SYNE1):c.21531A>T (p.Gln7177His) rs1554227607
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.21903T>G (p.Phe7301Leu) rs1415687146
NM_182961.4(SYNE1):c.21903_21904delinsGG (p.Phe7301_Phe7302delinsLeuVal) rs1554223069
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.22303C>T (p.Arg7435Cys) rs371642308
NM_182961.4(SYNE1):c.22304G>A (p.Arg7435His) rs748260996
NM_182961.4(SYNE1):c.22346+6G>T rs368678916
NM_182961.4(SYNE1):c.22495-9A>T rs762256509
NM_182961.4(SYNE1):c.22559G>A (p.Arg7520His) rs752057121
NM_182961.4(SYNE1):c.22663C>T (p.Arg7555Trp) rs755302191
NM_182961.4(SYNE1):c.22986A>C (p.Glu7662Asp) rs763100950
NM_182961.4(SYNE1):c.23240T>A (p.Ile7747Asn) rs1435183530
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.23645A>G (p.Glu7882Gly) rs1057518415
NM_182961.4(SYNE1):c.23704G>A (p.Ala7902Thr) rs372990463
NM_182961.4(SYNE1):c.23791-6del rs757124573
NM_182961.4(SYNE1):c.23791-7C>T rs375558499
NM_182961.4(SYNE1):c.23969G>A (p.Arg7990Lys) rs777371816
NM_182961.4(SYNE1):c.24349C>T (p.Arg8117Trp) rs144056525
NM_182961.4(SYNE1):c.24555C>G (p.Ile8185Met) rs201799566
NM_182961.4(SYNE1):c.245G>T (p.Arg82Leu) rs143900928
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.24865T>C (p.Tyr8289His) rs1016679896
NM_182961.4(SYNE1):c.25246+3G>A rs765849365
NM_182961.4(SYNE1):c.25381G>A (p.Glu8461Lys) rs119103248
NM_182961.4(SYNE1):c.25568G>A (p.Arg8523His) rs759577495
NM_182961.4(SYNE1):c.25583A>G (p.Asn8528Ser) rs1554393115
NM_182961.4(SYNE1):c.25706T>C (p.Ile8569Thr) rs760698113
NM_182961.4(SYNE1):c.25C>T (p.Arg9Trp) rs200346529
NM_182961.4(SYNE1):c.2728A>T (p.Ser910Cys) rs141214076
NM_182961.4(SYNE1):c.2889C>T (p.His963=) rs747231741
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.3473C>T (p.Ala1158Val) rs746060505
NM_182961.4(SYNE1):c.361A>G (p.Ile121Val) rs1554830234
NM_182961.4(SYNE1):c.3855C>T (p.Ile1285=) rs1592776784
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.3949C>G (p.Leu1317Val) rs1554709399
NM_182961.4(SYNE1):c.4107T>A (p.Phe1369Leu) rs149109801
NM_182961.4(SYNE1):c.4298C>T (p.Thr1433Met) rs139798419
NM_182961.4(SYNE1):c.4524G>T (p.Gln1508His) rs1378400021
NM_182961.4(SYNE1):c.4822G>A (p.Ala1608Thr) rs138617999
NM_182961.4(SYNE1):c.5282A>G (p.Gln1761Arg) rs146244669
NM_182961.4(SYNE1):c.5369C>T (p.Thr1790Ile) rs1554666956
NM_182961.4(SYNE1):c.5421+9G>T rs376218204
NM_182961.4(SYNE1):c.6154T>C (p.Phe2052Leu) rs147511500
NM_182961.4(SYNE1):c.7052G>A (p.Ser2351Asn) rs151039167
NM_182961.4(SYNE1):c.736G>A (p.Ala246Thr) rs1251834592
NM_182961.4(SYNE1):c.7592T>C (p.Ile2531Thr) rs138766629
NM_182961.4(SYNE1):c.7657A>G (p.Lys2553Glu) rs777368779
NM_182961.4(SYNE1):c.8005-3C>T rs117084693
NM_182961.4(SYNE1):c.8454A>T (p.Lys2818Asn) rs764853272
NM_182961.4(SYNE1):c.8557A>G (p.Thr2853Ala) rs77853132
NM_182961.4(SYNE1):c.8839C>G (p.Leu2947Val) rs756300560
NM_182961.4(SYNE1):c.9091A>G (p.Arg3031Gly) rs144643941
NM_182961.4(SYNE1):c.9148C>G (p.Leu3050Val) rs117360770
NM_182961.4(SYNE1):c.9377C>G (p.Ser3126Cys) rs139089832
NM_182961.4(SYNE1):c.9509A>G (p.Asn3170Ser) rs1554563052
NM_182961.4(SYNE1):c.9715C>G (p.Gln3239Glu) rs149901087
NM_182961.4(SYNE1):c.9799T>A (p.Leu3267Ile) rs1554560113
NM_182961.4(SYNE1):c.9847A>C (p.Asn3283His) rs745707616
NM_182961.4(SYNE1):c.9857C>T (p.Ser3286Phe) rs770774159

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