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: 142
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HGVS dbSNP gnomAD frequency
NM_182961.4(SYNE1):c.23315G>A (p.Arg7772Gln) rs138787771 0.00432
NM_182961.4(SYNE1):c.4107T>A (p.Phe1369Leu) rs149109801 0.00172
NM_182961.4(SYNE1):c.4822G>A (p.Ala1608Thr) rs138617999 0.00106
NM_182961.4(SYNE1):c.17827T>C (p.Ser5943Pro) rs147998933 0.00101
NM_182961.4(SYNE1):c.14263C>T (p.Leu4755Phe) rs41301343 0.00100
NM_182961.4(SYNE1):c.25381G>A (p.Glu8461Lys) rs119103248 0.00083
NM_182961.4(SYNE1):c.5282A>G (p.Gln1761Arg) rs146244669 0.00060
NM_182961.4(SYNE1):c.5421+9G>T rs376218204 0.00060
NM_182961.4(SYNE1):c.15337G>A (p.Val5113Ile) rs139170018 0.00054
NM_182961.4(SYNE1):c.24488T>C (p.Ile8163Thr) rs139643725 0.00045
NM_182961.4(SYNE1):c.21149G>A (p.Arg7050Gln) rs143639400 0.00043
NM_182961.4(SYNE1):c.12391G>T (p.Gly4131Cys) rs139139296 0.00038
NM_182961.4(SYNE1):c.4732C>T (p.Pro1578Ser) rs199769508 0.00034
NM_182961.4(SYNE1):c.9091A>G (p.Arg3031Gly) rs144643941 0.00031
NM_182961.4(SYNE1):c.21782G>A (p.Arg7261Gln) rs61742716 0.00030
NM_182961.4(SYNE1):c.7435A>G (p.Lys2479Glu) rs188146577 0.00027
NM_182961.4(SYNE1):c.15202A>G (p.Lys5068Glu) rs139805184 0.00021
NM_182961.4(SYNE1):c.18662C>T (p.Thr6221Ile) rs150335599 0.00021
NM_182961.4(SYNE1):c.22346+6G>T rs368678916 0.00020
NM_182961.4(SYNE1):c.15863G>C (p.Gly5288Ala) rs201313856 0.00018
NM_182961.4(SYNE1):c.24815G>A (p.Arg8272Gln) rs201029723 0.00018
NM_182961.4(SYNE1):c.13724G>T (p.Cys4575Phe) rs199701902 0.00011
NM_182961.4(SYNE1):c.21377A>G (p.Lys7126Arg) rs145882956 0.00011
NM_182961.4(SYNE1):c.8005-3C>T rs117084693 0.00011
NM_182961.4(SYNE1):c.19534G>T (p.Ala6512Ser) rs149272010 0.00010
NM_182961.4(SYNE1):c.23791-7C>T rs375558499 0.00010
NM_182961.4(SYNE1):c.4298C>T (p.Thr1433Met) rs139798419 0.00010
NM_182961.4(SYNE1):c.14018G>A (p.Arg4673Gln) rs144963785 0.00009
NM_182961.4(SYNE1):c.17930C>T (p.Thr5977Met) rs767144952 0.00009
NM_182961.4(SYNE1):c.19255C>G (p.Gln6419Glu) rs150700669 0.00009
NM_182961.4(SYNE1):c.20182C>T (p.Arg6728Cys) rs150063353 0.00009
NM_182961.4(SYNE1):c.24635G>A (p.Arg8212His) rs766462111 0.00008
NM_182961.4(SYNE1):c.7052G>A (p.Ser2351Asn) rs151039167 0.00008
NM_182961.4(SYNE1):c.23704G>A (p.Ala7902Thr) rs372990463 0.00007
NM_182961.4(SYNE1):c.3934G>A (p.Glu1312Lys) rs200276242 0.00007
NM_182961.4(SYNE1):c.12355G>A (p.Glu4119Lys) rs148935596 0.00006
NM_182961.4(SYNE1):c.1330C>T (p.Arg444Trp) rs75153800 0.00006
NM_182961.4(SYNE1):c.20027G>A (p.Arg6676Gln) rs190673256 0.00006
NM_182961.4(SYNE1):c.21706G>A (p.Ala7236Thr) rs202121741 0.00006
NM_182961.4(SYNE1):c.245G>A (p.Arg82Gln) rs143900928 0.00006
NM_182961.4(SYNE1):c.17848G>C (p.Val5950Leu) rs200589166 0.00005
NM_182961.4(SYNE1):c.21322G>A (p.Gly7108Ser) rs777227521 0.00005
NM_182961.4(SYNE1):c.6231-12T>C rs370687503 0.00005
NM_182961.4(SYNE1):c.11627T>C (p.Val3876Ala) rs372944688 0.00004
NM_182961.4(SYNE1):c.13331G>A (p.Arg4444Gln) rs139075013 0.00004
NM_182961.4(SYNE1):c.17825G>A (p.Arg5942His) rs746220387 0.00004
NM_182961.4(SYNE1):c.24717C>G (p.His8239Gln) rs201548223 0.00004
NM_182961.4(SYNE1):c.4075A>G (p.Thr1359Ala) rs377718960 0.00004
NM_182961.4(SYNE1):c.7592T>C (p.Ile2531Thr) rs138766629 0.00004
NM_182961.4(SYNE1):c.10766C>T (p.Thr3589Ile) rs201487756 0.00003
NM_182961.4(SYNE1):c.11702G>C (p.Ser3901Thr) rs376327805 0.00003
NM_182961.4(SYNE1):c.13436G>A (p.Arg4479His) rs768085752 0.00003
NM_182961.4(SYNE1):c.15489G>A (p.Glu5163=) rs750155092 0.00003
NM_182961.4(SYNE1):c.21815A>G (p.Lys7272Arg) rs764715827 0.00003
NM_182961.4(SYNE1):c.21903T>G (p.Phe7301Leu) rs1415687146 0.00003
NM_182961.4(SYNE1):c.22559G>A (p.Arg7520His) rs752057121 0.00003
NM_182961.4(SYNE1):c.22663C>T (p.Arg7555Trp) rs755302191 0.00003
NM_182961.4(SYNE1):c.24865T>C (p.Tyr8289His) rs1016679896 0.00003
NM_182961.4(SYNE1):c.3404A>C (p.Glu1135Ala) rs764928878 0.00003
NM_182961.4(SYNE1):c.736G>A (p.Ala246Thr) rs1251834592 0.00003
NM_182961.4(SYNE1):c.12658G>A (p.Asp4220Asn) rs201449723 0.00002
NM_182961.4(SYNE1):c.13181T>G (p.Leu4394Arg) rs763501028 0.00002
NM_182961.4(SYNE1):c.14335G>T (p.Ala4779Ser) rs368490158 0.00002
NM_182961.4(SYNE1):c.18972+4T>C rs774096623 0.00002
NM_182961.4(SYNE1):c.2066G>A (p.Arg689Gln) rs769628070 0.00002
NM_182961.4(SYNE1):c.21271A>C (p.Asn7091His) rs777618601 0.00002
NM_182961.4(SYNE1):c.23240T>A (p.Ile7747Asn) rs1435183530 0.00002
NM_182961.4(SYNE1):c.23403C>G (p.Ser7801Arg) rs886043281 0.00002
NM_182961.4(SYNE1):c.2889C>T (p.His963=) rs747231741 0.00002
NM_182961.4(SYNE1):c.3473C>T (p.Ala1158Val) rs746060505 0.00002
NM_182961.4(SYNE1):c.3916C>A (p.Leu1306Met) rs1454797342 0.00002
NM_182961.4(SYNE1):c.9847A>C (p.Asn3283His) rs745707616 0.00002
NM_182961.4(SYNE1):c.1097A>C (p.Glu366Ala) rs372327585 0.00001
NM_182961.4(SYNE1):c.11496A>G (p.Ile3832Met) rs1554518035 0.00001
NM_182961.4(SYNE1):c.12272A>G (p.Asp4091Gly) rs767294741 0.00001
NM_182961.4(SYNE1):c.14565G>C (p.Arg4855Ser) rs1237053788 0.00001
NM_182961.4(SYNE1):c.17332A>G (p.Ile5778Val) rs762422242 0.00001
NM_182961.4(SYNE1):c.20417A>C (p.Asp6806Ala) rs753654674 0.00001
NM_182961.4(SYNE1):c.20645C>T (p.Ser6882Leu) rs373012438 0.00001
NM_182961.4(SYNE1):c.21199C>G (p.Leu7067Val) rs749058571 0.00001
NM_182961.4(SYNE1):c.22304G>A (p.Arg7435His) rs748260996 0.00001
NM_182961.4(SYNE1):c.22495-9A>T rs762256509 0.00001
NM_182961.4(SYNE1):c.226-10C>T rs1353706819 0.00001
NM_182961.4(SYNE1):c.22986A>C (p.Glu7662Asp) rs763100950 0.00001
NM_182961.4(SYNE1):c.23969G>A (p.Arg7990Lys) rs777371816 0.00001
NM_182961.4(SYNE1):c.25246+3G>A rs765849365 0.00001
NM_182961.4(SYNE1):c.25568G>A (p.Arg8523His) rs759577495 0.00001
NM_182961.4(SYNE1):c.25706T>C (p.Ile8569Thr) rs760698113 0.00001
NM_182961.4(SYNE1):c.3949C>G (p.Leu1317Val) rs1554709399 0.00001
NM_182961.4(SYNE1):c.4196T>C (p.Leu1399Pro) rs754773565 0.00001
NM_182961.4(SYNE1):c.4524G>T (p.Gln1508His) rs1378400021 0.00001
NM_182961.4(SYNE1):c.6031C>T (p.Arg2011Cys) rs767563434 0.00001
NM_182961.4(SYNE1):c.8454A>T (p.Lys2818Asn) rs764853272 0.00001
NM_182961.4(SYNE1):c.9857C>T (p.Ser3286Phe) rs770774159 0.00001
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.10818G>T (p.Lys3606Asn) rs752187409
NM_182961.4(SYNE1):c.10981A>G (p.Arg3661Gly) rs767172575
NM_182961.4(SYNE1):c.11625A>G (p.Ser3875=) rs1057518265
NM_182961.4(SYNE1):c.11680G>C (p.Asp3894His) rs2154032071
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.12226-4C>T
NM_182961.4(SYNE1):c.12371A>C (p.Gln4124Pro) rs911413208
NM_182961.4(SYNE1):c.1343A>G (p.Gln448Arg)
NM_182961.4(SYNE1):c.13825C>A (p.Leu4609Ile) rs2153972296
NM_182961.4(SYNE1):c.13828G>C (p.Glu4610Gln) rs1590224228
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.16657A>G (p.Thr5553Ala)
NM_182961.4(SYNE1):c.17203-5C>A rs886044642
NM_182961.4(SYNE1):c.17545A>G (p.Thr5849Ala) rs2095126393
NM_182961.4(SYNE1):c.17603G>A (p.Gly5868Glu) rs2153809671
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.18658C>A (p.Arg6220Ser) rs201685248
NM_182961.4(SYNE1):c.1951C>T (p.Pro651Ser) rs1455678689
NM_182961.4(SYNE1):c.19663C>G (p.Pro6555Ala)
NM_182961.4(SYNE1):c.19735A>T (p.Ser6579Cys) rs1554264075
NM_182961.4(SYNE1):c.2097+3_2097+15del rs1593220945
NM_182961.4(SYNE1):c.21903_21904delinsGG (p.Phe7301_Phe7302delinsLeuVal) rs1554223069
NM_182961.4(SYNE1):c.225G>C (p.Leu75=)
NM_182961.4(SYNE1):c.23645A>G (p.Glu7882Gly) rs1057518415
NM_182961.4(SYNE1):c.23791-6del rs757124573
NM_182961.4(SYNE1):c.23999T>C (p.Leu8000Ser)
NM_182961.4(SYNE1):c.24555C>G (p.Ile8185Met) rs201799566
NM_182961.4(SYNE1):c.25229C>T (p.Thr8410Ile) rs2058481714
NM_182961.4(SYNE1):c.25583A>G (p.Asn8528Ser) rs1554393115
NM_182961.4(SYNE1):c.2728A>T (p.Ser910Cys) rs141214076
NM_182961.4(SYNE1):c.281C>T (p.Thr94Met)
NM_182961.4(SYNE1):c.310-13C>T
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.4570G>A (p.Ala1524Thr)
NM_182961.4(SYNE1):c.5267G>A (p.Arg1756Lys)
NM_182961.4(SYNE1):c.5369C>T (p.Thr1790Ile) rs1554666956
NM_182961.4(SYNE1):c.7657A>G (p.Lys2553Glu) rs777368779
NM_182961.4(SYNE1):c.943G>A (p.Glu315Lys)
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

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