ClinVar Miner

List of variants in gene NRXN1 reported as uncertain significance for not provided

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Gene type:
ClinVar version:
Total variants: 165
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HGVS dbSNP
GRCh37/hg19 2p16.3(chr2:50130275-50213678)x3
GRCh37/hg19 2p16.3(chr2:50524623-50686003)x3
GRCh37/hg19 2p16.3(chr2:50598358-50625932)x1
GRCh37/hg19 2p16.3(chr2:50612570-50671502)x1
GRCh37/hg19 2p16.3(chr2:50878157-50948464)x1
GRCh37/hg19 2p16.3(chr2:50941283-51098920)x1
GRCh37/hg19 2p16.3(chr2:50983186-51082754)x1
GRCh37/hg19 2p16.3(chr2:51153883-51326497)x1
NM_001135659.2(NRXN1):c.1322C>T (p.Thr441Met) rs796052764
NM_001135659.2(NRXN1):c.1364A>G (p.Tyr455Cys) rs371321580
NM_001135659.2(NRXN1):c.1406C>T (p.Pro469Leu) rs886042697
NM_001135659.2(NRXN1):c.1408G>A (p.Val470Ile) rs753832133
NM_001135659.2(NRXN1):c.1412G>A (p.Ser471Asn) rs796052788
NM_001135659.2(NRXN1):c.1427G>A (p.Gly476Asp) rs1057520337
NM_001135659.2(NRXN1):c.1440+10G>A rs113028018
NM_001135659.2(NRXN1):c.1446A>C (p.Val482=) rs201485014
NM_001135659.2(NRXN1):c.1502C>T (p.Pro501Leu) rs530674644
NM_001135659.2(NRXN1):c.1547T>G (p.Val516Gly) rs1553778755
NM_001135659.2(NRXN1):c.1564A>T (p.Ile522Phe) rs796052767
NM_001135659.2(NRXN1):c.1600C>T (p.Pro534Ser) rs199834999
NM_001135659.2(NRXN1):c.1651A>G (p.Thr551Ala) rs794726985
NM_001135659.2(NRXN1):c.1686C>T (p.Gly562=) rs199701804
NM_001135659.2(NRXN1):c.1709C>A (p.Ala570Asp) rs529697285
NM_001135659.2(NRXN1):c.1712A>G (p.Lys571Arg) rs796052769
NM_001135659.2(NRXN1):c.1850A>G (p.His617Arg) rs886042974
NM_001135659.2(NRXN1):c.1898C>T (p.Thr633Met) rs201530175
NM_001135659.2(NRXN1):c.1904G>A (p.Arg635His) rs761279630
NM_001135659.2(NRXN1):c.1909C>G (p.Pro637Ala) rs1553760276
NM_001135659.2(NRXN1):c.1918G>T (p.Ala640Ser) rs796052770
NM_001135659.2(NRXN1):c.192C>T (p.Arg64=) rs748944452
NM_001135659.2(NRXN1):c.1942G>A (p.Asp648Asn) rs796052771
NM_001135659.2(NRXN1):c.1970G>C (p.Gly657Ala) rs780931684
NM_001135659.2(NRXN1):c.2033A>G (p.Tyr678Cys) rs727504051
NM_001135659.2(NRXN1):c.2078G>A (p.Ser693Asn) rs587780406
NM_001135659.2(NRXN1):c.208T>C (p.Phe70Leu) rs796052773
NM_001135659.2(NRXN1):c.2128C>G (p.Pro710Ala) rs762326241
NM_001135659.2(NRXN1):c.2157G>A (p.Pro719=) rs199714221
NM_001135659.2(NRXN1):c.219G>C (p.Glu73Asp) rs201031680
NM_001135659.2(NRXN1):c.2230G>A (p.Gly744Arg) rs757547387
NM_001135659.2(NRXN1):c.2240A>C (p.Tyr747Ser) rs752073539
NM_001135659.2(NRXN1):c.2330C>T (p.Thr777Met) rs199970666
NM_001135659.2(NRXN1):c.2348C>A (p.Ser783Tyr) rs796052774
NM_001135659.2(NRXN1):c.2369G>A (p.Arg790His) rs200776618
NM_001135659.2(NRXN1):c.23G>T (p.Arg8Leu) rs796052765
NM_001135659.2(NRXN1):c.2437G>A (p.Ala813Thr) rs199548487
NM_001135659.2(NRXN1):c.2495-10T>A rs1085307863
NM_001135659.2(NRXN1):c.2495-7T>A rs199673405
NM_001135659.2(NRXN1):c.252G>A (p.Thr84=) rs886042465
NM_001135659.2(NRXN1):c.2542G>A (p.Glu848Lys) rs202145311
NM_001135659.2(NRXN1):c.2617+3A>G rs202074070
NM_001135659.2(NRXN1):c.2618-8T>C rs775167794
NM_001135659.2(NRXN1):c.262C>G (p.Arg88Gly) rs748684256
NM_001135659.2(NRXN1):c.2652C>G (p.Phe884Leu) rs796052789
NM_001135659.2(NRXN1):c.2686C>T (p.Arg896Trp) rs796052777
NM_001135659.2(NRXN1):c.2690A>G (p.Tyr897Cys) rs796052778
NM_001135659.2(NRXN1):c.2717T>C (p.Ile906Thr) rs796052779
NM_001135659.2(NRXN1):c.2779G>A (p.Asp927Asn) rs796052780
NM_001135659.2(NRXN1):c.2850G>A (p.Lys950=) rs192909520
NM_001135659.2(NRXN1):c.28G>A (p.Gly10Ser) rs777530225
NM_001135659.2(NRXN1):c.2902C>T (p.His968Tyr) rs1057524516
NM_001135659.2(NRXN1):c.2905C>A (p.Leu969Ile) rs794727140
NM_001135659.2(NRXN1):c.2905C>T (p.Leu969Phe) rs794727140
NM_001135659.2(NRXN1):c.2935G>A (p.Asp979Asn) rs796052781
NM_001135659.2(NRXN1):c.2999+7A>G rs200468214
NM_001135659.2(NRXN1):c.3013G>T (p.Val1005Leu) rs1057524337
NM_001135659.2(NRXN1):c.3099A>G (p.Ile1033Met) rs796052782
NM_001135659.2(NRXN1):c.3132G>A (p.Lys1044=) rs201118246
NM_001135659.2(NRXN1):c.3150_3161dup (p.Thr1051_Thr1054dup) rs1553698269
NM_001135659.2(NRXN1):c.3152C>T (p.Thr1051Met) rs199980022
NM_001135659.2(NRXN1):c.3191-10C>T rs398123573
NM_001135659.2(NRXN1):c.3223A>G (p.Thr1075Ala) rs753262049
NM_001135659.2(NRXN1):c.322C>G (p.Pro108Ala) rs199784029
NM_001135659.2(NRXN1):c.3249A>G (p.Val1083=) rs200698497
NM_001135659.2(NRXN1):c.325G>A (p.Val109Ile) rs779979011
NM_001135659.2(NRXN1):c.3285A>G (p.Ser1095=) rs1553656447
NM_001135659.2(NRXN1):c.32G>A (p.Cys11Tyr) rs796052766
NM_001135659.2(NRXN1):c.3339C>T (p.Asn1113=) rs563089155
NM_001135659.2(NRXN1):c.3374C>T (p.Thr1125Ile) rs796052784
NM_001135659.2(NRXN1):c.339C>T (p.Ala113=) rs767682431
NM_001135659.2(NRXN1):c.3401A>G (p.Asn1134Ser) rs201963074
NM_001135659.2(NRXN1):c.3464G>A (p.Ser1155Asn) rs201871194
NM_001135659.2(NRXN1):c.3485-109897G>C rs777054372
NM_001135659.2(NRXN1):c.3485-109897G>T rs777054372
NM_001135659.2(NRXN1):c.3485-109912G>A rs1057524649
NM_001135659.2(NRXN1):c.3485-109922G>C rs1188018101
NM_001135659.2(NRXN1):c.3485-109939C>T rs766942777
NM_001135659.2(NRXN1):c.3523A>G (p.Ile1175Val) rs765360600
NM_001135659.2(NRXN1):c.353G>A (p.Arg118His) rs796052775
NM_001135659.2(NRXN1):c.3599A>G (p.Gln1200Arg) rs768319291
NM_001135659.2(NRXN1):c.3662A>G (p.His1221Arg) rs200915287
NM_001135659.2(NRXN1):c.369C>A (p.Phe123Leu) rs879210752
NM_001135659.2(NRXN1):c.3736A>G (p.Ile1246Val) rs751778015
NM_001135659.2(NRXN1):c.374A>G (p.Asn125Ser) rs770641207
NM_001135659.2(NRXN1):c.3773C>T (p.Thr1258Met) rs201720955
NM_001135659.2(NRXN1):c.407A>G (p.Lys136Arg) rs202118977
NM_001135659.2(NRXN1):c.4122G>A (p.Met1374Ile) rs1553534743
NM_001135659.2(NRXN1):c.4124C>T (p.Thr1375Ile) rs200672080
NM_001135659.2(NRXN1):c.4131G>C (p.Glu1377Asp) rs200935246
NM_001135659.2(NRXN1):c.4132T>G (p.Ser1378Ala) rs1064796707
NM_001135659.2(NRXN1):c.4149G>A (p.Met1383Ile) rs146100580
NM_001135659.2(NRXN1):c.4322G>A (p.Ser1441Asn) rs796052762
NM_001135659.2(NRXN1):c.4394G>A (p.Arg1465Gln) rs201559515
NM_001135659.2(NRXN1):c.476C>T (p.Pro159Leu) rs373070672
NM_001135659.2(NRXN1):c.498G>A (p.Ala166=) rs201212909
NM_001135659.2(NRXN1):c.503A>G (p.Lys168Arg) rs200625614
NM_001135659.2(NRXN1):c.518C>G (p.Ser173Trp) rs775907305
NM_001135659.2(NRXN1):c.570C>A (p.Asn190Lys) rs564945882
NM_001135659.2(NRXN1):c.588C>A (p.Pro196=) rs201644834
NM_001135659.2(NRXN1):c.609G>C (p.Lys203Asn) rs759842391
NM_001135659.2(NRXN1):c.609_610delinsCA (p.Lys203_Leu204delinsAsnMet) rs886042534
NM_001135659.2(NRXN1):c.610C>A (p.Leu204Met) rs777133701
NM_001135659.2(NRXN1):c.637G>A (p.Gly213Arg) rs199561088
NM_001135659.2(NRXN1):c.656_664del (p.Ala219_Glu221del) rs546508545
NM_001135659.2(NRXN1):c.76G>C (p.Glu26Gln) rs201847846
NM_001135659.2(NRXN1):c.772G>A (p.Glu258Lys) rs746465882
NM_001135659.2(NRXN1):c.821A>G (p.Asn274Ser) rs759434607
NM_001135659.2(NRXN1):c.876C>T (p.Asp292=) rs587780407
NM_001135659.2(NRXN1):c.878A>C (p.Asn293Thr) rs779434583
NM_001135659.2(NRXN1):c.880A>G (p.Asn294Asp) rs781179797
NM_001135659.2(NRXN1):c.881A>G (p.Asn294Ser) rs141903943
NM_001135659.2(NRXN1):c.904A>T (p.Met302Leu) rs776779952
NM_001135659.2(NRXN1):c.981C>T (p.Tyr327=) rs200464704
NM_001330078.2(NRXN1):c.105C>A (p.Gly35=) rs55640811
NM_001330078.2(NRXN1):c.1158+26A>T rs201802152
NM_001330078.2(NRXN1):c.1365T>C (p.Leu455=) rs201727684
NM_001330078.2(NRXN1):c.1541A>G (p.Asn514Ser) rs770389634
NM_001330078.2(NRXN1):c.1688T>C (p.Ile563Thr) rs201837579
NM_001330078.2(NRXN1):c.1700T>G (p.Leu567Trp) rs372311299
NM_001330078.2(NRXN1):c.1843C>T (p.Leu615=) rs201029409
NM_001330078.2(NRXN1):c.1945A>G (p.Ile649Val) rs200074974
NM_001330078.2(NRXN1):c.1969C>T (p.Arg657Trp) rs200844126
NM_001330078.2(NRXN1):c.1978G>A (p.Ala660Thr) rs199939303
NM_001330078.2(NRXN1):c.2332C>A (p.Leu778Met) rs374942732
NM_001330078.2(NRXN1):c.2414A>G (p.Asn805Ser) rs753087756
NM_001330078.2(NRXN1):c.2459G>A (p.Ser820Asn) rs80293130
NM_001330078.2(NRXN1):c.24C>T (p.Arg8=) rs200113281
NM_001330078.2(NRXN1):c.2502A>G (p.Gln834=) rs770632900
NM_001330078.2(NRXN1):c.2533C>T (p.His845Tyr) rs199784139
NM_001330078.2(NRXN1):c.2567G>A (p.Arg856Gln) rs200249774
NM_001330078.2(NRXN1):c.2605C>A (p.Leu869Met) rs201818223
NM_001330078.2(NRXN1):c.270G>T (p.Gln90His) rs199960045
NM_001330078.2(NRXN1):c.2772C>T (p.Tyr924=) rs200182626
NM_001330078.2(NRXN1):c.302C>G (p.Ala101Gly) rs200184823
NM_001330078.2(NRXN1):c.3042C>T (p.Thr1014=) rs75137449
NM_001330078.2(NRXN1):c.3045C>T (p.Ala1015=) rs56402642
NM_001330078.2(NRXN1):c.3201C>T (p.Ser1067=) rs75275592
NM_001330078.2(NRXN1):c.3202G>A (p.Asp1068Asn) rs200722697
NM_001330078.2(NRXN1):c.322C>T (p.Pro108Ser) rs199784029
NM_001330078.2(NRXN1):c.3245-4G>T rs1057520338
NM_001330078.2(NRXN1):c.3307G>T (p.Asp1103Tyr) rs1295880908
NM_001330078.2(NRXN1):c.3364+3A>G rs762891600
NM_001330078.2(NRXN1):c.3489C>T (p.Ala1163=) rs147580960
NM_001330078.2(NRXN1):c.3499C>T (p.Arg1167Ter) rs199546979
NM_001330078.2(NRXN1):c.3905A>G (p.Tyr1302Cys) rs761776814
NM_001330078.2(NRXN1):c.4254A>G (p.Pro1418=) rs55923848
NM_001330078.2(NRXN1):c.569A>G (p.Asn190Ser) rs200792504
NM_001330078.2(NRXN1):c.600C>T (p.Gly200=) rs201481698
NM_001330078.2(NRXN1):c.739C>G (p.Arg247Gly) rs200009780
NM_001330078.2(NRXN1):c.744C>T (p.Thr248=)
NM_001330078.2(NRXN1):c.749T>A (p.Phe250Tyr) rs200646155
NM_001330078.2(NRXN1):c.752G>A (p.Arg251His) rs780954241
NM_001330078.2(NRXN1):c.772+1043C>G rs1179583246
NM_001330078.2(NRXN1):c.772+1050C>A rs367919055
NM_001330078.2(NRXN1):c.779A>G (p.Asn260Ser)
NM_138735.4(NRXN1):c.49GGC[11] (p.Gly17[11]) rs750165040

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