ClinVar Miner

List of variants in gene NRXN1 reported as likely benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 210
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HGVS dbSNP
GRCh37/hg19 2p16.3(chr2:50573838-50579293)x3
GRCh37/hg19 2p16.3(chr2:50847100-50847341)x3
GRCh37/hg19 2p16.3(chr2:50918448-50982113)x1
GRCh37/hg19 2p16.3(chr2:50937444-50970662)x1
GRCh38/hg38 2p16.3(chr2:49910893-49943628)x3
GRCh38/hg38 2p16.3(chr2:50004126-50041370)x3
GRCh38/hg38 2p16.3(chr2:50008168-50041168)x1
GRCh38/hg38 2p16.3(chr2:50265501-50274792)x1
GRCh38/hg38 2p16.3(chr2:50716342-50801952)x1
GRCh38/hg38 2p16.3(chr2:50751318-50856339)x1
GRCh38/hg38 2p16.3(chr2:50794314-50801971)x1
GRCh38/hg38 2p16.3(chr2:50839917-50873340)x1
GRCh38/hg38 2p16.3(chr2:50856272-50882552)x1
GRCh38/hg38 2p16.3(chr2:50931078-51009926)x3
GRCh38/hg38 2p16.3(chr2:50974455-50999101)x1
NM_001135659.2(NRXN1):c.*13A>C rs199777715
NM_001135659.2(NRXN1):c.*1T>A rs567887770
NM_001135659.2(NRXN1):c.*2511G>C rs148938313
NM_001135659.2(NRXN1):c.*941dup rs3839057
NM_001135659.2(NRXN1):c.-22C>A rs1057520336
NM_001135659.2(NRXN1):c.-563G>C rs62143025
NM_001135659.2(NRXN1):c.-602G>A rs62143026
NM_001135659.2(NRXN1):c.-7C>A rs202002348
NM_001135659.2(NRXN1):c.-883T>C rs10188340
NM_001135659.2(NRXN1):c.-906A>C rs1057522918
NM_001135659.2(NRXN1):c.-919G>C rs1341735881
NM_001135659.2(NRXN1):c.1029G>A (p.Leu343=) rs200532412
NM_001135659.2(NRXN1):c.105C>A (p.Gly35=) rs55640811
NM_001135659.2(NRXN1):c.108C>T (p.Ala36=) rs199871750
NM_001135659.2(NRXN1):c.1149C>G (p.Ala383=) rs201397488
NM_001135659.2(NRXN1):c.1158A>C (p.Ala386=) rs200259338
NM_001135659.2(NRXN1):c.1233+8C>T rs200448187
NM_001135659.2(NRXN1):c.1234-8C>T rs1430859209
NM_001135659.2(NRXN1):c.1278+5A>T rs201802152
NM_001135659.2(NRXN1):c.1314G>A (p.Thr438=) rs202166616
NM_001135659.2(NRXN1):c.1338C>A (p.Thr446=) rs768225503
NM_001135659.2(NRXN1):c.1347G>A (p.Gly449=) rs779819227
NM_001135659.2(NRXN1):c.1389C>T (p.Ala463=) rs753264637
NM_001135659.2(NRXN1):c.1395T>C (p.Leu465=)
NM_001135659.2(NRXN1):c.1405C>T (p.Pro469Ser) rs78540316
NM_001135659.2(NRXN1):c.1440+10G>A rs113028018
NM_001135659.2(NRXN1):c.1440+19A>G rs201399154
NM_001135659.2(NRXN1):c.1440+4_1440+7dup rs1259067816
NM_001135659.2(NRXN1):c.1446A>C (p.Val482=) rs201485014
NM_001135659.2(NRXN1):c.1458T>C (p.Asn486=) rs1057523256
NM_001135659.2(NRXN1):c.1485T>C (p.Leu495=) rs201727684
NM_001135659.2(NRXN1):c.1497A>G (p.Gly499=)
NM_001135659.2(NRXN1):c.159G>A (p.Glu53=) rs1057524126
NM_001135659.2(NRXN1):c.162G>A (p.Met54Ile) rs1057519409
NM_001135659.2(NRXN1):c.1695A>G (p.Arg565=) rs201941844
NM_001135659.2(NRXN1):c.1808T>C (p.Ile603Thr) rs201837579
NM_001135659.2(NRXN1):c.1816C>T (p.Leu606=) rs754703742
NM_001135659.2(NRXN1):c.1857C>T (p.Asp619=) rs1202295736
NM_001135659.2(NRXN1):c.1869C>T (p.Asp623=) rs199934259
NM_001135659.2(NRXN1):c.1880-11C>G rs199550097
NM_001135659.2(NRXN1):c.1880-15_1880-13delCTC rs1255783166
NM_001135659.2(NRXN1):c.1880-8T>C rs1057522281
NM_001135659.2(NRXN1):c.1899G>A (p.Thr633=) rs200817371
NM_001135659.2(NRXN1):c.1920T>C (p.Ala640=) rs1553760251
NM_001135659.2(NRXN1):c.1963C>T (p.Leu655=) rs201029409
NM_001135659.2(NRXN1):c.1989T>G (p.Ala663=) rs201816600
NM_001135659.2(NRXN1):c.2007C>T (p.Thr669=) rs200603742
NM_001135659.2(NRXN1):c.2065A>G (p.Ile689Val) rs200074974
NM_001135659.2(NRXN1):c.2067C>T (p.Ile689=) rs539484479
NM_001135659.2(NRXN1):c.2157G>A (p.Pro719=) rs199714221
NM_001135659.2(NRXN1):c.222C>T (p.Gly74=) rs201592993
NM_001135659.2(NRXN1):c.2242C>A (p.Leu748Ile) rs56086732
NM_001135659.2(NRXN1):c.2264-22_2264-20del rs779214382
NM_001135659.2(NRXN1):c.2264-4C>A rs1340313788
NM_001135659.2(NRXN1):c.2271G>T (p.Thr757=)
NM_001135659.2(NRXN1):c.2313C>T (p.Leu771=) rs201466898
NM_001135659.2(NRXN1):c.2316C>T (p.Pro772=) rs549242356
NM_001135659.2(NRXN1):c.2364C>G (p.Ser788=) rs761608592
NM_001135659.2(NRXN1):c.2367G>A (p.Gln789=) rs1057521319
NM_001135659.2(NRXN1):c.2394C>A (p.Thr798=) rs78030925
NM_001135659.2(NRXN1):c.2421C>A (p.Leu807=) rs1553750260
NM_001135659.2(NRXN1):c.2436C>T (p.Asp812=) rs200449662
NM_001135659.2(NRXN1):c.2468-6A>G rs758131961
NM_001135659.2(NRXN1):c.2495-20C>G rs776794965
NM_001135659.2(NRXN1):c.2495-4A>G rs747910295
NM_001135659.2(NRXN1):c.249G>T (p.Leu83=) rs565771336
NM_001135659.2(NRXN1):c.2505C>G (p.Pro835=) rs147984237
NM_001135659.2(NRXN1):c.2511T>A (p.Thr837=) rs750156118
NM_001135659.2(NRXN1):c.2541C>T (p.Asn847=) rs115211871
NM_001135659.2(NRXN1):c.2566C>A (p.Arg856=) rs200325059
NM_001135659.2(NRXN1):c.2579G>A (p.Ser860Asn) rs80293130
NM_001135659.2(NRXN1):c.2618-7C>T rs369071366
NM_001135659.2(NRXN1):c.261C>A (p.Gly87=) rs587781102
NM_001135659.2(NRXN1):c.261C>T (p.Gly87=) rs587781102
NM_001135659.2(NRXN1):c.2627C>T (p.Ala876Val) rs199557987
NM_001135659.2(NRXN1):c.2646G>A (p.Leu882=) rs868353645
NM_001135659.2(NRXN1):c.2725C>A (p.Leu909Met) rs201818223
NM_001135659.2(NRXN1):c.273C>T (p.Leu91=) rs201997966
NM_001135659.2(NRXN1):c.2745T>C (p.Asn915=) rs764347791
NM_001135659.2(NRXN1):c.2748A>G (p.Gly916=)
NM_001135659.2(NRXN1):c.276C>T (p.Ser92=) rs1553516780
NM_001135659.2(NRXN1):c.2850G>A (p.Lys950=) rs192909520
NM_001135659.2(NRXN1):c.285C>T (p.Ile95=) rs759011919
NM_001135659.2(NRXN1):c.2892C>T (p.Tyr964=) rs200182626
NM_001135659.2(NRXN1):c.2934A>G (p.Leu978=)
NM_001135659.2(NRXN1):c.2949A>G (p.Leu983=) rs754048752
NM_001135659.2(NRXN1):c.297G>A (p.Glu99=) rs1553516705
NM_001135659.2(NRXN1):c.3000-22_3000-14del rs755734707
NM_001135659.2(NRXN1):c.300T>G (p.Pro100=) rs753793668
NM_001135659.2(NRXN1):c.3015G>T (p.Val1005=) rs199734638
NM_001135659.2(NRXN1):c.3103A>C (p.Arg1035=) rs780193876
NM_001135659.2(NRXN1):c.3129A>T (p.Val1043=) rs781048514
NM_001135659.2(NRXN1):c.3150A>G (p.Thr1050=) rs201085950
NM_001135659.2(NRXN1):c.3162C>T (p.Thr1054=) rs75137449
NM_001135659.2(NRXN1):c.3165C>T (p.Ala1055=) rs56402642
NM_001135659.2(NRXN1):c.3191-10C>T rs398123573
NM_001135659.2(NRXN1):c.3191-17C>G rs200354492
NM_001135659.2(NRXN1):c.3210A>C (p.Gly1070=) rs201886024
NM_001135659.2(NRXN1):c.321G>T (p.Thr107=) rs776382029
NM_001135659.2(NRXN1):c.322C>T (p.Pro108Ser) rs199784029
NM_001135659.2(NRXN1):c.3249A>G (p.Val1083=) rs200698497
NM_001135659.2(NRXN1):c.324G>A (p.Pro108=) rs199595253
NM_001135659.2(NRXN1):c.3285A>G (p.Ser1095=) rs1553656447
NM_001135659.2(NRXN1):c.3288T>G (p.Val1096=) rs1553656429
NM_001135659.2(NRXN1):c.330C>T (p.Asn110=) rs756402228
NM_001135659.2(NRXN1):c.3312C>T (p.Asp1104=) rs199580594
NM_001135659.2(NRXN1):c.3318C>T (p.Ile1106=) rs1553656308
NM_001135659.2(NRXN1):c.3321C>T (p.Ser1107=) rs75275592
NM_001135659.2(NRXN1):c.3339C>T (p.Asn1113=) rs563089155
NM_001135659.2(NRXN1):c.3348C>A (p.Ile1116=) rs201241923
NM_001135659.2(NRXN1):c.3364+18T>A rs371530345
NM_001135659.2(NRXN1):c.3365-4G>T rs1057520338
NM_001135659.2(NRXN1):c.3369C>T (p.Pro1123=) rs116236999
NM_001135659.2(NRXN1):c.3450T>C (p.Ser1150=) rs1057522160
NM_001135659.2(NRXN1):c.3485-109705C>G rs1227805288
NM_001135659.2(NRXN1):c.3485-109758A>G rs142041427
NM_001135659.2(NRXN1):c.3485-109836G>A rs747566761
NM_001135659.2(NRXN1):c.3485-109836G>T rs747566761
NM_001135659.2(NRXN1):c.3485-109863C>T rs1057521027
NM_001135659.2(NRXN1):c.3485-109899A>G rs562219421
NM_001135659.2(NRXN1):c.3485-109902_3485-109900dup rs1440459434
NM_001135659.2(NRXN1):c.3485-109992C>T rs796052761
NM_001135659.2(NRXN1):c.3485-110011C>T rs1446478264
NM_001135659.2(NRXN1):c.3485-110014del rs1064794179
NM_001135659.2(NRXN1):c.3485-110016C>T rs1057521771
NM_001135659.2(NRXN1):c.3485-110131T>G rs193267438
NM_001135659.2(NRXN1):c.3495A>G (p.Thr1165=) rs757748286
NM_001135659.2(NRXN1):c.3498T>C (p.Tyr1166=) rs1420076341
NM_001135659.2(NRXN1):c.3504T>C (p.Phe1168=) rs751894635
NM_001135659.2(NRXN1):c.3528G>A (p.Thr1176=) rs80094872
NM_001135659.2(NRXN1):c.3609C>T (p.Ala1203=) rs147580960
NM_001135659.2(NRXN1):c.3667-16C>G rs756210249
NM_001135659.2(NRXN1):c.3667-18T>C rs754285936
NM_001135659.2(NRXN1):c.3715G>A (p.Ala1239Thr) rs201336161
NM_001135659.2(NRXN1):c.3774G>C (p.Thr1258=) rs765748728
NM_001135659.2(NRXN1):c.3792C>A (p.Ala1264=) rs201129779
NM_001135659.2(NRXN1):c.3795G>T (p.Thr1265=) rs200179221
NM_001135659.2(NRXN1):c.3837A>T (p.Ala1279=) rs145558855
NM_001135659.2(NRXN1):c.3838+11G>A rs1057522566
NM_001135659.2(NRXN1):c.3838+7A>G rs752561425
NM_001135659.2(NRXN1):c.3928+8dup rs770051379
NM_001135659.2(NRXN1):c.4008G>A (p.Gln1336=) rs1553535081
NM_001135659.2(NRXN1):c.4053A>G (p.Ala1351=) rs79970751
NM_001135659.2(NRXN1):c.4056C>T (p.Ala1352=) rs1309946041
NM_001135659.2(NRXN1):c.4077C>T (p.Ala1359=) rs1553534825
NM_001135659.2(NRXN1):c.417G>A (p.Glu139=) rs757453009
NM_001135659.2(NRXN1):c.4180A>T (p.Thr1394Ser) rs202006815
NM_001135659.2(NRXN1):c.4188G>A (p.Thr1396=) rs74714098
NM_001135659.2(NRXN1):c.4227G>A (p.Pro1409=) rs183440866
NM_001135659.2(NRXN1):c.4287C>G (p.Pro1429=) rs143446587
NM_001135659.2(NRXN1):c.4296T>C (p.Asp1432=) rs201135028
NM_001135659.2(NRXN1):c.4368G>A (p.Pro1456=) rs151195816
NM_001135659.2(NRXN1):c.4374A>G (p.Pro1458=) rs55923848
NM_001135659.2(NRXN1):c.4395G>T (p.Arg1465=) rs143495349
NM_001135659.2(NRXN1):c.4458T>C (p.Leu1486=) rs796052759
NM_001135659.2(NRXN1):c.4512T>C (p.His1504=) rs112536447
NM_001135659.2(NRXN1):c.4525C>A (p.Arg1509=)
NM_001135659.2(NRXN1):c.4548A>G (p.Ala1516=) rs184343684
NM_001135659.2(NRXN1):c.4593G>A (p.Ala1531=) rs113380721
NM_001135659.2(NRXN1):c.4605C>T (p.Asn1535=) rs200814948
NM_001135659.2(NRXN1):c.498G>A (p.Ala166=) rs201212909
NM_001135659.2(NRXN1):c.501C>G (p.Leu167=) rs200248561
NM_001135659.2(NRXN1):c.511C>T (p.Leu171=) rs1045874
NM_001135659.2(NRXN1):c.537C>T (p.Pro179=) rs771019713
NM_001135659.2(NRXN1):c.546G>A (p.Gly182=) rs1464488808
NM_001135659.2(NRXN1):c.583C>T (p.Leu195=) rs923508164
NM_001135659.2(NRXN1):c.588C>T (p.Pro196=) rs201644834
NM_001135659.2(NRXN1):c.684C>T (p.Cys228=) rs1057520920
NM_001135659.2(NRXN1):c.6G>T (p.Gly2=) rs1015367549
NM_001135659.2(NRXN1):c.702C>T (p.Cys234=) rs200357811
NM_001135659.2(NRXN1):c.723C>G (p.Ala241=) rs200153066
NM_001135659.2(NRXN1):c.726G>A (p.Val242=) rs201349397
NM_001135659.2(NRXN1):c.753C>A (p.Arg251=) rs770481343
NM_001135659.2(NRXN1):c.75G>A (p.Ala25=) rs376641324
NM_001135659.2(NRXN1):c.772+16C>T rs1038056478
NM_001135659.2(NRXN1):c.772+6G>C rs777461875
NM_001135659.2(NRXN1):c.772+9C>T rs1297063034
NM_001135659.2(NRXN1):c.773-9C>G rs199645252
NM_001135659.2(NRXN1):c.818A>G (p.Asp273Gly) rs144049982
NM_001135659.2(NRXN1):c.843T>C (p.Cys281=) rs1553513259
NM_001135659.2(NRXN1):c.858G>A (p.Lys286=) rs201194822
NM_001135659.2(NRXN1):c.871+9G>A rs61658382
NM_001135659.2(NRXN1):c.872-19C>T rs569755194
NM_001135659.2(NRXN1):c.897G>A (p.Ala299=) rs201027928
NM_001135659.2(NRXN1):c.903G>C (p.Leu301=) rs1553364040
NM_001135659.2(NRXN1):c.931+14T>G rs1057524092
NM_001135659.2(NRXN1):c.932-5T>G rs199712573
NM_001135659.2(NRXN1):c.93G>T (p.Leu31=) rs201539806
NM_001135659.2(NRXN1):c.963A>G (p.Gly321=) rs373654735
NM_001135659.2(NRXN1):c.999C>T (p.Pro333=) rs2303298
NM_001135659.2(NRXN1):c.9G>C (p.Thr3=) rs770820205
NM_138735.4(NRXN1):c.49GCC[12] (p.Gly17[12]) rs750165040
NM_138735.4(NRXN1):c.49GGC[11] (p.Gly17[11]) rs750165040
NM_138735.4(NRXN1):c.77_79del (p.Gly26del)
NM_138735.4:(NRXN1):c.49GGC[13] (p.Gly17[13]) rs750165040

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