ClinVar Miner

List of variants in gene NRXN1 reported as likely benign for not specified

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Gene type:
ClinVar version:
Total variants: 100
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HGVS dbSNP gnomAD frequency
NM_001330078.2(NRXN1):c.511C>T (p.Leu171=) rs1045874 0.17452
NM_001330078.2(NRXN1):c.900C>T (p.Pro300=) rs2303298 0.01844
NM_001330078.2(NRXN1):c.4068G>A (p.Thr1356=) rs74714098 0.01437
NM_001330078.2(NRXN1):c.772+1140G>A rs61658382 0.00837
NM_001330078.2(NRXN1):c.3408G>A (p.Thr1136=) rs80094872 0.00737
NM_001330078.2(NRXN1):c.3249C>T (p.Pro1083=) rs116236999 0.00578
NM_001330078.2(NRXN1):c.3933A>G (p.Ala1311=) rs79970751 0.00503
NM_001330078.2(NRXN1):c.1285C>T (p.Pro429Ser) rs78540316 0.00323
NM_001330078.2(NRXN1):c.4473G>A (p.Ala1491=) rs113380721 0.00191
NM_001330078.2(NRXN1):c.2385C>G (p.Pro795=) rs147984237 0.00166
NM_001330078.2(NRXN1):c.772+1078A>G rs144049982 0.00153
NM_001330078.2(NRXN1):c.501C>G (p.Leu167=) rs200248561 0.00145
NM_001330078.2(NRXN1):c.222C>T (p.Gly74=) rs201592993 0.00135
NM_001330078.2(NRXN1):c.3045C>T (p.Ala1015=) rs56402642 0.00109
NM_001330078.2(NRXN1):c.4254A>G (p.Pro1418=) rs55923848 0.00109
NM_001330078.2(NRXN1):c.1158+26A>T rs201802152 0.00069
NM_001330078.2(NRXN1):c.1365T>C (p.Leu455=) rs201727684 0.00051
NM_001330078.2(NRXN1):c.723C>G (p.Ala241=) rs200153066 0.00045
NM_001330078.2(NRXN1):c.4392T>C (p.His1464=) rs112536447 0.00035
NM_001330078.2(NRXN1):c.1050C>G (p.Ala350=) rs201397488 0.00010
NM_001330078.2(NRXN1):c.3090A>C (p.Gly1030=) rs201886024 0.00010
NM_001330078.2(NRXN1):c.321G>T (p.Thr107=) rs776382029 0.00008
NM_001330078.2(NRXN1):c.3365-109836G>T rs747566761 0.00008
NM_001330078.2(NRXN1):c.1320+19A>G rs201399154 0.00007
NM_001330078.2(NRXN1):c.3717A>T (p.Ala1239=) rs145558855 0.00006
NM_001330078.2(NRXN1):c.3219C>T (p.Asn1073=) rs563089155 0.00005
NM_001330078.2(NRXN1):c.1779G>A (p.Thr593=) rs200817371 0.00004
NM_001330078.2(NRXN1):c.93G>T (p.Leu31=) rs201539806 0.00004
NM_001330078.2(NRXN1):c.-7C>A rs202002348 0.00003
NM_001330078.2(NRXN1):c.-919G>C rs1341735881 0.00003
NM_001330078.2(NRXN1):c.1194G>A (p.Thr398=) rs202166616 0.00003
NM_001330078.2(NRXN1):c.3071-17C>G rs200354492 0.00003
NM_001330078.2(NRXN1):c.3365-109758A>G rs142041427 0.00003
NM_001330078.2(NRXN1):c.3365-110011C>T rs1446478264 0.00003
NM_001330078.2(NRXN1):c.3365-110016C>T rs1057521771 0.00003
NM_001330078.2(NRXN1):c.773-19C>T rs569755194 0.00003
NM_001330078.2(NRXN1):c.930G>A (p.Leu310=) rs200532412 0.00003
NM_001330078.2(NRXN1):c.*13A>C rs199777715 0.00002
NM_001330078.2(NRXN1):c.-22C>A rs1057520336 0.00002
NM_001330078.2(NRXN1):c.1320+10G>A rs113028018 0.00002
NM_001330078.2(NRXN1):c.2211G>A (p.Thr737=) rs755177932 0.00002
NM_001330078.2(NRXN1):c.3244+18T>A rs371530345 0.00002
NM_001330078.2(NRXN1):c.*1T>A rs567887770 0.00001
NM_001330078.2(NRXN1):c.1326A>C (p.Val442=) rs201485014 0.00001
NM_001330078.2(NRXN1):c.159G>A (p.Glu53=) rs1057524126 0.00001
NM_001330078.2(NRXN1):c.2247G>A (p.Gln749=) rs1057521319 0.00001
NM_001330078.2(NRXN1):c.2316C>T (p.Asp772=) rs200449662 0.00001
NM_001330078.2(NRXN1):c.2391T>A (p.Thr797=) rs750156118 0.00001
NM_001330078.2(NRXN1):c.2983A>C (p.Arg995=) rs780193876 0.00001
NM_001330078.2(NRXN1):c.3042C>T (p.Thr1014=) rs75137449 0.00001
NM_001330078.2(NRXN1):c.3365-110014del rs1064794179 0.00001
NM_001330078.2(NRXN1):c.3375A>G (p.Thr1125=) rs757748286 0.00001
NM_001330078.2(NRXN1):c.3547-16C>G rs756210249 0.00001
NM_001330078.2(NRXN1):c.3547-18T>C rs754285936 0.00001
NM_001330078.2(NRXN1):c.537C>T (p.Pro179=) rs771019713 0.00001
NM_001330078.2(NRXN1):c.6G>T (p.Gly2=) rs1015367549 0.00001
NM_001330078.2(NRXN1):c.772+1024C>G rs199645252 0.00001
NM_001330078.2(NRXN1):c.772+1103T>C rs1553513259 0.00001
NM_001330078.2(NRXN1):c.772+6G>C rs777461875 0.00001
NM_001330078.2(NRXN1):c.864A>G (p.Gly288=) rs373654735 0.00001
NM_001330078.2(NRXN1):c.-906A>C rs1057522918
NM_001330078.2(NRXN1):c.1320+4_1320+7dup rs1259067816
NM_001330078.2(NRXN1):c.1338T>C (p.Asn446=) rs1057523256
NM_001330078.2(NRXN1):c.1696C>T (p.Leu566=) rs754703742
NM_001330078.2(NRXN1):c.1760-15_1760-13del rs1255783166
NM_001330078.2(NRXN1):c.1760-8T>C rs1057522281
NM_001330078.2(NRXN1):c.1869T>G (p.Ala623=) rs201816600
NM_001330078.2(NRXN1):c.2144-22_2144-20del rs779214382
NM_001330078.2(NRXN1):c.2144-4C>A rs1340313788
NM_001330078.2(NRXN1):c.2301C>A (p.Leu767=) rs1553750260
NM_001330078.2(NRXN1):c.2375-20C>G rs776794965
NM_001330078.2(NRXN1):c.2507C>T (p.Ala836Val) rs199557987
NM_001330078.2(NRXN1):c.261C>T (p.Gly87=) rs587781102
NM_001330078.2(NRXN1):c.285C>T (p.Ile95=) rs759011919
NM_001330078.2(NRXN1):c.2880-22_2880-14del rs755734707
NM_001330078.2(NRXN1):c.297G>A (p.Glu99=) rs1553516705
NM_001330078.2(NRXN1):c.3009A>T (p.Val1003=) rs781048514
NM_001330078.2(NRXN1):c.300T>G (p.Pro100=) rs753793668
NM_001330078.2(NRXN1):c.3168T>G (p.Val1056=) rs1553656429
NM_001330078.2(NRXN1):c.3192C>T (p.Asp1064=) rs199580594
NM_001330078.2(NRXN1):c.3198C>T (p.Ile1066=) rs1553656308
NM_001330078.2(NRXN1):c.3228C>A (p.Ile1076=) rs201241923
NM_001330078.2(NRXN1):c.3330T>C (p.Ser1110=) rs1057522160
NM_001330078.2(NRXN1):c.3365-109705C>G rs1227805288
NM_001330078.2(NRXN1):c.3365-109836G>A rs747566761
NM_001330078.2(NRXN1):c.3365-109863C>T rs1057521027
NM_001330078.2(NRXN1):c.3365-109992C>T rs796052761
NM_001330078.2(NRXN1):c.3654G>C (p.Thr1218=) rs765748728
NM_001330078.2(NRXN1):c.3675G>T (p.Thr1225=) rs200179221
NM_001330078.2(NRXN1):c.3718+11G>A rs1057522566
NM_001330078.2(NRXN1):c.3808+8dup rs770051379
NM_001330078.2(NRXN1):c.3888G>A (p.Gln1296=) rs1553535081
NM_001330078.2(NRXN1):c.3957C>T (p.Ala1319=) rs1553534825
NM_001330078.2(NRXN1):c.588C>T (p.Pro196=) rs201644834
NM_001330078.2(NRXN1):c.684C>T (p.Cys228=) rs1057520920
NM_001330078.2(NRXN1):c.75G>A (p.Ala25=) rs376641324
NM_001330078.2(NRXN1):c.772+16C>T rs1038056478
NM_001330078.2(NRXN1):c.772+9C>T rs1297063034
NM_001330078.2(NRXN1):c.832+14T>G rs1057524092
NM_138735.4(NRXN1):c.49GCC[12] (p.Gly17[12]) rs750165040

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