ClinVar Miner

List of variants in gene NRXN1 reported by Genetic Services Laboratory, University of Chicago

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Total variants: 63
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HGVS dbSNP
NM_001135659.2(NRXN1):c.1149C>G (p.Ala383=) rs201397488
NM_001135659.2(NRXN1):c.1416C>T (p.Asn472=) rs1259694734
NM_001135659.2(NRXN1):c.1446A>C (p.Val482=) rs201485014
NM_001135659.2(NRXN1):c.1544A>C (p.Asn515Thr) rs751754721
NM_001135659.2(NRXN1):c.1712A>G (p.Lys571Arg) rs796052769
NM_001135659.2(NRXN1):c.1768C>G (p.Leu590Val) rs1295091945
NM_001135659.2(NRXN1):c.1869C>T (p.Asp623=) rs199934259
NM_001135659.2(NRXN1):c.2078G>A (p.Ser693Asn) rs587780406
NM_001135659.2(NRXN1):c.2195G>A (p.Arg732Lys) rs797045796
NM_001135659.2(NRXN1):c.2627C>T (p.Ala876Val) rs199557987
NM_001135659.2(NRXN1):c.2657A>C (p.Asn886Thr) rs797045797
NM_001135659.2(NRXN1):c.3129A>T (p.Val1043=) rs781048514
NM_001135659.2(NRXN1):c.316G>A (p.Asp106Asn) rs200576486
NM_001135659.2(NRXN1):c.3312C>T (p.Asp1104=) rs199580594
NM_001135659.2(NRXN1):c.3339C>T (p.Asn1113=) rs563089155
NM_001135659.2(NRXN1):c.338C>T (p.Ala113Val) rs201542547
NM_001135659.2(NRXN1):c.3464G>A (p.Ser1155Asn) rs201871194
NM_001135659.2(NRXN1):c.3736A>G (p.Ile1246Val) rs751778015
NM_001135659.2(NRXN1):c.3795G>A (p.Thr1265=) rs200179221
NM_001135659.2(NRXN1):c.4124C>T (p.Thr1375Ile) rs200672080
NM_001135659.2(NRXN1):c.4356C>T (p.Gly1452=) rs587781101
NM_001135659.2(NRXN1):c.4368G>A (p.Pro1456=) rs151195816
NM_001135659.2(NRXN1):c.637G>A (p.Gly213Arg) rs199561088
NM_001135659.2(NRXN1):c.656_664dup (p.Ala219_Glu221dup) rs546508545
NM_001135659.2(NRXN1):c.668G>A (p.Gly223Asp) rs200490872
NM_001135659.2(NRXN1):c.772+9del rs755130575
NM_001135659.2(NRXN1):c.773-9C>G rs199645252
NM_001135659.2(NRXN1):c.876C>T (p.Asp292=) rs587780407
NM_001135659.2(NRXN1):c.946A>G (p.Ile316Val) rs748218169
NM_001330078.2(NRXN1):c.105C>A (p.Gly35=) rs55640811
NM_001330078.2(NRXN1):c.1158+26A>T rs201802152
NM_001330078.2(NRXN1):c.1285C>T (p.Pro429Ser) rs78540316
NM_001330078.2(NRXN1):c.1365T>C (p.Leu455=) rs201727684
NM_001330078.2(NRXN1):c.1575A>G (p.Arg525=) rs201941844
NM_001330078.2(NRXN1):c.1945A>G (p.Ile649Val) rs200074974
NM_001330078.2(NRXN1):c.2036C>T (p.Pro679Leu) rs201735573
NM_001330078.2(NRXN1):c.2122C>A (p.Leu708Ile) rs56086732
NM_001330078.2(NRXN1):c.2190G>T (p.Gln730His) rs199978276
NM_001330078.2(NRXN1):c.222C>T (p.Gly74=) rs201592993
NM_001330078.2(NRXN1):c.2421C>T (p.Asn807=) rs115211871
NM_001330078.2(NRXN1):c.2459G>A (p.Ser820Asn) rs80293130
NM_001330078.2(NRXN1):c.2533C>T (p.His845Tyr) rs199784139
NM_001330078.2(NRXN1):c.2605C>A (p.Leu869Met) rs201818223
NM_001330078.2(NRXN1):c.2772C>T (p.Tyr924=) rs200182626
NM_001330078.2(NRXN1):c.3045C>T (p.Ala1015=) rs56402642
NM_001330078.2(NRXN1):c.3090A>C (p.Gly1030=) rs201886024
NM_001330078.2(NRXN1):c.320C>T (p.Thr107Met) rs368549770
NM_001330078.2(NRXN1):c.3249C>T (p.Pro1083=) rs116236999
NM_001330078.2(NRXN1):c.3408G>A (p.Thr1136=) rs80094872
NM_001330078.2(NRXN1):c.3933A>G (p.Ala1311=) rs79970751
NM_001330078.2(NRXN1):c.4068G>A (p.Thr1356=) rs74714098
NM_001330078.2(NRXN1):c.4167C>G (p.Pro1389=) rs143446587
NM_001330078.2(NRXN1):c.4254A>G (p.Pro1418=) rs55923848
NM_001330078.2(NRXN1):c.4275G>T (p.Arg1425=) rs143495349
NM_001330078.2(NRXN1):c.4392T>C (p.His1464=) rs112536447
NM_001330078.2(NRXN1):c.4473G>A (p.Ala1491=) rs113380721
NM_001330078.2(NRXN1):c.501C>G (p.Leu167=) rs200248561
NM_001330078.2(NRXN1):c.511C>T (p.Leu171=) rs1045874
NM_001330078.2(NRXN1):c.569A>G (p.Asn190Ser) rs200792504
NM_001330078.2(NRXN1):c.749T>A (p.Phe250Tyr) rs200646155
NM_001330078.2(NRXN1):c.772+1050C>A rs367919055
NM_001330078.2(NRXN1):c.772+1140G>A rs61658382
NM_001330078.2(NRXN1):c.900C>T (p.Pro300=) rs2303298

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