ClinVar Miner

List of variants in gene NRXN1 reported by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 87
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HGVS dbSNP
NM_001135659.2(NRXN1):c.1149C>G (p.Ala383=) rs201397488
NM_001135659.2(NRXN1):c.2067C>T (p.Ile689=) rs539484479
NM_001135659.2(NRXN1):c.2271G>T (p.Thr757=)
NM_001135659.2(NRXN1):c.2313C>T (p.Leu771=) rs201466898
NM_001135659.2(NRXN1):c.2394C>A (p.Thr798=) rs78030925
NM_001135659.2(NRXN1):c.2570G>T (p.Arg857Leu)
NM_001135659.2(NRXN1):c.2850G>A (p.Lys950=) rs192909520
NM_001135659.2(NRXN1):c.300T>G (p.Pro100=) rs753793668
NM_001135659.2(NRXN1):c.3249A>G (p.Val1083=) rs200698497
NM_001135659.2(NRXN1):c.3285A>G (p.Ser1095=) rs1553656447
NM_001135659.2(NRXN1):c.3339C>T (p.Asn1113=) rs563089155
NM_001135659.2(NRXN1):c.3485-109836G>T rs747566761
NM_001135659.2(NRXN1):c.3485-109897G>C rs777054372
NM_001135659.2(NRXN1):c.3485-109939C>T rs766942777
NM_001135659.2(NRXN1):c.4124C>T (p.Thr1375Ile) rs200672080
NM_001135659.2(NRXN1):c.4368G>A (p.Pro1456=) rs151195816
NM_001135659.2(NRXN1):c.589G>C (p.Val197Leu) rs369183287
NM_001135659.2(NRXN1):c.665_673dup (p.Glu222_Glu224dup) rs774230140
NM_001135659.2(NRXN1):c.780A>T (p.Lys260Asn) rs201741449
NM_001330078.2(NRXN1):c.-4G>A rs1558617962
NM_001330078.2(NRXN1):c.105C>A (p.Gly35=) rs55640811
NM_001330078.2(NRXN1):c.1158+26A>T rs201802152
NM_001330078.2(NRXN1):c.1275T>C (p.Leu425=) rs1559029940
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.1377A>G (p.Gly459=) rs1352621512
NM_001330078.2(NRXN1):c.1575A>G (p.Arg525=) rs201941844
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.1885A>C (p.Thr629Pro)
NM_001330078.2(NRXN1):c.1887C>T (p.Thr629=) rs200603742
NM_001330078.2(NRXN1):c.1945A>G (p.Ile649Val) rs200074974
NM_001330078.2(NRXN1):c.1978G>A (p.Ala660Thr) rs199939303
NM_001330078.2(NRXN1):c.2036C>T (p.Pro679Leu) rs201735573
NM_001330078.2(NRXN1):c.20A>G (p.Gln7Arg) rs1558617775
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.2288C>G (p.Ser763Cys) rs1558889761
NM_001330078.2(NRXN1):c.2385C>G (p.Pro795=) rs147984237
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.2569T>C (p.Tyr857His) rs1558834284
NM_001330078.2(NRXN1):c.2605C>A (p.Leu869Met) rs201818223
NM_001330078.2(NRXN1):c.2628A>G (p.Gly876=)
NM_001330078.2(NRXN1):c.2772C>T (p.Tyr924=) rs200182626
NM_001330078.2(NRXN1):c.2814A>G (p.Leu938=)
NM_001330078.2(NRXN1):c.2888A>G (p.His963Arg) rs1558830787
NM_001330078.2(NRXN1):c.302C>G (p.Ala101Gly) rs200184823
NM_001330078.2(NRXN1):c.3045C>T (p.Ala1015=) rs56402642
NM_001330078.2(NRXN1):c.3076T>A (p.Leu1026Ile) rs1558790614
NM_001330078.2(NRXN1):c.3124C>T (p.Leu1042Phe) rs1558790367
NM_001330078.2(NRXN1):c.3201C>T (p.Ser1067=) rs75275592
NM_001330078.2(NRXN1):c.322C>T (p.Pro108Ser) rs199784029
NM_001330078.2(NRXN1):c.3249C>T (p.Pro1083=) rs116236999
NM_001330078.2(NRXN1):c.3353T>G (p.Leu1118Arg)
NM_001330078.2(NRXN1):c.3365-109865C>T
NM_001330078.2(NRXN1):c.3365-109899A>G rs562219421
NM_001330078.2(NRXN1):c.3365-109930G>T rs13413205
NM_001330078.2(NRXN1):c.3365-109930GCG[9] rs750165040
NM_001330078.2(NRXN1):c.3408G>A (p.Thr1136=) rs80094872
NM_001330078.2(NRXN1):c.347G>C (p.Ser116Thr)
NM_001330078.2(NRXN1):c.35T>G (p.Phe12Cys) rs1298445857
NM_001330078.2(NRXN1):c.370C>T (p.Arg124Cys)
NM_001330078.2(NRXN1):c.37C>T (p.Leu13Phe)
NM_001330078.2(NRXN1):c.3919G>A (p.Val1307Ile) rs200044811
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.412G>T (p.Val138Leu)
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.4405C>A (p.Arg1469=) rs1331703447
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.723C>G (p.Ala241=) rs200153066
NM_001330078.2(NRXN1):c.772+1050C>A rs367919055
NM_001330078.2(NRXN1):c.772+1078A>G rs144049982
NM_001330078.2(NRXN1):c.833-5T>G rs199712573
NM_001330078.2(NRXN1):c.900C>T (p.Pro300=) rs2303298
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.49GGC[7] (p.Gly17[7]) rs750165040
NM_138735.4(NRXN1):c.49[5] (p.Gly17[5]) rs750165040

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