ClinVar Miner

List of variants in gene NRXN1 reported as likely benign for History of neurodevelopmental disorder

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Total variants: 44
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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.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.4368G>A (p.Pro1456=) rs151195816
NM_001330078.2(NRXN1):c.105C>A (p.Gly35=) rs55640811
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.1887C>T (p.Thr629=) rs200603742
NM_001330078.2(NRXN1):c.1945A>G (p.Ile649Val) rs200074974
NM_001330078.2(NRXN1):c.2122C>A (p.Leu708Ile) rs56086732
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.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.3045C>T (p.Ala1015=) rs56402642
NM_001330078.2(NRXN1):c.3201C>T (p.Ser1067=) rs75275592
NM_001330078.2(NRXN1):c.3249C>T (p.Pro1083=) rs116236999
NM_001330078.2(NRXN1):c.3365-109899A>G rs562219421
NM_001330078.2(NRXN1):c.3365-109930GCG[9] rs750165040
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.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.723C>G (p.Ala241=) rs200153066
NM_138735.4(NRXN1):c.49GCC[12] (p.Gly17[12]) rs750165040
NM_138735.4(NRXN1):c.49GGC[11] (p.Gly17[11]) rs750165040

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