ClinVar Miner

List of variants in gene NRXN1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_001330078.2(NRXN1):c.3933A>G (p.Ala1311=) rs79970751 0.00503
NM_001330078.2(NRXN1):c.1760-16C>T rs79422704 0.00472
NM_001330078.2(NRXN1):c.2122C>A (p.Leu708Ile) rs56086732 0.00458
NM_001135659.2(NRXN1):c.-1273G>A rs186103615 0.00373
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.1575A>G (p.Arg525=) rs201941844 0.00155
NM_001330078.2(NRXN1):c.501C>G (p.Leu167=) rs200248561 0.00145
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.2772C>T (p.Tyr924=) rs200182626 0.00083
NM_001330078.2(NRXN1):c.1158+26A>T rs201802152 0.00069
NM_001330078.2(NRXN1):c.3201C>T (p.Ser1067=) rs75275592 0.00069
NM_001330078.2(NRXN1):c.105C>A (p.Gly35=) rs55640811 0.00059
NM_001330078.2(NRXN1):c.1365T>C (p.Leu455=) rs201727684 0.00051
NM_001330078.2(NRXN1):c.4392T>C (p.His1464=) rs112536447 0.00035
NM_001330078.2(NRXN1):c.772+1118G>A rs201194822 0.00026
NM_001330078.2(NRXN1):c.3365-109939C>T rs766942777 0.00024
NM_001330078.2(NRXN1):c.3129A>G (p.Val1043=) rs200698497 0.00019
NM_001330078.2(NRXN1):c.3365-109899A>G rs562219421 0.00012
NM_001330078.2(NRXN1):c.1749C>T (p.Asp583=) rs199934259 0.00006
NM_001330078.2(NRXN1):c.2109C>T (p.Ser703=) rs200456688 0.00006
NM_001330078.2(NRXN1):c.2253A>G (p.Ala751=) rs199648817 0.00006
NM_001330078.2(NRXN1):c.1353A>G (p.Glu451=) rs368788040 0.00004
NM_001330078.2(NRXN1):c.3384T>C (p.Phe1128=) rs751894635 0.00004
NM_001330078.2(NRXN1):c.315C>T (p.Ala105=) rs767271650 0.00003
NM_001135659.1(NRXN1):c.-1461_-1452dupCTCTCTCTCT rs70958640
NM_001330078.2(NRXN1):c.210C>T (p.Phe70=)
NM_001330078.2(NRXN1):c.2946T>A (p.Pro982=)
NM_001330078.2(NRXN1):c.297G>A (p.Glu99=) rs1553516705
NM_001330078.2(NRXN1):c.3365-109764T>C rs2078010493
NM_001330078.2(NRXN1):c.3365-109930GCG[6] rs750165040
NM_001330078.2(NRXN1):c.4275G>A (p.Arg1425=) rs143495349
NM_001330078.2(NRXN1):c.4317C>T (p.Ala1439=)
NM_001330078.2(NRXN1):c.648G>A (p.Pro216=)
NM_138735.4(NRXN1):c.49GCC[12] (p.Gly17[12]) rs750165040
NM_138735.4(NRXN1):c.49GGC[7] (p.Gly17[7]) rs750165040

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