ClinVar Miner

List of variants in gene NRXN1 reported as likely benign by PreventionGenetics, part of Exact Sciences

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Total variants: 36
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HGVS dbSNP gnomAD frequency
NM_001330078.2(NRXN1):c.4473G>A (p.Ala1491=) rs113380721 0.00191
NM_001330078.2(NRXN1):c.772+1078A>G rs144049982 0.00153
NM_001330078.2(NRXN1):c.322C>T (p.Pro108Ser) rs199784029 0.00131
NM_001330078.2(NRXN1):c.820+50G>A rs199971485 0.00114
NM_001330078.2(NRXN1):c.3045C>T (p.Ala1015=) rs56402642 0.00110
NM_001330078.2(NRXN1):c.3365-109830G>A rs148517834 0.00074
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.820+35G>C rs201734514 0.00017
NM_001330078.2(NRXN1):c.4176T>C (p.Asp1392=) rs201135028 0.00016
NM_001330078.2(NRXN1):c.324G>A (p.Pro108=) rs199595253 0.00011
NM_001330078.2(NRXN1):c.1050C>G (p.Ala350=) rs201397488 0.00010
NM_001330078.2(NRXN1):c.498G>A (p.Ala166=) rs201212909 0.00008
NM_001330078.2(NRXN1):c.1688T>C (p.Ile563Thr) rs201837579 0.00007
NM_001330078.2(NRXN1):c.2037G>A (p.Pro679=) rs199714221 0.00007
NM_001330078.2(NRXN1):c.1749C>T (p.Asp583=) rs199934259 0.00006
NM_001330078.2(NRXN1):c.492C>T (p.Ala164=) rs201180707 0.00005
NM_001330078.2(NRXN1):c.798G>A (p.Ala266=) rs201027928 0.00005
NM_001330078.2(NRXN1):c.3675G>A (p.Thr1225=) rs200179221 0.00004
NM_001330078.2(NRXN1):c.378C>G (p.Thr126=) rs181121858 0.00004
NM_001330078.2(NRXN1):c.1779G>A (p.Thr593=) rs200817371 0.00003
NM_001330078.2(NRXN1):c.3228C>T (p.Ile1076=) rs201241923 0.00003
NM_001330078.2(NRXN1):c.576G>A (p.Ser192=) rs1165324585 0.00003
NM_001330078.2(NRXN1):c.3070+9A>G rs763508293 0.00002
NM_001330078.2(NRXN1):c.702C>T (p.Cys234=) rs200357811 0.00002
NM_001330078.2(NRXN1):c.2196C>T (p.Pro732=) rs549242356 0.00001
NM_001330078.2(NRXN1):c.363C>T (p.Arg121=) rs1265535501 0.00001
NM_001330078.2(NRXN1):c.414G>C (p.Val138=) rs962050724 0.00001
NM_001330078.2(NRXN1):c.864A>G (p.Gly288=) rs373654735 0.00001
NM_001330078.2(NRXN1):c.-31G>C rs774347162
NM_001330078.2(NRXN1):c.3000C>T (p.Leu1000=) rs2468898740
NM_001330078.2(NRXN1):c.3365-109930GCG[6] rs750165040
NM_001330078.2(NRXN1):c.772+9del rs755130575
NM_001330078.2(NRXN1):c.832+2683A>G rs1206765024
NM_138735.4(NRXN1):c.49GGC[11] (p.Gly17[11]) rs750165040
NM_138735.4(NRXN1):c.49GGC[7] (p.Gly17[7]) rs750165040

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