ClinVar Miner

List of variants in gene NRXN1 reported as uncertain significance for History of neurodevelopmental disorder

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Total variants: 35
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HGVS dbSNP
NM_001135659.2(NRXN1):c.-4G>A
NM_001135659.2(NRXN1):c.1278+5A>T rs201802152
NM_001135659.2(NRXN1):c.1820T>G (p.Leu607Trp) rs372311299
NM_001135659.2(NRXN1):c.2005A>C (p.Thr669Pro)
NM_001135659.2(NRXN1):c.2098G>A (p.Ala700Thr) rs199939303
NM_001135659.2(NRXN1):c.20A>G (p.Gln7Arg)
NM_001135659.2(NRXN1):c.2156C>T (p.Pro719Leu) rs201735573
NM_001135659.2(NRXN1):c.2310G>T (p.Gln770His) rs199978276
NM_001135659.2(NRXN1):c.2408C>G (p.Ser803Cys)
NM_001135659.2(NRXN1):c.2570G>T (p.Arg857Leu)
NM_001135659.2(NRXN1):c.2579G>A (p.Ser860Asn) rs80293130
NM_001135659.2(NRXN1):c.2653C>T (p.His885Tyr) rs199784139
NM_001135659.2(NRXN1):c.2689T>C (p.Tyr897His)
NM_001135659.2(NRXN1):c.2725C>A (p.Leu909Met) rs201818223
NM_001135659.2(NRXN1):c.3008A>G (p.His1003Arg)
NM_001135659.2(NRXN1):c.302C>G (p.Ala101Gly) rs200184823
NM_001135659.2(NRXN1):c.3196T>A (p.Leu1066Ile)
NM_001135659.2(NRXN1):c.322C>T (p.Pro108Ser) rs199784029
NM_001135659.2(NRXN1):c.3244C>T (p.Leu1082Phe)
NM_001135659.2(NRXN1):c.3473T>G (p.Leu1158Arg)
NM_001135659.2(NRXN1):c.347G>C (p.Ser116Thr)
NM_001135659.2(NRXN1):c.3485-109897G>C rs777054372
NM_001135659.2(NRXN1):c.3485-109939C>T rs766942777
NM_001135659.2(NRXN1):c.35T>G (p.Phe12Cys)
NM_001135659.2(NRXN1):c.370C>T (p.Arg124Cys)
NM_001135659.2(NRXN1):c.37C>T (p.Leu13Phe)
NM_001135659.2(NRXN1):c.4039G>A (p.Val1347Ile) rs200044811
NM_001135659.2(NRXN1):c.412G>T (p.Val138Leu)
NM_001135659.2(NRXN1):c.569A>G (p.Asn190Ser) rs200792504
NM_001135659.2(NRXN1):c.665_673dup (p.Glu224_Gly225insGluGlyGlu) rs774230140
NM_001135659.2(NRXN1):c.780A>T (p.Lys260Asn) rs201741449
NM_001135659.2(NRXN1):c.790C>A (p.Gln264Lys) rs367919055
NM_001135659.2(NRXN1):c.818A>G (p.Asp273Gly) rs144049982
NM_001135659.2(NRXN1):c.932-5T>G rs199712573
NM_138735.4(NRXN1):c.115C>T (p.Leu39Phe)

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