ClinVar Miner

List of variants in gene NRXN1 reported as likely benign by Ambry Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 90
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HGVS dbSNP gnomAD frequency
NM_001330078.2(NRXN1):c.3408G>A (p.Thr1136=) rs80094872 0.00737
NM_001330078.2(NRXN1):c.3249C>T (p.Pro1083=) rs116236999 0.00578
NM_001330078.2(NRXN1):c.2421C>T (p.Asn807=) rs115211871 0.00535
NM_001330078.2(NRXN1):c.3933A>G (p.Ala1311=) rs79970751 0.00503
NM_001330078.2(NRXN1):c.2122C>A (p.Leu708Ile) rs56086732 0.00458
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.222C>T (p.Gly74=) rs201592993 0.00135
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.4275G>T (p.Arg1425=) rs143495349 0.00096
NM_001330078.2(NRXN1):c.2772C>T (p.Tyr924=) rs200182626 0.00083
NM_001330078.2(NRXN1):c.3365-109830G>A rs148517834 0.00074
NM_001330078.2(NRXN1):c.3201C>T (p.Ser1067=) rs75275592 0.00069
NM_001330078.2(NRXN1):c.1945A>G (p.Ile649Val) rs200074974 0.00062
NM_001330078.2(NRXN1):c.105C>A (p.Gly35=) rs55640811 0.00059
NM_001330078.2(NRXN1):c.24C>T (p.Arg8=) rs200113281 0.00057
NM_001330078.2(NRXN1):c.4167C>G (p.Pro1389=) rs143446587 0.00053
NM_001330078.2(NRXN1):c.1365T>C (p.Leu455=) rs201727684 0.00051
NM_001330078.2(NRXN1):c.723C>G (p.Ala241=) rs200153066 0.00045
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.3129A>G (p.Val1043=) rs200698497 0.00019
NM_001330078.2(NRXN1):c.4176T>C (p.Asp1392=) rs201135028 0.00016
NM_001330078.2(NRXN1):c.108C>T (p.Ala36=) rs199871750 0.00014
NM_001330078.2(NRXN1):c.2193C>T (p.Leu731=) rs201466898 0.00014
NM_001330078.2(NRXN1):c.3365-109899A>G rs562219421 0.00012
NM_001330078.2(NRXN1):c.1050C>G (p.Ala350=) rs201397488 0.00010
NM_001330078.2(NRXN1):c.3090A>C (p.Gly1030=) rs201886024 0.00010
NM_001330078.2(NRXN1):c.2037G>A (p.Pro679=) rs199714221 0.00008
NM_001330078.2(NRXN1):c.2628A>G (p.Gly876=) rs781698676 0.00008
NM_001330078.2(NRXN1):c.3365-109836G>T rs747566761 0.00008
NM_001330078.2(NRXN1):c.847A>G (p.Ile283Val) rs748218169 0.00007
NM_001330078.2(NRXN1):c.1688T>C (p.Ile563Thr) rs201837579 0.00006
NM_001330078.2(NRXN1):c.1887C>T (p.Thr629=) rs200603742 0.00006
NM_001330078.2(NRXN1):c.2109C>T (p.Ser703=) rs200456688 0.00006
NM_001330078.2(NRXN1):c.2730G>A (p.Lys910=) rs192909520 0.00006
NM_001330078.2(NRXN1):c.4248G>A (p.Pro1416=) rs151195816 0.00006
NM_001330078.2(NRXN1):c.3219C>T (p.Asn1073=) rs563089155 0.00005
NM_001330078.2(NRXN1):c.1779G>A (p.Thr593=) rs200817371 0.00004
NM_001330078.2(NRXN1):c.1947C>T (p.Ile649=) rs539484479 0.00004
NM_001330078.2(NRXN1):c.2196C>T (p.Pro732=) rs549242356 0.00004
NM_001330078.2(NRXN1):c.4236C>T (p.Gly1412=) rs587781101 0.00004
NM_001330078.2(NRXN1):c.420C>G (p.Val140=) rs751401940 0.00003
NM_001330078.2(NRXN1):c.600C>T (p.Gly200=) rs201481698 0.00003
NM_001330078.2(NRXN1):c.2643C>T (p.Asp881=) rs1196816567 0.00002
NM_001330078.2(NRXN1):c.2970C>T (p.Asn990=) rs534591485 0.00002
NM_001330078.2(NRXN1):c.4428A>G (p.Ala1476=) rs184343684 0.00002
NM_001330078.2(NRXN1):c.450C>T (p.Phe150=) rs766193025 0.00002
NM_001330078.2(NRXN1):c.690C>T (p.Asn230=) rs200930363 0.00002
NM_001330078.2(NRXN1):c.1326A>C (p.Val442=) rs201485014 0.00001
NM_001330078.2(NRXN1):c.2658C>T (p.Gly886=) rs752920557 0.00001
NM_001330078.2(NRXN1):c.2698A>C (p.Arg900=) rs574531814 0.00001
NM_001330078.2(NRXN1):c.2967C>T (p.His989=) rs1449052965 0.00001
NM_001330078.2(NRXN1):c.3165A>G (p.Ser1055=) rs1553656447 0.00001
NM_001330078.2(NRXN1):c.771A>G (p.Gln257=) rs1307802785 0.00001
NM_001330078.2(NRXN1):c.864A>G (p.Gly288=) rs373654735 0.00001
NM_001330078.2(NRXN1):c.987T>C (p.Asp329=) rs1404653942 0.00001
NM_001330078.2(NRXN1):c.1215T>C (p.Tyr405=)
NM_001330078.2(NRXN1):c.1275T>C (p.Leu425=) rs1559029940
NM_001330078.2(NRXN1):c.12G>A (p.Ala4=)
NM_001330078.2(NRXN1):c.1362A>G (p.Arg454=)
NM_001330078.2(NRXN1):c.1377A>G (p.Gly459=) rs1352621512
NM_001330078.2(NRXN1):c.1512A>T (p.Ile504=)
NM_001330078.2(NRXN1):c.1536G>A (p.Glu512=)
NM_001330078.2(NRXN1):c.1995T>G (p.Thr665=)
NM_001330078.2(NRXN1):c.2151G>T (p.Thr717=) rs200768648
NM_001330078.2(NRXN1):c.2274C>A (p.Thr758=) rs78030925
NM_001330078.2(NRXN1):c.2814A>G (p.Leu938=) rs902243141
NM_001330078.2(NRXN1):c.300T>G (p.Pro100=) rs753793668
NM_001330078.2(NRXN1):c.3033G>T (p.Thr1011=) rs764611037
NM_001330078.2(NRXN1):c.3172T>C (p.Leu1058=)
NM_001330078.2(NRXN1):c.3357C>T (p.Cys1119=)
NM_001330078.2(NRXN1):c.3365-109737C>T
NM_001330078.2(NRXN1):c.3365-109930GCG[8] rs750165040
NM_001330078.2(NRXN1):c.3365-109930GCG[9] rs750165040
NM_001330078.2(NRXN1):c.3365-109932_3365-109927dup rs2078032746
NM_001330078.2(NRXN1):c.3365-109941C>A
NM_001330078.2(NRXN1):c.4405C>A (p.Arg1469=) rs1331703447
NM_001330078.2(NRXN1):c.4416C>A (p.Ile1472=)
NM_001330078.2(NRXN1):c.51G>T (p.Ser17=) rs200631737
NM_001330078.2(NRXN1):c.588C>T (p.Pro196=) rs201644834
NM_001330078.2(NRXN1):c.705C>G (p.Ser235=)
NM_001330078.2(NRXN1):c.753C>T (p.Arg251=) rs770481343
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[13] (p.Gly17[13]) rs750165040

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