ClinVar Miner

List of variants in gene NRXN1 reported as uncertain significance by Genetic Services Laboratory, University of Chicago

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 41
Download table as spreadsheet
HGVS dbSNP
NM_001135659.2(NRXN1):c.1416C>T (p.Asn472=) rs1259694734
NM_001135659.2(NRXN1):c.1544A>C (p.Asn515Thr) rs751754721
NM_001135659.2(NRXN1):c.1712A>G (p.Lys571Arg) rs796052769
NM_001135659.2(NRXN1):c.1768C>G (p.Leu590Val) rs1295091945
NM_001135659.2(NRXN1):c.1869C>T (p.Asp623=) rs199934259
NM_001135659.2(NRXN1):c.2078G>A (p.Ser693Asn) rs587780406
NM_001135659.2(NRXN1):c.2195G>A (p.Arg732Lys) rs797045796
NM_001135659.2(NRXN1):c.2627C>T (p.Ala876Val) rs199557987
NM_001135659.2(NRXN1):c.2657A>C (p.Asn886Thr) rs797045797
NM_001135659.2(NRXN1):c.316G>A (p.Asp106Asn) rs200576486
NM_001135659.2(NRXN1):c.3339C>T (p.Asn1113=) rs563089155
NM_001135659.2(NRXN1):c.338C>T (p.Ala113Val) rs201542547
NM_001135659.2(NRXN1):c.3464G>A (p.Ser1155Asn) rs201871194
NM_001135659.2(NRXN1):c.3736A>G (p.Ile1246Val) rs751778015
NM_001135659.2(NRXN1):c.3795G>A (p.Thr1265=) rs200179221
NM_001135659.2(NRXN1):c.4124C>T (p.Thr1375Ile) rs200672080
NM_001135659.2(NRXN1):c.4356C>T (p.Gly1452=) rs587781101
NM_001135659.2(NRXN1):c.4368G>A (p.Pro1456=) rs151195816
NM_001135659.2(NRXN1):c.637G>A (p.Gly213Arg) rs199561088
NM_001135659.2(NRXN1):c.656_664dup (p.Ala219_Glu221dup) rs546508545
NM_001135659.2(NRXN1):c.668G>A (p.Gly223Asp) rs200490872
NM_001135659.2(NRXN1):c.772+9del rs755130575
NM_001135659.2(NRXN1):c.773-9C>G rs199645252
NM_001135659.2(NRXN1):c.876C>T (p.Asp292=) rs587780407
NM_001135659.2(NRXN1):c.946A>G (p.Ile316Val) rs748218169
NM_001330078.2(NRXN1):c.105C>A (p.Gly35=) rs55640811
NM_001330078.2(NRXN1):c.1158+26A>T rs201802152
NM_001330078.2(NRXN1):c.1575A>G (p.Arg525=) rs201941844
NM_001330078.2(NRXN1):c.1945A>G (p.Ile649Val) rs200074974
NM_001330078.2(NRXN1):c.2036C>T (p.Pro679Leu) rs201735573
NM_001330078.2(NRXN1):c.2190G>T (p.Gln730His) rs199978276
NM_001330078.2(NRXN1):c.2459G>A (p.Ser820Asn) rs80293130
NM_001330078.2(NRXN1):c.2533C>T (p.His845Tyr) rs199784139
NM_001330078.2(NRXN1):c.2605C>A (p.Leu869Met) rs201818223
NM_001330078.2(NRXN1):c.2772C>T (p.Tyr924=) rs200182626
NM_001330078.2(NRXN1):c.320C>T (p.Thr107Met) rs368549770
NM_001330078.2(NRXN1):c.4167C>G (p.Pro1389=) rs143446587
NM_001330078.2(NRXN1):c.4275G>T (p.Arg1425=) rs143495349
NM_001330078.2(NRXN1):c.569A>G (p.Asn190Ser) rs200792504
NM_001330078.2(NRXN1):c.749T>A (p.Phe250Tyr) rs200646155
NM_001330078.2(NRXN1):c.772+1050C>A rs367919055

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.