ClinVar Miner

List of variants in gene NRXN1 reported by EGL Genetic Diagnostics,Eurofins Clinical Diagnostics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 84
Download table as spreadsheet
HGVS dbSNP
NM_001135659.2(NRXN1):c.1406C>T (p.Pro469Leu) rs886042697
NM_001135659.2(NRXN1):c.1408G>A (p.Val470Ile) rs753832133
NM_001135659.2(NRXN1):c.1440+10G>A rs113028018
NM_001135659.2(NRXN1):c.1446A>C (p.Val482=) rs201485014
NM_001135659.2(NRXN1):c.1502C>T (p.Pro501Leu) rs530674644
NM_001135659.2(NRXN1):c.1651A>G (p.Thr551Ala) rs794726985
NM_001135659.2(NRXN1):c.1850A>G (p.His617Arg) rs886042974
NM_001135659.2(NRXN1):c.1909C>G (p.Pro637Ala) rs1553760276
NM_001135659.2(NRXN1):c.192C>T (p.Arg64=) rs748944452
NM_001135659.2(NRXN1):c.2033A>G (p.Tyr678Cys) rs727504051
NM_001135659.2(NRXN1):c.2128C>G (p.Pro710Ala) rs762326241
NM_001135659.2(NRXN1):c.2157G>A (p.Pro719=) rs199714221
NM_001135659.2(NRXN1):c.2369G>A (p.Arg790His) rs200776618
NM_001135659.2(NRXN1):c.252G>A (p.Thr84=) rs886042465
NM_001135659.2(NRXN1):c.2617+3A>G rs202074070
NM_001135659.2(NRXN1):c.2618-8T>C rs775167794
NM_001135659.2(NRXN1):c.2627C>T (p.Ala876Val) rs199557987
NM_001135659.2(NRXN1):c.2850G>A (p.Lys950=) rs192909520
NM_001135659.2(NRXN1):c.2905C>T (p.Leu969Phe) rs794727140
NM_001135659.2(NRXN1):c.2999+7A>G rs200468214
NM_001135659.2(NRXN1):c.3132G>A (p.Lys1044=) rs201118246
NM_001135659.2(NRXN1):c.3191-10C>T rs398123573
NM_001135659.2(NRXN1):c.3223A>G (p.Thr1075Ala) rs753262049
NM_001135659.2(NRXN1):c.3249A>G (p.Val1083=) rs200698497
NM_001135659.2(NRXN1):c.3285A>G (p.Ser1095=) rs1553656447
NM_001135659.2(NRXN1):c.3365-2A>G rs886042846
NM_001135659.2(NRXN1):c.3523A>G (p.Ile1175Val) rs765360600
NM_001135659.2(NRXN1):c.3619C>T (p.Arg1207Ter) rs199546979
NM_001135659.2(NRXN1):c.4131G>C (p.Glu1377Asp) rs200935246
NM_001135659.2(NRXN1):c.498G>A (p.Ala166=) rs201212909
NM_001135659.2(NRXN1):c.518C>G (p.Ser173Trp) rs775907305
NM_001135659.2(NRXN1):c.588C>A (p.Pro196=) rs201644834
NM_001135659.2(NRXN1):c.609G>C (p.Lys203Asn) rs759842391
NM_001135659.2(NRXN1):c.609_610delinsCA (p.Lys203_Leu204delinsAsnMet) rs886042534
NM_001135659.2(NRXN1):c.610C>A (p.Leu204Met) rs777133701
NM_001135659.2(NRXN1):c.880A>G (p.Asn294Asp) rs781179797
NM_001135659.2(NRXN1):c.881A>G (p.Asn294Ser) rs141903943
NM_001135659.2(NRXN1):c.981C>T (p.Tyr327=) rs200464704
NM_001330078.2(NRXN1):c.105C>A (p.Gly35=) rs55640811
NM_001330078.2(NRXN1):c.1285C>T (p.Pro429Ser) rs78540316
NM_001330078.2(NRXN1):c.1365T>C (p.Leu455=) rs201727684
NM_001330078.2(NRXN1):c.1688T>C (p.Ile563Thr) rs201837579
NM_001330078.2(NRXN1):c.1700T>G (p.Leu567Trp) rs372311299
NM_001330078.2(NRXN1):c.1760-16C>T rs79422704
NM_001330078.2(NRXN1):c.1843C>T (p.Leu615=) rs201029409
NM_001330078.2(NRXN1):c.1945A>G (p.Ile649Val) rs200074974
NM_001330078.2(NRXN1):c.1969C>T (p.Arg657Trp) rs200844126
NM_001330078.2(NRXN1):c.2122C>A (p.Leu708Ile) rs56086732
NM_001330078.2(NRXN1):c.222C>T (p.Gly74=) rs201592993
NM_001330078.2(NRXN1):c.2332C>A (p.Leu778Met) rs374942732
NM_001330078.2(NRXN1):c.2385C>G (p.Pro795=) rs147984237
NM_001330078.2(NRXN1):c.2421C>T (p.Asn807=) rs115211871
NM_001330078.2(NRXN1):c.2459G>A (p.Ser820Asn) rs80293130
NM_001330078.2(NRXN1):c.24C>T (p.Arg8=) rs200113281
NM_001330078.2(NRXN1):c.2502A>G (p.Gln834=) rs770632900
NM_001330078.2(NRXN1):c.2533C>T (p.His845Tyr) rs199784139
NM_001330078.2(NRXN1):c.2567G>A (p.Arg856Gln) rs200249774
NM_001330078.2(NRXN1):c.2605C>A (p.Leu869Met) rs201818223
NM_001330078.2(NRXN1):c.270G>T (p.Gln90His) rs199960045
NM_001330078.2(NRXN1):c.2772C>T (p.Tyr924=) rs200182626
NM_001330078.2(NRXN1):c.3042C>T (p.Thr1014=) rs75137449
NM_001330078.2(NRXN1):c.3045C>T (p.Ala1015=) rs56402642
NM_001330078.2(NRXN1):c.322C>T (p.Pro108Ser) rs199784029
NM_001330078.2(NRXN1):c.3245-4G>T rs1057520338
NM_001330078.2(NRXN1):c.3307G>T (p.Asp1103Tyr) rs1295880908
NM_001330078.2(NRXN1):c.3364+20T>C rs3213756
NM_001330078.2(NRXN1):c.3364+3A>G rs762891600
NM_001330078.2(NRXN1):c.3365-109930G>T rs13413205
NM_001330078.2(NRXN1):c.3489C>T (p.Ala1163=) rs147580960
NM_001330078.2(NRXN1):c.3933A>G (p.Ala1311=) rs79970751
NM_001330078.2(NRXN1):c.4254A>G (p.Pro1418=) rs55923848
NM_001330078.2(NRXN1):c.4473G>A (p.Ala1491=) rs113380721
NM_001330078.2(NRXN1):c.501C>G (p.Leu167=) rs200248561
NM_001330078.2(NRXN1):c.511C>T (p.Leu171=) rs1045874
NM_001330078.2(NRXN1):c.569A>G (p.Asn190Ser) rs200792504
NM_001330078.2(NRXN1):c.744C>T (p.Thr248=)
NM_001330078.2(NRXN1):c.752G>A (p.Arg251His) rs780954241
NM_001330078.2(NRXN1):c.772+1043C>G rs1179583246
NM_001330078.2(NRXN1):c.772+1078A>G rs144049982
NM_001330078.2(NRXN1):c.779A>G (p.Asn260Ser)
NM_001330078.2(NRXN1):c.900C>T (p.Pro300=) rs2303298
NM_138735.4(NRXN1):c.49GGC[11] (p.Gly17[11]) rs750165040
NM_138735.4(NRXN1):c.49GGC[7] (p.Gly17[7]) rs750165040
NM_138735.4(NRXN1):c.49[5] (p.Gly17[5]) rs750165040

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.