ClinVar Miner

List of variants in gene NRXN1 reported as uncertain significance for not specified

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Gene type:
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Total variants: 53
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HGVS dbSNP gnomAD frequency
NM_001330078.2(NRXN1):c.1575A>G (p.Arg525=) rs201941844 0.00155
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.569A>G (p.Asn190Ser) rs200792504 0.00074
NM_001330078.2(NRXN1):c.2533C>T (p.His845Tyr) rs199784139 0.00064
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.4167C>G (p.Pro1389=) rs143446587 0.00053
NM_001330078.2(NRXN1):c.2605C>A (p.Leu869Met) rs201818223 0.00044
NM_001330078.2(NRXN1):c.2190G>T (p.Gln730His) rs199978276 0.00025
NM_001330078.2(NRXN1):c.320C>T (p.Thr107Met) rs368549770 0.00016
NM_001330078.2(NRXN1):c.2036C>T (p.Pro679Leu) rs201735573 0.00014
NM_001330078.2(NRXN1):c.2459G>A (p.Ser820Asn) rs80293130 0.00013
NM_001330078.2(NRXN1):c.749T>A (p.Phe250Tyr) rs200646155 0.00010
NM_001330078.2(NRXN1):c.847A>G (p.Ile283Val) rs748218169 0.00007
NM_001330078.2(NRXN1):c.1749C>T (p.Asp583=) rs199934259 0.00006
NM_001330078.2(NRXN1):c.4004C>T (p.Thr1335Ile) rs200672080 0.00006
NM_001330078.2(NRXN1):c.4248G>A (p.Pro1416=) rs151195816 0.00006
NM_001330078.2(NRXN1):c.3675G>A (p.Thr1225=) rs200179221 0.00004
NM_001330078.2(NRXN1):c.4236C>T (p.Gly1412=) rs587781101 0.00004
NM_001330078.2(NRXN1):c.4237G>A (p.Gly1413Ser) rs200604893 0.00004
NM_001330078.2(NRXN1):c.782A>G (p.Asn261Ser) rs141903943 0.00004
NM_001330078.2(NRXN1):c.338C>T (p.Ala113Val) rs201542547 0.00003
NM_001330078.2(NRXN1):c.2497+3A>G rs202074070 0.00002
NM_001330078.2(NRXN1):c.3616A>G (p.Ile1206Val) rs751778015 0.00002
NM_001330078.2(NRXN1):c.1296C>T (p.Asn432=) rs1259694734 0.00001
NM_001330078.2(NRXN1):c.1361G>A (p.Arg454Gln) rs199592328 0.00001
NM_001330078.2(NRXN1):c.2075G>A (p.Arg692Lys) rs797045796 0.00001
NM_001330078.2(NRXN1):c.3365-109977G>A rs1057517946 0.00001
NM_001330078.2(NRXN1):c.668G>A (p.Gly223Asp) rs200490872 0.00001
NM_001330078.2(NRXN1):c.772+1024C>G rs199645252 0.00001
NM_001330078.2(NRXN1):c.859A>C (p.Lys287Gln) rs1257232783 0.00001
GRCh37/hg19 2p16.3(chr2:50130766-50170284)x3
GRCh37/hg19 2p16.3(chr2:51181652-51343169)
NM_001330078.2(NRXN1):c.*18G>A
NM_001330078.2(NRXN1):c.1400_1401inv (p.Gly467Val)
NM_001330078.2(NRXN1):c.1424A>C (p.Asn475Thr) rs751754721
NM_001330078.2(NRXN1):c.150C>G (p.Cys50Trp) rs1057518563
NM_001330078.2(NRXN1):c.1592A>G (p.Lys531Arg) rs796052769
NM_001330078.2(NRXN1):c.1648C>G (p.Leu550Val) rs1295091945
NM_001330078.2(NRXN1):c.2044A>G (p.Ser682Gly) rs2105259007
NM_001330078.2(NRXN1):c.2507C>T (p.Ala836Val) rs199557987
NM_001330078.2(NRXN1):c.2537A>C (p.Asn846Thr) rs797045797
NM_001330078.2(NRXN1):c.2827C>A (p.Leu943Ile) rs864309567
NM_001330078.2(NRXN1):c.2843A>G (p.Asp948Gly) rs1057518283
NM_001330078.2(NRXN1):c.2953G>A (p.Asp985Asn) rs1553698631
NM_001330078.2(NRXN1):c.316G>A (p.Asp106Asn) rs200576486
NM_001330078.2(NRXN1):c.3618C>T (p.Ile1206=) rs1573859191
NM_001330078.2(NRXN1):c.4173_4188delinsGTGTCCCTAA (p.Asp1391_Asp1396delinsGluCysProTer) rs1553400438
NM_001330078.2(NRXN1):c.4494_4496del (p.Lys1499del) rs796052785
NM_001330078.2(NRXN1):c.637G>A (p.Gly213Arg) rs199561088
NM_001330078.2(NRXN1):c.656_664dup (p.Ala219_Glu221dup) rs546508545
NM_001330078.2(NRXN1):c.772+9del rs755130575

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