ClinVar Miner

List of variants in gene NRXN1 reported as benign for not specified

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Gene type:
ClinVar version:
Total variants: 60
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HGVS dbSNP
NM_001135659.2(NRXN1):c.*18G>C rs201303041
NM_001135659.2(NRXN1):c.-28A>C rs796052760
NM_001135659.2(NRXN1):c.1233+8C>T rs200448187
NM_001135659.2(NRXN1):c.2157G>A (p.Pro719=) rs199714221
NM_001135659.2(NRXN1):c.2313C>T (p.Leu771=) rs201466898
NM_001135659.2(NRXN1):c.2394C>A (p.Thr798=) rs78030925
NM_001135659.2(NRXN1):c.261C>A (p.Gly87=) rs587781102
NM_001135659.2(NRXN1):c.2850G>A (p.Lys950=) rs192909520
NM_001135659.2(NRXN1):c.3249A>G (p.Val1083=) rs200698497
NM_001135659.2(NRXN1):c.324G>A (p.Pro108=) rs199595253
NM_001135659.2(NRXN1):c.3485-109893G>A rs546558752
NM_001135659.2(NRXN1):c.4336+17T>A rs200836763
NM_001135659.2(NRXN1):c.4356C>T (p.Gly1452=) rs587781101
NM_001135659.2(NRXN1):c.4458T>C (p.Leu1486=) rs796052759
NM_001135659.2(NRXN1):c.498G>A (p.Ala166=) rs201212909
NM_001135659.2(NRXN1):c.981C>T (p.Tyr327=) rs200464704
NM_001330078.2(NRXN1):c.-21C>A rs576405440
NM_001330078.2(NRXN1):c.-34C>A rs200335720
NM_001330078.2(NRXN1):c.-922+7A>C rs200115353
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.1575A>G (p.Arg525=) rs201941844
NM_001330078.2(NRXN1):c.1760-16C>T rs79422704
NM_001330078.2(NRXN1):c.1833T>C (p.Asp611=) rs190377845
NM_001330078.2(NRXN1):c.2109C>T (p.Ser703=) rs200456688
NM_001330078.2(NRXN1):c.2122C>A (p.Leu708Ile) rs56086732
NM_001330078.2(NRXN1):c.2143+19A>G rs150513096
NM_001330078.2(NRXN1):c.222C>T (p.Gly74=) rs201592993
NM_001330078.2(NRXN1):c.2347+18C>A rs150460414
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.2772C>T (p.Tyr924=) rs200182626
NM_001330078.2(NRXN1):c.2879+20A>G rs200986624
NM_001330078.2(NRXN1):c.3045C>T (p.Ala1015=) rs56402642
NM_001330078.2(NRXN1):c.3090A>C (p.Gly1030=) rs201886024
NM_001330078.2(NRXN1):c.3201C>T (p.Ser1067=) rs75275592
NM_001330078.2(NRXN1):c.3249C>T (p.Pro1083=) rs116236999
NM_001330078.2(NRXN1):c.3364+20T>C rs3213756
NM_001330078.2(NRXN1):c.3365-109703A>T rs199700602
NM_001330078.2(NRXN1):c.3365-109709A>G rs13023114
NM_001330078.2(NRXN1):c.3365-109830G>A rs148517834
NM_001330078.2(NRXN1):c.3365-109930G>T rs13413205
NM_001330078.2(NRXN1):c.3408G>A (p.Thr1136=) rs80094872
NM_001330078.2(NRXN1):c.3933A>G (p.Ala1311=) rs79970751
NM_001330078.2(NRXN1):c.4068G>A (p.Thr1356=) rs74714098
NM_001330078.2(NRXN1):c.4217-13C>T rs376269786
NM_001330078.2(NRXN1):c.4217-16A>C rs74520052
NM_001330078.2(NRXN1):c.4254A>G (p.Pro1418=) rs55923848
NM_001330078.2(NRXN1):c.4275G>T (p.Arg1425=) rs143495349
NM_001330078.2(NRXN1):c.4392T>C (p.His1464=) rs112536447
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.772+1015C>A rs200375396
NM_001330078.2(NRXN1):c.772+1140G>A rs61658382
NM_001330078.2(NRXN1):c.798G>A (p.Ala266=) rs201027928
NM_001330078.2(NRXN1):c.900C>T (p.Pro300=) rs2303298
NM_138735.4(NRXN1):c.49GGC[7] (p.Gly17[7]) rs750165040
NM_138735.4(NRXN1):c.49[5] (p.Gly17[5]) rs750165040

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