ClinVar Miner

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

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Total variants: 54
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HGVS dbSNP
NM_144573.3(NEXN):c.-10T>C rs727505219
NM_144573.3(NEXN):c.1053+1G>A rs397517843
NM_144573.3(NEXN):c.1108A>G (p.Thr370Ala) rs1557988169
NM_144573.3(NEXN):c.1112C>T (p.Pro371Leu) rs200067011
NM_144573.3(NEXN):c.1174C>T (p.Arg392Ter) rs750076188
NM_144573.3(NEXN):c.1179_1180AG[1] (p.Glu394fs) rs727504874
NM_144573.3(NEXN):c.1190G>A (p.Arg397Gln) rs201806320
NM_144573.3(NEXN):c.1234A>G (p.Arg412Gly) rs768693715
NM_144573.3(NEXN):c.1252-10T>G rs201019553
NM_144573.3(NEXN):c.1366G>A (p.Gly456Arg) rs397517844
NM_144573.3(NEXN):c.1401_1403AGA[2] (p.Glu470del) rs397517846
NM_144573.3(NEXN):c.1415C>G (p.Ala472Gly) rs539665448
NM_144573.3(NEXN):c.1416_1418AAG[1] (p.Arg475del) rs794729091
NM_144573.3(NEXN):c.1430T>G (p.Ile477Ser) rs727504658
NM_144573.3(NEXN):c.1435C>T (p.Leu479Phe) rs181520023
NM_144573.3(NEXN):c.1453G>A (p.Glu485Lys) rs368812830
NM_144573.3(NEXN):c.1457C>G (p.Ala486Gly) rs397517847
NM_144573.3(NEXN):c.1528A>G (p.Lys510Glu) rs727504758
NM_144573.3(NEXN):c.1573_1575GAA[3] (p.Glu528del) rs764505909
NM_144573.3(NEXN):c.1609_1610insA (p.Leu537fs) rs779350415
NM_144573.3(NEXN):c.1660-11_1660-7del rs727503344
NM_144573.3(NEXN):c.1671_1673GGA[2] (p.Glu561_Glu562del) rs397517848
NM_144573.3(NEXN):c.1671_1673GGA[5] (p.Glu562dup) rs397517848
NM_144573.3(NEXN):c.1753_1755AAG[1] (p.Lys586del) rs397517851
NM_144573.3(NEXN):c.1788T>G (p.Ser596Arg) rs199738750
NM_144573.3(NEXN):c.1820_1822del (p.Gly607del) rs876657928
NM_144573.3(NEXN):c.1935C>G (p.Phe645Leu) rs794729086
NM_144573.3(NEXN):c.1937C>A (p.Pro646Gln) rs397517852
NM_144573.3(NEXN):c.1946_1948GAG[1] (p.Gly650del) rs397517853
NM_144573.3(NEXN):c.1955A>G (p.Tyr652Cys) rs137853197
NM_144573.3(NEXN):c.1981G>A (p.Gly661Arg) rs876657929
NM_144573.3(NEXN):c.1996A>G (p.Thr666Ala) rs374000722
NM_144573.3(NEXN):c.2015A>G (p.Glu672Gly) rs876657930
NM_144573.3(NEXN):c.2026_*1del rs794729094
NM_144573.3(NEXN):c.220A>C (p.Ile74Leu) rs727503342
NM_144573.3(NEXN):c.249G>C (p.Glu83Asp) rs372532824
NM_144573.3(NEXN):c.299-3T>C rs397517856
NM_144573.3(NEXN):c.341_342del (p.Gln114fs) rs397517857
NM_144573.3(NEXN):c.379C>T (p.Arg127Cys) rs771113424
NM_144573.3(NEXN):c.392A>G (p.Gln131Arg) rs397517858
NM_144573.3(NEXN):c.447+5C>T rs727503343
NM_144573.3(NEXN):c.586C>T (p.Arg196Cys) rs369486891
NM_144573.3(NEXN):c.613G>A (p.Glu205Lys) rs201447781
NM_144573.3(NEXN):c.65A>G (p.Tyr22Cys) rs1057518512
NM_144573.3(NEXN):c.677del (p.Ser226fs) rs397517859
NM_144573.3(NEXN):c.687+4A>T rs754061340
NM_144573.3(NEXN):c.836G>A (p.Arg279His) rs750349053
NM_144573.3(NEXN):c.856C>T (p.Arg286Trp) rs199917913
NM_144573.3(NEXN):c.864G>T (p.Met288Ile) rs371666396
NM_144573.3(NEXN):c.865-5G>A rs727505353
NM_144573.3(NEXN):c.86G>T (p.Gly29Val) rs876657931
NM_144573.3(NEXN):c.893C>G (p.Thr298Arg) rs200753280
NM_144573.3(NEXN):c.989_991AAG[2] (p.Glu332del) rs727505124
NM_144573.3(NEXN):c.995A>C (p.Glu332Ala) rs201763096

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