ClinVar Miner

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

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Gene type:
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Total variants: 53
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HGVS dbSNP
NM_144573.3(NEXN):c.1002_1004del (p.Arg336del) rs794729090
NM_144573.3(NEXN):c.1010T>C (p.Ile337Thr) rs749553777
NM_144573.3(NEXN):c.1028C>T (p.Ala343Val) rs769073940
NM_144573.3(NEXN):c.1094C>G (p.Ser365Cys) rs772491358
NM_144573.3(NEXN):c.1252-11T>G rs781115798
NM_144573.3(NEXN):c.1271C>T (p.Thr424Ile) rs200442502
NM_144573.3(NEXN):c.1435C>T (p.Leu479Phe) rs181520023
NM_144573.3(NEXN):c.1471G>C (p.Glu491Gln) rs373057251
NM_144573.3(NEXN):c.157G>A (p.Glu53Lys) rs373778361
NM_144573.3(NEXN):c.1595T>C (p.Ile532Thr) rs754656961
NM_144573.3(NEXN):c.1615C>T (p.Arg539Cys) rs373680705
NM_144573.3(NEXN):c.1640T>C (p.Ile547Thr) rs753636624
NM_144573.3(NEXN):c.1653A>G (p.Leu551=) rs794727078
NM_144573.3(NEXN):c.1684G>C (p.Glu562Gln) rs794729085
NM_144573.3(NEXN):c.1733G>C (p.Arg578Thr) rs374878979
NM_144573.3(NEXN):c.1784A>G (p.Asp595Gly) rs1131691984
NM_144573.3(NEXN):c.1805C>T (p.Thr602Met) rs756709134
NM_144573.3(NEXN):c.1820_1822del (p.Gly607del) rs876657928
NM_144573.3(NEXN):c.1911C>A (p.Tyr637Ter) rs772833406
NM_144573.3(NEXN):c.1918_1922del (p.Tyr640fs) rs1222794437
NM_144573.3(NEXN):c.1997C>A (p.Thr666Asn) rs749271412
NM_144573.3(NEXN):c.2000G>A (p.Cys667Tyr) rs794729087
NM_144573.3(NEXN):c.2005C>T (p.Leu669Phe) rs774194309
NM_144573.3(NEXN):c.242A>T (p.Asp81Val) rs367871780
NM_144573.3(NEXN):c.370G>A (p.Glu124Lys) rs372745590
NM_144573.3(NEXN):c.380G>A (p.Arg127His) rs776891268
NM_144573.3(NEXN):c.442G>A (p.Glu148Lys) rs794729082
NM_144573.3(NEXN):c.450T>A (p.Ile150=) rs1064797051
NM_144573.3(NEXN):c.542C>A (p.Thr181Lys) rs764640427
NM_144573.3(NEXN):c.571del (p.Asp191fs) rs794729089
NM_144573.3(NEXN):c.62C>T (p.Thr21Ile) rs794729081
NM_144573.3(NEXN):c.64T>A (p.Tyr22Asn) rs1553236590
NM_144573.3(NEXN):c.680T>C (p.Leu227Ser) rs756273801
NM_144573.3(NEXN):c.874G>A (p.Asp292Asn) rs373377525
NM_144573.3(NEXN):c.906T>A (p.Phe302Leu) rs767740199
NM_144573.4(NEXN):c.1053+1G>A rs397517843
NM_144573.4(NEXN):c.1112C>T (p.Pro371Leu) rs200067011
NM_144573.4(NEXN):c.1174C>T (p.Arg392Ter) rs750076188
NM_144573.4(NEXN):c.1252-5del rs768326968
NM_144573.4(NEXN):c.1401AGA[2] (p.Glu470del) rs397517846
NM_144573.4(NEXN):c.1453G>A (p.Glu485Lys) rs368812830
NM_144573.4(NEXN):c.1478ATG[1] (p.Asp494del) rs1064796362
NM_144573.4(NEXN):c.1573GAA[3] (p.Glu528del) rs764505909
NM_144573.4(NEXN):c.1609_1610insA (p.Leu537fs) rs779350415
NM_144573.4(NEXN):c.1671GGA[2] (p.Glu561_Glu562del) rs397517848
NM_144573.4(NEXN):c.1671GGA[5] (p.Glu562dup) rs397517848
NM_144573.4(NEXN):c.1751_1757del (p.Phe584fs)
NM_144573.4(NEXN):c.1788T>G (p.Ser596Arg) rs199738750
NM_144573.4(NEXN):c.1946GAG[1] (p.Gly650del) rs397517853
NM_144573.4(NEXN):c.1955A>G (p.Tyr652Cys) rs137853197
NM_144573.4(NEXN):c.249G>A (p.Glu83=) rs372532824
NM_144573.4(NEXN):c.511dup (p.Ile171fs)
NM_144573.4(NEXN):c.613G>A (p.Glu205Lys) rs201447781

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