ClinVar Miner

List of variants in gene NEXN reported as uncertain significance by GeneDx

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Gene type:
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Total variants: 44
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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.1053+1G>A rs397517843
NM_144573.3(NEXN):c.1094C>G (p.Ser365Cys) rs772491358
NM_144573.3(NEXN):c.1112C>T (p.Pro371Leu) rs200067011
NM_144573.3(NEXN):c.1252-10T>G rs201019553
NM_144573.3(NEXN):c.1252-11T>G rs781115798
NM_144573.3(NEXN):c.1271C>T (p.Thr424Ile) rs200442502
NM_144573.3(NEXN):c.1416_1418AAG[1] (p.Arg475del) rs794729091
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.1478_1480ATG[1] (p.Asp494del) rs1064796362
NM_144573.3(NEXN):c.1573_1575GAA[3] (p.Glu528del) rs764505909
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.1671_1673GGA[2] (p.Glu561_Glu562del) rs397517848
NM_144573.3(NEXN):c.1671_1673GGA[5] (p.Glu562dup) rs397517848
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.1946_1948GAG[1] (p.Gly650del) rs397517853
NM_144573.3(NEXN):c.1955A>G (p.Tyr652Cys) rs137853197
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.2026_*1del rs794729094
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.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.613G>A (p.Glu205Lys) rs201447781
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.65A>G (p.Tyr22Cys) rs1057518512
NM_144573.3(NEXN):c.680T>C (p.Leu227Ser) rs756273801
NM_144573.3(NEXN):c.687+4A>T rs754061340
NM_144573.3(NEXN):c.856C>T (p.Arg286Trp) rs199917913
NM_144573.3(NEXN):c.874G>A (p.Asp292Asn) rs373377525

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