ClinVar Miner

List of variants in gene NEXN reported by GeneDx

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Gene type:
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Total variants: 104
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HGVS dbSNP
NC_000001.11:g.77935818dup
NM_144573.3(NEXN):c.-34C>A rs758434911
NM_144573.3(NEXN):c.-43T>A rs765499984
NM_144573.3(NEXN):c.-52-16T>C rs557864364
NM_144573.3(NEXN):c.-52-4delT rs972673849
NM_144573.3(NEXN):c.-58T>C rs587781100
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.1029G>A (p.Ala343=) rs374260457
NM_144573.3(NEXN):c.1042A>C (p.Arg348=) rs752036618
NM_144573.3(NEXN):c.1053+128T>C
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.1251+43C>G
NM_144573.3(NEXN):c.1251+48T>C
NM_144573.3(NEXN):c.1252-10T>G rs201019553
NM_144573.3(NEXN):c.1252-11T>G rs781115798
NM_144573.3(NEXN):c.1252-13A>C rs372603998
NM_144573.3(NEXN):c.1252-16T>C rs915475936
NM_144573.3(NEXN):c.1252-16_1252-12delTTAATinsA rs1064796194
NM_144573.3(NEXN):c.1252-20C>A rs776869661
NM_144573.3(NEXN):c.1252-301T>C
NM_144573.3(NEXN):c.1271C>T (p.Thr424Ile) rs200442502
NM_144573.3(NEXN):c.1275T>C (p.Phe425=) rs759257757
NM_144573.3(NEXN):c.1408G>C (p.Glu470Gln) rs35366555
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.1445_1446del (p.Lys482fs) rs794729092
NM_144573.3(NEXN):c.1471G>C (p.Glu491Gln) rs373057251
NM_144573.3(NEXN):c.1473+15T>C rs757028785
NM_144573.3(NEXN):c.1474-10T>C rs374541562
NM_144573.3(NEXN):c.1478_1480ATG[1] (p.Asp494del) rs1064796362
NM_144573.3(NEXN):c.1488T>C (p.Asp496=) rs754485056
NM_144573.3(NEXN):c.156C>T (p.Asp52=) rs371431782
NM_144573.3(NEXN):c.1573_1575GAA[3] (p.Glu528del) rs764505909
NM_144573.3(NEXN):c.1582G>C (p.Glu528Gln) rs200071700
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.1618A>G (p.Met540Val) rs201390657
NM_144573.3(NEXN):c.1640T>C (p.Ile547Thr) rs753636624
NM_144573.3(NEXN):c.1659+18C>G rs147422621
NM_144573.3(NEXN):c.1671_1673GGA[2] (p.Glu561_Glu562del) rs397517848
NM_144573.3(NEXN):c.1671_1673GGA[3] (p.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.1785C>T (p.Asp595=) rs182998780
NM_144573.3(NEXN):c.1805C>T (p.Thr602Met) rs756709134
NM_144573.3(NEXN):c.1806G>A (p.Thr602=) rs373102543
NM_144573.3(NEXN):c.1820_1822del (p.Gly607del) rs876657928
NM_144573.3(NEXN):c.1887A>G (p.Gln629=) rs727503346
NM_144573.3(NEXN):c.1890T>C (p.Tyr630=) rs1057523025
NM_144573.3(NEXN):c.1911C>A (p.Tyr637Ter) rs772833406
NM_144573.3(NEXN):c.1935C>G (p.Phe645Leu) rs794729086
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.219+25G>A
NM_144573.3(NEXN):c.220-6A>G rs374762720
NM_144573.3(NEXN):c.242A>T (p.Asp81Val) rs367871780
NM_144573.3(NEXN):c.249G>A (p.Glu83=) rs372532824
NM_144573.3(NEXN):c.27+200T>C
NM_144573.3(NEXN):c.27+220A>C
NM_144573.3(NEXN):c.299-14T>C rs921990698
NM_144573.3(NEXN):c.363G>A (p.Thr121=) rs35117963
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.447+105A>G
NM_144573.3(NEXN):c.450T>A (p.Ile150=) rs1064797051
NM_144573.3(NEXN):c.461_464del (p.Asn154fs) rs794729088
NM_144573.3(NEXN):c.468G>A (p.Thr156=) rs199988442
NM_144573.3(NEXN):c.483A>C (p.Ala161=)
NM_144573.3(NEXN):c.512T>C (p.Ile171Thr) rs372065024
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+19_687+22delGTTT rs768486390
NM_144573.3(NEXN):c.687+20delT rs141957231
NM_144573.3(NEXN):c.687+4A>T rs754061340
NM_144573.3(NEXN):c.688-10G>A rs370574269
NM_144573.3(NEXN):c.732C>A (p.Pro244=) rs201171783
NM_144573.3(NEXN):c.733G>A (p.Gly245Arg) rs1166698
NM_144573.3(NEXN):c.777A>G (p.Gln259=) rs375544798
NM_144573.3(NEXN):c.78T>C (p.Leu26=) rs376535223
NM_144573.3(NEXN):c.835C>T (p.Arg279Cys) rs146245480
NM_144573.3(NEXN):c.856C>T (p.Arg286Trp) rs199917913
NM_144573.3(NEXN):c.864+12T>A rs188416492
NM_144573.3(NEXN):c.864+231A>G
NM_144573.3(NEXN):c.864+290C>T
NM_144573.3(NEXN):c.864+294A>G
NM_144573.3(NEXN):c.865-5G>A rs727505353
NM_144573.3(NEXN):c.874G>A (p.Asp292Asn) rs373377525
NM_144573.3(NEXN):c.893C>G (p.Thr298Arg) rs200753280
NM_144573.3(NEXN):c.949A>C (p.Met317Leu) rs559464457
NM_144573.3(NEXN):c.995A>C (p.Glu332Ala) rs201763096

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