ClinVar Miner

List of variants in gene NEXN studied for not specified

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Gene type:
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Total variants: 95
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HGVS dbSNP gnomAD frequency
NM_144573.4(NEXN):c.733G>A (p.Gly245Arg) rs1166698 0.15380
NM_144573.4(NEXN):c.1408G>C (p.Glu470Gln) rs35366555 0.00302
NM_144573.4(NEXN):c.995A>C (p.Glu332Ala) rs201763096 0.00262
NM_144573.4(NEXN):c.1659+18C>G rs147422621 0.00228
NM_144573.4(NEXN):c.864+12T>A rs188416492 0.00141
NM_144573.4(NEXN):c.156C>T (p.Asp52=) rs371431782 0.00128
NM_144573.4(NEXN):c.1618A>G (p.Met540Val) rs201390657 0.00113
NM_144573.4(NEXN):c.1252-10T>G rs201019553 0.00088
NM_144573.4(NEXN):c.777A>G (p.Gln259=) rs375544798 0.00077
NM_144573.4(NEXN):c.-52-16T>C rs557864364 0.00047
NM_144573.4(NEXN):c.732C>A (p.Pro244=) rs201171783 0.00045
NM_144573.4(NEXN):c.1785C>T (p.Asp595=) rs182998780 0.00041
NM_144573.4(NEXN):c.512T>C (p.Ile171Thr) rs372065024 0.00035
NM_144573.4(NEXN):c.613G>A (p.Glu205Lys) rs201447781 0.00034
NM_144573.4(NEXN):c.-58T>C rs587781100 0.00030
NM_144573.4(NEXN):c.1788T>G (p.Ser596Arg) rs199738750 0.00029
NM_144573.4(NEXN):c.242A>T (p.Asp81Val) rs367871780 0.00028
NM_144573.4(NEXN):c.835C>T (p.Arg279Cys) rs146245480 0.00025
NM_144573.4(NEXN):c.1029G>A (p.Ala343=) rs374260457 0.00023
NM_144573.4(NEXN):c.865-17A>G rs201771600 0.00016
NM_144573.4(NEXN):c.893C>G (p.Thr298Arg) rs200753280 0.00016
NM_144573.4(NEXN):c.1806G>A (p.Thr602=) rs373102543 0.00014
NM_144573.4(NEXN):c.1042A>C (p.Arg348=) rs752036618 0.00011
NM_144573.4(NEXN):c.1582G>C (p.Glu528Gln) rs200071700 0.00011
NM_144573.4(NEXN):c.1955A>G (p.Tyr652Cys) rs137853197 0.00011
NM_144573.4(NEXN):c.688-10G>A rs370574269 0.00011
NM_144573.4(NEXN):c.1435C>T (p.Leu479Phe) rs181520023 0.00009
NM_144573.4(NEXN):c.949A>C (p.Met317Leu) rs559464457 0.00009
NM_144573.4(NEXN):c.1488T>C (p.Asp496=) rs754485056 0.00008
NM_144573.4(NEXN):c.78T>C (p.Leu26=) rs376535223 0.00008
NM_144573.4(NEXN):c.1190G>A (p.Arg397Gln) rs201806320 0.00007
NM_144573.4(NEXN):c.1996A>G (p.Thr666Ala) rs374000722 0.00007
NM_144573.4(NEXN):c.586C>T (p.Arg196Cys) rs369486891 0.00007
NM_144573.4(NEXN):c.1453G>A (p.Glu485Lys) rs368812830 0.00006
NM_144573.4(NEXN):c.865-5G>A rs727505353 0.00005
NM_144573.4(NEXN):c.1065T>C (p.Asp355=) rs369897647 0.00004
NM_144573.4(NEXN):c.1174C>T (p.Arg392Ter) rs750076188 0.00004
NM_144573.4(NEXN):c.1252-20C>A rs776869661 0.00004
NM_144573.4(NEXN):c.249G>A (p.Glu83=) rs372532824 0.00004
NM_144573.4(NEXN):c.836G>A (p.Arg279His) rs750349053 0.00004
NM_144573.4(NEXN):c.1053+1G>A rs397517843 0.00003
NM_144573.4(NEXN):c.468G>A (p.Thr156=) rs199988442 0.00003
NM_144573.4(NEXN):c.634T>A (p.Tyr212Asn) rs769549962 0.00003
NM_144573.4(NEXN):c.-10T>C rs727505219 0.00002
NM_144573.4(NEXN):c.1368A>C (p.Gly456=) rs397517845 0.00002
NM_144573.4(NEXN):c.1234A>G (p.Arg412Gly) rs768693715 0.00001
NM_144573.4(NEXN):c.1252-13A>C rs372603998 0.00001
NM_144573.4(NEXN):c.1252-16T>C rs915475936 0.00001
NM_144573.4(NEXN):c.1366G>A (p.Gly456Arg) rs397517844 0.00001
NM_144573.4(NEXN):c.1415C>G (p.Ala472Gly) rs539665448 0.00001
NM_144573.4(NEXN):c.1528A>G (p.Lys510Glu) rs727504758 0.00001
NM_144573.4(NEXN):c.1609_1610insA (p.Leu537fs) rs779350415 0.00001
NM_144573.4(NEXN):c.1704C>T (p.Gly568=) rs397517850 0.00001
NM_144573.4(NEXN):c.1805C>T (p.Thr602Met) rs756709134 0.00001
NM_144573.4(NEXN):c.1981G>A (p.Gly661Arg) rs876657929 0.00001
NM_144573.4(NEXN):c.220-6A>G rs374762720 0.00001
NM_144573.4(NEXN):c.237T>C (p.Ala79=) rs727504549 0.00001
NM_144573.4(NEXN):c.65A>G (p.Tyr22Cys) rs1057518512 0.00001
NM_144573.4(NEXN):c.66T>C (p.Tyr22=) rs749182975 0.00001
NM_144573.3(NEXN):c.2026_*1del rs794729094
NM_144573.4(NEXN):c.-34C>A rs758434911
NM_144573.4(NEXN):c.-43T>A rs765499984
NM_144573.4(NEXN):c.1108A>G (p.Thr370Ala) rs1557988169
NM_144573.4(NEXN):c.1112C>T (p.Pro371Leu) rs200067011
NM_144573.4(NEXN):c.1181_1182del (p.Glu394fs) rs727504874
NM_144573.4(NEXN):c.1252-16_1252-12delinsA rs1064796194
NM_144573.4(NEXN):c.1252-1G>A rs1650708891
NM_144573.4(NEXN):c.1275T>C (p.Phe425=) rs759257757
NM_144573.4(NEXN):c.1399dup (p.Ile467fs) rs1365488625
NM_144573.4(NEXN):c.1401AGA[2] (p.Glu470del) rs397517846
NM_144573.4(NEXN):c.1416AAG[1] (p.Arg475del) rs794729091
NM_144573.4(NEXN):c.1430T>G (p.Ile477Ser) rs727504658
NM_144573.4(NEXN):c.1457C>G (p.Ala486Gly) rs397517847
NM_144573.4(NEXN):c.1573GAA[3] (p.Glu528del) rs764505909
NM_144573.4(NEXN):c.1660-11_1660-7del rs727503344
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.1753AAG[1] (p.Lys586del) rs397517851
NM_144573.4(NEXN):c.1773A>G (p.Thr591=) rs727503345
NM_144573.4(NEXN):c.1814del (p.Val605fs)
NM_144573.4(NEXN):c.1820_1822del (p.Gly607del) rs876657928
NM_144573.4(NEXN):c.1887A>G (p.Gln629=) rs727503346
NM_144573.4(NEXN):c.1890T>C (p.Tyr630=) rs1057523025
NM_144573.4(NEXN):c.1935C>G (p.Phe645Leu) rs794729086
NM_144573.4(NEXN):c.1937C>A (p.Pro646Gln) rs397517852
NM_144573.4(NEXN):c.1946GAG[1] (p.Gly650del) rs397517853
NM_144573.4(NEXN):c.2015A>G (p.Glu672Gly) rs876657930
NM_144573.4(NEXN):c.220A>C (p.Ile74Leu) rs727503342
NM_144573.4(NEXN):c.249G>C (p.Glu83Asp) rs372532824
NM_144573.4(NEXN):c.677del (p.Ser226fs) rs397517859
NM_144573.4(NEXN):c.687+23del rs141957231
NM_144573.4(NEXN):c.687+8TTTG[2] rs768486390
NM_144573.4(NEXN):c.864G>T (p.Met288Ile) rs371666396
NM_144573.4(NEXN):c.86G>T (p.Gly29Val) rs876657931
NM_144573.4(NEXN):c.989AAG[2] (p.Glu332del) rs727505124

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