ClinVar Miner

List of variants in gene NEXN reported as likely benign by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 73
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HGVS dbSNP gnomAD frequency
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.777A>G (p.Gln259=) rs375544798 0.00077
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.1029G>A (p.Ala343=) rs374260457 0.00023
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.1582G>C (p.Glu528Gln) rs200071700 0.00011
NM_144573.4(NEXN):c.856C>T (p.Arg286Trp) rs199917913 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.222T>C (p.Ile74=) rs767610015 0.00005
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.1450C>A (p.Arg484=) rs767792289 0.00004
NM_144573.4(NEXN):c.249G>A (p.Glu83=) rs372532824 0.00004
NM_144573.4(NEXN):c.739T>C (p.Leu247=) rs781118443 0.00004
NM_144573.4(NEXN):c.1368A>C (p.Gly456=) rs397517845 0.00002
NM_144573.4(NEXN):c.1651C>T (p.Leu551=) rs1346328853 0.00002
NM_144573.4(NEXN):c.507A>G (p.Leu169=) rs776106290 0.00002
NM_144573.4(NEXN):c.1266T>C (p.Asn422=) rs1200707526 0.00001
NM_144573.4(NEXN):c.1332A>G (p.Gln444=) rs1385609119 0.00001
NM_144573.4(NEXN):c.1419A>G (p.Arg473=) rs140900323 0.00001
NM_144573.4(NEXN):c.141A>G (p.Gln47=) rs1459232585 0.00001
NM_144573.4(NEXN):c.1489G>A (p.Val497Ile) rs778330292 0.00001
NM_144573.4(NEXN):c.1605A>G (p.Gln535=) rs778477679 0.00001
NM_144573.4(NEXN):c.1653A>G (p.Leu551=) rs794727078 0.00001
NM_144573.4(NEXN):c.1731C>G (p.Thr577=) rs371743669 0.00001
NM_144573.4(NEXN):c.237T>C (p.Ala79=) rs727504549 0.00001
NM_144573.4(NEXN):c.456C>T (p.Asp152=) rs760312569 0.00001
NM_144573.4(NEXN):c.579A>G (p.Glu193=) rs1476054611 0.00001
NM_144573.4(NEXN):c.66T>C (p.Tyr22=) rs749182975 0.00001
NM_144573.4(NEXN):c.711A>C (p.Ala237=) rs754009978 0.00001
NM_144573.4(NEXN):c.987A>C (p.Ala329=) rs1270187994 0.00001
NM_144573.4(NEXN):c.108A>G (p.Glu36=)
NM_144573.4(NEXN):c.1113G>A (p.Pro371=)
NM_144573.4(NEXN):c.1252-5dup rs768326968
NM_144573.4(NEXN):c.1275T>C (p.Phe425=) rs759257757
NM_144573.4(NEXN):c.1342C>T (p.Leu448=)
NM_144573.4(NEXN):c.1416AAG[1] (p.Arg475del) rs794729091
NM_144573.4(NEXN):c.1431T>C (p.Ile477=)
NM_144573.4(NEXN):c.1491T>C (p.Val497=)
NM_144573.4(NEXN):c.1533G>A (p.Val511=)
NM_144573.4(NEXN):c.1611A>G (p.Leu537=)
NM_144573.4(NEXN):c.1671GGA[2] (p.Glu561_Glu562del) rs397517848
NM_144573.4(NEXN):c.1671GGA[3] (p.Glu562del) rs397517848
NM_144573.4(NEXN):c.1677G>A (p.Glu559=)
NM_144573.4(NEXN):c.1680G>A (p.Glu560=)
NM_144573.4(NEXN):c.1704C>G (p.Gly568=) rs397517850
NM_144573.4(NEXN):c.1719T>C (p.Asp573=)
NM_144573.4(NEXN):c.1737A>G (p.Ser579=)
NM_144573.4(NEXN):c.1773A>G (p.Thr591=) rs727503345
NM_144573.4(NEXN):c.1839T>A (p.Ile613=)
NM_144573.4(NEXN):c.1887A>G (p.Gln629=) rs727503346
NM_144573.4(NEXN):c.1921T>C (p.Leu641=) rs1321925816
NM_144573.4(NEXN):c.1950A>G (p.Gly650=) rs2102182136
NM_144573.4(NEXN):c.1965A>G (p.Lys655=)
NM_144573.4(NEXN):c.2010C>A (p.Thr670=)
NM_144573.4(NEXN):c.246T>C (p.Asp82=)
NM_144573.4(NEXN):c.255T>G (p.Asp85Glu)
NM_144573.4(NEXN):c.45T>C (p.Ser15=)
NM_144573.4(NEXN):c.522A>C (p.Val174=)
NM_144573.4(NEXN):c.561G>A (p.Lys187=)
NM_144573.4(NEXN):c.616G>A (p.Glu206Lys) rs370428679
NM_144573.4(NEXN):c.651A>G (p.Pro217=)
NM_144573.4(NEXN):c.711A>G (p.Ala237=)
NM_144573.4(NEXN):c.732C>T (p.Pro244=) rs201171783
NM_144573.4(NEXN):c.816A>G (p.Lys272=)
NM_144573.4(NEXN):c.820T>C (p.Leu274=)
NM_144573.4(NEXN):c.989AAG[2] (p.Glu332del) rs727505124
NM_144573.4(NEXN):c.996A>G (p.Glu332=)

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