ClinVar Miner

List of variants in gene NEXN reported as likely benign

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Gene type:
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Total variants: 71
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HGVS dbSNP
NC_000001.11:g.77935818dup
NM_144573.3(NEXN):c.*22C>G rs3767028
NM_144573.3(NEXN):c.*417_*418insC rs201203673
NM_144573.3(NEXN):c.*418dup rs368295679
NM_144573.3(NEXN):c.*511dup rs5775432
NM_144573.3(NEXN):c.*716_*722delTGTTGAG rs145017889
NM_144573.3(NEXN):c.-43T>A rs765499984
NM_144573.3(NEXN):c.-52-4del rs972673849
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.1065T>C (p.Asp355=) rs369897647
NM_144573.3(NEXN):c.1083T>C (p.Tyr361=) rs1060504549
NM_144573.3(NEXN):c.1089A>C (p.Thr363=) rs878855209
NM_144573.3(NEXN):c.1137A>G (p.Glu379=) rs1553240026
NM_144573.3(NEXN):c.1252-10T>G rs201019553
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_1252-12delinsA rs1064796194
NM_144573.3(NEXN):c.1252-20C>A rs776869661
NM_144573.3(NEXN):c.1275T>C (p.Phe425=) rs759257757
NM_144573.3(NEXN):c.1332A>G (p.Gln444=) rs1385609119
NM_144573.3(NEXN):c.1368A>C (p.Gly456=) rs397517845
NM_144573.3(NEXN):c.141A>G (p.Gln47=) rs1459232585
NM_144573.3(NEXN):c.1473+15T>C rs757028785
NM_144573.3(NEXN):c.1474-10T>C rs374541562
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.1582G>C (p.Glu528Gln) rs200071700
NM_144573.3(NEXN):c.1593A>G (p.Arg531=)
NM_144573.3(NEXN):c.1605A>G (p.Gln535=) rs778477679
NM_144573.3(NEXN):c.1618A>G (p.Met540Val) rs201390657
NM_144573.3(NEXN):c.1671_1673GGA[2] (p.Glu561_Glu562del) rs397517848
NM_144573.3(NEXN):c.1704C>G (p.Gly568=) rs397517850
NM_144573.3(NEXN):c.1704C>T (p.Gly568=) rs397517850
NM_144573.3(NEXN):c.1743T>G (p.Ala581=) rs772313224
NM_144573.3(NEXN):c.1773A>G (p.Thr591=) rs727503345
NM_144573.3(NEXN):c.1785C>T (p.Asp595=) rs182998780
NM_144573.3(NEXN):c.1806G>A (p.Thr602=) rs373102543
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.216G>A (p.Gln72=) rs531315786
NM_144573.3(NEXN):c.220-6A>G rs374762720
NM_144573.3(NEXN):c.222T>C (p.Ile74=) rs767610015
NM_144573.3(NEXN):c.237T>C (p.Ala79=) rs727504549
NM_144573.3(NEXN):c.249G>A (p.Glu83=) rs372532824
NM_144573.3(NEXN):c.298+10T>C rs397517854
NM_144573.3(NEXN):c.299-10A>G rs1452768769
NM_144573.3(NEXN):c.299-14T>C rs921990698
NM_144573.3(NEXN):c.299-14del rs397517855
NM_144573.3(NEXN):c.321T>A (p.Ala107=) rs1553236762
NM_144573.3(NEXN):c.363G>A (p.Thr121=) rs35117963
NM_144573.3(NEXN):c.447+105A>G
NM_144573.3(NEXN):c.468G>A (p.Thr156=) rs199988442
NM_144573.3(NEXN):c.483A>C (p.Ala161=)
NM_144573.3(NEXN):c.507A>G (p.Leu169=) rs776106290
NM_144573.3(NEXN):c.512T>C (p.Ile171Thr) rs372065024
NM_144573.3(NEXN):c.687+8TTTG[2] rs768486390
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.739T>C (p.Leu247=) rs781118443
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.865-5G>A rs727505353
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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