ClinVar Miner

List of variants in gene NEXN reported as likely benign by GeneDx

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Total variants: 33
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HGVS dbSNP
NC_000001.11:g.77935818dup
NM_144573.3(NEXN):c.-43T>A rs765499984
NM_144573.3(NEXN):c.-52-4del rs972673849
NM_144573.3(NEXN):c.1042A>C (p.Arg348=) rs752036618
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.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.1582G>C (p.Glu528Gln) rs200071700
NM_144573.3(NEXN):c.1618A>G (p.Met540Val) rs201390657
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.220-6A>G rs374762720
NM_144573.3(NEXN):c.249G>A (p.Glu83=) rs372532824
NM_144573.3(NEXN):c.299-14T>C rs921990698
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.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.78T>C (p.Leu26=) rs376535223
NM_144573.3(NEXN):c.835C>T (p.Arg279Cys) rs146245480
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

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