ClinVar Miner

List of variants in gene NEXN reported as likely benign for not provided

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Total variants: 23
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HGVS dbSNP
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.1252-6T>C rs1571156994
NM_144573.3(NEXN):c.1413A>G (p.Arg471=) rs780858511
NM_144573.3(NEXN):c.1422G>A (p.Arg474=) rs775204901
NM_144573.3(NEXN):c.1533G>T (p.Val511=) rs765353395
NM_144573.3(NEXN):c.1593A>G (p.Arg531=) rs1359392123
NM_144573.3(NEXN):c.1809T>G (p.Val603=) rs1571175311
NM_144573.3(NEXN):c.1938A>C (p.Pro646=) rs1571176052
NM_144573.3(NEXN):c.292T>C (p.Leu98=) rs539220077
NM_144573.3(NEXN):c.447+105A>G rs76755414
NM_144573.3(NEXN):c.456C>T (p.Asp152=) rs760312569
NM_144573.3(NEXN):c.483A>C (p.Ala161=) rs1290445861
NM_144573.3(NEXN):c.492A>G (p.Glu164=) rs1571134764
NM_144573.3(NEXN):c.579A>G (p.Glu193=) rs1476054611
NM_144573.3(NEXN):c.732C>T (p.Pro244=) rs201171783
NM_144573.3(NEXN):c.864+231A>G rs111357417
NM_144573.3(NEXN):c.987A>C (p.Ala329=) rs1270187994
NM_144573.4(NEXN):c.1252-5dup rs768326968
NM_144573.4(NEXN):c.1368A>C (p.Gly456=) rs397517845
NM_144573.4(NEXN):c.237T>C (p.Ala79=) rs727504549
NM_144573.4(NEXN):c.688-10G>A rs370574269
NM_144573.4(NEXN):c.865-5G>A rs727505353

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