ClinVar Miner

List of variants in gene NEXN reported as likely benign by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Total variants: 21
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HGVS dbSNP
NM_144573.3(NEXN):c.242A>T (p.Asp81Val) rs367871780
NM_144573.3(NEXN):c.299-14del rs397517855
NM_144573.4(NEXN):c.1029G>A (p.Ala343=) rs374260457
NM_144573.4(NEXN):c.1065T>C (p.Asp355=) rs369897647
NM_144573.4(NEXN):c.1252-10T>G rs201019553
NM_144573.4(NEXN):c.1368A>C (p.Gly456=) rs397517845
NM_144573.4(NEXN):c.1618A>G (p.Met540Val) rs201390657
NM_144573.4(NEXN):c.1704C>T (p.Gly568=) rs397517850
NM_144573.4(NEXN):c.1773A>G (p.Thr591=) rs727503345
NM_144573.4(NEXN):c.1785C>T (p.Asp595=) rs182998780
NM_144573.4(NEXN):c.1887A>G (p.Gln629=) rs727503346
NM_144573.4(NEXN):c.237T>C (p.Ala79=) rs727504549
NM_144573.4(NEXN):c.249G>A (p.Glu83=) rs372532824
NM_144573.4(NEXN):c.298+10T>C rs397517854
NM_144573.4(NEXN):c.512T>C (p.Ile171Thr) rs372065024
NM_144573.4(NEXN):c.688-10G>A rs370574269
NM_144573.4(NEXN):c.732C>A (p.Pro244=) rs201171783
NM_144573.4(NEXN):c.777A>G (p.Gln259=) rs375544798
NM_144573.4(NEXN):c.835C>T (p.Arg279Cys) rs146245480
NM_144573.4(NEXN):c.864+12T>A rs188416492
NM_144573.4(NEXN):c.949A>C (p.Met317Leu) rs559464457

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