ClinVar Miner

List of variants in gene NEXN reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_144573.4(NEXN):c.864+12T>A rs188416492 0.00141
NM_144573.4(NEXN):c.1618A>G (p.Met540Val) rs201390657 0.00113
NM_144573.4(NEXN):c.1252-10T>G rs201019553 0.00088
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.242A>T (p.Asp81Val) rs367871780 0.00028
NM_144573.4(NEXN):c.835C>T (p.Arg279Cys) rs146245480 0.00025
NM_144573.4(NEXN):c.1029G>A (p.Ala343=) rs374260457 0.00023
NM_144573.4(NEXN):c.688-10G>A rs370574269 0.00011
NM_144573.4(NEXN):c.949A>C (p.Met317Leu) rs559464457 0.00009
NM_144573.4(NEXN):c.1065T>C (p.Asp355=) rs369897647 0.00004
NM_144573.4(NEXN):c.249G>A (p.Glu83=) rs372532824 0.00004
NM_144573.4(NEXN):c.1368A>C (p.Gly456=) rs397517845 0.00002
NM_144573.4(NEXN):c.1704C>T (p.Gly568=) rs397517850 0.00001
NM_144573.4(NEXN):c.237T>C (p.Ala79=) rs727504549 0.00001
NM_144573.4(NEXN):c.1773A>G (p.Thr591=) rs727503345
NM_144573.4(NEXN):c.1887A>G (p.Gln629=) rs727503346

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