ClinVar Miner

List of variants in gene NEXN reported as benign for not specified

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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_144573.4(NEXN):c.733G>A (p.Gly245Arg) rs1166698 0.15380
NM_144573.4(NEXN):c.1408G>C (p.Glu470Gln) rs35366555 0.00302
NM_144573.4(NEXN):c.995A>C (p.Glu332Ala) rs201763096 0.00262
NM_144573.4(NEXN):c.1659+18C>G rs147422621 0.00228
NM_144573.4(NEXN):c.864+12T>A rs188416492 0.00141
NM_144573.4(NEXN):c.156C>T (p.Asp52=) rs371431782 0.00128
NM_144573.4(NEXN):c.1618A>G (p.Met540Val) rs201390657 0.00113
NM_144573.4(NEXN):c.777A>G (p.Gln259=) rs375544798 0.00077
NM_144573.4(NEXN):c.-52-16T>C rs557864364 0.00047
NM_144573.4(NEXN):c.732C>A (p.Pro244=) rs201171783 0.00045
NM_144573.4(NEXN):c.512T>C (p.Ile171Thr) rs372065024 0.00035
NM_144573.4(NEXN):c.-58T>C rs587781100 0.00030
NM_144573.4(NEXN):c.1029G>A (p.Ala343=) rs374260457 0.00023
NM_144573.4(NEXN):c.865-17A>G rs201771600 0.00016
NM_144573.4(NEXN):c.78T>C (p.Leu26=) rs376535223 0.00008
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.66T>C (p.Tyr22=) rs749182975 0.00001
NM_144573.4(NEXN):c.-34C>A rs758434911
NM_144573.4(NEXN):c.1573GAA[3] (p.Glu528del) rs764505909
NM_144573.4(NEXN):c.687+23del rs141957231

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