ClinVar Miner

List of variants in gene NEXN reported by Illumina Clinical Services Laboratory,Illumina

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Gene type:
ClinVar version:
Total variants: 42
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HGVS dbSNP
NM_144573.3(NEXN):c.*1020T>A rs150511446
NM_144573.3(NEXN):c.*209A>G rs530666449
NM_144573.3(NEXN):c.*22C>G rs3767028
NM_144573.3(NEXN):c.*279G>A rs11558429
NM_144573.3(NEXN):c.*314A>C rs78105746
NM_144573.3(NEXN):c.*356A>G rs865984102
NM_144573.3(NEXN):c.*362G>C rs796447682
NM_144573.3(NEXN):c.*414A>C rs1359518
NM_144573.3(NEXN):c.*417_*418insC rs201203673
NM_144573.3(NEXN):c.*418A>C rs886046539
NM_144573.3(NEXN):c.*418delA rs368295679
NM_144573.3(NEXN):c.*418dupA rs368295679
NM_144573.3(NEXN):c.*511dupA rs5775432
NM_144573.3(NEXN):c.*661A>G rs886046541
NM_144573.3(NEXN):c.*6_*7delCT rs553696163
NM_144573.3(NEXN):c.*716_*722delTGTTGAG rs145017889
NM_144573.3(NEXN):c.*759T>A rs192101966
NM_144573.3(NEXN):c.*809T>G rs569415834
NM_144573.3(NEXN):c.*899G>A rs886046543
NM_144573.3(NEXN):c.-128A>G rs886046532
NM_144573.3(NEXN):c.-194A>G rs886046531
NM_144573.3(NEXN):c.-197_-195dupGGC rs528439602
NM_144573.3(NEXN):c.-230A>C rs886046529
NM_144573.3(NEXN):c.-233T>C rs886046528
NM_144573.3(NEXN):c.1029G>A (p.Ala343=) rs374260457
NM_144573.3(NEXN):c.1065T>C (p.Asp355=) rs369897647
NM_144573.3(NEXN):c.1189C>T (p.Arg397Trp) rs754281087
NM_144573.3(NEXN):c.1228C>T (p.Gln410Ter)
NM_144573.3(NEXN):c.1408G>C (p.Glu470Gln) rs35366555
NM_144573.3(NEXN):c.1435C>T (p.Leu479Phe) rs181520023
NM_144573.3(NEXN):c.1892T>C (p.Ile631Thr) rs775292649
NM_144573.3(NEXN):c.2021A>C (p.Lys674Thr) rs886046535
NM_144573.3(NEXN):c.363G>A (p.Thr121=) rs35117963
NM_144573.3(NEXN):c.593A>T (p.Glu198Val) rs886046533
NM_144573.3(NEXN):c.671G>A (p.Cys224Tyr) rs886046534
NM_144573.3(NEXN):c.732C>A (p.Pro244=) rs201171783
NM_144573.3(NEXN):c.733G>A (p.Gly245Arg) rs1166698
NM_144573.3(NEXN):c.864+12T>A rs188416492
NM_144573.3(NEXN):c.893C>G (p.Thr298Arg) rs200753280
NM_144573.3(NEXN):c.949A>C (p.Met317Leu) rs559464457
NM_144573.3(NEXN):c.995A>C (p.Glu332Ala) rs201763096
NM_144573.3:c.1606_1607delAA

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