ClinVar Miner

List of variants in gene NEXN reported as uncertain significance for Cardiomyopathy

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Total variants: 34
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HGVS dbSNP
NM_001172309.1(NEXN):c.*4_*5CT[1] rs553696163
NM_001172309.1(NEXN):c.1390_1393delinsCAAA (p.Glu464_Gln465delinsGlnLys) rs1557996950
NM_001172309.1(NEXN):c.797_799AAG[2] (p.Glu268del) rs727505124
NM_144573.3(NEXN):c.1271C>T (p.Thr424Ile) rs200442502
NM_144573.3(NEXN):c.1430T>C (p.Ile477Thr) rs727504658
NM_144573.3(NEXN):c.1489G>A (p.Val497Ile) rs778330292
NM_144573.3(NEXN):c.1550T>A (p.Phe517Tyr) rs1557996817
NM_144573.3(NEXN):c.1572_1574delAGA rs764505909
NM_144573.3(NEXN):c.1585C>A (p.Gln529Lys) rs766323670
NM_144573.3(NEXN):c.1642G>A (p.Asp548Asn) rs1404772841
NM_144573.3(NEXN):c.1653A>G (p.Leu551=) rs794727078
NM_144573.3(NEXN):c.1664_1666del (p.Arg555_Glu556delinsLys) rs1221963637
NM_144573.3(NEXN):c.166_169del (p.Arg56fs) rs765396527
NM_144573.3(NEXN):c.1770C>T (p.Asn590=) rs1557998187
NM_144573.3(NEXN):c.1894G>C (p.Glu632Gln) rs370965740
NM_144573.3(NEXN):c.1922T>C (p.Leu641Ser) rs760119697
NM_144573.3(NEXN):c.257T>C (p.Val86Ala) rs1557974419
NM_144573.3(NEXN):c.341_342del (p.Gln114fs) rs397517857
NM_144573.3(NEXN):c.421C>T (p.Arg141Cys) rs536537549
NM_144573.3(NEXN):c.535T>C (p.Tyr179His) rs1557981610
NM_144573.3(NEXN):c.60A>C (p.Lys20Asn) rs1557973780
NM_144573.3(NEXN):c.865-4T>C rs542794485
NM_144573.3(NEXN):c.874G>A (p.Asp292Asn) rs373377525
NM_144573.4(NEXN):c.1112C>T (p.Pro371Leu) rs200067011
NM_144573.4(NEXN):c.1190G>A (p.Arg397Gln) rs201806320
NM_144573.4(NEXN):c.1416AAG[1] (p.Arg475del) rs794729091
NM_144573.4(NEXN):c.1788T>G (p.Ser596Arg) rs199738750
NM_144573.4(NEXN):c.1946_1948GAG[1] (p.Gly650del) rs397517853
NM_144573.4(NEXN):c.1981G>A (p.Gly661Arg) rs876657929
NM_144573.4(NEXN):c.1996A>G (p.Thr666Ala) rs374000722
NM_144573.4(NEXN):c.373C>T (p.Arg125Ter)
NM_144573.4(NEXN):c.512T>C (p.Ile171Thr) rs372065024
NM_144573.4(NEXN):c.586C>T (p.Arg196Cys) rs369486891
NM_144573.4(NEXN):c.613G>A (p.Glu205Lys) rs201447781

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