List of variants in gene NEXN studied for Cardiomyopathy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 82

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HGVS	dbSNP	gnomAD frequency
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.156C>T (p.Asp52=)	rs371431782	0.00128
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.732C>A (p.Pro244=)	rs201171783	0.00045
NM_144573.4(NEXN):c.512T>C (p.Ile171Thr)	rs372065024	0.00035
NM_144573.4(NEXN):c.613G>A (p.Glu205Lys)	rs201447781	0.00034
NM_144573.4(NEXN):c.1788T>G (p.Ser596Arg)	rs199738750	0.00029
NM_144573.4(NEXN):c.835C>T (p.Arg279Cys)	rs146245480	0.00025
NM_144573.4(NEXN):c.893C>G (p.Thr298Arg)	rs200753280	0.00016
NM_144573.4(NEXN):c.1582G>C (p.Glu528Gln)	rs200071700	0.00011
NM_144573.4(NEXN):c.1955A>G (p.Tyr652Cys)	rs137853197	0.00011
NM_144573.4(NEXN):c.856C>T (p.Arg286Trp)	rs199917913	0.00009
NM_144573.4(NEXN):c.949A>C (p.Met317Leu)	rs559464457	0.00009
NM_144573.4(NEXN):c.78T>C (p.Leu26=)	rs376535223	0.00008
NM_144573.4(NEXN):c.1190G>A (p.Arg397Gln)	rs201806320	0.00007
NM_144573.4(NEXN):c.1996A>G (p.Thr666Ala)	rs374000722	0.00007
NM_144573.4(NEXN):c.586C>T (p.Arg196Cys)	rs369486891	0.00007
NM_144573.4(NEXN):c.1422G>A (p.Arg474=)	rs775204901	0.00006
NM_144573.4(NEXN):c.1453G>A (p.Glu485Lys)	rs368812830	0.00006
NM_144573.4(NEXN):c.687+4A>T	rs754061340	0.00006
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.818G>A (p.Arg273His)	rs765385072	0.00004
NM_144573.4(NEXN):c.967G>A (p.Glu323Lys)	rs1196365963	0.00004
NM_144573.4(NEXN):c.1053+1G>A	rs397517843	0.00003
NM_144573.4(NEXN):c.1894G>C (p.Glu632Gln)	rs370965740	0.00003
NM_144573.4(NEXN):c.216G>A (p.Gln72=)	rs531315786	0.00003
NM_144573.4(NEXN):c.1368A>C (p.Gly456=)	rs397517845	0.00002
NM_144573.4(NEXN):c.874G>A (p.Asp292Asn)	rs373377525	0.00002
NM_144573.4(NEXN):c.1234A>G (p.Arg412Gly)	rs768693715	0.00001
NM_144573.4(NEXN):c.1271C>T (p.Thr424Ile)	rs200442502	0.00001
NM_144573.4(NEXN):c.1364T>C (p.Ile455Thr)	rs1338886488	0.00001
NM_144573.4(NEXN):c.1430T>C (p.Ile477Thr)	rs727504658	0.00001
NM_144573.4(NEXN):c.1489G>A (p.Val497Ile)	rs778330292	0.00001
NM_144573.4(NEXN):c.1605A>G (p.Gln535=)	rs778477679	0.00001
NM_144573.4(NEXN):c.1642G>A (p.Asp548Asn)	rs1404772841	0.00001
NM_144573.4(NEXN):c.1653A>G (p.Leu551=)	rs794727078	0.00001
NM_144573.4(NEXN):c.1664_1666del (p.Arg555_Glu556delinsLys)	rs1221963637	0.00001
NM_144573.4(NEXN):c.1683A>G (p.Glu561=)	rs1403473507	0.00001
NM_144573.4(NEXN):c.1720G>A (p.Glu574Lys)	rs756408591	0.00001
NM_144573.4(NEXN):c.1731C>G (p.Thr577=)	rs371743669	0.00001
NM_144573.4(NEXN):c.1981G>A (p.Gly661Arg)	rs876657929	0.00001
NM_144573.4(NEXN):c.1995T>C (p.Ser665=)	rs757311272	0.00001
NM_144573.4(NEXN):c.2019T>A (p.Ser673Arg)	rs539689450	0.00001
NM_144573.4(NEXN):c.620A>G (p.Asp207Gly)	rs570946423	0.00001
NM_144573.4(NEXN):c.906T>A (p.Phe302Leu)	rs767740199	0.00001
NM_144573.4(NEXN):c.916C>T (p.Arg306Cys)	rs765051104	0.00001
NM_144573.4(NEXN):c.917G>A (p.Arg306His)	rs758055856	0.00001
NM_144573.4(NEXN):c.*4CT[1]	rs553696163
NM_144573.4(NEXN):c.1112C>T (p.Pro371Leu)	rs200067011
NM_144573.4(NEXN):c.1251+1G>A	rs1650474978
NM_144573.4(NEXN):c.1271C>A (p.Thr424Asn)
NM_144573.4(NEXN):c.1416AAG[1] (p.Arg475del)	rs794729091
NM_144573.4(NEXN):c.1473+5A>G	rs1650735272
NM_144573.4(NEXN):c.1499C>A (p.Ala500Glu)	rs2102176895
NM_144573.4(NEXN):c.1527C>T (p.His509=)
NM_144573.4(NEXN):c.1550T>A (p.Phe517Tyr)	rs1557996817
NM_144573.4(NEXN):c.1573GAA[3] (p.Glu528del)	rs764505909
NM_144573.4(NEXN):c.1582_1585delinsCAAA (p.Glu528_Gln529delinsGlnLys)	rs1557996950
NM_144573.4(NEXN):c.1585C>A (p.Gln529Lys)	rs766323670
NM_144573.4(NEXN):c.166_169del (p.Arg56fs)	rs765396527
NM_144573.4(NEXN):c.1671GGA[2] (p.Glu561_Glu562del)	rs397517848
NM_144573.4(NEXN):c.1678G>C (p.Glu560Gln)
NM_144573.4(NEXN):c.1770C>T (p.Asn590=)	rs1557998187
NM_144573.4(NEXN):c.1922T>C (p.Leu641Ser)	rs760119697
NM_144573.4(NEXN):c.1946GAG[1] (p.Gly650del)	rs397517853
NM_144573.4(NEXN):c.201G>A (p.Trp67Ter)	rs999958582
NM_144573.4(NEXN):c.257T>C (p.Val86Ala)	rs1557974419
NM_144573.4(NEXN):c.43T>C (p.Ser15Pro)
NM_144573.4(NEXN):c.492A>G (p.Glu164=)	rs1571134764
NM_144573.4(NEXN):c.52G>A (p.Val18Ile)	rs2102091643
NM_144573.4(NEXN):c.535T>C (p.Tyr179His)	rs1557981610
NM_144573.4(NEXN):c.60A>C (p.Lys20Asn)	rs1557973780
NM_144573.4(NEXN):c.685A>G (p.Met229Val)	rs1179163117
NM_144573.4(NEXN):c.687+23del	rs141957231
NM_144573.4(NEXN):c.732C>T (p.Pro244=)	rs201171783
NM_144573.4(NEXN):c.817del (p.Arg273fs)	rs2102125160
NM_144573.4(NEXN):c.821T>C (p.Leu274Ser)	rs2102125189
NM_144573.4(NEXN):c.865-4T>C	rs542794485
NM_144573.4(NEXN):c.989AAG[2] (p.Glu332del)	rs727505124

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