ClinVar Miner

List of variants reported as uncertain significance for Dilated cardiomyopathy 1CC; Hypertrophic cardiomyopathy 20 by Fulgent Genetics, Fulgent Genetics

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Total variants: 54
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HGVS dbSNP gnomAD frequency
NM_144573.4(NEXN):c.392A>G (p.Gln131Arg) rs397517858 0.00009
NM_144573.4(NEXN):c.1190G>A (p.Arg397Gln) rs201806320 0.00007
NM_144573.4(NEXN):c.157G>A (p.Glu53Lys) rs373778361 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.1453G>A (p.Glu485Lys) rs368812830 0.00006
NM_144573.4(NEXN):c.2012T>C (p.Ile671Thr) rs747781785 0.00006
NM_144573.4(NEXN):c.250G>A (p.Glu84Lys) rs547319928 0.00006
NM_144573.4(NEXN):c.687+4A>T rs754061340 0.00006
NM_144573.4(NEXN):c.1010T>C (p.Ile337Thr) rs749553777 0.00004
NM_144573.4(NEXN):c.1174C>T (p.Arg392Ter) rs750076188 0.00004
NM_144573.4(NEXN):c.1471G>C (p.Glu491Gln) rs373057251 0.00004
NM_144573.4(NEXN):c.1595T>C (p.Ile532Thr) rs754656961 0.00004
NM_144573.4(NEXN):c.836G>A (p.Arg279His) rs750349053 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.379C>T (p.Arg127Cys) rs771113424 0.00003
NM_144573.4(NEXN):c.817C>T (p.Arg273Cys) rs757571525 0.00003
NM_144573.4(NEXN):c.857G>A (p.Arg286Gln) rs910594117 0.00003
NM_144573.4(NEXN):c.1046G>C (p.Arg349Thr) rs898035834 0.00002
NM_144573.4(NEXN):c.874G>A (p.Asp292Asn) rs373377525 0.00002
NM_144573.4(NEXN):c.1171C>T (p.Arg391Ter) rs200106758 0.00001
NM_144573.4(NEXN):c.1222T>C (p.Phe408Leu) rs794729083 0.00001
NM_144573.4(NEXN):c.1271C>T (p.Thr424Ile) rs200442502 0.00001
NM_144573.4(NEXN):c.1415C>G (p.Ala472Gly) rs539665448 0.00001
NM_144573.4(NEXN):c.1609_1610insA (p.Leu537fs) rs779350415 0.00001
NM_144573.4(NEXN):c.1805C>T (p.Thr602Met) rs756709134 0.00001
NM_144573.4(NEXN):c.328G>C (p.Glu110Gln) rs754671609 0.00001
NM_144573.4(NEXN):c.364G>C (p.Glu122Gln) rs748518328 0.00001
NM_144573.4(NEXN):c.421C>T (p.Arg141Cys) rs536537549 0.00001
NM_144573.4(NEXN):c.620A>G (p.Asp207Gly) rs570946423 0.00001
NM_144573.4(NEXN):c.671G>A (p.Cys224Tyr) rs886046534 0.00001
NM_144573.4(NEXN):c.688-1G>C rs761030548 0.00001
NM_144573.4(NEXN):c.772A>G (p.Arg258Gly) rs1308264799 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.*418del rs368295679
NM_144573.4(NEXN):c.1055T>C (p.Val352Ala) rs1040085867
NM_144573.4(NEXN):c.1111C>A (p.Pro371Thr) rs1223883098
NM_144573.4(NEXN):c.1112C>T (p.Pro371Leu) rs200067011
NM_144573.4(NEXN):c.137del (p.Asn46fs) rs2102092061
NM_144573.4(NEXN):c.1401AGA[2] (p.Glu470del) rs397517846
NM_144573.4(NEXN):c.1450C>T (p.Arg484Ter) rs767792289
NM_144573.4(NEXN):c.1481A>T (p.Asp494Val) rs750183004
NM_144573.4(NEXN):c.1573GAA[3] (p.Glu528del) rs764505909
NM_144573.4(NEXN):c.1640T>A (p.Ile547Asn) rs753636624
NM_144573.4(NEXN):c.1661A>G (p.Lys554Arg) rs1651445427
NM_144573.4(NEXN):c.1671GGA[5] (p.Glu562dup) rs397517848
NM_144573.4(NEXN):c.1678G>A (p.Glu560Lys) rs377257742
NM_144573.4(NEXN):c.784C>T (p.Arg262Ter) rs1002648603
NM_144573.4(NEXN):c.864G>T (p.Met288Ile) rs371666396
NM_144573.4(NEXN):c.86G>T (p.Gly29Val) rs876657931
NM_144573.4(NEXN):c.962del (p.Arg321fs) rs915318065
NM_144573.4(NEXN):c.989AAG[2] (p.Glu332del) rs727505124

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