ClinVar Miner

List of variants reported as uncertain significance for Dilated cardiomyopathy 1W by Illumina Laboratory Services, Illumina

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Total variants: 75
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HGVS dbSNP gnomAD frequency
NM_014000.3(VCL):c.1317T>C (p.Ser439=) rs71579355 0.00442
NM_014000.3(VCL):c.3258+10A>T rs71579379 0.00267
NM_014000.3(VCL):c.2025G>A (p.Val675=) rs140766884 0.00256
NM_014000.3(VCL):c.*148A>G rs528724911 0.00243
NM_014000.3(VCL):c.1907A>G (p.His636Arg) rs71579374 0.00240
NM_014000.3(VCL):c.*1751C>T rs372750308 0.00198
NM_014000.3(VCL):c.*652T>C rs79816413 0.00159
NM_014000.3(VCL):c.*646C>G rs41280414 0.00112
NM_014000.3(VCL):c.1555A>C (p.Ile519Leu) rs141033098 0.00064
NM_014000.3(VCL):c.*1659C>T rs1804893 0.00040
NM_014000.3(VCL):c.*698C>A rs182637339 0.00037
NM_014000.3(VCL):c.492T>G (p.Leu164=) rs143702799 0.00033
NM_014000.3(VCL):c.*1285C>T rs879813349 0.00027
NM_014000.3(VCL):c.*864C>T rs536381894 0.00024
NM_014000.3(VCL):c.*1526A>G rs752039786 0.00021
NM_014000.3(VCL):c.2427C>T (p.Ser809=) rs183739128 0.00019
NM_014000.3(VCL):c.2969C>T (p.Ala990Val) rs150595117 0.00019
NM_014000.3(VCL):c.81C>T (p.His27=) rs200733607 0.00018
NM_014000.3(VCL):c.1716T>G (p.Leu572=) rs189781480 0.00016
NM_014000.3(VCL):c.*212C>A rs757322860 0.00012
NM_014000.3(VCL):c.2796T>C (p.Asp932=) rs140308982 0.00012
NM_014000.3(VCL):c.378C>T (p.Phe126=) rs148966602 0.00012
NM_014000.3(VCL):c.*1793C>T rs575785254 0.00011
NM_014000.3(VCL):c.*1761A>G rs886047230 0.00010
NM_014000.3(VCL):c.*491C>T rs915076132 0.00009
NM_014000.3(VCL):c.1290C>T (p.Asp430=) rs576271894 0.00009
NM_014000.3(VCL):c.3066C>T (p.Ile1022=) rs138619320 0.00009
NM_014000.3(VCL):c.2802C>T (p.Ala934=) rs372381809 0.00007
NM_014000.3(VCL):c.*1403C>T rs886047225 0.00006
NM_014000.3(VCL):c.*1540A>C rs886047226 0.00006
NM_014000.3(VCL):c.2468G>A (p.Arg823Gln) rs759202535 0.00006
NM_014000.3(VCL):c.592G>A (p.Val198Met) rs760340545 0.00006
NM_014000.3(VCL):c.1287T>A (p.Asp429Glu) rs139371702 0.00005
NM_014000.3(VCL):c.1177-14G>A rs778137720 0.00004
NM_014000.3(VCL):c.1390A>G (p.Lys464Glu) rs200710859 0.00004
NM_014000.3(VCL):c.1607C>A (p.Pro536His) rs200624351 0.00004
NM_014000.3(VCL):c.2472C>G (p.Ile824Met) rs140381835 0.00004
NM_014000.3(VCL):c.2746-8C>T rs532645343 0.00004
NM_014000.3(VCL):c.*1891G>A rs529702817 0.00003
NM_014000.3(VCL):c.-58G>T rs1189528818 0.00003
NM_014000.3(VCL):c.1015C>T (p.Arg339Cys) rs759961842 0.00003
NM_014000.3(VCL):c.1040C>T (p.Pro347Leu) rs148619523 0.00003
NM_014000.3(VCL):c.2006G>A (p.Arg669Gln) rs759771302 0.00003
NM_014000.3(VCL):c.1404G>A (p.Thr468=) rs772104870 0.00002
NM_014000.3(VCL):c.808T>C (p.Leu270=) rs727505339 0.00002
NM_014000.3(VCL):c.*1143A>G rs886047224 0.00001
NM_014000.3(VCL):c.*1708A>G rs886047229 0.00001
NM_014000.3(VCL):c.*207G>T rs1035762300 0.00001
NM_014000.3(VCL):c.1223T>C (p.Ile408Thr) rs878854969 0.00001
NM_014000.3(VCL):c.1433A>G (p.Asn478Ser) rs763235691 0.00001
NM_014000.3(VCL):c.1543+8C>G rs886047218 0.00001
NM_014000.3(VCL):c.1613G>A (p.Arg538Gln) rs566596830 0.00001
NM_014000.3(VCL):c.2338C>T (p.Arg780Cys) rs753445972 0.00001
NM_014000.3(VCL):c.2807C>T (p.Ala936Val) rs754681045 0.00001
NM_014000.3(VCL):c.2924G>A (p.Arg975Gln) rs767325003 0.00001
NM_014000.3(VCL):c.3186G>A (p.Gln1062=) rs761534024 0.00001
NM_014000.3(VCL):c.36C>T (p.Ile12=) rs774195260 0.00001
NM_014000.2(VCL):c.-96C>T rs1591641543
NM_014000.3(VCL):c.*1794G>A rs577038840
NM_014000.3(VCL):c.*279T>C rs1840344849
NM_014000.3(VCL):c.-62T>G rs886047215
NM_014000.3(VCL):c.1379G>A (p.Arg460Gln) rs753026034
NM_014000.3(VCL):c.1472T>C (p.Val491Ala) rs1839933596
NM_014000.3(VCL):c.155G>C (p.Ser52Thr) rs886047216
NM_014000.3(VCL):c.1599G>C (p.Met533Ile) rs775532849
NM_014000.3(VCL):c.1704G>A (p.Gln568=) rs1839959715
NM_014000.3(VCL):c.1856C>T (p.Ala619Val) rs771628544
NM_014000.3(VCL):c.1918C>T (p.Leu640Phe) rs886047219
NM_014000.3(VCL):c.1998G>T (p.Lys666Asn) rs886047220
NM_014000.3(VCL):c.2110G>A (p.Asp704Asn) rs1840094833
NM_014000.3(VCL):c.256A>G (p.Thr86Ala) rs1841649925
NM_014000.3(VCL):c.378C>A (p.Phe126Leu) rs148966602
NM_014000.3(VCL):c.622+4C>T rs201020802
NM_014000.3(VCL):c.789T>C (p.Thr263=) rs538002543
NM_014000.3(VCL):c.901C>T (p.Gln301Ter) rs886047217

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