ClinVar Miner

List of variants in gene VCL reported as uncertain significance for Dilated cardiomyopathy 1W

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Total variants: 121
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HGVS dbSNP
NC_000010.10:g.(?_75757946)_(75758153_?)del
NM_014000.2(VCL):c.1015C>T (p.Arg339Cys) rs759961842
NM_014000.2(VCL):c.1031G>C (p.Gly344Ala) rs778875353
NM_014000.2(VCL):c.1039C>T (p.Pro347Ser)
NM_014000.2(VCL):c.1040C>T (p.Pro347Leu) rs148619523
NM_014000.2(VCL):c.1046C>T (p.Ala349Val)
NM_014000.2(VCL):c.1050G>A (p.Met350Ile)
NM_014000.2(VCL):c.1115G>A (p.Arg372His) rs377289804
NM_014000.2(VCL):c.113C>T (p.Pro38Leu) rs1060502194
NM_014000.2(VCL):c.1195A>C (p.Asn399His) rs377228795
NM_014000.2(VCL):c.1223T>C (p.Ile408Thr) rs878854969
NM_014000.2(VCL):c.1225C>T (p.Arg409Ter) rs202005455
NM_014000.2(VCL):c.1237G>A (p.Ala413Thr) rs146278697
NM_014000.2(VCL):c.1247G>A (p.Arg416Gln) rs758811315
NM_014000.2(VCL):c.1268A>G (p.Asp423Gly) rs769504902
NM_014000.2(VCL):c.1287T>A (p.Asp429Glu) rs139371702
NM_014000.2(VCL):c.1294C>G (p.Leu432Val) rs144146254
NM_014000.2(VCL):c.1296_1297inv (p.Arg433Cys)
NM_014000.2(VCL):c.1298G>A (p.Arg433His) rs754046223
NM_014000.2(VCL):c.1319C>T (p.Ala440Val) rs1554817862
NM_014000.2(VCL):c.1352+5G>A rs374522164
NM_014000.2(VCL):c.1403C>T (p.Thr468Met) rs147957747
NM_014000.2(VCL):c.1490T>C (p.Ile497Thr) rs572757800
NM_014000.2(VCL):c.1511T>C (p.Ile504Thr) rs745343813
NM_014000.2(VCL):c.1534C>T (p.Arg512Cys) rs781079975
NM_014000.2(VCL):c.1543G>A (p.Gly515Ser) rs1215494764
NM_014000.2(VCL):c.1559G>A (p.Arg520Gln) rs757009736
NM_014000.2(VCL):c.1582C>T (p.Arg528Cys) rs923960592
NM_014000.2(VCL):c.1583G>A (p.Arg528His) rs746095066
NM_014000.2(VCL):c.1612C>T (p.Arg538Trp)
NM_014000.2(VCL):c.1620T>A (p.Asp540Glu)
NM_014000.2(VCL):c.1621C>G (p.Leu541Val) rs370229150
NM_014000.2(VCL):c.1648C>G (p.Gln550Glu) rs1406371942
NM_014000.2(VCL):c.166C>T (p.Arg56Trp) rs1555112641
NM_014000.2(VCL):c.1708C>T (p.Arg570Ter) rs794729191
NM_014000.2(VCL):c.1713del (p.Ala573fs) rs779488376
NM_014000.2(VCL):c.1715T>C (p.Leu572Pro) rs1060502197
NM_014000.2(VCL):c.1743+6A>G
NM_014000.2(VCL):c.1803T>A (p.Asp601Glu)
NM_014000.2(VCL):c.1814C>G (p.Pro605Arg) rs960761223
NM_014000.2(VCL):c.1819A>C (p.Lys607Gln) rs794729192
NM_014000.2(VCL):c.1835C>T (p.Ala612Val)
NM_014000.2(VCL):c.1844C>T (p.Ala615Val) rs148669762
NM_014000.2(VCL):c.1856C>T (p.Ala619Val)
NM_014000.2(VCL):c.185T>C (p.Val62Ala) rs769799445
NM_014000.2(VCL):c.1861A>C (p.Asn621His) rs374309823
NM_014000.2(VCL):c.1863C>G (p.Asn621Lys) rs746293391
NM_014000.2(VCL):c.1865G>A (p.Arg622Lys) rs771590749
NM_014000.2(VCL):c.1868A>C (p.Glu623Ala) rs1060502193
NM_014000.2(VCL):c.1917G>T (p.Lys639Asn) rs915381122
NM_014000.2(VCL):c.1928C>T (p.Thr643Met) rs150643310
NM_014000.2(VCL):c.1961A>G (p.Asn654Ser)
NM_014000.2(VCL):c.1999A>G (p.Thr667Ala)
NM_014000.2(VCL):c.2000C>T (p.Thr667Met) rs794729187
NM_014000.2(VCL):c.2006G>A (p.Arg669Gln) rs759771302
NM_014000.2(VCL):c.2022+5G>T rs1050797785
NM_014000.2(VCL):c.2046A>T (p.Leu682Phe) rs565398652
NM_014000.2(VCL):c.20G>T (p.Arg7Leu)
NM_014000.2(VCL):c.2173G>A (p.Ala725Thr) rs1554818884
NM_014000.2(VCL):c.2182G>A (p.Glu728Lys)
NM_014000.2(VCL):c.224C>T (p.Pro75Leu) rs373830664
NM_014000.2(VCL):c.2273G>A (p.Arg758His)
NM_014000.2(VCL):c.2275C>A (p.Arg759=) rs774477633
NM_014000.2(VCL):c.2276G>A (p.Arg759Gln) rs1425397914
NM_014000.2(VCL):c.2285G>A (p.Arg762Gln)
NM_014000.2(VCL):c.2330C>T (p.Pro777Leu) rs1564532927
NM_014000.2(VCL):c.2365G>A (p.Glu789Lys) rs745419923
NM_014000.2(VCL):c.2387del (p.Pro796fs) rs1241654679
NM_014000.2(VCL):c.2443A>G (p.Lys815Glu) rs960017518
NM_014000.2(VCL):c.2444A>G (p.Lys815Arg) rs373010557
NM_014000.2(VCL):c.2468G>A (p.Arg823Gln) rs759202535
NM_014000.2(VCL):c.2531C>T (p.Pro844Leu) rs145393322
NM_014000.2(VCL):c.2543A>G (p.Asp848Gly)
NM_014000.2(VCL):c.2566G>A (p.Asp856Asn) rs1554819202
NM_014000.2(VCL):c.2649A>C (p.Glu883Asp) rs752902180
NM_014000.2(VCL):c.2699T>C (p.Met900Thr) rs1554819236
NM_014000.2(VCL):c.2746-8C>T rs532645343
NM_014000.2(VCL):c.2803G>A (p.Asp935Asn) rs746658025
NM_014000.2(VCL):c.2807C>T (p.Ala936Val) rs754681045
NM_014000.2(VCL):c.2823_2824delinsGT (p.Pro942Ser) rs1060502196
NM_014000.2(VCL):c.2828_2829del (p.Pro943fs) rs781036800
NM_014000.2(VCL):c.2853del (p.Glu952fs) rs878854972
NM_014000.2(VCL):c.2866A>G (p.Met956Val) rs761830073
NM_014000.2(VCL):c.2875A>C (p.Asn959His) rs758969419
NM_014000.2(VCL):c.2875A>G (p.Asn959Asp) rs758969419
NM_014000.2(VCL):c.2887A>G (p.Asn963Asp) rs777702397
NM_014000.2(VCL):c.2924G>A (p.Arg975Gln) rs767325003
NM_014000.2(VCL):c.2969C>T (p.Ala990Val) rs150595117
NM_014000.2(VCL):c.2978G>T (p.Arg993Leu) rs1554819624
NM_014000.2(VCL):c.3039_3043dup (p.Leu1015fs)
NM_014000.2(VCL):c.3092G>A (p.Arg1031Gln) rs397517238
NM_014000.2(VCL):c.3164G>A (p.Arg1055Gln)
NM_014000.2(VCL):c.3226C>T (p.Arg1076Trp) rs397517241
NM_014000.2(VCL):c.3245A>C (p.Glu1082Ala) rs1554819693
NM_014000.2(VCL):c.3258+4T>C rs1268605937
NM_014000.2(VCL):c.3267G>C (p.Glu1089Asp) rs149300310
NM_014000.2(VCL):c.32G>A (p.Ser11Asn) rs777811020
NM_014000.2(VCL):c.3358G>A (p.Ala1120Thr)
NM_014000.2(VCL):c.3373C>T (p.Arg1125Cys) rs373317423
NM_014000.2(VCL):c.390+4G>A rs1060502195
NM_014000.2(VCL):c.437C>A (p.Thr146Lys) rs1421034616
NM_014000.2(VCL):c.458C>T (p.Thr153Ile) rs1554816691
NM_014000.2(VCL):c.511A>G (p.Met171Val)
NM_014000.2(VCL):c.536A>C (p.Gln179Pro) rs1564523578
NM_014000.2(VCL):c.562C>T (p.Arg188Ter) rs397517244
NM_014000.2(VCL):c.592G>A (p.Val198Met) rs760340545
NM_014000.2(VCL):c.622+4C>A
NM_014000.2(VCL):c.622+4C>G rs201020802
NM_014000.2(VCL):c.625A>T (p.Met209Leu) rs144683137
NM_014000.2(VCL):c.688C>T (p.Arg230Cys) rs139312390
NM_014000.2(VCL):c.695T>A (p.Phe232Tyr) rs200956572
NM_014000.2(VCL):c.701T>C (p.Val234Ala)
NM_014000.2(VCL):c.737G>A (p.Arg246His) rs746577068
NM_014000.2(VCL):c.768T>A (p.Asp256Glu) rs56413529
NM_014000.2(VCL):c.780C>T (p.Ser260=) rs774377548
NM_014000.2(VCL):c.783+5G>A
NM_014000.2(VCL):c.787A>T (p.Thr263Ser) rs142233726
NM_014000.2(VCL):c.829C>A (p.Leu277Met) rs71579353
NM_014000.2(VCL):c.853C>T (p.Arg285Cys) rs757517552
NM_014000.2(VCL):c.901C>T (p.Gln301Ter) rs886047217
NM_014000.2(VCL):c.952C>T (p.Arg318Cys) rs397517247

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