ClinVar Miner

List of variants in gene VCL reported as uncertain significance for Cardiovascular phenotype

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 235
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_014000.3(VCL):c.1294C>G (p.Leu432Val) rs144146254 0.00025
NM_014000.3(VCL):c.2969C>T (p.Ala990Val) rs150595117 0.00019
NM_014000.3(VCL):c.2828_2829del (p.Pro943fs) rs781036800 0.00014
NM_014000.3(VCL):c.1403C>T (p.Thr468Met) rs147957747 0.00013
NM_014000.3(VCL):c.829C>A (p.Leu277Met) rs71579353 0.00010
NM_014000.3(VCL):c.1490T>C (p.Ile497Thr) rs572757800 0.00008
NM_014000.3(VCL):c.1621C>G (p.Leu541Val) rs370229150 0.00008
NM_014000.3(VCL):c.2444A>G (p.Lys815Arg) rs373010557 0.00008
NM_014000.3(VCL):c.1195A>C (p.Asn399His) rs377228795 0.00006
NM_014000.3(VCL):c.2467C>T (p.Arg823Trp) rs779047174 0.00006
NM_014000.3(VCL):c.2468G>A (p.Arg823Gln) rs759202535 0.00006
NM_014000.3(VCL):c.2531C>T (p.Pro844Leu) rs145393322 0.00006
NM_014000.3(VCL):c.1205C>T (p.Pro402Leu) rs766393966 0.00005
NM_014000.3(VCL):c.1287T>A (p.Asp429Glu) rs139371702 0.00005
NM_014000.3(VCL):c.1583G>A (p.Arg528His) rs746095066 0.00005
NM_014000.3(VCL):c.2273G>A (p.Arg758His) rs371970354 0.00005
NM_014000.3(VCL):c.1176+4G>C rs1286302808 0.00004
NM_014000.3(VCL):c.1192C>T (p.Pro398Ser) rs201528612 0.00004
NM_014000.3(VCL):c.1390A>G (p.Lys464Glu) rs200710859 0.00004
NM_014000.3(VCL):c.1505G>A (p.Arg502Gln) rs201808867 0.00004
NM_014000.3(VCL):c.1511T>C (p.Ile504Thr) rs745343813 0.00004
NM_014000.3(VCL):c.1534C>T (p.Arg512Cys) rs781079975 0.00004
NM_014000.3(VCL):c.185T>C (p.Val62Ala) rs769799445 0.00004
NM_014000.3(VCL):c.1928C>T (p.Thr643Met) rs150643310 0.00004
NM_014000.3(VCL):c.2046A>T (p.Leu682Phe) rs565398652 0.00004
NM_014000.3(VCL):c.2399A>T (p.Asp800Val) rs919509789 0.00004
NM_014000.3(VCL):c.2887A>G (p.Asn963Asp) rs777702397 0.00004
NM_014000.3(VCL):c.3373C>T (p.Arg1125Cys) rs373317423 0.00004
NM_014000.3(VCL):c.788C>G (p.Thr263Ser) rs150443513 0.00004
NM_014000.3(VCL):c.1015C>T (p.Arg339Cys) rs759961842 0.00003
NM_014000.3(VCL):c.1039C>T (p.Pro347Ser) rs566961713 0.00003
NM_014000.3(VCL):c.1040C>T (p.Pro347Leu) rs148619523 0.00003
NM_014000.3(VCL):c.1247G>A (p.Arg416Gln) rs758811315 0.00003
NM_014000.3(VCL):c.1352+5G>A rs374522164 0.00003
NM_014000.3(VCL):c.1917G>T (p.Lys639Asn) rs915381122 0.00003
NM_014000.3(VCL):c.1940C>T (p.Ala647Val) rs534449109 0.00003
NM_014000.3(VCL):c.2006G>A (p.Arg669Gln) rs759771302 0.00003
NM_014000.3(VCL):c.2875A>C (p.Asn959His) rs758969419 0.00003
NM_014000.3(VCL):c.3267G>C (p.Glu1089Asp) rs149300310 0.00003
NM_014000.3(VCL):c.1019C>T (p.Ala340Val) rs374928228 0.00002
NM_014000.3(VCL):c.1558C>T (p.Arg520Trp) rs377722209 0.00002
NM_014000.3(VCL):c.158A>G (p.Asn53Ser) rs751938777 0.00002
NM_014000.3(VCL):c.1606C>A (p.Pro536Thr) rs370058111 0.00002
NM_014000.3(VCL):c.1803T>A (p.Asp601Glu) rs1235063893 0.00002
NM_014000.3(VCL):c.1814C>G (p.Pro605Arg) rs960761223 0.00002
NM_014000.3(VCL):c.2038C>T (p.Arg680Cys) rs759356162 0.00002
NM_014000.3(VCL):c.2204A>G (p.Asp735Gly) rs1426976613 0.00002
NM_014000.3(VCL):c.224C>T (p.Pro75Leu) rs373830664 0.00002
NM_014000.3(VCL):c.2747C>T (p.Pro916Leu) rs143321584 0.00002
NM_014000.3(VCL):c.676G>A (p.Ala226Thr) rs146910007 0.00002
NM_014000.3(VCL):c.783+5G>A rs767694507 0.00002
NM_014000.3(VCL):c.1006G>A (p.Ala336Thr) rs565546734 0.00001
NM_014000.3(VCL):c.1046C>T (p.Ala349Val) rs777709634 0.00001
NM_014000.3(VCL):c.1050G>A (p.Met350Ile) rs771542436 0.00001
NM_014000.3(VCL):c.1114C>T (p.Arg372Cys) rs770954415 0.00001
NM_014000.3(VCL):c.1147A>G (p.Ser383Gly) rs1444969965 0.00001
NM_014000.3(VCL):c.1223T>C (p.Ile408Thr) rs878854969 0.00001
NM_014000.3(VCL):c.1238C>T (p.Ala413Val) rs794729190 0.00001
NM_014000.3(VCL):c.1246C>T (p.Arg416Trp) rs746004026 0.00001
NM_014000.3(VCL):c.1292T>G (p.Ile431Ser) rs766192312 0.00001
NM_014000.3(VCL):c.1298G>A (p.Arg433His) rs754046223 0.00001
NM_014000.3(VCL):c.1382C>G (p.Ala461Gly) rs886038800 0.00001
NM_014000.3(VCL):c.1433A>G (p.Asn478Ser) rs763235691 0.00001
NM_014000.3(VCL):c.1435C>T (p.Arg479Trp) rs369055603 0.00001
NM_014000.3(VCL):c.1604G>A (p.Gly535Glu) rs1342547968 0.00001
NM_014000.3(VCL):c.1612C>T (p.Arg538Trp) rs1371212023 0.00001
NM_014000.3(VCL):c.1640G>A (p.Arg547Gln) rs748044427 0.00001
NM_014000.3(VCL):c.1816A>G (p.Ile606Val) rs750293810 0.00001
NM_014000.3(VCL):c.1838C>T (p.Ala613Val) rs781520177 0.00001
NM_014000.3(VCL):c.184G>A (p.Val62Ile) rs147809878 0.00001
NM_014000.3(VCL):c.1863C>G (p.Asn621Lys) rs746293391 0.00001
NM_014000.3(VCL):c.1918C>G (p.Leu640Val) rs886047219 0.00001
NM_014000.3(VCL):c.1999A>G (p.Thr667Ala) rs1233764253 0.00001
NM_014000.3(VCL):c.2000C>T (p.Thr667Met) rs794729187 0.00001
NM_014000.3(VCL):c.2159A>T (p.Lys720Ile) rs1554818881 0.00001
NM_014000.3(VCL):c.2182G>A (p.Glu728Lys) rs144717954 0.00001
NM_014000.3(VCL):c.2284C>T (p.Arg762Trp) rs1334643090 0.00001
NM_014000.3(VCL):c.2285G>A (p.Arg762Gln) rs540039788 0.00001
NM_014000.3(VCL):c.2305A>G (p.Arg769Gly) rs566257885 0.00001
NM_014000.3(VCL):c.2332A>G (p.Lys778Glu) rs1840113067 0.00001
NM_014000.3(VCL):c.2338C>T (p.Arg780Cys) rs753445972 0.00001
NM_014000.3(VCL):c.2365G>A (p.Glu789Lys) rs745419923 0.00001
NM_014000.3(VCL):c.2378C>A (p.Thr793Asn) rs773421444 0.00001
NM_014000.3(VCL):c.238A>C (p.Lys80Gln) rs775532257 0.00001
NM_014000.3(VCL):c.239+3G>A rs372571288 0.00001
NM_014000.3(VCL):c.2602G>A (p.Gly868Ser) rs960636997 0.00001
NM_014000.3(VCL):c.2803G>A (p.Asp935Asn) rs746658025 0.00001
NM_014000.3(VCL):c.2807C>T (p.Ala936Val) rs754681045 0.00001
NM_014000.3(VCL):c.2829del (p.Asp944fs) rs750347797 0.00001
NM_014000.3(VCL):c.2834T>C (p.Met945Thr) rs1443843519 0.00001
NM_014000.3(VCL):c.2852C>G (p.Pro951Arg) rs368570586 0.00001
NM_014000.3(VCL):c.2867T>G (p.Met956Arg) rs765717598 0.00001
NM_014000.3(VCL):c.2893C>T (p.Pro965Ser) rs749236817 0.00001
NM_014000.3(VCL):c.2923C>T (p.Arg975Trp) rs121917776 0.00001
NM_014000.3(VCL):c.292G>A (p.Asp98Asn) rs794729193 0.00001
NM_014000.3(VCL):c.3007C>T (p.Arg1003Trp) rs753166628 0.00001
NM_014000.3(VCL):c.3259-5T>C rs1057523095 0.00001
NM_014000.3(VCL):c.457A>C (p.Thr153Pro) rs376921881 0.00001
NM_014000.3(VCL):c.527A>G (p.Asp176Gly) rs573623641 0.00001
NM_014000.3(VCL):c.529G>A (p.Glu177Lys) rs1007055332 0.00001
NM_014000.3(VCL):c.562C>T (p.Arg188Ter) rs397517244 0.00001
NM_014000.3(VCL):c.581C>T (p.Ser194Leu) rs921627346 0.00001
NM_014000.3(VCL):c.689G>A (p.Arg230His) rs749628307 0.00001
NM_014000.3(VCL):c.739G>A (p.Val247Met) rs545372383 0.00001
NM_014000.3(VCL):c.844G>T (p.Gly282Cys) rs766091503 0.00001
NM_014000.3(VCL):c.952C>T (p.Arg318Cys) rs397517247 0.00001
NM_014000.3(VCL):c.997G>A (p.Asp333Asn) rs778677392 0.00001
NM_014000.3(VCL):c.1001_1015del (p.Gln334_Leu338del) rs1554817370
NM_014000.3(VCL):c.1016G>A (p.Arg339His)
NM_014000.3(VCL):c.1031G>T (p.Gly344Val)
NM_014000.3(VCL):c.1040C>A (p.Pro347Gln)
NM_014000.3(VCL):c.1064A>G (p.Gln355Arg)
NM_014000.3(VCL):c.1108G>C (p.Ala370Pro)
NM_014000.3(VCL):c.1115G>A (p.Arg372His) rs377289804
NM_014000.3(VCL):c.1171G>T (p.Ala391Ser)
NM_014000.3(VCL):c.1195A>G (p.Asn399Asp) rs377228795
NM_014000.3(VCL):c.1198G>T (p.Gly400Cys) rs201361282
NM_014000.3(VCL):c.1228G>A (p.Gly410Ser)
NM_014000.3(VCL):c.1312A>G (p.Ile438Val)
NM_014000.3(VCL):c.1332A>C (p.Lys444Asn)
NM_014000.3(VCL):c.1345C>T (p.Arg449Ter)
NM_014000.3(VCL):c.1349G>C (p.Arg450Thr)
NM_014000.3(VCL):c.1354G>A (p.Gly452Arg) rs1015527957
NM_014000.3(VCL):c.1359A>C (p.Lys453Asn)
NM_014000.3(VCL):c.1379G>A (p.Arg460Gln) rs753026034
NM_014000.3(VCL):c.1391A>G (p.Lys464Arg)
NM_014000.3(VCL):c.1395G>T (p.Gln465His)
NM_014000.3(VCL):c.142C>T (p.Gln48Ter)
NM_014000.3(VCL):c.1445C>A (p.Ala482Asp)
NM_014000.3(VCL):c.145G>A (p.Ala49Thr)
NM_014000.3(VCL):c.146C>G (p.Ala49Gly)
NM_014000.3(VCL):c.1472T>C (p.Val491Ala) rs1839933596
NM_014000.3(VCL):c.1495C>G (p.Gln499Glu)
NM_014000.3(VCL):c.1538G>A (p.Gly513Glu)
NM_014000.3(VCL):c.1543+2dup
NM_014000.3(VCL):c.1589C>G (p.Ala530Gly)
NM_014000.3(VCL):c.1591A>G (p.Asn531Asp)
NM_014000.3(VCL):c.1594G>A (p.Val532Ile)
NM_014000.3(VCL):c.1627G>A (p.Ala543Thr)
NM_014000.3(VCL):c.1639C>T (p.Arg547Ter) rs397517234
NM_014000.3(VCL):c.1648C>G (p.Gln550Glu) rs1406371942
NM_014000.3(VCL):c.1655C>A (p.Thr552Lys)
NM_014000.3(VCL):c.1661A>G (p.Gln554Arg)
NM_014000.3(VCL):c.1666G>T (p.Ala556Ser)
NM_014000.3(VCL):c.168+1del
NM_014000.3(VCL):c.1685G>A (p.Gly562Glu)
NM_014000.3(VCL):c.1699C>T (p.Pro567Ser)
NM_014000.3(VCL):c.1718C>G (p.Ala573Gly)
NM_014000.3(VCL):c.173G>C (p.Gly58Ala)
NM_014000.3(VCL):c.1791T>A (p.Asp597Glu) rs1839983396
NM_014000.3(VCL):c.1801G>A (p.Asp601Asn)
NM_014000.3(VCL):c.1807A>T (p.Thr603Ser)
NM_014000.3(VCL):c.1810A>G (p.Thr604Ala) rs754470470
NM_014000.3(VCL):c.1856C>A (p.Ala619Glu) rs771628544
NM_014000.3(VCL):c.1856C>T (p.Ala619Val) rs771628544
NM_014000.3(VCL):c.1877T>C (p.Phe626Ser)
NM_014000.3(VCL):c.1880_1881insGGA (p.Phe626_Asp627insGlu)
NM_014000.3(VCL):c.1921G>A (p.Gly641Ser) rs765123545
NM_014000.3(VCL):c.1938G>T (p.Lys646Asn)
NM_014000.3(VCL):c.2021A>C (p.Gln674Pro)
NM_014000.3(VCL):c.2021A>G (p.Gln674Arg)
NM_014000.3(VCL):c.2023-1177_2051del
NM_014000.3(VCL):c.2035G>T (p.Ala679Ser) rs375392559
NM_014000.3(VCL):c.2132-3C>A rs1840110148
NM_014000.3(VCL):c.2137G>T (p.Val713Leu) rs374737519
NM_014000.3(VCL):c.2143G>A (p.Glu715Lys) rs1022329091
NM_014000.3(VCL):c.2219C>T (p.Ala740Val)
NM_014000.3(VCL):c.2255G>A (p.Gly752Glu) rs2131928418
NM_014000.3(VCL):c.2275C>T (p.Arg759Trp)
NM_014000.3(VCL):c.227C>T (p.Pro76Leu)
NM_014000.3(VCL):c.2330C>T (p.Pro777Leu) rs1564532927
NM_014000.3(VCL):c.2339G>A (p.Arg780His)
NM_014000.3(VCL):c.2386C>A (p.Pro796Thr) rs749471739
NM_014000.3(VCL):c.2388_2389delinsAG (p.Met797Val) rs1840114333
NM_014000.3(VCL):c.2389A>G (p.Met797Val)
NM_014000.3(VCL):c.2393T>C (p.Val798Ala)
NM_014000.3(VCL):c.2395A>G (p.Met799Val)
NM_014000.3(VCL):c.2407G>A (p.Ala803Thr) rs754294941
NM_014000.3(VCL):c.2435-2A>C
NM_014000.3(VCL):c.2453T>A (p.Leu818Gln) rs794727192
NM_014000.3(VCL):c.2455G>A (p.Asp819Asn)
NM_014000.3(VCL):c.2521G>A (p.Asp841Asn)
NM_014000.3(VCL):c.254G>T (p.Cys85Phe)
NM_014000.3(VCL):c.256A>T (p.Thr86Ser)
NM_014000.3(VCL):c.2656C>T (p.Pro886Ser)
NM_014000.3(VCL):c.2671G>A (p.Gly891Arg) rs2131933634
NM_014000.3(VCL):c.2700G>A (p.Met900Ile)
NM_014000.3(VCL):c.2771G>A (p.Gly924Asp)
NM_014000.3(VCL):c.2775A>G (p.Ile925Met)
NM_014000.3(VCL):c.2775_2780del (p.Gly926_Val927del) rs757018106
NM_014000.3(VCL):c.2777G>A (p.Gly926Asp)
NM_014000.3(VCL):c.2788G>A (p.Glu930Lys)
NM_014000.3(VCL):c.2809G>A (p.Ala937Thr) rs1314540118
NM_014000.3(VCL):c.2818C>T (p.Pro940Ser)
NM_014000.3(VCL):c.2825C>A (p.Pro942His)
NM_014000.3(VCL):c.2827C>A (p.Pro943Thr) rs71579375
NM_014000.3(VCL):c.2828del (p.Pro943fs) rs1840230101
NM_014000.3(VCL):c.2828dup (p.Pro943_Asp944insTer)
NM_014000.3(VCL):c.2866A>G (p.Met956Val) rs761830073
NM_014000.3(VCL):c.2882C>T (p.Pro961Leu) rs754591130
NM_014000.3(VCL):c.2918T>C (p.Leu973Ser)
NM_014000.3(VCL):c.2929G>C (p.Ala977Pro)
NM_014000.3(VCL):c.2940G>T (p.Trp980Cys)
NM_014000.3(VCL):c.3025A>G (p.Ser1009Gly)
NM_014000.3(VCL):c.3212C>T (p.Ala1071Val)
NM_014000.3(VCL):c.3250T>C (p.Ser1084Pro)
NM_014000.3(VCL):c.3297G>A (p.Met1099Ile)
NM_014000.3(VCL):c.3373C>G (p.Arg1125Gly)
NM_014000.3(VCL):c.3380T>C (p.Val1127Ala)
NM_014000.3(VCL):c.448G>T (p.Val150Leu)
NM_014000.3(VCL):c.451G>T (p.Val151Leu)
NM_014000.3(VCL):c.530A>G (p.Glu177Gly)
NM_014000.3(VCL):c.535C>G (p.Gln179Glu)
NM_014000.3(VCL):c.562C>G (p.Arg188Gly)
NM_014000.3(VCL):c.565G>A (p.Val189Met) rs151045204
NM_014000.3(VCL):c.565G>T (p.Val189Leu) rs151045204
NM_014000.3(VCL):c.585G>A (p.Met195Ile)
NM_014000.3(VCL):c.597del (p.Glu200fs) rs777492997
NM_014000.3(VCL):c.622+4C>G rs201020802
NM_014000.3(VCL):c.709dup (p.Met237fs)
NM_014000.3(VCL):c.731T>A (p.Ile244Lys) rs886038819
NM_014000.3(VCL):c.732A>G (p.Ile244Met)
NM_014000.3(VCL):c.773G>A (p.Trp258Ter)
NM_014000.3(VCL):c.780C>G (p.Ser260Arg) rs774377548
NM_014000.3(VCL):c.818T>C (p.Ile273Thr) rs762380935
NM_014000.3(VCL):c.854G>T (p.Arg285Leu)
NM_014000.3(VCL):c.868T>A (p.Ser290Thr)
NM_014000.3(VCL):c.873A>G (p.Pro291=)
NM_014000.3(VCL):c.889C>T (p.Gln297Ter)
NM_014000.3(VCL):c.898A>G (p.Arg300Gly)
NM_014000.3(VCL):c.923A>T (p.Lys308Ile)
NM_014000.3(VCL):c.949G>C (p.Glu317Gln)
NM_014000.3(VCL):c.960G>C (p.Glu320Asp)
NM_014000.3(VCL):c.964C>G (p.Leu322Val)
NM_014000.3(VCL):c.981G>A (p.Met327Ile)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.