ClinVar Miner

List of variants in gene VCAN reported as uncertain significance for Wagner syndrome

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Gene type:
ClinVar version:
Total variants: 87
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HGVS dbSNP gnomAD frequency
NM_004385.5(VCAN):c.*905A>G rs796702160 0.01288
NM_004385.5(VCAN):c.*813_*816dup rs140261411 0.00522
NM_004385.5(VCAN):c.*1031T>C rs548595991 0.00264
NM_004385.5(VCAN):c.-75A>G rs886060816 0.00195
NM_004385.5(VCAN):c.*1408G>A rs886060837 0.00024
NM_004385.5(VCAN):c.6034G>A (p.Gly2012Ser) rs138550552 0.00014
NM_004385.5(VCAN):c.*819T>C rs757423230 0.00012
NM_004385.5(VCAN):c.5489C>T (p.Ser1830Phe) rs141725839 0.00011
NM_004385.5(VCAN):c.7035G>A (p.Thr2345=) rs200757689 0.00010
NM_004385.5(VCAN):c.5201C>T (p.Thr1734Met) rs200941140 0.00009
NM_004385.5(VCAN):c.*1091C>T rs886060836 0.00006
NM_004385.5(VCAN):c.*2C>T rs370984795 0.00006
NM_004385.5(VCAN):c.*1671C>T rs776524825 0.00005
NM_004385.5(VCAN):c.9481C>G (p.Leu3161Val) rs765359111 0.00005
NM_004385.5(VCAN):c.*93G>A rs560274180 0.00004
NM_004385.5(VCAN):c.-135G>A rs886060814 0.00004
NM_004385.5(VCAN):c.109T>G (p.Ser37Ala) rs142740596 0.00004
NM_004385.5(VCAN):c.5836C>T (p.His1946Tyr) rs886060825 0.00004
NM_004385.5(VCAN):c.-259C>T rs886060813 0.00003
NM_004385.5(VCAN):c.6727A>G (p.Thr2243Ala) rs751656177 0.00003
NM_004385.5(VCAN):c.1240G>A (p.Ala414Thr) rs749795455 0.00002
NM_004385.5(VCAN):c.5482C>T (p.Pro1828Ser) rs886060823 0.00002
NM_004385.5(VCAN):c.8063C>T (p.Pro2688Leu) rs755806449 0.00002
NM_004385.5(VCAN):c.1874G>A (p.Arg625Lys) rs779485029 0.00001
NM_004385.5(VCAN):c.2741G>A (p.Gly914Asp) rs200429289 0.00001
NM_004385.5(VCAN):c.3202G>A (p.Gly1068Ser) rs1231605869 0.00001
NM_004385.5(VCAN):c.3204C>T (p.Gly1068=) rs142805131 0.00001
NM_004385.5(VCAN):c.3540A>G (p.Leu1180=) rs141764458 0.00001
NM_004385.5(VCAN):c.4248C>T (p.Leu1416=) rs758617685 0.00001
NM_004385.5(VCAN):c.4292G>A (p.Arg1431His) rs747887033 0.00001
NM_004385.5(VCAN):c.5427C>T (p.His1809=) rs779803420 0.00001
NM_004385.5(VCAN):c.5801T>G (p.Phe1934Cys) rs886060824 0.00001
NM_004385.5(VCAN):c.6169A>C (p.Arg2057=) rs886060826 0.00001
NM_004385.5(VCAN):c.7895C>T (p.Thr2632Ile) rs767660495 0.00001
NM_004385.5(VCAN):c.8454G>A (p.Ala2818=) rs773474075 0.00001
NM_004385.4(VCAN):c.-334C>T rs886060812
NM_004385.5(VCAN):c.*160A>G rs886060828
NM_004385.5(VCAN):c.*1717C>T rs537687030
NM_004385.5(VCAN):c.*1753C>T rs904583529
NM_004385.5(VCAN):c.*446T>C rs886060829
NM_004385.5(VCAN):c.*625G>A rs939870012
NM_004385.5(VCAN):c.*881_*883del rs886060831
NM_004385.5(VCAN):c.*883_*885del rs886060832
NM_004385.5(VCAN):c.*898_*905delinsG rs886060833
NM_004385.5(VCAN):c.*905_*912del rs886060834
NM_004385.5(VCAN):c.*909del rs886060835
NM_004385.5(VCAN):c.-87A>G rs1744205658
NM_004385.5(VCAN):c.-89T>C rs886060815
NM_004385.5(VCAN):c.10157G>A (p.Arg3386His) rs370521277
NM_004385.5(VCAN):c.1112C>T (p.Pro371Leu) rs1745984120
NM_004385.5(VCAN):c.2381G>C (p.Ser794Thr) rs2112409816
NM_004385.5(VCAN):c.2937C>T (p.Pro979=) rs886060819
NM_004385.5(VCAN):c.297G>C (p.Gly99=) rs886060817
NM_004385.5(VCAN):c.3046A>G (p.Ile1016Val) rs139937202
NM_004385.5(VCAN):c.3067A>G (p.Thr1023Ala) rs886060820
NM_004385.5(VCAN):c.3103T>G (p.Phe1035Val) rs886060821
NM_004385.5(VCAN):c.3264A>G (p.Pro1088=) rs767745674
NM_004385.5(VCAN):c.3340G>A (p.Val1114Met) rs1746106150
NM_004385.5(VCAN):c.3673C>A (p.Pro1225Thr) rs1746123738
NM_004385.5(VCAN):c.375G>A (p.Ala125=) rs762753715
NM_004385.5(VCAN):c.3956A>G (p.His1319Arg) rs886060822
NM_004385.5(VCAN):c.4022G>A (p.Ser1341Asn) rs1746739066
NM_004385.5(VCAN):c.4236T>C (p.Asn1412=) rs752922531
NM_004385.5(VCAN):c.4545C>T (p.Ala1515=) rs1746771607
NM_004385.5(VCAN):c.4761T>A (p.Val1587=) rs1746783267
NM_004385.5(VCAN):c.4805C>A (p.Thr1602Asn) rs1386946213
NM_004385.5(VCAN):c.6138A>G (p.Gly2046=) rs1746854455
NM_004385.5(VCAN):c.6201A>G (p.Glu2067=) rs780184359
NM_004385.5(VCAN):c.6277G>C (p.Glu2093Gln) rs756371655
NM_004385.5(VCAN):c.6704A>T (p.His2235Leu) rs1746887068
NM_004385.5(VCAN):c.6829G>A (p.Glu2277Lys) rs1746893996
NM_004385.5(VCAN):c.7337C>T (p.Ala2446Val) rs1561257553
NM_004385.5(VCAN):c.7434T>G (p.Thr2478=) rs1746925822
NM_004385.5(VCAN):c.7447C>G (p.Pro2483Ala) rs1746926635
NM_004385.5(VCAN):c.7462A>G (p.Met2488Val) rs2112447405
NM_004385.5(VCAN):c.8052C>T (p.Asp2684=) rs184452501
NM_004385.5(VCAN):c.8058A>C (p.Leu2686Phe) rs780717994
NM_004385.5(VCAN):c.8064C>T (p.Pro2688=) rs886060827
NM_004385.5(VCAN):c.8474C>T (p.Pro2825Leu) rs969739770
NM_004385.5(VCAN):c.8482C>T (p.Pro2828Ser) rs1746988417
NM_004385.5(VCAN):c.9218T>C (p.Ile3073Thr) rs200780028
NM_004385.5(VCAN):c.9265+4A>G rs1747036627
NM_004385.5(VCAN):c.9266-14C>T rs1747170920
NM_004385.5(VCAN):c.930G>A (p.Val310=) rs886060818
NM_004385.5(VCAN):c.9403C>A (p.Pro3135Thr) rs1747300004
NM_004385.5(VCAN):c.9494-9T>G rs1747543997
NM_004385.5(VCAN):c.9918G>C (p.Lys3306Asn) rs1748612637

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