ClinVar Miner

List of variants in gene VCAN reported as likely benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 82
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HGVS dbSNP gnomAD frequency
NM_004385.5(VCAN):c.*31A>G rs17206014 0.02076
NM_004385.5(VCAN):c.2875A>T (p.Ser959Cys) rs78164236 0.00525
NM_004385.5(VCAN):c.*1614G>T rs145490018 0.00455
NM_004385.5(VCAN):c.*1652G>C rs148439157 0.00406
NM_004385.5(VCAN):c.4604A>G (p.Glu1535Gly) rs61749614 0.00315
NM_004385.5(VCAN):c.5187G>A (p.Glu1729=) rs35648048 0.00302
NM_004385.5(VCAN):c.1523T>A (p.Ile508Asn) rs143368552 0.00271
NM_004385.5(VCAN):c.9234G>A (p.Glu3078=) rs139453864 0.00270
NM_004385.5(VCAN):c.574G>A (p.Gly192Arg) rs141008923 0.00245
NM_004385.5(VCAN):c.5750A>T (p.Tyr1917Phe) rs141477510 0.00225
NM_004385.5(VCAN):c.2159T>C (p.Val720Ala) rs76418670 0.00222
NM_004385.5(VCAN):c.7551C>T (p.Asp2517=) rs77870162 0.00182
NM_004385.5(VCAN):c.*961T>C rs531984651 0.00097
NM_004385.5(VCAN):c.6767T>C (p.Leu2256Pro) rs146630369 0.00072
NM_004385.5(VCAN):c.*18A>G rs187567161 0.00071
NM_004385.5(VCAN):c.3713G>C (p.Arg1238Thr) rs146560021 0.00071
NM_004385.5(VCAN):c.854C>T (p.Ala285Val) rs144939909 0.00066
NM_004385.5(VCAN):c.1931C>T (p.Pro644Leu) rs148104757 0.00051
NM_004385.5(VCAN):c.591C>T (p.Asp197=) rs148875090 0.00051
NM_004385.5(VCAN):c.7489A>G (p.Lys2497Glu) rs140606678 0.00044
NM_004385.5(VCAN):c.3201G>A (p.Glu1067=) rs201157092 0.00043
NM_004385.5(VCAN):c.9124G>A (p.Asp3042Asn) rs144214095 0.00041
NM_004385.5(VCAN):c.7374A>G (p.Thr2458=) rs148715382 0.00040
NM_004385.5(VCAN):c.4272A>G (p.Pro1424=) rs150960939 0.00039
NM_004385.5(VCAN):c.7480G>C (p.Glu2494Gln) rs147255921 0.00038
NM_004385.5(VCAN):c.9380-4T>A rs139854446 0.00038
NM_004385.5(VCAN):c.*835G>A rs184855903 0.00035
NM_004385.5(VCAN):c.5859G>T (p.Thr1953=) rs80028865 0.00035
NM_004385.5(VCAN):c.-119A>C rs557823406 0.00030
NM_004385.5(VCAN):c.1895C>T (p.Thr632Met) rs143729093 0.00030
NM_004385.5(VCAN):c.9025G>A (p.Glu3009Lys) rs146090207 0.00024
NM_004385.5(VCAN):c.2315C>G (p.Ala772Gly) rs141007991 0.00019
NM_004385.5(VCAN):c.2943A>T (p.Thr981=) rs144070403 0.00019
NM_004385.5(VCAN):c.7715C>T (p.Ser2572Leu) rs149032014 0.00019
NM_004385.5(VCAN):c.7893A>T (p.Leu2631Phe) rs148063549 0.00019
NM_004385.5(VCAN):c.2234A>C (p.Lys745Thr) rs144502710 0.00018
NM_004385.5(VCAN):c.3094C>G (p.Gln1032Glu) rs201255257 0.00016
NM_004385.5(VCAN):c.6127G>A (p.Glu2043Lys) rs138937534 0.00015
NM_004385.5(VCAN):c.9291G>A (p.Pro3097=) rs375652154 0.00015
NM_004385.5(VCAN):c.4546A>G (p.Lys1516Glu) rs144610900 0.00014
NM_004385.5(VCAN):c.5615C>T (p.Pro1872Leu) rs150017263 0.00014
NM_004385.5(VCAN):c.7638C>T (p.Asp2546=) rs144914004 0.00014
NM_004385.5(VCAN):c.7966A>G (p.Thr2656Ala) rs756823982 0.00014
NM_004385.5(VCAN):c.7581C>T (p.Phe2527=) rs149880697 0.00013
NM_004385.5(VCAN):c.8634A>G (p.Pro2878=) rs200031614 0.00011
NM_004385.5(VCAN):c.2220T>C (p.Ser740=) rs201834775 0.00010
NM_004385.5(VCAN):c.5190A>G (p.Gly1730=) rs201888251 0.00010
NM_004385.5(VCAN):c.7493G>T (p.Ser2498Ile) rs761405097 0.00010
NM_004385.5(VCAN):c.*707G>A rs545081931 0.00009
NM_004385.5(VCAN):c.2542G>A (p.Glu848Lys) rs188853533 0.00009
NM_004385.5(VCAN):c.5526C>T (p.Ala1842=) rs150593011 0.00009
NM_004385.5(VCAN):c.*218G>A rs532122355 0.00007
NM_004385.5(VCAN):c.1192G>A (p.Val398Met) rs186214606 0.00007
NM_004385.5(VCAN):c.5202G>A (p.Thr1734=) rs138599596 0.00006
NM_004385.5(VCAN):c.7884C>A (p.Asn2628Lys) rs201327923 0.00006
NM_004385.5(VCAN):c.249C>A (p.Val83=) rs751640388 0.00005
NM_004385.5(VCAN):c.9049G>C (p.Ala3017Pro) rs774896703 0.00005
NM_004385.5(VCAN):c.9481C>G (p.Leu3161Val) rs765359111 0.00005
NM_004385.5(VCAN):c.109T>G (p.Ser37Ala) rs142740596 0.00004
NM_004385.5(VCAN):c.8338C>T (p.Leu2780=) rs541755820 0.00004
NM_004385.5(VCAN):c.8683G>C (p.Asp2895His) rs202198791 0.00004
NM_004385.5(VCAN):c.9275G>C (p.Arg3092Pro) rs528022086 0.00004
NM_004385.5(VCAN):c.9880+11C>A rs373723999 0.00004
NM_004385.5(VCAN):c.690T>C (p.Tyr230=) rs539798172 0.00003
NM_004385.5(VCAN):c.6943G>C (p.Val2315Leu) rs3734094 0.00003
NM_004385.5(VCAN):c.1127A>C (p.Asp376Ala) rs181669993 0.00001
NM_004385.5(VCAN):c.1794G>A (p.Glu598=) rs760822691 0.00001
NM_004385.5(VCAN):c.3204C>T (p.Gly1068=) rs142805131 0.00001
NM_004385.5(VCAN):c.3282A>G (p.Pro1094=) rs140613404 0.00001
NM_004385.5(VCAN):c.3683C>T (p.Ala1228Val) rs200685807 0.00001
NM_004385.5(VCAN):c.4248C>T (p.Leu1416=) rs758617685 0.00001
NM_004385.5(VCAN):c.6269A>G (p.Gln2090Arg) rs767918859 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_004385.5(VCAN):c.*1266G>C rs544686778
NM_004385.5(VCAN):c.*232_*235del rs372079782
NM_004385.5(VCAN):c.*816C>A rs111455323
NM_004385.5(VCAN):c.3188T>C (p.Leu1063Pro) rs61754532
NM_004385.5(VCAN):c.6672T>C (p.Asp2224=) rs183187115
NM_004385.5(VCAN):c.6902T>G (p.Phe2301Cys) rs160278
NM_004385.5(VCAN):c.8272G>T (p.Gly2758Cys) rs577603057
NM_004385.5(VCAN):c.8362A>G (p.Met2788Val) rs201444192

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