ClinVar Miner

List of variants in gene VCAN reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 129
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HGVS dbSNP gnomAD frequency
NM_004385.5(VCAN):c.9882C>T (p.Val3294=) rs308365 0.97301
NM_004385.5(VCAN):c.9380-181G>A rs7728751 0.81081
NM_004385.5(VCAN):c.4323G>A (p.Gln1441=) rs2548541 0.67722
NM_004385.5(VCAN):c.9494-63T>A rs6873404 0.57304
NM_004385.5(VCAN):c.4547A>G (p.Lys1516Arg) rs309559 0.50554
NM_004385.5(VCAN):c.5808T>C (p.Gly1936=) rs309557 0.50487
NM_004385.5(VCAN):c.6723A>G (p.Arg2241=) rs160279 0.50384
NM_004385.5(VCAN):c.9380-78_9380-76dup rs3842065 0.48314
NM_004385.5(VCAN):c.348T>C (p.Thr116=) rs12332199 0.40199
NM_004385.5(VCAN):c.71-176G>T rs4339334 0.39903
NM_004385.5(VCAN):c.5477G>A (p.Arg1826His) rs188703 0.38473
NM_004385.5(VCAN):c.645A>G (p.Val215=) rs4470745 0.33601
NM_004385.5(VCAN):c.9736-62G>A rs309585 0.29443
NM_004385.5(VCAN):c.1283G>A (p.Gly428Asp) rs2287926 0.16841
NM_004385.5(VCAN):c.9379+7T>C rs695103 0.09623
NM_004385.5(VCAN):c.4569A>G (p.Thr1523=) rs16900528 0.06757
NM_004385.5(VCAN):c.9630C>T (p.His3210=) rs16900564 0.05374
NM_004385.5(VCAN):c.9033C>A (p.Asn3011Lys) rs16900532 0.05068
NM_004385.5(VCAN):c.*730A>G rs8061 0.03976
NM_004385.5(VCAN):c.7030C>T (p.Pro2344Ser) rs61733401 0.02963
NM_004385.5(VCAN):c.9075G>A (p.Thr3025=) rs113014073 0.02820
NM_004385.5(VCAN):c.1043-10A>G rs115912456 0.02772
NM_004385.5(VCAN):c.1045A>G (p.Lys349Glu) rs61749613 0.02772
NM_004385.5(VCAN):c.8090G>A (p.Arg2697His) rs61733389 0.02711
NM_004385.5(VCAN):c.9266-129T>A rs60367526 0.02462
NM_004385.5(VCAN):c.393C>T (p.Asp131=) rs35042106 0.01920
NM_004385.5(VCAN):c.426G>A (p.Thr142=) rs35031282 0.01806
NM_004385.5(VCAN):c.5155A>T (p.Thr1719Ser) rs113965318 0.01319
NM_004385.5(VCAN):c.5576C>A (p.Ala1859Glu) rs34050047 0.01316
NM_004385.5(VCAN):c.6123C>T (p.Ile2041=) rs113659987 0.01282
NM_004385.5(VCAN):c.6237G>A (p.Lys2079=) rs80200229 0.01278
NM_004385.5(VCAN):c.8622G>A (p.Ala2874=) rs3096171 0.01237
NM_004385.5(VCAN):c.899C>T (p.Ser300Leu) rs2652098 0.00988
NM_004385.5(VCAN):c.4422T>C (p.Thr1474=) rs61733395 0.00980
NM_004385.5(VCAN):c.9104C>T (p.Ala3035Val) rs111512368 0.00955
NM_004385.5(VCAN):c.2065A>G (p.Thr689Ala) rs61754531 0.00895
NM_004385.5(VCAN):c.7419C>T (p.Ser2473=) rs61754536 0.00819
NM_004385.5(VCAN):c.2378T>C (p.Leu793Ser) rs76165877 0.00793
NM_004385.5(VCAN):c.2887C>T (p.Pro963Ser) rs76914270 0.00597
NM_004385.5(VCAN):c.2875A>T (p.Ser959Cys) rs78164236 0.00525
NM_004385.5(VCAN):c.*813_*816dup rs140261411 0.00522
NM_004385.5(VCAN):c.9652+20G>C rs77559437 0.00448
NM_004385.5(VCAN):c.1458G>A (p.Ser486=) rs150735474 0.00363
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.5750A>T (p.Tyr1917Phe) rs141477510 0.00225
NM_004385.5(VCAN):c.2159T>C (p.Val720Ala) rs76418670 0.00222
NM_004385.5(VCAN):c.4701A>G (p.Glu1567=) rs201926758 0.00202
NM_004385.5(VCAN):c.7551C>T (p.Asp2517=) rs77870162 0.00182
NM_004385.5(VCAN):c.71-18A>G rs143037679 0.00177
NM_004385.5(VCAN):c.9960G>C (p.Leu3320=) rs1802711 0.00171
NM_004385.5(VCAN):c.7743T>C (p.Asp2581=) rs75771891 0.00160
NM_004385.5(VCAN):c.9018T>A (p.Ser3006=) rs142894260 0.00156
NM_004385.5(VCAN):c.763C>T (p.Leu255Phe) rs36065652 0.00148
NM_004385.5(VCAN):c.1864T>C (p.Trp622Arg) rs147152203 0.00142
NM_004385.5(VCAN):c.1281T>C (p.Thr427=) rs144399722 0.00140
NM_004385.5(VCAN):c.7176C>T (p.Asn2392=) rs148114239 0.00138
NM_004385.5(VCAN):c.2666C>T (p.Thr889Ile) rs149153726 0.00128
NM_004385.5(VCAN):c.1243A>G (p.Ile415Val) rs141268824 0.00127
NM_004385.5(VCAN):c.2028A>G (p.Leu676=) rs147286274 0.00127
NM_004385.5(VCAN):c.2668G>T (p.Gly890Cys) rs146527005 0.00088
NM_004385.5(VCAN):c.4003+16C>G rs200855770 0.00083
NM_004385.5(VCAN):c.7568G>A (p.Arg2523His) rs139938317 0.00080
NM_004385.5(VCAN):c.6767T>C (p.Leu2256Pro) rs146630369 0.00072
NM_004385.5(VCAN):c.8067G>A (p.Thr2689=) rs113287237 0.00069
NM_004385.5(VCAN):c.591C>T (p.Asp197=) rs148875090 0.00051
NM_004385.5(VCAN):c.2262A>T (p.Thr754=) rs113094612 0.00048
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.7374A>G (p.Thr2458=) rs148715382 0.00040
NM_004385.5(VCAN):c.4272A>G (p.Pro1424=) rs150960939 0.00039
NM_004385.5(VCAN):c.9380-4T>A rs139854446 0.00038
NM_004385.5(VCAN):c.5859G>T (p.Thr1953=) rs80028865 0.00035
NM_004385.5(VCAN):c.394G>A (p.Val132Ile) rs201515722 0.00032
NM_004385.5(VCAN):c.1895C>T (p.Thr632Met) rs143729093 0.00030
NM_004385.5(VCAN):c.4762C>A (p.Pro1588Thr) rs151102598 0.00028
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.5863A>G (p.Met1955Val) rs574024586 0.00017
NM_004385.5(VCAN):c.3094C>G (p.Gln1032Glu) rs201255257 0.00016
NM_004385.5(VCAN):c.3076A>G (p.Ile1026Val) rs570423677 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.1396G>A (p.Val466Ile) rs147551428 0.00012
NM_004385.5(VCAN):c.2925T>C (p.Leu975=) rs139028655 0.00012
NM_004385.5(VCAN):c.5240C>T (p.Ser1747Leu) rs376380721 0.00012
NM_004385.5(VCAN):c.4599A>T (p.Ala1533=) rs540210222 0.00011
NM_004385.5(VCAN):c.1251T>C (p.Asp417=) rs371700683 0.00010
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.1230C>G (p.Val410=) rs148253316 0.00009
NM_004385.5(VCAN):c.5526C>T (p.Ala1842=) rs150593011 0.00009
NM_004385.5(VCAN):c.2067A>G (p.Thr689=) rs576246409 0.00008
NM_004385.5(VCAN):c.7371C>T (p.Thr2457=) rs199626605 0.00008
NM_004385.5(VCAN):c.1192G>A (p.Val398Met) rs186214606 0.00007
NM_004385.5(VCAN):c.9454C>G (p.Leu3152Val) rs183984308 0.00007
NM_004385.5(VCAN):c.1413G>A (p.Thr471=) rs182822707 0.00006
NM_004385.5(VCAN):c.5202G>A (p.Thr1734=) rs138599596 0.00006
NM_004385.5(VCAN):c.7456T>C (p.Ser2486Pro) rs771294587 0.00006
NM_004385.5(VCAN):c.9954C>T (p.Asn3318=) rs368432759 0.00006
NM_004385.5(VCAN):c.10122G>A (p.Lys3374=) rs375208337 0.00004
NM_004385.5(VCAN):c.7626T>C (p.Asn2542=) rs751601623 0.00004
NM_004385.5(VCAN):c.8338C>T (p.Leu2780=) rs541755820 0.00004
NM_004385.5(VCAN):c.3096G>A (p.Gln1032=) rs552692378 0.00003
NM_004385.5(VCAN):c.690T>C (p.Tyr230=) rs539798172 0.00003
NM_004385.5(VCAN):c.5289A>T (p.Thr1763=) rs190587279 0.00002
NM_004385.5(VCAN):c.1191C>T (p.Pro397=) rs762666146 0.00001
NM_004385.5(VCAN):c.1775C>T (p.Thr592Ile) rs536252273 0.00001
NM_004385.5(VCAN):c.9366C>T (p.Asp3122=) rs528024400 0.00001
NM_004385.5(VCAN):c.*816C>A rs111455323
NM_004385.5(VCAN):c.*900_*908del rs70975508
NM_004385.5(VCAN):c.*901_*908del rs70975508
NM_004385.5(VCAN):c.1042+21dup
NM_004385.5(VCAN):c.1400C>T (p.Ser467Phe) rs115336789
NM_004385.5(VCAN):c.3188T>C (p.Leu1063Pro) rs61754532
NM_004385.5(VCAN):c.4004-4dup rs1206862567
NM_004385.5(VCAN):c.6126C>T (p.Asp2042=) rs138910265
NM_004385.5(VCAN):c.630C>T (p.Ile210=) rs538498172
NM_004385.5(VCAN):c.6902T>A (p.Phe2301Tyr) rs160278
NM_004385.5(VCAN):c.6902T>G (p.Phe2301Cys) rs160278
NM_004385.5(VCAN):c.7329C>T (p.His2443=)
NM_004385.5(VCAN):c.749-5dup
NM_004385.5(VCAN):c.849C>T (p.Leu283=) rs142777690
NM_004385.5(VCAN):c.8809G>T (p.Asp2937Tyr) rs160277
NM_004385.5(VCAN):c.927T>C (p.Thr309=) rs536465380

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