ClinVar Miner

Variants in gene VCAN with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 29
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HGVS dbSNP gnomAD frequency
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.7419C>T (p.Ser2473=) rs61754536 0.00819
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.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.6767T>C (p.Leu2256Pro) rs146630369 0.00072
NM_004385.5(VCAN):c.8067G>A (p.Thr2689=) rs113287237 0.00069
NM_004385.5(VCAN):c.7489A>G (p.Lys2497Glu) rs140606678 0.00044
NM_004385.5(VCAN):c.9380-4T>A rs139854446 0.00038
NM_004385.5(VCAN):c.4762C>A (p.Pro1588Thr) rs151102598 0.00028
NM_004385.5(VCAN):c.7715C>T (p.Ser2572Leu) rs149032014 0.00019
NM_004385.5(VCAN):c.3076A>G (p.Ile1026Val) rs570423677 0.00015
NM_004385.5(VCAN):c.7638C>T (p.Asp2546=) rs144914004 0.00014
NM_004385.5(VCAN):c.7581C>T (p.Phe2527=) rs149880697 0.00013
NM_004385.5(VCAN):c.9454C>G (p.Leu3152Val) rs183984308 0.00007
NM_004385.5(VCAN):c.2618T>G (p.Ile873Arg) rs150395515 0.00006
NM_004385.5(VCAN):c.1775C>T (p.Thr592Ile) rs536252273 0.00001
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.6902T>G (p.Phe2301Cys) rs160278
NM_004385.5(VCAN):c.849C>T (p.Leu283=) rs142777690

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