ClinVar Miner

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

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 48
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HGVS dbSNP gnomAD frequency
NM_014000.3(VCL):c.1506G>A (p.Arg502=) rs2228373 0.06736
NM_014000.3(VCL):c.945C>A (p.Gly315=) rs61731180 0.02850
NM_014000.3(VCL):c.2950-22C>G rs71579378 0.00753
NM_014000.3(VCL):c.2801C>T (p.Ala934Val) rs16931179 0.00658
NM_014000.3(VCL):c.1317T>C (p.Ser439=) rs71579355 0.00442
NM_014000.3(VCL):c.1177-15C>T rs115083446 0.00414
NM_014000.3(VCL):c.1542C>T (p.Val514=) rs7904077 0.00380
NM_014000.3(VCL):c.3258+10A>T rs71579379 0.00267
NM_014000.3(VCL):c.2025G>A (p.Val675=) rs140766884 0.00256
NM_014000.3(VCL):c.2023-20A>G rs143756084 0.00247
NM_014000.3(VCL):c.1907A>G (p.His636Arg) rs71579374 0.00240
NM_014000.3(VCL):c.1671C>T (p.Asp557=) rs137877092 0.00228
NM_014000.3(VCL):c.1353-19G>A rs145537824 0.00193
NM_014000.3(VCL):c.660C>T (p.Asn220=) rs56264452 0.00091
NM_014000.3(VCL):c.1572C>T (p.Ala524=) rs138566234 0.00086
NM_014000.3(VCL):c.1348A>C (p.Arg450=) rs142128712 0.00075
NM_014000.3(VCL):c.1555A>C (p.Ile519Leu) rs141033098 0.00064
NM_014000.3(VCL):c.2521G>C (p.Asp841His) rs150385900 0.00051
NM_014000.3(VCL):c.492T>G (p.Leu164=) rs143702799 0.00033
NM_014000.3(VCL):c.1626C>T (p.Leu542=) rs150402791 0.00031
NM_014000.3(VCL):c.366G>A (p.Leu122=) rs199562976 0.00029
NM_014000.3(VCL):c.1744-19T>G rs201488697 0.00022
NM_014000.3(VCL):c.1788A>C (p.Ser596=) rs199582103 0.00021
NM_014000.3(VCL):c.1716T>G (p.Leu572=) rs189781480 0.00016
NM_014000.3(VCL):c.1842G>A (p.Thr614=) rs144117013 0.00016
NM_014000.3(VCL):c.2796T>C (p.Asp932=) rs140308982 0.00012
NM_014000.3(VCL):c.1290C>T (p.Asp430=) rs576271894 0.00009
NM_014000.3(VCL):c.2142C>T (p.Asp714=) rs373790383 0.00009
NM_014000.3(VCL):c.2799G>A (p.Ala933=) rs199507346 0.00009
NM_014000.3(VCL):c.3066C>T (p.Ile1022=) rs138619320 0.00009
NM_014000.3(VCL):c.3333T>C (p.Ala1111=) rs147415627 0.00008
NM_014000.3(VCL):c.2349G>A (p.Val783=) rs558040780 0.00006
NM_014000.3(VCL):c.404T>C (p.Ile135Thr) rs373744314 0.00006
NM_014000.3(VCL):c.528C>T (p.Asp176=) rs746453891 0.00005
NM_014000.3(VCL):c.1177-14G>A rs778137720 0.00004
NM_014000.3(VCL):c.2265T>C (p.Ser755=) rs147887754 0.00004
NM_014000.3(VCL):c.1164C>T (p.Ile388=) rs370852950 0.00003
NM_014000.3(VCL):c.3154-6C>T rs371257509 0.00001
NM_014000.3(VCL):c.424T>C (p.Leu142=) rs762497815 0.00001
NM_014000.3(VCL):c.874+13T>C rs777617736 0.00001
NM_014000.3(VCL):c.875-5T>C rs1225977039 0.00001
NM_014000.3(VCL):c.1294C>T (p.Leu432=) rs144146254
NM_014000.3(VCL):c.168+9G>T rs997516030
NM_014000.3(VCL):c.2529G>A (p.Pro843=) rs1591714816
NM_014000.3(VCL):c.2560C>T (p.Leu854=) rs551463686
NM_014000.3(VCL):c.2862_2864del (p.Leu955del) rs397517237
NM_014000.3(VCL):c.622+4C>G rs201020802
NM_014000.3(VCL):c.622+4C>T rs201020802

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