ClinVar Miner

List of variants in gene VCL reported as likely benign by Invitae

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Gene type:
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Total variants: 48
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HGVS dbSNP
NM_014000.2(VCL):c.1177-5T>C rs370860265
NM_014000.2(VCL):c.1206G>A (p.Pro402=) rs779265817
NM_014000.2(VCL):c.120C>T (p.Leu40=) rs144080529
NM_014000.2(VCL):c.1234T>C (p.Leu412=) rs1554817846
NM_014000.2(VCL):c.1308G>A (p.Gly436=) rs878854970
NM_014000.2(VCL):c.1543+8C>G rs886047218
NM_014000.2(VCL):c.1544-6G>A rs1554818318
NM_014000.2(VCL):c.1555A>C (p.Ile519Leu) rs141033098
NM_014000.2(VCL):c.1575A>C (p.Glu525Asp) rs548487697
NM_014000.2(VCL):c.1607C>A (p.Pro536His) rs200624351
NM_014000.2(VCL):c.1626C>T (p.Leu542=) rs150402791
NM_014000.2(VCL):c.169-10C>G rs778769534
NM_014000.2(VCL):c.169-7C>G rs370213146
NM_014000.2(VCL):c.1767G>A (p.Glu589=) rs878854971
NM_014000.2(VCL):c.1842G>A (p.Thr614=) rs144117013
NM_014000.2(VCL):c.1932C>T (p.Ala644=) rs762594014
NM_014000.2(VCL):c.1947G>A (p.Ala649=) rs200168992
NM_014000.2(VCL):c.2142C>T (p.Asp714=) rs373790383
NM_014000.2(VCL):c.225A>G (p.Pro75=) rs759937112
NM_014000.2(VCL):c.2368T>C (p.Leu790=) rs780172945
NM_014000.2(VCL):c.2427C>T (p.Ser809=) rs183739128
NM_014000.2(VCL):c.2472C>G (p.Ile824Met) rs140381835
NM_014000.2(VCL):c.255C>T (p.Cys85=) rs117384664
NM_014000.2(VCL):c.2560C>T (p.Leu854=) rs551463686
NM_014000.2(VCL):c.2748G>A (p.Pro916=) rs761794669
NM_014000.2(VCL):c.2769G>C (p.Val923=) rs1057521313
NM_014000.2(VCL):c.2796T>C (p.Asp932=) rs140308982
NM_014000.2(VCL):c.2799G>A (p.Ala933=) rs199507346
NM_014000.2(VCL):c.2802C>T (p.Ala934=) rs372381809
NM_014000.2(VCL):c.2827C>G (p.Pro943Ala) rs71579375
NM_014000.2(VCL):c.2841C>T (p.Asp947=) rs566296495
NM_014000.2(VCL):c.2950-6C>T rs771375471
NM_014000.2(VCL):c.2967A>G (p.Ala989=) rs1010419468
NM_014000.2(VCL):c.3033C>T (p.Thr1011=) rs537877002
NM_014000.2(VCL):c.3066C>T (p.Ile1022=) rs138619320
NM_014000.2(VCL):c.3102G>A (p.Lys1034=) rs373584575
NM_014000.2(VCL):c.3237C>T (p.Ile1079=) rs201526599
NM_014000.2(VCL):c.3339A>C (p.Ser1113=) rs1060504504
NM_014000.2(VCL):c.366G>A (p.Leu122=) rs199562976
NM_014000.2(VCL):c.404T>C (p.Ile135Thr) rs373744314
NM_014000.2(VCL):c.424T>C (p.Leu142=) rs762497815
NM_014000.2(VCL):c.45G>A (p.Pro15=) rs775062250
NM_014000.2(VCL):c.519G>A (p.Lys173=) rs1060504505
NM_014000.2(VCL):c.528C>T (p.Asp176=) rs746453891
NM_014000.2(VCL):c.582G>A (p.Ser194=) rs773725513
NM_014000.2(VCL):c.590C>T (p.Thr197Ile) rs189242810
NM_014000.2(VCL):c.804A>G (p.Arg268=) rs556334319
NM_014000.2(VCL):c.808T>C (p.Leu270=) rs727505339

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