ClinVar Miner

List of variants in gene VIM studied for cataract 30

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Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_003380.5(VIM):c.-22G>C rs3758410 0.34400
NM_003380.5(VIM):c.813C>T (p.Asp271=) rs4903 0.05252
NM_003380.5(VIM):c.879C>G (p.Ser293=) rs11254467 0.01153
NM_003380.5(VIM):c.1009-10C>T rs79719081 0.00570
NM_003380.5(VIM):c.542A>C (p.Asp181Ala) rs149942621 0.00115
NM_003380.5(VIM):c.749A>G (p.Gln250Arg) rs145152785 0.00111
NM_003380.5(VIM):c.282C>T (p.Thr94=) rs144539901 0.00107
NM_003380.5(VIM):c.1008+18A>G rs368836644 0.00103
NM_003380.5(VIM):c.987A>G (p.Glu329=) rs147429387 0.00026
NM_003380.5(VIM):c.911G>A (p.Arg304Gln) rs552165238 0.00021
NM_003380.5(VIM):c.384T>C (p.Asn128=) rs147857896 0.00016
NM_003380.5(VIM):c.1360-17T>G rs764183925 0.00010
NM_003380.5(VIM):c.758A>G (p.His253Arg) rs773762488 0.00004
NM_003380.5(VIM):c.1009-8C>A rs372984113 0.00003
NM_003380.5(VIM):c.451G>A (p.Glu151Lys) rs121917775 0.00003
NM_003380.5(VIM):c.1141C>T (p.Arg381Cys) rs749084801 0.00002
NM_003380.5(VIM):c.134G>A (p.Arg45His) rs778098458 0.00001
NM_003380.5(VIM):c.99G>T (p.Thr33=) rs531385322 0.00001
NM_003380.5(VIM):c.1024C>G (p.Arg342Gly)
NM_003380.5(VIM):c.1122G>A (p.Glu374=)
NM_003380.5(VIM):c.1133G>A (p.Arg378His)
NM_003380.5(VIM):c.1360-18G>T
NM_003380.5(VIM):c.1360-7del
NM_003380.5(VIM):c.1360-7dup rs750651760
NM_003380.5(VIM):c.1368C>T (p.Asn456=)
NM_003380.5(VIM):c.1372A>G (p.Thr458Ala)
NM_003380.5(VIM):c.1374_1375dup (p.Ser459fs) rs1846907790
NM_003380.5(VIM):c.15del (p.Val6fs) rs864309690
NM_003380.5(VIM):c.423A>G (p.Gln141=) rs2131679660
NM_003380.5(VIM):c.451GAG[2] (p.Glu153del)
NM_003380.5(VIM):c.468G>C (p.Glu156Asp) rs1846752790
NM_003380.5(VIM):c.46G>A (p.Gly16Ser) rs773471865
NM_003380.5(VIM):c.598G>C (p.Glu200Gln) rs1037734535
NM_003380.5(VIM):c.623A>G (p.Gln208Arg) rs1085307141
NM_003380.5(VIM):c.624+17C>G
NM_003380.5(VIM):c.624+7A>C rs376197279
NM_003380.5(VIM):c.624+7A>G
NM_003380.5(VIM):c.626A>G (p.Asp209Gly)
NM_003380.5(VIM):c.720+18C>T rs7096093
NM_003380.5(VIM):c.807G>T (p.Leu269=) rs745874397
NM_003380.5(VIM):c.814G>A (p.Val272Ile)
NM_003380.5(VIM):c.82C>G (p.Arg28Gly)
NM_003380.5(VIM):c.882+20G>A
NM_003380.5(VIM):c.990G>C (p.Val330=)

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