ClinVar Miner

List of variants in gene GLB1 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 54
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HGVS dbSNP gnomAD frequency
NM_000404.4(GLB1):c.457+235A>G rs9865113 0.98130
NM_000404.4(GLB1):c.246-194A>G rs7610916 0.97490
NM_000404.4(GLB1):c.553-119A>G rs7637435 0.97005
NM_000404.4(GLB1):c.1561T>C (p.Cys521Arg) rs4302331 0.93112
NM_000404.4(GLB1):c.955+60A>G rs12632196 0.75289
NM_000404.4(GLB1):c.793-132T>G rs6550200 0.68532
NC_000003.12:g.33097518del rs35744352 0.48743
NM_000404.4(GLB1):c.396+122C>A rs11129543 0.47988
NM_000404.4(GLB1):c.1233+174G>T rs13093517 0.31462
NM_000404.4(GLB1):c.1347+208A>G rs4371463 0.25375
NM_000404.4(GLB1):c.1233+8T>C rs13093698 0.21250
NM_000404.4(GLB1):c.1734+233C>T rs62252531 0.21080
NM_000404.4(GLB1):c.956-190C>G rs34173901 0.17958
NM_000404.4(GLB1):c.1068+264G>A rs34840292 0.17566
NM_000404.4(GLB1):c.1068+217G>T rs35480293 0.17555
NM_000404.4(GLB1):c.956-118G>C rs35000357 0.16700
NM_000404.4(GLB1):c.955+144T>C rs13062239 0.12963
NM_000404.4(GLB1):c.76-4746T>C rs9827863 0.11214
NM_000404.4(GLB1):c.76-4426C>T rs9865342 0.11155
NM_000404.4(GLB1):c.458-11T>C rs34204221 0.10591
NM_000404.4(GLB1):c.457+283T>C rs9882717 0.10136
NM_000404.4(GLB1):c.457+154C>T rs9845695 0.10068
NM_000404.4(GLB1):c.1480-149T>C rs57857629 0.08553
NM_000404.4(GLB1):c.1480-320C>A rs57739080 0.08528
NM_000404.4(GLB1):c.1479+204A>G rs12054351 0.08163
NM_000404.4(GLB1):c.792+231G>A rs75764209 0.07312
NM_000404.4(GLB1):c.792+250G>C rs4493381 0.07312
NM_000404.4(GLB1):c.734-112T>C rs80059915 0.07289
NM_000404.4(GLB1):c.1069-231G>A rs73826342 0.06953
NM_000404.4(GLB1):c.793-185C>G rs77890945 0.06842
NM_000404.4(GLB1):c.1347+194G>T rs112116560 0.06822
NM_000404.4(GLB1):c.1144-256C>G rs76705613 0.06456
NM_000404.4(GLB1):c.1233+218C>T rs80045472 0.06454
NM_000404.4(GLB1):c.1234-177C>T rs55970801 0.06264
NM_000404.4(GLB1):c.734-80G>A rs75639377 0.05351
NM_000404.4(GLB1):c.1594A>G (p.Ser532Gly) rs73826339 0.05158
NM_000404.4(GLB1):c.1480-74C>G rs73826340 0.05149
NM_000404.4(GLB1):c.1480-272T>C rs75119558 0.02174
NM_000404.4(GLB1):c.1734+188C>T rs73826338 0.02054
NM_000404.4(GLB1):c.325C>T (p.Arg109Trp) rs35289681 0.01618
NM_000404.4(GLB1):c.1824G>C (p.Leu608=) rs77226678 0.01441
NM_000404.4(GLB1):c.1306C>T (p.Leu436Phe) rs34421970 0.00952
NM_000404.4(GLB1):c.*319G>A rs139730198 0.00851
NM_000404.4(GLB1):c.793-19C>T rs114082733 0.00619
NM_000404.4(GLB1):c.246-252A>C rs7610931
NM_000404.4(GLB1):c.733+78A>G rs77452319
NM_000404.4(GLB1):c.734-99G>T rs72856120
NM_000404.4(GLB1):c.76-4483G>A
NM_000404.4(GLB1):c.792+10G>T rs79518579
NM_000404.4(GLB1):c.955+123dup rs71630561
NM_000404.4(GLB1):c.955+139dup rs59740209
NM_000404.4(GLB1):c.955+142_955+143insTTTTCTTTT rs764769471
NM_000404.4(GLB1):c.955+154del rs59740209
NM_000404.4(GLB1):c.955+93del rs143982364

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