ClinVar Miner

List of variants in gene MANBA reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 63
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HGVS dbSNP gnomAD frequency
NM_005908.4(MANBA):c.674-115A>G rs227370 0.64221
NM_005908.4(MANBA):c.674-209C>T rs227371 0.59880
NM_005908.4(MANBA):c.674-90C>A rs227369 0.59679
NM_005908.4(MANBA):c.850-31T>C rs227365 0.58834
NM_005908.4(MANBA):c.849+220T>A rs227367 0.56588
NM_005908.4(MANBA):c.2415+269A>G rs6839064 0.55357
NM_005908.4(MANBA):c.2158-166dup rs11436517 0.55343
NM_005908.4(MANBA):c.2015-28G>A rs4547797 0.55331
NM_005908.4(MANBA):c.2415+124C>T rs2272696 0.55328
NM_005908.4(MANBA):c.2416-105G>A rs735403 0.55317
NM_005908.4(MANBA):c.2368T>C (p.Leu790=) rs2272697 0.55313
NM_005908.4(MANBA):c.*124T>C rs3194585 0.55297
NM_005908.4(MANBA):c.*161C>T rs1054029 0.55296
NM_005908.4(MANBA):c.2416-227C>T rs735404 0.55112
NM_005908.4(MANBA):c.2015-55G>A rs2866414 0.54971
NM_005908.4(MANBA):c.2015-87C>T rs10027437 0.54401
NM_005908.4(MANBA):c.2415+142C>G rs2272695 0.54119
NM_005908.4(MANBA):c.2415+326G>C rs6813322 0.53653
NM_005908.4(MANBA):c.2158-114A>G rs909349 0.53612
NM_005908.4(MANBA):c.2015-147C>G rs4496586 0.53186
NM_005908.4(MANBA):c.1112+138C>T rs227277 0.51495
NM_005908.4(MANBA):c.1704+202C>T rs228614 0.49770
NM_005908.4(MANBA):c.1318-968G>A rs227361 0.49751
NM_005908.4(MANBA):c.1112+158A>G rs227276 0.44913
NM_005908.4(MANBA):c.757G>A (p.Val253Ile) rs227368 0.39095
NM_005908.4(MANBA):c.2014+125T>A rs765789 0.23027
NM_005908.4(MANBA):c.2015-299T>A rs10007196 0.17237
NM_005908.4(MANBA):c.960+213del rs200722092 0.12481
NM_005908.4(MANBA):c.315G>A (p.Thr105=) rs6857760 0.10011
NM_005908.4(MANBA):c.960+213A>T rs944261438 0.09546
NM_005908.4(MANBA):c.960+194C>T rs111412346 0.08652
NM_005908.4(MANBA):c.961-62T>A rs41276945 0.07392
NM_005908.4(MANBA):c.1317+71G>C rs59822982 0.07121
NM_005908.4(MANBA):c.1230+164_1230+165insAG rs10684965 0.06890
NM_005908.4(MANBA):c.1113-97T>C rs6812484 0.06888
NM_005908.4(MANBA):c.1112+126C>T rs6827148 0.06423
NM_005908.4(MANBA):c.961-301G>A rs60220347 0.06417
NM_005908.4(MANBA):c.1317+107G>T rs78025722 0.05862
NM_005908.4(MANBA):c.1317+106T>A rs74842201 0.05859
NM_005908.4(MANBA):c.831A>G (p.Leu277=) rs17033168 0.04331
NM_005908.4(MANBA):c.177+183G>A rs17033246 0.03214
NM_005908.4(MANBA):c.272+185T>C rs76080811 0.03003
NM_005908.4(MANBA):c.*317A>G rs78514870 0.02873
NM_005908.4(MANBA):c.1482G>T (p.Leu494=) rs74718667 0.02182
NM_005908.4(MANBA):c.272+61G>T rs78238035 0.01516
NM_005908.4(MANBA):c.1113-77_1113-76dup rs10684966
NM_005908.4(MANBA):c.1705-13C>A rs34754408
NM_005908.4(MANBA):c.1869+267= rs228622
NM_005908.4(MANBA):c.2102C>T (p.Thr701Met) rs2866413
NM_005908.4(MANBA):c.2157+161A>G rs3733202
NM_005908.4(MANBA):c.2158-260C>G rs4586937
NM_005908.4(MANBA):c.2415+299del rs10712070
NM_005908.4(MANBA):c.2416-10del rs5860729
NM_005908.4(MANBA):c.272+103TGTTT[5] rs149166963
NM_005908.4(MANBA):c.378+32del rs375744268
NM_005908.4(MANBA):c.673+255G>T rs17033204
NM_005908.4(MANBA):c.674-41AT[6] rs143832054
NM_005908.4(MANBA):c.674-41AT[8] rs143832054
NM_005908.4(MANBA):c.960+186CA[3] rs34188354
NM_005908.4(MANBA):c.960+186CA[4] rs34188354
NM_005908.4(MANBA):c.960+214_960+215insA rs1321343795
NM_005908.4(MANBA):c.960+223_960+225del rs35110858
NM_005908.4(MANBA):c.960+225del rs35110858

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