ClinVar Miner

List of variants in gene APC reported as likely benign by University of Washington Department of Laboratory Medicine, University of Washington

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 64
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HGVS dbSNP gnomAD frequency
NM_000038.6(APC):c.-19+985A>G rs111717700 0.01410
NM_000038.6(APC):c.835-452G>C rs17134956 0.01344
NM_000038.6(APC):c.-19+968C>T rs149097203 0.01178
NM_000038.6(APC):c.835-259A>T rs114873746 0.01146
NM_000038.6(APC):c.1743+959C>T rs56218335 0.01113
NM_000038.6(APC):c.729+183C>T rs58529934 0.00882
NM_001127511.3(APC):c.165+370A>G rs191729416 0.00653
NM_001127511.3(APC):c.165+22164T>C rs114176051 0.00623
NM_001127511.3(APC):c.165+434T>C rs141935736 0.00550
NM_001127511.3(APC):c.166-28546T>C rs113017087 0.00548
NM_000038.6(APC):c.1959-121A>T rs140289188 0.00547
NM_000038.6(APC):c.-18-871T>C rs115198624 0.00530
NM_000038.6(APC):c.1743+1075A>G rs181983752 0.00516
NM_000038.6(APC):c.1743+494C>A rs115039927 0.00469
NM_001127511.3(APC):c.165+19920A>G rs182207994 0.00447
NM_000038.6(APC):c.646-1462G>A rs138766550 0.00436
NM_000038.6(APC):c.645+3642A>G rs143426216 0.00402
NM_000038.6(APC):c.645+691A>C rs144533215 0.00312
NM_000038.6(APC):c.-18-952T>C rs145308873 0.00274
NM_000038.6(APC):c.1312+163C>G rs151219923 0.00116
NM_000038.6(APC):c.1312+1239T>G rs146819357 0.00096
NM_000038.6(APC):c.646-1437A>G rs74496175 0.00096
NM_001127511.3(APC):c.165+915C>T rs554976891 0.00092
NM_000038.6(APC):c.834+4088G>A rs180882590 0.00088
NM_000038.6(APC):c.-19+679T>A rs79491077 0.00086
NM_000038.6(APC):c.1408+1262T>A rs182458072 0.00081
NM_000038.6(APC):c.645+663G>C rs142806675 0.00076
NM_000038.6(APC):c.1312+778G>A rs548408102 0.00075
NM_000038.6(APC):c.934-219A>G rs148659221 0.00066
NM_000038.6(APC):c.645+646A>G rs373975906 0.00063
NM_000038.6(APC):c.-19+1592A>C rs191565835 0.00048
NM_000038.6(APC):c.607C>G (p.Gln203Glu) rs141576417 0.00034
NM_000038.6(APC):c.1549-208A>G rs528500907 0.00032
NM_000038.6(APC):c.1744-144A>G rs573935628 0.00031
NM_000038.6(APC):c.-19+2392A>G rs869312466 0.00022
NM_000038.6(APC):c.-19+310G>C rs76537511 0.00019
NM_000038.6(APC):c.1958+126G>T rs368368751 0.00019
NM_000038.6(APC):c.135+1150C>G rs115110409 0.00013
NM_000038.6(APC):c.422+2773C>T rs548786690 0.00013
NM_000038.6(APC):c.-18-931T>C rs550427653 0.00012
NM_000038.6(APC):c.-19+6497A>G rs181436331 0.00012
NM_000038.6(APC):c.2204C>T (p.Ala735Val) rs147655929 0.00012
NM_000038.6(APC):c.646-1104T>A rs140046325 0.00012
NM_000038.6(APC):c.1409-320T>G rs536225490 0.00011
NM_000038.6(APC):c.-18-1815T>G rs769073607 0.00008
NM_000038.6(APC):c.6724A>G (p.Ser2242Gly) rs201375478 0.00008
NM_000038.6(APC):c.-18-112A>G rs765486151 0.00007
NM_001127511.3(APC):c.165+1074A>C rs869312475 0.00005
NM_001127511.3(APC):c.166-28616G>A rs869312470 0.00005
NM_000038.6(APC):c.729+4358G>A rs869312473 0.00004
NM_000038.6(APC):c.934-1409A>G rs371624693 0.00002
NM_000038.6(APC):c.1312+46T>C rs747389686 0.00001
NM_000038.6(APC):c.220+208C>A rs869312468 0.00001
NM_000038.6(APC):c.323G>A (p.Gly108Glu) rs1114167456 0.00001
NM_000038.6(APC):c.532-1605T>G rs869312467 0.00001
NM_001127511.3(APC):c.165+25G>A rs869312472 0.00001
NM_000038.6(APC):c.-18-93T>C rs182529004
NM_000038.6(APC):c.136-646A>T rs869312471
NM_000038.6(APC):c.1409-2354A>C rs869312474
NM_000038.6(APC):c.1549-212C>A rs869312469
NM_000038.6(APC):c.2658G>T (p.Gln886His) rs587780593
NM_000038.6(APC):c.645+655A>G rs869312465
NM_001127511.3(APC):c.165+16249G>A rs376613947
NM_001127511.3(APC):c.165+636G>C rs368544993

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