ClinVar Miner

List of variants in gene ANO5 reported as benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 79
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HGVS dbSNP gnomAD frequency
NM_213599.3(ANO5):c.267T>C (p.Asp89=) rs4312063 0.83210
NM_213599.3(ANO5):c.180+223G>A rs4620717 0.83192
NM_213599.3(ANO5):c.-136G>C rs12792259 0.83191
NM_213599.3(ANO5):c.*3178C>G rs6483841 0.72187
NM_213599.3(ANO5):c.180+279T>C rs4543996 0.69131
NM_213599.3(ANO5):c.138+169G>A rs4922980 0.67443
NM_213599.3(ANO5):c.138+206T>C rs4922981 0.67232
NM_213599.3(ANO5):c.364-300T>C rs4617581 0.67070
NM_213599.3(ANO5):c.*1286G>T rs7925081 0.65457
NM_213599.3(ANO5):c.*496A>G rs10766930 0.53080
NM_213599.3(ANO5):c.2520+25G>C rs11026488 0.16418
NM_213599.3(ANO5):c.879-76T>A rs7104736 0.16088
NM_213599.3(ANO5):c.762+87G>A rs11026471 0.15642
NM_213599.3(ANO5):c.762+321T>C rs10833726 0.15632
NM_213599.3(ANO5):c.649-114T>A rs11820954 0.15623
NM_213599.3(ANO5):c.649-166A>G rs4534588 0.15597
NM_213599.3(ANO5):c.648+257G>A rs7951567 0.14470
NM_213599.3(ANO5):c.649-249C>G rs4254072 0.14172
NM_213599.3(ANO5):c.*1521T>C rs73483433 0.09970
NM_213599.3(ANO5):c.*1313A>G rs73483432 0.09785
NM_213599.3(ANO5):c.364-283T>C rs11827827 0.09032
NM_213599.3(ANO5):c.2415-148A>G rs7124079 0.07502
NM_213599.3(ANO5):c.1630+181A>G rs7108392 0.07152
NM_213599.3(ANO5):c.88-281C>A rs75162101 0.06518
NM_213599.3(ANO5):c.1333-238T>C rs7937378 0.06446
NM_213599.3(ANO5):c.879-18T>C rs7104758 0.06440
NM_213599.3(ANO5):c.40+64G>T rs112145196 0.06408
NM_213599.3(ANO5):c.138+166G>A rs77546698 0.05088
NM_213599.3(ANO5):c.*3152G>A rs79486036 0.04921
NM_213599.3(ANO5):c.2520+206T>C rs75315439 0.04395
NM_213599.3(ANO5):c.139-226T>G rs116738367 0.03636
NM_213599.3(ANO5):c.1333-303C>G rs74834281 0.03179
NM_213599.3(ANO5):c.1898+182T>A rs114770419 0.03053
NM_213599.3(ANO5):c.648+208A>G rs75126999 0.03014
NM_213599.3(ANO5):c.879-132A>G rs116274417 0.03008
NM_213599.3(ANO5):c.1898+29G>T rs76084798 0.02917
NM_213599.3(ANO5):c.2521-13A>G rs76850415 0.02660
NM_213599.3(ANO5):c.181-318T>C rs79402446 0.02464
NM_213599.3(ANO5):c.1013+143del rs148611587 0.02223
NM_213599.3(ANO5):c.1630+216A>G rs114322625 0.02219
NM_213599.3(ANO5):c.1631-127C>T rs7939120 0.02219
NM_213599.3(ANO5):c.1333-264G>A rs80249417 0.02213
NM_213599.3(ANO5):c.878+215C>A rs77977104 0.01976
NM_213599.3(ANO5):c.2029+147A>G rs7925115 0.01786
NM_213599.3(ANO5):c.2235+138G>A rs77581966 0.01782
NM_213599.3(ANO5):c.2029+238A>C rs7925231 0.01781
NM_213599.3(ANO5):c.2259A>G (p.Ser753=) rs61746201 0.01772
NM_213599.3(ANO5):c.1899-288C>T rs80267696 0.01768
NM_213599.3(ANO5):c.181-220T>C rs80159991 0.01552
NM_213599.3(ANO5):c.1029C>T (p.Asp343=) rs78899595 0.00992
NM_213599.3(ANO5):c.604G>A (p.Glu202Lys) rs115750596 0.00971
NM_213599.3(ANO5):c.616A>G (p.Thr206Ala) rs78266558 0.00922
NM_213599.3(ANO5):c.763-46G>T rs76657996 0.00909
NM_213599.3(ANO5):c.2387C>T (p.Ser796Leu) rs61910685 0.00804
NM_213599.3(ANO5):c.800C>G (p.Thr267Ser) rs138144479 0.00727
NM_213599.3(ANO5):c.1545A>G (p.Ser515=) rs35843353 0.00699
NM_213599.3(ANO5):c.2354T>G (p.Leu785Arg) rs146136277 0.00524
NM_213599.3(ANO5):c.680G>C (p.Gly227Ala) rs140903276 0.00320
NM_213599.3(ANO5):c.259G>A (p.Val87Ile) rs34994927 0.00293
NM_213599.3(ANO5):c.879-41A>T rs144743605 0.00215
NM_213599.3(ANO5):c.*112_*113del rs5790246
NM_213599.3(ANO5):c.*113del rs5790246
NM_213599.3(ANO5):c.*1762del rs398015552
NM_213599.3(ANO5):c.*1890AAGA[1] rs397786204
NM_213599.3(ANO5):c.*3481dup rs147581685
NM_213599.3(ANO5):c.-217G>T rs73479393
NM_213599.3(ANO5):c.139-164del rs60388835
NM_213599.3(ANO5):c.1630+220_1630+221dup rs36077990
NM_213599.3(ANO5):c.1630+221dup rs36077990
NM_213599.3(ANO5):c.1630+228T>G rs7124796
NM_213599.3(ANO5):c.2029+219C>T rs7925323
NM_213599.3(ANO5):c.2236-10del rs72105710
NM_213599.3(ANO5):c.2236-10dup rs72105710
NM_213599.3(ANO5):c.2236-13_2236-10del rs72105710
NM_213599.3(ANO5):c.2415-22del rs5790245
NM_213599.3(ANO5):c.2646C>G (p.Asn882Lys) rs34969327
NM_213599.3(ANO5):c.364-166_364-165del rs34515704
NM_213599.3(ANO5):c.364-8del rs146983312
NM_213599.3(ANO5):c.966A>T (p.Leu322Phe) rs7481951

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