ClinVar Miner

List of variants in gene ANO5 reported as benign

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Total variants: 68
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HGVS dbSNP
GRCh37/hg19 11p14.3(chr11:22221534-22257284)x3
NC_000011.10:g.22218076del rs60388835
NM_213599.2(ANO5):c.*1286G>T rs7925081
NM_213599.2(ANO5):c.*1313A>G rs73483432
NM_213599.2(ANO5):c.*1328C>T rs78089375
NM_213599.2(ANO5):c.*1429A>G rs78143145
NM_213599.2(ANO5):c.*1521T>C rs73483433
NM_213599.2(ANO5):c.*1661C>T rs12284506
NM_213599.2(ANO5):c.*279G>A rs72982058
NM_213599.2(ANO5):c.*3152G>A rs79486036
NM_213599.2(ANO5):c.*3178C>G rs6483841
NM_213599.2(ANO5):c.*496A>G rs10766930
NM_213599.2(ANO5):c.*554C>T rs117180492
NM_213599.2(ANO5):c.-136G>C rs12792259
NM_213599.2(ANO5):c.-156_-155insAGGGGAATGAGGAGGAGGAGGAGG rs71034576
NM_213599.2(ANO5):c.-217G>T rs73479393
NM_213599.2(ANO5):c.-261A>C rs114897158
NM_213599.2(ANO5):c.1095A>G (p.Leu365=) rs35804601
NM_213599.2(ANO5):c.1120-24A>T rs11026476
NM_213599.2(ANO5):c.1333-238T>C rs7937378
NM_213599.2(ANO5):c.138+10G>A rs78987921
NM_213599.2(ANO5):c.138+166G>A rs77546698
NM_213599.2(ANO5):c.138+169G>A rs4922980
NM_213599.2(ANO5):c.138+206T>C rs4922981
NM_213599.2(ANO5):c.139-226T>G rs116738367
NM_213599.2(ANO5):c.1545A>G (p.Ser515=) rs35843353
NM_213599.2(ANO5):c.155A>G rs143777403
NM_213599.2(ANO5):c.1630+181A>G rs7108392
NM_213599.2(ANO5):c.1630+228T>G rs7124796
NM_213599.2(ANO5):c.180+223G>A rs4620717
NM_213599.2(ANO5):c.180+279T>C rs4543996
NM_213599.2(ANO5):c.2236-11_2236-10dup rs72105710
NM_213599.2(ANO5):c.2236-13_2236-10del rs72105710
NM_213599.2(ANO5):c.2256G>A (p.Thr752=) rs144048656
NM_213599.2(ANO5):c.2259A>G (p.Ser753=) rs61746201
NM_213599.2(ANO5):c.2354T>G (p.Leu785Arg) rs146136277
NM_213599.2(ANO5):c.2387C>T (p.Ser796Leu) rs61910685
NM_213599.2(ANO5):c.2415-148A>G rs7124079
NM_213599.2(ANO5):c.2520+206T>C rs75315439
NM_213599.2(ANO5):c.2520+25G>C rs11026488
NM_213599.2(ANO5):c.2521-13A>G rs76850415
NM_213599.2(ANO5):c.2521-7C>T rs201438159
NM_213599.2(ANO5):c.2646C>G (p.Asn882Lys) rs34969327
NM_213599.2(ANO5):c.364-283T>C rs11827827
NM_213599.2(ANO5):c.364-300T>C rs4617581
NM_213599.2(ANO5):c.364-8del rs146983312
NM_213599.2(ANO5):c.40+64G>T rs112145196
NM_213599.2(ANO5):c.604G>A (p.Glu202Lys) rs115750596
NM_213599.2(ANO5):c.616A>G (p.Thr206Ala) rs78266558
NM_213599.2(ANO5):c.648+257G>A rs7951567
NM_213599.2(ANO5):c.649-114T>A rs11820954
NM_213599.2(ANO5):c.649-166A>G rs4534588
NM_213599.2(ANO5):c.649-249C>G rs4254072
NM_213599.2(ANO5):c.762+321T>C rs10833726
NM_213599.2(ANO5):c.762+87G>A rs11026471
NM_213599.2(ANO5):c.879-18T>C rs7104758
NM_213599.2(ANO5):c.879-76T>A rs7104736
NM_213599.2(ANO5):c.879-7_879-6del rs143977836
NM_213599.2(ANO5):c.88-281C>A rs75162101
NM_213599.3(ANO5):c.*113del rs5790246
NM_213599.3(ANO5):c.*3121A>G
NM_213599.3(ANO5):c.1029C>T (p.Asp343=) rs78899595
NM_213599.3(ANO5):c.2236-10dup rs72105710
NM_213599.3(ANO5):c.2236-12_2236-10del rs72105710
NM_213599.3(ANO5):c.267T>C (p.Asp89=) rs4312063
NM_213599.3(ANO5):c.364-8dup rs146983312
NM_213599.3(ANO5):c.800C>G (p.Thr267Ser) rs138144479
NM_213599.3(ANO5):c.966A>T (p.Leu322Phe) rs7481951

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