ClinVar Miner

List of variants in gene ANO5 reported as likely benign by Illumina Laboratory Services, Illumina

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Gene type:
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Total variants: 34
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HGVS dbSNP gnomAD frequency
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.*1521T>C rs73483433 0.09970
NM_213599.3(ANO5):c.*1313A>G rs73483432 0.09785
NM_213599.3(ANO5):c.*3152G>A rs79486036 0.04921
NM_213599.3(ANO5):c.*3168C>T rs35892535 0.01843
NM_213599.3(ANO5):c.*2095G>A rs142192440 0.01610
NM_213599.3(ANO5):c.*3155T>C rs78929863 0.01340
NM_213599.3(ANO5):c.*930C>T rs78428314 0.01204
NM_213599.3(ANO5):c.*2251A>G rs114636071 0.01015
NM_213599.3(ANO5):c.*2723A>T rs116278349 0.01013
NM_213599.3(ANO5):c.*2674A>C rs115846873 0.01002
NM_213599.3(ANO5):c.*1429A>G rs78143145 0.00911
NM_213599.3(ANO5):c.2387C>T (p.Ser796Leu) rs61910685 0.00804
NM_213599.3(ANO5):c.*3350T>G rs144806967 0.00723
NM_213599.3(ANO5):c.*2357A>T rs151218419 0.00715
NM_213599.3(ANO5):c.*3564A>T rs7933026 0.00682
NM_213599.3(ANO5):c.*2869A>G rs115249135 0.00608
NM_213599.3(ANO5):c.*199T>C rs190481523 0.00453
NM_213599.3(ANO5):c.*111T>C rs543256905 0.00442
NM_213599.3(ANO5):c.*2711T>C rs137887236 0.00440
NM_213599.3(ANO5):c.*948C>T rs189525296 0.00434
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.*1712T>C rs530413127 0.00216
NM_213599.3(ANO5):c.1095A>G (p.Leu365=) rs35804601 0.00183
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.138+10G>A rs78987921
NM_213599.3(ANO5):c.2646C>G (p.Asn882Lys) rs34969327
NM_213599.3(ANO5):c.364-8del rs146983312
NM_213599.3(ANO5):c.966A>T (p.Leu322Phe) rs7481951

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