ClinVar Miner

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

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Gene type:
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Total variants: 34
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HGVS dbSNP
NM_001142649.2(ANO5):c.*1890_*1893AAGA[1] rs397786204
NM_213599.2(ANO5):c.*1286G>T rs7925081
NM_213599.2(ANO5):c.*1313A>G rs73483432
NM_213599.2(ANO5):c.*1429A>G rs78143145
NM_213599.2(ANO5):c.*1521T>C rs73483433
NM_213599.2(ANO5):c.*1712T>C rs530413127
NM_213599.2(ANO5):c.*1762del rs398015552
NM_213599.2(ANO5):c.*2095G>A rs142192440
NM_213599.2(ANO5):c.*2357A>T rs151218419
NM_213599.2(ANO5):c.*2869A>G rs115249135
NM_213599.2(ANO5):c.*3152G>A rs79486036
NM_213599.2(ANO5):c.*3155T>C rs78929863
NM_213599.2(ANO5):c.*3168C>T rs35892535
NM_213599.2(ANO5):c.*3350T>G rs144806967
NM_213599.2(ANO5):c.*3481dup rs147581685
NM_213599.2(ANO5):c.*496A>G rs10766930
NM_213599.2(ANO5):c.*930C>T rs78428314
NM_213599.2(ANO5):c.-217G>T rs73479393
NM_213599.2(ANO5):c.1095A>G (p.Leu365=) rs35804601
NM_213599.2(ANO5):c.138+10G>A rs78987921
NM_213599.2(ANO5):c.2387C>T (p.Ser796Leu) rs61910685
NM_213599.2(ANO5):c.259G>A (p.Val87Ile) rs34994927
NM_213599.2(ANO5):c.2646C>G (p.Asn882Lys) rs34969327
NM_213599.2(ANO5):c.364-8del rs146983312
NM_213599.2(ANO5):c.680G>C (p.Gly227Ala) rs140903276
NM_213599.3(ANO5):c.*111T>C
NM_213599.3(ANO5):c.*199T>C
NM_213599.3(ANO5):c.*2251A>G
NM_213599.3(ANO5):c.*2674A>C
NM_213599.3(ANO5):c.*2711T>C
NM_213599.3(ANO5):c.*2723A>T
NM_213599.3(ANO5):c.*3564A>T
NM_213599.3(ANO5):c.*948C>T
NM_213599.3(ANO5):c.966A>T (p.Leu322Phe) rs7481951

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