ClinVar Miner

List of variants in gene ANO5 reported as benign by EGL Genetic Diagnostics,Eurofins Clinical Diagnostics

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Total variants: 19
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HGVS dbSNP
NM_213599.2(ANO5):c.-136G>C rs12792259
NM_213599.2(ANO5):c.1029C>T (p.Asp343=) rs78899595
NM_213599.2(ANO5):c.1545A>G (p.Ser515=) rs35843353
NM_213599.2(ANO5):c.2236-10dupT rs72105710
NM_213599.2(ANO5):c.2236-11_2236-10dup rs72105710
NM_213599.2(ANO5):c.2236-12_2236-10delTTT rs72105710
NM_213599.2(ANO5):c.2236-13_2236-10delTTTT rs72105710
NM_213599.2(ANO5):c.2256G>A (p.Thr752=) rs144048656
NM_213599.2(ANO5):c.2387C>T (p.Ser796Leu) rs61910685
NM_213599.2(ANO5):c.2521-13A>G rs76850415
NM_213599.2(ANO5):c.2646C>G (p.Asn882Lys) rs34969327
NM_213599.2(ANO5):c.267T>C (p.Asp89=) rs4312063
NM_213599.2(ANO5):c.364-8del rs146983312
NM_213599.2(ANO5):c.364-8dupT rs146983312
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.800C>G (p.Thr267Ser) rs138144479
NM_213599.2(ANO5):c.879-18T>C rs7104758
NM_213599.2(ANO5):c.966A>T (p.Leu322Phe) rs7481951

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