ClinVar Miner

List of variants in gene ANO5 reported by PreventionGenetics, part of Exact Sciences

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Total variants: 44
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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.879-18T>C rs7104758 0.06440
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.1120-24A>T rs11026476 0.02147
NM_213599.3(ANO5):c.2259A>G (p.Ser753=) rs61746201 0.01772
NM_213599.3(ANO5):c.1181-21T>A rs114582774 0.01015
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.2387C>T (p.Ser796Leu) rs61910685 0.00804
NM_213599.3(ANO5):c.1181-48T>A rs150412089 0.00767
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.1631-35G>A rs72982041 0.00334
NM_213599.3(ANO5):c.692G>T (p.Gly231Val) rs137854523 0.00098
NM_213599.3(ANO5):c.1013+29G>C rs371272245 0.00039
NM_213599.3(ANO5):c.279C>T (p.Asp93=) rs148516756 0.00015
NM_213599.3(ANO5):c.1364G>A (p.Arg455His) rs772899863 0.00011
NM_213599.3(ANO5):c.1332+8A>G rs368857740 0.00009
NM_213599.3(ANO5):c.1210C>T (p.Arg404Ter) rs566415362 0.00004
NM_213599.3(ANO5):c.1482C>T (p.Phe494=) rs745446244 0.00004
NM_213599.3(ANO5):c.1227A>G (p.Glu409=) rs781554633 0.00003
NM_213599.3(ANO5):c.1314A>G (p.Lys438=) rs764893392 0.00003
NM_213599.3(ANO5):c.1254A>G (p.Glu418=) rs368092838 0.00002
NM_213599.3(ANO5):c.53A>G (p.Asn18Ser) rs1010958758 0.00002
NM_213599.3(ANO5):c.1800+5G>A rs794727179 0.00001
NM_213599.3(ANO5):c.1801-9T>C rs202034123 0.00001
NM_213599.3(ANO5):c.2139C>T (p.Thr713=) rs767479331 0.00001
NM_213599.3(ANO5):c.2470del (p.Gln824fs) rs770694933 0.00001
NM_213599.3(ANO5):c.632C>T (p.Ser211Leu) rs142939381 0.00001
NM_213599.3(ANO5):c.1037T>C (p.Ile346Thr)
NM_213599.3(ANO5):c.1079G>T (p.Cys360Phe)
NM_213599.3(ANO5):c.1445_1450dup (p.Tyr483_Arg484insLeuTyr)
NM_213599.3(ANO5):c.181-5T>C rs765995011
NM_213599.3(ANO5):c.191dup (p.Asn64fs) rs137854521
NM_213599.3(ANO5):c.2043A>G (p.Gly681=)
NM_213599.3(ANO5):c.2236-13_2236-10del rs72105710
NM_213599.3(ANO5):c.2587G>A (p.Glu863Lys)
NM_213599.3(ANO5):c.2646C>G (p.Asn882Lys) rs34969327
NM_213599.3(ANO5):c.2688C>G (p.Ala896=) rs377549896
NM_213599.3(ANO5):c.364-8del rs146983312
NM_213599.3(ANO5):c.966A>G (p.Leu322=) rs7481951
NM_213599.3(ANO5):c.966A>T (p.Leu322Phe) rs7481951

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