ClinVar Miner

List of variants in gene ANO5 reported as likely benign for not specified

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Total variants: 35
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HGVS dbSNP
NM_213599.2(ANO5):c.1013+29G>C rs371272245
NM_213599.2(ANO5):c.1029C>T (p.Asp343=) rs78899595
NM_213599.2(ANO5):c.1095A>G (p.Leu365=) rs35804601
NM_213599.2(ANO5):c.1181-21T>A rs114582774
NM_213599.2(ANO5):c.1181-48T>A rs150412089
NM_213599.2(ANO5):c.1222C>T (p.Leu408=) rs997655691
NM_213599.2(ANO5):c.1227A>G (p.Glu409=) rs781554633
NM_213599.2(ANO5):c.1545A>G (p.Ser515=) rs35843353
NM_213599.2(ANO5):c.155A>G rs143777403
NM_213599.2(ANO5):c.1631-35G>A rs72982041
NM_213599.2(ANO5):c.181-16T>C rs762760550
NM_213599.2(ANO5):c.181-18C>T rs1350082012
NM_213599.2(ANO5):c.1898+29G>T rs76084798
NM_213599.2(ANO5):c.1962A>G (p.Arg654=) rs1057521970
NM_213599.2(ANO5):c.2139C>T (p.Thr713=) rs767479331
NM_213599.2(ANO5):c.2175T>C (p.His725=) rs1057522538
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.2415-7T>C rs1554935084
NM_213599.2(ANO5):c.2521-7C>T rs201438159
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.2688C>G (p.Ala896=) rs377549896
NM_213599.2(ANO5):c.2698A>C (p.Met900Leu) rs148293985
NM_213599.2(ANO5):c.276A>G (p.Lys92=) rs201678262
NM_213599.2(ANO5):c.295-16T>A rs746448319
NM_213599.2(ANO5):c.295-8dup rs778435515
NM_213599.2(ANO5):c.616A>G (p.Thr206Ala) rs78266558
NM_213599.2(ANO5):c.680G>C (p.Gly227Ala) rs140903276
NM_213599.2(ANO5):c.720G>T (p.Leu240=) rs147121216
NM_213599.2(ANO5):c.878+17G>A rs749031281
NM_213599.2(ANO5):c.879-7_879-6del rs143977836

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