ClinVar Miner

List of variants in gene ANO10 reported as uncertain significance for Autosomal recessive cerebellar ataxia

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Total variants: 35
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HGVS dbSNP
NM_001204831.2(ANO10):c.-140G>A rs886058485
NM_018075.5(ANO10):c.*179C>T rs111871863
NM_018075.5(ANO10):c.*368C>T rs114561351
NM_018075.5(ANO10):c.*372G>T rs145489333
NM_018075.5(ANO10):c.*438A>T rs376644560
NM_018075.5(ANO10):c.*447G>A rs112787589
NM_018075.5(ANO10):c.*452A>G rs886058476
NM_018075.5(ANO10):c.*464C>T rs886058475
NM_018075.5(ANO10):c.*74dup rs556549778
NM_018075.5(ANO10):c.*82G>A rs560234921
NM_018075.5(ANO10):c.*91G>A rs776954907
NM_018075.5(ANO10):c.-102C>A rs886058484
NM_018075.5(ANO10):c.-31G>C rs533146042
NM_018075.5(ANO10):c.-67C>T rs563565187
NM_018075.5(ANO10):c.-74C>T rs886058482
NM_018075.5(ANO10):c.-83T>C rs760135054
NM_018075.5(ANO10):c.-95del rs886058483
NM_018075.5(ANO10):c.1012G>A (p.Asp338Asn) rs187425614
NM_018075.5(ANO10):c.1133G>A (p.Arg378Gln) rs61732728
NM_018075.5(ANO10):c.1218+4A>T rs886058479
NM_018075.5(ANO10):c.1294-3del rs778730043
NM_018075.5(ANO10):c.1339A>T (p.Met447Leu) rs745940196
NM_018075.5(ANO10):c.1416A>C (p.Ala472=) rs886058478
NM_018075.5(ANO10):c.1559C>T (p.Ala520Val) rs150026260
NM_018075.5(ANO10):c.1595C>T (p.Ser532Leu) rs886058477
NM_018075.5(ANO10):c.1628G>A (p.Arg543His) rs372086237
NM_018075.5(ANO10):c.1669-8T>G rs115769245
NM_018075.5(ANO10):c.1683G>C (p.Thr561=) rs141040660
NM_018075.5(ANO10):c.1817A>G (p.Lys606Arg) rs761659935
NM_018075.5(ANO10):c.1864A>G (p.Met622Val) rs141806947
NM_018075.5(ANO10):c.192A>G (p.Leu64=) rs146432615
NM_018075.5(ANO10):c.338-11T>C rs774494441
NM_018075.5(ANO10):c.632A>G (p.Tyr211Cys) rs886058480
NM_018075.5(ANO10):c.676G>A (p.Ala226Thr) rs188443010
NM_018075.5(ANO10):c.980A>G (p.Tyr327Cys) rs146569520

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