ClinVar Miner

List of variants in gene ANO10 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 57
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HGVS dbSNP gnomAD frequency
NM_018075.5(ANO10):c.1915-5852T>C rs6441771 0.97895
NM_018075.5(ANO10):c.140-53G>T rs6441785 0.77750
NM_018075.5(ANO10):c.593-227A>C rs9883169 0.77625
NM_018075.5(ANO10):c.593-228C>G rs9863479 0.77600
NM_018075.5(ANO10):c.1385G>A (p.Arg462Gln) rs3772165 0.58882
NM_018075.5(ANO10):c.1293+9A>G rs7616708 0.56196
NM_018075.5(ANO10):c.1797+70C>T rs12638282 0.48151
NM_018075.5(ANO10):c.1914+189T>G rs11710107 0.18495
NM_018075.5(ANO10):c.1914+237T>C rs11710079 0.18475
NM_018075.5(ANO10):c.1669-65A>G rs1842805 0.15235
NM_018075.5(ANO10):c.-11-218T>C rs6769241 0.10935
NM_018075.5(ANO10):c.1797+238A>G rs17075814 0.09939
NM_018075.5(ANO10):c.1293+282T>G rs17075829 0.09769
NM_018075.5(ANO10):c.1066A>G (p.Ser356Gly) rs56389778 0.05750
NM_018075.5(ANO10):c.1682C>T (p.Thr561Met) rs17409162 0.04859
NM_018075.5(ANO10):c.1915-270G>A rs74804865 0.03382
NM_018075.5(ANO10):c.593-123G>A rs75854701 0.03303
NM_018075.5(ANO10):c.1915-79A>C rs73831275 0.02785
NM_018075.5(ANO10):c.*196C>A rs73831274 0.02784
NM_018075.5(ANO10):c.*246A>G rs73831273 0.02628
NM_018075.5(ANO10):c.140-83G>A rs2068969 0.02366
NM_018075.5(ANO10):c.486C>T (p.Leu162=) rs34829628 0.02348
NM_018075.5(ANO10):c.1293+182A>T rs9847454 0.02078
NM_018075.5(ANO10):c.1477-14G>A rs78884042 0.02011
NM_018075.5(ANO10):c.1293+283A>G rs80171035 0.02008
NM_018075.5(ANO10):c.1219-231T>C rs112573059 0.02004
NM_018075.5(ANO10):c.338-323T>G rs17075851 0.01995
NM_018075.5(ANO10):c.592+264T>C rs113130026 0.01949
NM_018075.5(ANO10):c.-11-273A>G rs75808456 0.01921
NM_018075.5(ANO10):c.592+330del rs113754689 0.01910
NM_018075.5(ANO10):c.592+310C>G rs112774666 0.01901
NM_018075.5(ANO10):c.788G>A (p.Arg263His) rs41289586 0.01896
NM_018075.5(ANO10):c.-11-123G>A rs76110549 0.01829
NM_018075.5(ANO10):c.74A>C (p.Gln25Pro) rs112040665 0.01413
NM_018075.5(ANO10):c.1219-96C>T rs182153917 0.01380
NM_018075.5(ANO10):c.627T>C (p.Ala209=) rs61742945 0.01193
NM_018075.5(ANO10):c.*447G>A rs112787589 0.00714
NM_018075.5(ANO10):c.1669-8T>G rs115769245 0.00517
NM_018075.5(ANO10):c.1915-5863G>A rs141400669 0.00503
NM_018075.5(ANO10):c.1133G>A (p.Arg378Gln) rs61732728 0.00281
NM_018075.5(ANO10):c.963C>T (p.Phe321=) rs149196477 0.00097
NM_018075.5(ANO10):c.842T>C (p.Phe281Ser) rs184756780 0.00030
NM_018075.5(ANO10):c.1162+12G>A
NM_018075.5(ANO10):c.1219-23_1219-22dup rs367784953
NM_018075.5(ANO10):c.1219-23dup rs367784953
NM_018075.5(ANO10):c.1219-277T>C rs7616890
NM_018075.5(ANO10):c.1219-6del rs367784953
NM_018075.5(ANO10):c.1476+129C>T rs76708931
NM_018075.5(ANO10):c.1477-37T>G rs4682893
NM_018075.5(ANO10):c.159A>G (p.Arg53=) rs533186096
NM_018075.5(ANO10):c.1668+20del
NM_018075.5(ANO10):c.1669-1566A>G rs9829081
NM_018075.5(ANO10):c.1683G>C (p.Thr561=) rs141040660
NM_018075.5(ANO10):c.1797+78G>T rs9874278
NM_018075.5(ANO10):c.1798-4del
NM_018075.5(ANO10):c.592+193dup rs546649985
NM_018075.5(ANO10):c.592+210del rs546649985

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