ClinVar Miner

List of variants in gene ADAR reported as benign

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Gene type:
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Total variants: 70
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HGVS dbSNP gnomAD frequency
NM_001111.5(ADAR):c.78G>A (p.Arg26=) rs1802645 0.99723
NM_001111.5(ADAR):c.298A>G (p.Arg100Gly) rs1466731 0.99604
NM_001111.5(ADAR):c.16-234T>C rs4845381 0.99233
NM_001111.5(ADAR):c.3020-197C>G rs6683149 0.92153
NM_001111.5(ADAR):c.1151A>G (p.Lys384Arg) rs2229857 0.61729
NM_001111.5(ADAR):c.*1016C>T rs1127314 0.59417
NM_001111.5(ADAR):c.*1790A>G rs1127326 0.59410
NM_001111.5(ADAR):c.*619C>T rs1127311 0.41540
NM_001111.5(ADAR):c.*857C>T rs1127313 0.41404
NM_001111.5(ADAR):c.3443+8G>A rs9427094 0.40966
NM_001111.5(ADAR):c.*1242A>C rs1127317 0.29977
NM_001111.5(ADAR):c.16-219C>T rs3738029 0.29062
NM_001111.5(ADAR):c.1601+98G>A rs3738032 0.21987
NM_001111.5(ADAR):c.*1549T>A rs9616 0.21349
NM_001111.5(ADAR):c.16-213T>G rs3738030 0.10197
NM_001111.5(ADAR):c.16-323A>G rs12094866 0.07435
NM_001111.5(ADAR):c.15+257T>C rs561516155 0.06249
NM_001111.5(ADAR):c.1935-152C>G rs115800464 0.05153
NM_001111.5(ADAR):c.*943C>A rs34167604 0.02238
NM_001111.5(ADAR):c.1785+186C>T rs74115806 0.02228
NM_001111.5(ADAR):c.2270+102C>T rs116266783 0.01844
NM_001111.5(ADAR):c.2271-272T>C rs75308349 0.01550
NM_001111.5(ADAR):c.1760A>G (p.Tyr587Cys) rs17843865 0.01046
NM_001111.5(ADAR):c.*938A>C rs147862510 0.00621
NM_001111.5(ADAR):c.298= (p.Arg100=) rs1466731 0.00396
NM_001111.5(ADAR):c.*413A>T rs115205788 0.00367
NM_001111.5(ADAR):c.*1436G>T rs144500439 0.00255
NM_001111.5(ADAR):c.1003A>T (p.Ile335Phe) rs34154757 0.00235
NM_001111.5(ADAR):c.*2199C>T rs140535856 0.00229
NM_001111.5(ADAR):c.*2033G>A rs571724294 0.00210
NM_001111.5(ADAR):c.2079+8G>A rs376867928 0.00139
NM_001111.5(ADAR):c.1926T>C (p.His642=) rs150171059 0.00135
NM_001111.5(ADAR):c.2886-11_2886-10del rs557801982 0.00128
NM_001111.5(ADAR):c.*2623C>T rs112827019 0.00111
NM_001111.5(ADAR):c.*2643G>A rs539051807 0.00084
NM_001111.5(ADAR):c.*368G>A rs558906089 0.00079
NM_001111.5(ADAR):c.*245T>C rs376176238 0.00077
NM_001111.5(ADAR):c.*898G>A rs140910871 0.00063
NM_001111.5(ADAR):c.3018C>T (p.Asn1006=) rs151241634 0.00063
NM_001111.5(ADAR):c.3523A>C (p.Arg1175=) rs146625055 0.00042
NM_001111.5(ADAR):c.772G>A (p.Gly258Arg) rs201143561 0.00039
NM_001111.5(ADAR):c.1887C>G (p.Ser629=) rs747820726 0.00019
NM_001111.5(ADAR):c.2496+9G>A rs199698434 0.00017
NM_001111.5(ADAR):c.2497-15C>T rs113249520 0.00014
NM_001111.5(ADAR):c.1934+8C>T rs376025865 0.00013
NM_001111.5(ADAR):c.1935-20C>T rs17843867 0.00012
NM_001111.5(ADAR):c.1851C>A (p.Thr617=) rs764879657 0.00009
NM_001111.5(ADAR):c.57C>T (p.Gly19=) rs137983302 0.00006
NM_001111.5(ADAR):c.1934+12G>A rs776357782 0.00005
NM_001111.5(ADAR):c.2319C>T (p.Cys773=) rs750666914 0.00004
NM_001111.5(ADAR):c.1785+5G>A rs17843866 0.00002
NM_001111.5(ADAR):c.*1614T>A rs530015999 0.00001
NM_001111.5(ADAR):c.*25G>C rs780228174 0.00001
NM_001111.5(ADAR):c.1846G>A (p.Val616Ile) rs570647049 0.00001
NM_001111.5(ADAR):c.2496+8C>T rs770464278 0.00001
NM_001111.5(ADAR):c.650G>A (p.Ser217Asn) rs199906332 0.00001
NM_001025107.3(ADAR):c.-912T>C
NM_001111.5(ADAR):c.*517AG[1] rs16361
NM_001111.5(ADAR):c.15+104GT[9] rs71586026
NM_001111.5(ADAR):c.15+241TG[10] rs551880161
NM_001111.5(ADAR):c.15+258_15+269del rs71077960
NM_001111.5(ADAR):c.1577A>G (p.Gln526Arg) rs770224427
NM_001111.5(ADAR):c.1602-114_1602-112dup
NM_001111.5(ADAR):c.1602-116_1602-114dup rs4045821
NM_001111.5(ADAR):c.1897C>T (p.Arg633Cys)
NM_001111.5(ADAR):c.2361G>A (p.Ala787=)
NM_001111.5(ADAR):c.2496+31G>T rs60407842
NM_001111.5(ADAR):c.2496+35C>G rs7532276
NM_001111.5(ADAR):c.2496+36dup rs3215061
NM_001111.5(ADAR):c.3019+19dup

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