ClinVar Miner

List of variants in gene ADAR studied for not provided

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Gene type:
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Total variants: 123
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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.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.3443+8G>A rs9427094 0.40966
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.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.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.1601+317C>T rs142654985 0.00881
NM_001111.5(ADAR):c.*309T>G rs141369769 0.00402
NM_001111.5(ADAR):c.3020-137C>T rs141130161 0.00367
NM_001111.5(ADAR):c.1935-261G>C rs186653551 0.00355
NM_001111.5(ADAR):c.1003A>T (p.Ile335Phe) rs34154757 0.00235
NM_001111.5(ADAR):c.577C>G (p.Pro193Ala) rs145588689 0.00162
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.3018C>T (p.Asn1006=) rs151241634 0.00063
NM_001111.5(ADAR):c.518A>G (p.Asn173Ser) rs201331183 0.00048
NM_001111.5(ADAR):c.3523A>C (p.Arg1175=) rs146625055 0.00042
NM_001111.5(ADAR):c.2052G>A (p.Ala684=) rs148041309 0.00039
NM_001111.5(ADAR):c.772G>A (p.Gly258Arg) rs201143561 0.00039
NM_001111.5(ADAR):c.1229A>G (p.Glu410Gly) rs145652884 0.00022
NM_001111.5(ADAR):c.1625A>G (p.Asn542Ser) rs200242235 0.00016
NM_001111.5(ADAR):c.1725C>T (p.Ala575=) rs144279106 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.2274C>T (p.Phe758=) rs149039619 0.00011
NM_001111.5(ADAR):c.222G>A (p.Arg74=) rs150423721 0.00010
NM_001111.5(ADAR):c.1392T>C (p.Asn464=) rs370763473 0.00009
NM_001111.5(ADAR):c.1192A>G (p.Asn398Asp) rs371050239 0.00006
NM_001111.5(ADAR):c.1741T>C (p.Ser581Pro) rs142884797 0.00006
NM_001111.5(ADAR):c.1766C>G (p.Thr589Arg) rs373667326 0.00006
NM_001111.5(ADAR):c.1875A>G (p.Lys625=) rs771871176 0.00006
NM_001111.5(ADAR):c.2275G>A (p.Val759Ile) rs145849344 0.00006
NM_001111.5(ADAR):c.3171G>A (p.Leu1057=) rs149496690 0.00006
NM_001111.5(ADAR):c.57C>T (p.Gly19=) rs137983302 0.00006
NM_001111.5(ADAR):c.983G>A (p.Arg328Gln) rs371476324 0.00006
NM_001111.5(ADAR):c.1400G>A (p.Arg467His) rs192121167 0.00005
NM_001111.5(ADAR):c.3354C>T (p.Ser1118=) rs764381126 0.00004
NM_001111.5(ADAR):c.675G>A (p.Pro225=) rs771459105 0.00004
NM_001111.5(ADAR):c.1543G>T (p.Ala515Ser) rs200830156 0.00003
NM_001111.5(ADAR):c.3289C>A (p.His1097Asn) rs200537032 0.00003
NM_001111.5(ADAR):c.547G>A (p.Gly183Ser) rs779939725 0.00002
NM_001111.5(ADAR):c.1158C>T (p.Asn386=) rs752276168 0.00001
NM_001111.5(ADAR):c.1189T>A (p.Ser397Thr) rs1190740301 0.00001
NM_001111.5(ADAR):c.1542C>T (p.Phe514=) rs757137562 0.00001
NM_001111.5(ADAR):c.1846G>A (p.Val616Ile) rs570647049 0.00001
NM_001111.5(ADAR):c.2886-12C>G rs775018500 0.00001
NM_001111.5(ADAR):c.3095G>A (p.Arg1032His) rs773129591 0.00001
NM_001111.5(ADAR):c.30C>T (p.Ser10=) rs769752403 0.00001
NM_001111.5(ADAR):c.3351A>G (p.Gln1117=) rs1571047056 0.00001
NM_001111.5(ADAR):c.3463C>T (p.Arg1155Trp) rs1044845711 0.00001
NM_001111.5(ADAR):c.434A>G (p.Lys145Arg) rs763767761 0.00001
NM_001111.5(ADAR):c.474A>C (p.Ala158=) rs1434133622 0.00001
NM_001111.5(ADAR):c.1006G>A (p.Asp336Asn) rs763575197
NM_001111.5(ADAR):c.1103A>T (p.Asn368Ile) rs1553213121
NM_001111.5(ADAR):c.1267C>T (p.Gln423Ter)
NM_001111.5(ADAR):c.1304C>T (p.Pro435Leu)
NM_001111.5(ADAR):c.1491dup (p.Glu498fs) rs1697846493
NM_001111.5(ADAR):c.1493_1494del (p.Glu498fs) rs1064794324
NM_001111.5(ADAR):c.15+104GT[9] rs71586026
NM_001111.5(ADAR):c.15+241TG[10] rs551880161
NM_001111.5(ADAR):c.15+241TG[11] rs551880161
NM_001111.5(ADAR):c.15+258_15+269del rs71077960
NM_001111.5(ADAR):c.15+259_15+268del rs66550822
NM_001111.5(ADAR):c.1601+1G>T
NM_001111.5(ADAR):c.1602-116_1602-114dup rs4045821
NM_001111.5(ADAR):c.1630C>A (p.Arg544=) rs768943773
NM_001111.5(ADAR):c.1666G>C (p.Val556Leu) rs1557882037
NM_001111.5(ADAR):c.1675C>T (p.Gln559Ter) rs1553212090
NM_001111.5(ADAR):c.1696A>T (p.Met566Leu) rs777616553
NM_001111.5(ADAR):c.1714dup (p.Glu572fs) rs1571095986
NM_001111.5(ADAR):c.1780G>A (p.Glu594Lys) rs1203572202
NM_001111.5(ADAR):c.1798C>T (p.Gln600Ter)
NM_001111.5(ADAR):c.1832del (p.Ser611fs) rs1697611007
NM_001111.5(ADAR):c.1891G>A (p.Glu631Lys) rs756241513
NM_001111.5(ADAR):c.1910A>G (p.Lys637Arg) rs886045341
NM_001111.5(ADAR):c.2079+1G>C rs757819771
NM_001111.5(ADAR):c.2130dup (p.Asn711fs) rs1553211449
NM_001111.5(ADAR):c.2180del (p.Pro727fs) rs1571089005
NM_001111.5(ADAR):c.220A>G (p.Arg74Gly) rs1571112467
NM_001111.5(ADAR):c.2224G>A (p.Ala742Thr) rs2101619298
NM_001111.5(ADAR):c.224T>G (p.Phe75Cys) rs886045345
NM_001111.5(ADAR):c.2262C>T (p.His754=)
NM_001111.5(ADAR):c.2290G>T (p.Val764Phe)
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.2496+41_2496+42dup
NM_001111.5(ADAR):c.2497-91C>T rs115161953
NM_001111.5(ADAR):c.2771A>G (p.Tyr924Cys)
NM_001111.5(ADAR):c.2894C>T (p.Pro965Leu)
NM_001111.5(ADAR):c.3002_3003delinsTT (p.Arg1001Leu) rs1064795689
NM_001111.5(ADAR):c.3004A>C (p.Thr1002Pro) rs749167389
NM_001111.5(ADAR):c.3019G>A (p.Gly1007Arg) rs398122822
NM_001111.5(ADAR):c.3020-3C>G rs1085307951
NM_001111.5(ADAR):c.3058C>A (p.Pro1020Thr) rs1464239852
NM_001111.5(ADAR):c.3062C>T (p.Thr1021Met) rs772773296
NM_001111.5(ADAR):c.3091C>T (p.Leu1031Phe)
NM_001111.5(ADAR):c.3102G>A (p.Met1034Ile)
NM_001111.5(ADAR):c.3124C>T (p.Arg1042Cys) rs779004315
NM_001111.5(ADAR):c.3130A>T (p.Asn1044Tyr) rs1057523436
NM_001111.5(ADAR):c.3286C>T (p.Arg1096Ter) rs769148365
NM_001111.5(ADAR):c.3301G>A (p.Val1101Ile)
NM_001111.5(ADAR):c.3301G>T (p.Val1101Phe) rs2101563031
NM_001111.5(ADAR):c.3348del (p.Arg1116fs)
NM_001111.5(ADAR):c.3443+2T>A rs1571046516
NM_001111.5(ADAR):c.3556A>G (p.Lys1186Glu) rs2101557212
NM_001111.5(ADAR):c.3577G>A (p.Glu1193Lys) rs1064796761
NM_001111.5(ADAR):c.3623A>G (p.Tyr1208Cys) rs2101556911
NM_001111.5(ADAR):c.386A>G (p.His129Arg)
NM_001111.5(ADAR):c.615C>A (p.Asn205Lys) rs770367924
NM_001111.5(ADAR):c.658_804del (p.Ala220_Gly268del)
NM_001111.5(ADAR):c.787G>C (p.Asp263His) rs766779037
NM_001111.5(ADAR):c.909C>G (p.Ile303Met) rs1131691507

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