ClinVar Miner

List of variants in gene ADAR reported by PreventionGenetics, part of Exact Sciences

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Total variants: 30
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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.1151A>G (p.Lys384Arg) rs2229857 0.61729
NM_001111.5(ADAR):c.3443+8G>A rs9427094 0.40966
NM_001111.5(ADAR):c.577C>G (p.Pro193Ala) rs145588689 0.00162
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.2349A>G (p.Glu783=) rs77988942 0.00033
NM_001111.5(ADAR):c.2496+9G>A rs199698434 0.00017
NM_001111.5(ADAR):c.1625A>G (p.Asn542Ser) rs200242235 0.00016
NM_001111.5(ADAR):c.1934+8C>T rs376025865 0.00013
NM_001111.5(ADAR):c.2952A>G (p.Thr984=) rs765649485 0.00011
NM_001111.5(ADAR):c.222G>A (p.Arg74=) rs150423721 0.00010
NM_001111.5(ADAR):c.16-7T>A rs190022999 0.00007
NM_001111.5(ADAR):c.2275G>A (p.Val759Ile) rs145849344 0.00006
NM_001111.5(ADAR):c.2319C>T (p.Cys773=) rs750666914 0.00004
NM_001111.5(ADAR):c.3199T>C (p.Leu1067=) rs758120128 0.00004
NM_001111.5(ADAR):c.675G>A (p.Pro225=) rs771459105 0.00004
NM_001111.5(ADAR):c.643G>A (p.Gly215Ser) rs751532191 0.00003
NM_001111.5(ADAR):c.3316-4C>T rs765304172 0.00001
NM_001111.5(ADAR):c.*2A>G
NM_001111.5(ADAR):c.1006G>A (p.Asp336Asn) rs763575197
NM_001111.5(ADAR):c.1281A>G (p.Pro427=) rs147766807
NM_001111.5(ADAR):c.1483A>T (p.Lys495Ter)
NM_001111.5(ADAR):c.1600C>T (p.Arg534Ter)
NM_001111.5(ADAR):c.2203G>A (p.Ala735Thr) rs2101619399
NM_001111.5(ADAR):c.2361G>A (p.Ala787=)
NM_001111.5(ADAR):c.3148G>A (p.Gly1050Arg)
NM_001111.5(ADAR):c.3233G>A (p.Arg1078His)
NM_001111.5(ADAR):c.597C>G (p.Val199=)
NM_001365045.1(ADAR):c.42+3A>G

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