ClinVar Miner

List of variants in gene RAD21 reported as likely benign for Inborn genetic diseases

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Total variants: 32
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HGVS dbSNP gnomAD frequency
NM_006265.3(RAD21):c.786C>T (p.Asp262=) rs34653007 0.00300
NM_006265.3(RAD21):c.1515C>G (p.Pro505=) rs9297560 0.00266
NM_006265.3(RAD21):c.1564C>G (p.Leu522Val) rs199878247 0.00060
NM_006265.3(RAD21):c.1617A>G (p.Glu539=) rs138040512 0.00040
NM_006265.3(RAD21):c.1352T>G (p.Leu451Arg) rs144953114 0.00034
NM_006265.3(RAD21):c.735C>T (p.Pro245=) rs199767556 0.00029
NM_006265.3(RAD21):c.1185G>A (p.Pro395=) rs138247094 0.00026
NM_006265.3(RAD21):c.1503T>G (p.Pro501=) rs150935041 0.00017
NM_006265.3(RAD21):c.645T>C (p.Tyr215=) rs143910582 0.00010
NM_006265.3(RAD21):c.1479G>C (p.Gln493His) rs759030507 0.00009
NM_006265.3(RAD21):c.450G>A (p.Gly150=) rs188711205 0.00009
NM_006265.3(RAD21):c.582G>A (p.Glu194=) rs201468757 0.00008
NM_006265.3(RAD21):c.1620G>A (p.Glu540=) rs746050594 0.00006
NM_006265.3(RAD21):c.1471-3A>G rs202098276 0.00005
NM_006265.3(RAD21):c.1735A>G (p.Ile579Val) rs780599047 0.00004
NM_006265.3(RAD21):c.1801T>C (p.Leu601=) rs780662446 0.00004
NM_006265.3(RAD21):c.363G>C (p.Leu121=) rs959964243 0.00003
NM_006265.3(RAD21):c.849C>T (p.Pro283=) rs369661655 0.00003
NM_006265.3(RAD21):c.859A>G (p.Met287Val) rs141936111 0.00003
NM_006265.3(RAD21):c.1285G>A (p.Asp429Asn) rs147956016 0.00002
NM_006265.3(RAD21):c.1364T>C (p.Val455Ala) rs373625369 0.00002
NM_006265.3(RAD21):c.1441G>A (p.Gly481Arg) rs755168088 0.00002
NM_006265.3(RAD21):c.145-4A>G rs752213732 0.00002
NM_006265.3(RAD21):c.1629T>C (p.Asp543=) rs377080076 0.00002
NM_006265.3(RAD21):c.378C>T (p.Asp126=) rs763410561 0.00002
NM_006265.3(RAD21):c.1251C>T (p.Leu417=) rs1184536083 0.00001
NM_006265.3(RAD21):c.1320C>T (p.Ile440=) rs776397992 0.00001
NM_006265.3(RAD21):c.1347C>T (p.Ser449=) rs760592900 0.00001
NM_006265.3(RAD21):c.1349G>A (p.Arg450His) rs1051321465 0.00001
NM_006265.3(RAD21):c.1446A>T (p.Gln482His) rs756283022 0.00001
NM_006265.3(RAD21):c.1532A>G (p.Asn511Ser) rs1202371552 0.00001
NM_006265.3(RAD21):c.689-4del rs772388827

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