ClinVar Miner

List of variants in gene RANBP2 reported as likely benign by GeneDx

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Total variants: 32
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HGVS dbSNP
NM_006267.5(RANBP2):c.-41G>T rs372373398
NM_006267.5(RANBP2):c.-50C>T rs377140608
NM_006267.5(RANBP2):c.1209C>T (p.Ser403=) rs140275032
NM_006267.5(RANBP2):c.1274-14T>A rs201447069
NM_006267.5(RANBP2):c.1632-16T>C rs147266881
NM_006267.5(RANBP2):c.1920A>G (p.Ala640=) rs147080366
NM_006267.5(RANBP2):c.2173A>G (p.Ser725Gly) rs17414315
NM_006267.5(RANBP2):c.238G>A (p.Val80Ile) rs140785381
NM_006267.5(RANBP2):c.2466+17C>T rs760137862
NM_006267.5(RANBP2):c.2520T>C (p.Arg840=) rs150539591
NM_006267.5(RANBP2):c.3033G>A (p.Pro1011=) rs78215631
NM_006267.5(RANBP2):c.3934G>A (p.Val1312Ile) rs372722891
NM_006267.5(RANBP2):c.4239A>G (p.Pro1413=) rs1553495415
NM_006267.5(RANBP2):c.4530A>G (p.Leu1510=) rs111676038
NM_006267.5(RANBP2):c.4726A>T (p.Thr1576Ser) rs74821091
NM_006267.5(RANBP2):c.5217C>T (p.Ala1739=) rs146460294
NM_006267.5(RANBP2):c.5307G>A (p.Lys1769=) rs76221103
NM_006267.5(RANBP2):c.5394C>T (p.Ser1798=) rs368119755
NM_006267.5(RANBP2):c.543G>A (p.Leu181=) rs146460580
NM_006267.5(RANBP2):c.5489A>G (p.His1830Arg) rs760578682
NM_006267.5(RANBP2):c.6612C>A (p.Ala2204=) rs202005268
NM_006267.5(RANBP2):c.6643C>G (p.Pro2215Ala) rs775798185
NM_006267.5(RANBP2):c.73-6T>A rs201485597
NM_006267.5(RANBP2):c.7463T>C (p.Val2488Ala) rs189289937
NM_006267.5(RANBP2):c.7499C>T (p.Thr2500Ile) rs140280672
NM_006267.5(RANBP2):c.7617A>T (p.Ser2539=) rs143675099
NM_006267.5(RANBP2):c.7850-15dup rs573949870
NM_006267.5(RANBP2):c.7850-7G>C rs1057521363
NM_006267.5(RANBP2):c.8113+12G>A rs375754677
NM_006267.5(RANBP2):c.8670C>T (p.Ala2890=) rs199918785
NM_006267.5(RANBP2):c.9369+20T>C rs201669692
NM_006267.5(RANBP2):c.9369+4G>A rs139387463

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