ClinVar Miner

List of variants in gene RANBP2 reported as likely benign for not specified

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Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_006267.5(RANBP2):c.73-6T>A rs201485597 0.00516
NM_006267.5(RANBP2):c.5307G>A (p.Lys1769=) rs76221103 0.00493
NM_006267.5(RANBP2):c.4726A>T (p.Thr1576Ser) rs74821091 0.00490
NM_006267.5(RANBP2):c.3033G>A (p.Pro1011=) rs78215631 0.00478
NM_006267.5(RANBP2):c.1274-14T>A rs201447069 0.00399
NM_006267.5(RANBP2):c.-41G>T rs372373398 0.00331
NM_006267.5(RANBP2):c.9369+4G>A rs139387463 0.00108
NM_006267.5(RANBP2):c.1920A>G (p.Ala640=) rs147080366 0.00106
NM_006267.5(RANBP2):c.4530A>G (p.Leu1510=) rs111676038 0.00105
NM_006267.5(RANBP2):c.2520T>C (p.Arg840=) rs150539591 0.00071
NM_006267.5(RANBP2):c.7499C>T (p.Thr2500Ile) rs140280672 0.00061
NM_006267.5(RANBP2):c.238G>A (p.Val80Ile) rs140785381 0.00058
NM_006267.5(RANBP2):c.7463T>C (p.Val2488Ala) rs189289937 0.00051
NM_006267.5(RANBP2):c.2466+17C>T rs760137862 0.00018
NM_006267.5(RANBP2):c.543G>A (p.Leu181=) rs146460580 0.00012
NM_006267.5(RANBP2):c.3934G>A (p.Val1312Ile) rs372722891 0.00011
NM_006267.5(RANBP2):c.9369+20T>C rs201669692 0.00010
NM_006267.5(RANBP2):c.8670C>T (p.Ala2890=) rs199918785 0.00009
NM_006267.5(RANBP2):c.6643C>G (p.Pro2215Ala) rs775798185 0.00003
NM_006267.5(RANBP2):c.5489A>G (p.His1830Arg) rs760578682 0.00002
NM_006267.5(RANBP2):c.7850-7G>C rs1057521363 0.00002
NM_006267.5(RANBP2):c.4239A>G (p.Pro1413=) rs1553495415
NM_006267.5(RANBP2):c.5394C>T (p.Ser1798=) rs368119755
NM_006267.5(RANBP2):c.6612C>A (p.Ala2204=) rs202005268
NM_006267.5(RANBP2):c.7850-15dup rs573949870
NM_006267.5(RANBP2):c.8113+12G>A rs375754677

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