ClinVar Miner

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

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Total variants: 54
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HGVS dbSNP gnomAD frequency
NM_006267.5(RANBP2):c.5175A>G (p.Glu1725=) rs535428027 0.01063
NM_006267.5(RANBP2):c.2351G>A (p.Arg784Lys) rs2912838 0.00684
NM_006267.5(RANBP2):c.73-6T>A rs201485597 0.00516
NM_006267.5(RANBP2):c.7849+4A>G rs2949961 0.00502
NM_006267.5(RANBP2):c.7754T>C (p.Ile2585Thr) rs145886643 0.00488
NM_006267.5(RANBP2):c.2982A>T (p.Ala994=) rs61748148 0.00486
NM_006267.5(RANBP2):c.2339C>T (p.Pro780Leu) rs61758802 0.00418
NM_006267.5(RANBP2):c.3162G>T (p.Gln1054His) rs141230513 0.00290
NM_006267.5(RANBP2):c.3163C>T (p.Pro1055Ser) rs140860785 0.00290
NM_006267.5(RANBP2):c.8407A>G (p.Ile2803Val) rs61758804 0.00272
NM_006267.5(RANBP2):c.7850-6T>G rs183569993 0.00270
NM_006267.5(RANBP2):c.4760G>T (p.Gly1587Val) rs148677577 0.00204
NM_006267.5(RANBP2):c.4498G>C (p.Ala1500Pro) rs145284139 0.00133
NM_006267.5(RANBP2):c.5217C>T (p.Ala1739=) rs146460294 0.00129
NM_006267.5(RANBP2):c.7172C>G (p.Thr2391Ser) rs2433786 0.00117
NM_006267.5(RANBP2):c.783-6T>C rs138540027 0.00108
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.8599+16G>A rs145152325 0.00087
NM_006267.5(RANBP2):c.1284A>G (p.Arg428=) rs142514679 0.00076
NM_006267.5(RANBP2):c.2520T>C (p.Arg840=) rs150539591 0.00071
NM_006267.5(RANBP2):c.3226T>G (p.Leu1076Val) rs142768885 0.00068
NM_006267.5(RANBP2):c.7499C>T (p.Thr2500Ile) rs140280672 0.00061
NM_006267.5(RANBP2):c.3350C>T (p.Ser1117Leu) rs137976808 0.00036
NM_006267.5(RANBP2):c.7751A>G (p.Asp2584Gly) rs138022657 0.00036
NM_006267.5(RANBP2):c.2340G>A (p.Pro780=) rs2912839 0.00019
NM_006267.5(RANBP2):c.834G>A (p.Leu278=) rs199652721 0.00019
NM_006267.5(RANBP2):c.342A>T (p.Ala114=) rs140650569 0.00016
NM_006267.5(RANBP2):c.3419C>T (p.Ser1140Leu) rs756874724 0.00015
NM_006267.5(RANBP2):c.5979C>T (p.Ser1993=) rs757493880 0.00014
NM_006267.5(RANBP2):c.1225A>G (p.Ile409Val) rs201087513 0.00012
NM_006267.5(RANBP2):c.7617A>T (p.Ser2539=) rs143675099 0.00009
NM_006267.5(RANBP2):c.8859C>T (p.Arg2953=) rs779450120 0.00009
NM_006267.5(RANBP2):c.3170C>T (p.Pro1057Leu) rs150151795 0.00008
NM_006267.5(RANBP2):c.4791C>T (p.Ser1597=) rs547882747 0.00007
NM_006267.5(RANBP2):c.9035-4C>T rs753514543 0.00007
NM_006267.5(RANBP2):c.-50C>T rs377140608 0.00006
NM_006267.5(RANBP2):c.1911C>T (p.Asp637=) rs202210294 0.00004
NM_006267.5(RANBP2):c.6643C>G (p.Pro2215Ala) rs775798185 0.00003
NM_006267.5(RANBP2):c.1001_1003delinsGAG (p.Ile334_Lys335delinsArgGlu) rs2149198433
NM_006267.5(RANBP2):c.1023T>C (p.Asn341=)
NM_006267.5(RANBP2):c.1123A>T (p.Thr375Ser)
NM_006267.5(RANBP2):c.2268T>C (p.Tyr756=) rs1573780904
NM_006267.5(RANBP2):c.3363G>T (p.Lys1121Asn) rs112835359
NM_006267.5(RANBP2):c.3558T>A (p.Thr1186=)
NM_006267.5(RANBP2):c.4332T>C (p.Ala1444=) rs1573811420
NM_006267.5(RANBP2):c.4794A>G (p.Gly1598=)
NM_006267.5(RANBP2):c.6312A>G (p.Ala2104=) rs751303610
NM_006267.5(RANBP2):c.6612C>A (p.Ala2204=) rs202005268
NM_006267.5(RANBP2):c.6792A>C (p.Thr2264=) rs773147227
NM_006267.5(RANBP2):c.7224T>C (p.Asp2408=)
NM_006267.5(RANBP2):c.7790T>C (p.Phe2597Ser) rs2949962
NM_006267.5(RANBP2):c.8589T>C (p.Phe2863=) rs1573846232
NM_006267.5(RANBP2):c.8826A>G (p.Arg2942=)

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