ClinVar Miner

List of variants in gene RANBP2 reported as benign

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Gene type:
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Total variants: 95
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HGVS dbSNP gnomAD frequency
NM_006267.5(RANBP2):c.8253G>A (p.Glu2751=) rs826580 0.98708
NM_006267.5(RANBP2):c.405+17T>G rs826526 0.37500
NM_006267.5(RANBP2):c.637-18G>A rs826577 0.37494
NM_006267.5(RANBP2):c.2550A>G (p.Ser850=) rs826549 0.36200
NM_006267.5(RANBP2):c.1456-7A>G rs144029181 0.16005
NM_006267.5(RANBP2):c.4443A>G (p.Gly1481=) rs61748149 0.05119
NM_006267.5(RANBP2):c.9585C>T (p.Gly3195=) rs10185197 0.04909
NM_006267.5(RANBP2):c.72+11C>G rs113447280 0.04653
NM_006267.5(RANBP2):c.6609G>A (p.Ala2203=) rs60199637 0.04502
NM_006267.5(RANBP2):c.2562A>G (p.Gly854=) rs13426055 0.02567
NM_006267.5(RANBP2):c.-45C>T rs79379002 0.02350
NM_006267.5(RANBP2):c.3597G>A (p.Ala1199=) rs17036806 0.02270
NM_006267.5(RANBP2):c.2330A>G (p.His777Arg) rs61748146 0.02199
NM_006267.5(RANBP2):c.2056-19A>G rs199880095 0.02155
NM_006267.5(RANBP2):c.8600-14G>T rs57063709 0.01439
NM_006267.5(RANBP2):c.1064-13A>T rs192629843 0.01429
NM_006267.5(RANBP2):c.2559T>A (p.Asp853Glu) rs148999619 0.01352
NM_006267.5(RANBP2):c.8253= (p.Glu2751=) rs826580 0.01292
NM_006267.5(RANBP2):c.816G>C (p.Leu272Phe) rs76352345 0.01093
NM_006267.5(RANBP2):c.1209C>T (p.Ser403=) rs140275032 0.00951
NM_006267.5(RANBP2):c.1632-16T>C rs147266881 0.00948
NM_006267.5(RANBP2):c.2173A>G (p.Ser725Gly) rs17414315 0.00940
NM_006267.5(RANBP2):c.5941T>A (p.Ser1981Thr) rs61748150 0.00849
NM_006267.5(RANBP2):c.3411A>C (p.Pro1137=) rs76461420 0.00790
NM_006267.5(RANBP2):c.2351G>A (p.Arg784Lys) rs2912838 0.00684
NM_006267.5(RANBP2):c.1087C>T (p.Arg363Cys) rs149207118 0.00617
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.5307G>A (p.Lys1769=) rs76221103 0.00493
NM_006267.5(RANBP2):c.4726A>T (p.Thr1576Ser) rs74821091 0.00490
NM_006267.5(RANBP2):c.728T>C (p.Met243Thr) rs139151870 0.00489
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.3033G>A (p.Pro1011=) rs78215631 0.00478
NM_006267.5(RANBP2):c.2339C>T (p.Pro780Leu) rs61758802 0.00418
NM_006267.5(RANBP2):c.2955G>A (p.Pro985=) rs61748147 0.00417
NM_006267.5(RANBP2):c.1274-14T>A rs201447069 0.00399
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.3461A>T (p.His1154Leu) rs77443930 0.00272
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.225C>G (p.Asn75Lys) rs144278795 0.00227
NM_006267.5(RANBP2):c.4760G>T (p.Gly1587Val) rs148677577 0.00204
NM_006267.5(RANBP2):c.7670A>G (p.Asn2557Ser) rs145613015 0.00194
NM_006267.5(RANBP2):c.1536G>A (p.Pro512=) rs370400502 0.00193
NM_006267.5(RANBP2):c.3501T>C (p.Asp1167=) rs141352171 0.00140
NM_006267.5(RANBP2):c.4826A>T (p.Gln1609Leu) rs146669983 0.00132
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.2502C>G (p.Asn834Lys) rs144573168 0.00110
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.4530A>G (p.Leu1510=) rs111676038 0.00105
NM_006267.5(RANBP2):c.6663A>G (p.Thr2221=) rs150750548 0.00102
NM_006267.5(RANBP2):c.8599+16G>A rs145152325 0.00087
NM_006267.5(RANBP2):c.6270G>A (p.Thr2090=) rs138191683 0.00081
NM_006267.5(RANBP2):c.2243C>T (p.Ser748Leu) rs200940828 0.00072
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.1755+15A>G rs376409146 0.00051
NM_006267.5(RANBP2):c.2212C>T (p.Pro738Ser) rs201793011 0.00045
NM_006267.5(RANBP2):c.2405G>A (p.Arg802Gln) rs187011794 0.00036
NM_006267.5(RANBP2):c.7340C>T (p.Ser2447Phe) rs200750445 0.00022
NM_006267.5(RANBP2):c.2751T>C (p.Tyr917=) rs140567791 0.00021
NM_006267.5(RANBP2):c.834G>A (p.Leu278=) rs199652721 0.00019
NM_006267.5(RANBP2):c.2901A>G (p.Gln967=) rs376394926 0.00017
NM_006267.5(RANBP2):c.6203A>G (p.Asn2068Ser) rs150424672 0.00016
NM_006267.5(RANBP2):c.3955G>C (p.Ala1319Pro) rs374902910 0.00015
NM_006267.5(RANBP2):c.1108A>G (p.Lys370Glu) rs143137111 0.00012
NM_006267.5(RANBP2):c.8671G>A (p.Gly2891Ser) rs376940698 0.00009
NM_006267.5(RANBP2):c.9216G>A (p.Ala3072=) rs371443840 0.00009
NM_006267.5(RANBP2):c.1740A>G (p.Glu580=) rs554245982 0.00008
NM_006267.5(RANBP2):c.2625A>G (p.Val875=) rs200515712 0.00008
NM_006267.5(RANBP2):c.9035-4C>T rs753514543 0.00007
NM_006267.5(RANBP2):c.1644A>G (p.Val548=) rs1057955 0.00006
NM_006267.5(RANBP2):c.2202+14T>G rs202098901 0.00005
NM_006267.5(RANBP2):c.3612C>T (p.Phe1204=) rs749275095 0.00005
NM_006267.5(RANBP2):c.7863A>G (p.Lys2621=) rs749384165 0.00003
NM_006267.5(RANBP2):c.2754G>A (p.Pro918=) rs542711340 0.00001
NM_006267.5(RANBP2):c.3253A>C (p.Lys1085Gln) rs576035153 0.00001
NM_006267.5(RANBP2):c.1756-3del
NM_006267.5(RANBP2):c.2340G>T (p.Pro780=)
NM_006267.5(RANBP2):c.2383-3dup rs542446071
NM_006267.5(RANBP2):c.2467-11dup rs747860271
NM_006267.5(RANBP2):c.3162_3163delinsTT (p.Gln1054_Pro1055delinsHisSer) rs1553494411
NM_006267.5(RANBP2):c.5367T>G (p.Val1789=) rs200692090
NM_006267.5(RANBP2):c.6612C>A (p.Ala2204=) rs202005268
NM_006267.5(RANBP2):c.6612C>T (p.Ala2204=) rs202005268
NM_006267.5(RANBP2):c.6613G>C (p.Gly2205Arg) rs755789696
NM_006267.5(RANBP2):c.7474A>C (p.Thr2492Pro) rs2693103
NM_006267.5(RANBP2):c.7669A>G (p.Asn2557Asp)
NM_006267.5(RANBP2):c.7849+936G>T

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