ClinVar Miner

List of variants in gene RANBP2 studied for not specified

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Total variants: 55
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HGVS dbSNP
NM_006267.5(RANBP2):c.-41G>T rs372373398
NM_006267.5(RANBP2):c.-45C>T rs79379002
NM_006267.5(RANBP2):c.1064-13A>T rs192629843
NM_006267.5(RANBP2):c.1209C>T (p.Ser403=) rs140275032
NM_006267.5(RANBP2):c.1274-14T>A rs201447069
NM_006267.5(RANBP2):c.1456-7A>G rs144029181
NM_006267.5(RANBP2):c.1632-16T>C rs147266881
NM_006267.5(RANBP2):c.1920A>G (p.Ala640=) rs147080366
NM_006267.5(RANBP2):c.2056-19A>G rs199880095
NM_006267.5(RANBP2):c.2173A>G (p.Ser725Gly) rs17414315
NM_006267.5(RANBP2):c.2330A>G (p.His777Arg) rs61748146
NM_006267.5(RANBP2):c.2339C>T (p.Pro780Leu) rs61758802
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.2550A>G (p.Ser850=) rs826549
NM_006267.5(RANBP2):c.2559T>A (p.Asp853Glu) rs148999619
NM_006267.5(RANBP2):c.2562A>G (p.Gly854=) rs13426055
NM_006267.5(RANBP2):c.2955G>A (p.Pro985=) rs61748147
NM_006267.5(RANBP2):c.2982A>T (p.Ala994=) rs61748148
NM_006267.5(RANBP2):c.3033G>A (p.Pro1011=) rs78215631
NM_006267.5(RANBP2):c.3411A>C (p.Pro1137=) rs76461420
NM_006267.5(RANBP2):c.3597G>A (p.Ala1199=) rs17036806
NM_006267.5(RANBP2):c.3934G>A (p.Val1312Ile) rs372722891
NM_006267.5(RANBP2):c.405+17T>G rs826526
NM_006267.5(RANBP2):c.4239A>G (p.Pro1413=) rs1553495415
NM_006267.5(RANBP2):c.4443A>G (p.Gly1481=) rs61748149
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.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.5941T>A (p.Ser1981Thr) rs61748150
NM_006267.5(RANBP2):c.637-18G>A rs826577
NM_006267.5(RANBP2):c.6609G>A (p.Ala2203=) rs60199637
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.72+11C>G rs113447280
NM_006267.5(RANBP2):c.728T>C (p.Met243Thr) rs139151870
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.7754T>C (p.Ile2585Thr) rs145886643
NM_006267.5(RANBP2):c.7849+4A>G rs2949961
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.816G>C (p.Leu272Phe) rs76352345
NM_006267.5(RANBP2):c.8407A>G (p.Ile2803Val) rs61758804
NM_006267.5(RANBP2):c.8600-14G>T rs57063709
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
NM_006267.5(RANBP2):c.9585C>T (p.Gly3195=) rs10185197

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