ClinVar Miner

List of variants in gene RANBP2 reported as benign for Encephalopathy, acute, infection-induced, 3, suceptibility to

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Total variants: 47
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HGVS dbSNP
NM_006267.5(RANBP2):c.1087C>T (p.Arg363Cys) rs149207118
NM_006267.5(RANBP2):c.1209C>T (p.Ser403=) rs140275032
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.225C>G (p.Asn75Lys) rs144278795
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.2351G>A (p.Arg784Lys) rs2912838
NM_006267.5(RANBP2):c.2405G>A (p.Arg802Gln) rs187011794
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.2625A>G (p.Val875=) rs200515712
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.3162_3163delinsTT (p.Gln1054_Pro1055delinsHisSer) rs1553494411
NM_006267.5(RANBP2):c.3411A>C (p.Pro1137=) rs76461420
NM_006267.5(RANBP2):c.3461A>T (p.His1154Leu) rs77443930
NM_006267.5(RANBP2):c.3501T>C (p.Asp1167=) rs141352171
NM_006267.5(RANBP2):c.3597G>A (p.Ala1199=) rs17036806
NM_006267.5(RANBP2):c.3612C>T (p.Phe1204=) rs749275095
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.4760G>T (p.Gly1587Val) rs148677577
NM_006267.5(RANBP2):c.4826A>T (p.Gln1609Leu) rs146669983
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.5941T>A (p.Ser1981Thr) rs61748150
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.7172C>G (p.Thr2391Ser) rs2433786
NM_006267.5(RANBP2):c.728T>C (p.Met243Thr) rs139151870
NM_006267.5(RANBP2):c.73-6T>A rs201485597
NM_006267.5(RANBP2):c.7474A>C (p.Thr2492Pro) rs2693103
NM_006267.5(RANBP2):c.7499C>T (p.Thr2500Ile) rs140280672
NM_006267.5(RANBP2):c.7670A>G (p.Asn2557Ser) rs145613015
NM_006267.5(RANBP2):c.7754T>C (p.Ile2585Thr) rs145886643
NM_006267.5(RANBP2):c.783-6T>C rs138540027
NM_006267.5(RANBP2):c.7849+4A>G rs2949961
NM_006267.5(RANBP2):c.7850-6T>G rs183569993
NM_006267.5(RANBP2):c.816G>C (p.Leu272Phe) rs76352345
NM_006267.5(RANBP2):c.8253= (p.Glu2751=) rs826580
NM_006267.5(RANBP2):c.8407A>G (p.Ile2803Val) rs61758804
NM_006267.5(RANBP2):c.8671G>A (p.Gly2891Ser) rs376940698
NM_006267.5(RANBP2):c.9585C>T (p.Gly3195=) rs10185197

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