ClinVar Miner

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

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Total variants: 34
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HGVS dbSNP
NM_006267.5(RANBP2):c.1284A>G (p.Arg428=) rs142514679
NM_006267.5(RANBP2):c.1776T>C (p.Phe592=) rs755487849
NM_006267.5(RANBP2):c.2056-10A>G rs539183099
NM_006267.5(RANBP2):c.2056-4A>T rs372329184
NM_006267.5(RANBP2):c.2142C>T (p.Thr714=) rs371899344
NM_006267.5(RANBP2):c.2943C>T (p.Phe981=) rs1186427284
NM_006267.5(RANBP2):c.3153T>C (p.Val1051=) rs372530448
NM_006267.5(RANBP2):c.3351G>A (p.Ser1117=) rs746610775
NM_006267.5(RANBP2):c.3363G>T (p.Lys1121Asn) rs112835359
NM_006267.5(RANBP2):c.4498G>C (p.Ala1500Pro) rs145284139
NM_006267.5(RANBP2):c.4707G>A (p.Pro1569=) rs757396599
NM_006267.5(RANBP2):c.4752T>C (p.Phe1584=) rs1553495996
NM_006267.5(RANBP2):c.4950A>G (p.Thr1650=) rs1553496153
NM_006267.5(RANBP2):c.5175A>G (p.Glu1725=) rs535428027
NM_006267.5(RANBP2):c.5561A>G (p.Asn1854Ser) rs141379413
NM_006267.5(RANBP2):c.561C>T (p.His187=) rs761758022
NM_006267.5(RANBP2):c.5979C>T (p.Ser1993=) rs757493880
NM_006267.5(RANBP2):c.6033C>T (p.Ile2011=) rs1360566375
NM_006267.5(RANBP2):c.6060C>T (p.Pro2020=) rs4012040
NM_006267.5(RANBP2):c.6171G>A (p.Leu2057=) rs199917317
NM_006267.5(RANBP2):c.627G>A (p.Gln209=) rs1453197920
NM_006267.5(RANBP2):c.6342T>C (p.Asp2114=) rs529005450
NM_006267.5(RANBP2):c.7474A>G (p.Thr2492Ala) rs2693103
NM_006267.5(RANBP2):c.7602A>G (p.Ala2534=) rs759564858
NM_006267.5(RANBP2):c.8075G>A (p.Gly2692Asp) rs111958052
NM_006267.5(RANBP2):c.8166G>A (p.Glu2722=) rs895968968
NM_006267.5(RANBP2):c.8334A>G (p.Val2778=) rs758018669
NM_006267.5(RANBP2):c.8461A>C (p.Thr2821Pro) rs142231499
NM_006267.5(RANBP2):c.8599+16G>A rs145152325
NM_006267.5(RANBP2):c.8670C>T (p.Ala2890=) rs199918785
NM_006267.5(RANBP2):c.8916A>C (p.Leu2972=) rs1553502610
NM_006267.5(RANBP2):c.9354A>G (p.Pro3118=) rs201982385
NM_006267.5(RANBP2):c.9369+4G>A rs139387463
NM_006267.5(RANBP2):c.9405A>G (p.Gly3135=) rs1553503136

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