ClinVar Miner

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

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Total variants: 41
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HGVS dbSNP
NM_006267.5(RANBP2):c.-50C>T rs377140608
NM_006267.5(RANBP2):c.1770T>C (p.Asn590=) rs1573774225
NM_006267.5(RANBP2):c.2056-4A>T rs372329184
NM_006267.5(RANBP2):c.2142C>T (p.Thr714=) rs371899344
NM_006267.5(RANBP2):c.2148C>T (p.Asp716=) rs1573777630
NM_006267.5(RANBP2):c.2203-8A>G rs372713342
NM_006267.5(RANBP2):c.2244A>G (p.Ser748=) rs1488046156
NM_006267.5(RANBP2):c.2268T>C (p.Tyr756=) rs1573780904
NM_006267.5(RANBP2):c.2340G>A (p.Pro780=) rs2912839
NM_006267.5(RANBP2):c.2351G>A (p.Arg784Lys) rs2912838
NM_006267.5(RANBP2):c.2862A>G (p.Leu954=) rs374697321
NM_006267.5(RANBP2):c.288T>G (p.Leu96=) rs755002297
NM_006267.5(RANBP2):c.3060A>G (p.Pro1020=) rs1312609974
NM_006267.5(RANBP2):c.3226T>G (p.Leu1076Val) rs142768885
NM_006267.5(RANBP2):c.324T>C (p.Asp108=) rs375199174
NM_006267.5(RANBP2):c.3376C>T (p.Arg1126Trp) rs370285906
NM_006267.5(RANBP2):c.342A>T (p.Ala114=) rs140650569
NM_006267.5(RANBP2):c.4207A>G (p.Asn1403Asp) rs773879572
NM_006267.5(RANBP2):c.4332T>C (p.Ala1444=) rs1573811420
NM_006267.5(RANBP2):c.468A>G (p.Ser156=) rs1573715364
NM_006267.5(RANBP2):c.4791C>T (p.Ser1597=) rs547882747
NM_006267.5(RANBP2):c.5040C>T (p.Ala1680=) rs552993785
NM_006267.5(RANBP2):c.5217C>T (p.Ala1739=) rs146460294
NM_006267.5(RANBP2):c.6120A>G (p.Val2040=) rs1056562628
NM_006267.5(RANBP2):c.627G>A (p.Gln209=) rs1453197920
NM_006267.5(RANBP2):c.6312A>G (p.Ala2104=) rs751303610
NM_006267.5(RANBP2):c.6792A>C (p.Thr2264=) rs773147227
NM_006267.5(RANBP2):c.7039G>C (p.Gly2347Arg) rs151064332
NM_006267.5(RANBP2):c.73-6T>A rs201485597
NM_006267.5(RANBP2):c.7464A>G (p.Val2488=) rs368598843
NM_006267.5(RANBP2):c.7617A>T (p.Ser2539=) rs143675099
NM_006267.5(RANBP2):c.7751A>G (p.Asp2584Gly) rs138022657
NM_006267.5(RANBP2):c.8020+7C>T rs1573831757
NM_006267.5(RANBP2):c.8262A>G (p.Gln2754=) rs749840401
NM_006267.5(RANBP2):c.8385A>G (p.Glu2795=) rs774055387
NM_006267.5(RANBP2):c.8415A>G (p.Ser2805=) rs751209914
NM_006267.5(RANBP2):c.8589T>C (p.Phe2863=) rs1573846232
NM_006267.5(RANBP2):c.8700T>C (p.Ser2900=) rs750711827
NM_006267.5(RANBP2):c.8859C>T (p.Arg2953=) rs779450120
NM_006267.5(RANBP2):c.9243T>C (p.Thr3081=) rs752209534
NM_006267.5(RANBP2):c.9369+8T>C rs534483974

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