ClinVar Miner

List of variants in gene RANBP2 reported as uncertain significance by GeneDx

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Total variants: 73
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HGVS dbSNP gnomAD frequency
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.2230G>C (p.Glu744Gln) rs2912840 0.00104
NM_006267.5(RANBP2):c.3226T>G (p.Leu1076Val) rs142768885 0.00068
NM_006267.5(RANBP2):c.7966A>G (p.Thr2656Ala) rs148596328 0.00041
NM_006267.5(RANBP2):c.560A>G (p.His187Arg) rs2693122 0.00018
NM_006267.5(RANBP2):c.2818G>T (p.Gly940Cys) rs201001226 0.00017
NM_006267.5(RANBP2):c.4213C>G (p.Gln1405Glu) rs375021752 0.00009
NM_006267.5(RANBP2):c.1954A>G (p.Ile652Val) rs560038746 0.00007
NM_006267.5(RANBP2):c.4294G>A (p.Val1432Ile) rs1006499929 0.00005
NM_006267.5(RANBP2):c.2954C>T (p.Pro985Leu) rs368547122 0.00003
NM_006267.5(RANBP2):c.7982A>G (p.Lys2661Arg) rs746866652 0.00003
NM_006267.5(RANBP2):c.6349G>A (p.Ala2117Thr) rs769174532 0.00002
NM_006267.5(RANBP2):c.649T>C (p.Ser217Pro) rs760640664 0.00002
NM_006267.5(RANBP2):c.9154G>C (p.Val3052Leu) rs775739392 0.00002
NM_006267.5(RANBP2):c.9220G>A (p.Gly3074Ser) rs753643539 0.00002
NM_006267.5(RANBP2):c.2384A>G (p.Tyr795Cys) rs372122123 0.00001
NM_006267.5(RANBP2):c.2507C>T (p.Ala836Val) rs762106093 0.00001
NM_006267.5(RANBP2):c.309G>T (p.Leu103Phe) rs1695156914 0.00001
NM_006267.5(RANBP2):c.3134C>T (p.Thr1045Met) rs144270067 0.00001
NM_006267.5(RANBP2):c.4972T>G (p.Phe1658Val) rs755016899 0.00001
NM_006267.5(RANBP2):c.7850-5T>A rs756409669 0.00001
NM_006267.5(RANBP2):c.8076del (p.Ser2693fs) rs1164664766 0.00001
NM_006267.5(RANBP2):c.1064-12T>G
NM_006267.5(RANBP2):c.1126T>C (p.Phe376Leu)
NM_006267.5(RANBP2):c.1172C>G (p.Ser391Cys) rs1553487968
NM_006267.5(RANBP2):c.1282C>T (p.Arg428Ter)
NM_006267.5(RANBP2):c.1309C>T (p.Leu437Phe)
NM_006267.5(RANBP2):c.1685dup (p.Arg563fs) rs1558903136
NM_006267.5(RANBP2):c.1777T>C (p.Tyr593His)
NM_006267.5(RANBP2):c.1786C>T (p.Arg596Ter)
NM_006267.5(RANBP2):c.1894C>T (p.His632Tyr)
NM_006267.5(RANBP2):c.1953C>G (p.His651Gln) rs756288262
NM_006267.5(RANBP2):c.1955T>C (p.Ile652Thr) rs2149232531
NM_006267.5(RANBP2):c.1961_1962del (p.Phe654fs) rs2149232562
NM_006267.5(RANBP2):c.2048_2049dup (p.Ala684fs)
NM_006267.5(RANBP2):c.2055+1G>A rs2149233034
NM_006267.5(RANBP2):c.2061dup (p.His688fs)
NM_006267.5(RANBP2):c.217G>A (p.Glu73Lys) rs1695112403
NM_006267.5(RANBP2):c.2321A>G (p.Glu774Gly) rs1676189155
NM_006267.5(RANBP2):c.2363C>T (p.Ser788Leu)
NM_006267.5(RANBP2):c.2617C>A (p.Pro873Thr)
NM_006267.5(RANBP2):c.2808G>C (p.Gln936His)
NM_006267.5(RANBP2):c.2954C>G (p.Pro985Arg) rs368547122
NM_006267.5(RANBP2):c.2977T>G (p.Ser993Ala) rs1064796454
NM_006267.5(RANBP2):c.335G>A (p.Gly112Glu)
NM_006267.5(RANBP2):c.3388G>C (p.Asp1130His)
NM_006267.5(RANBP2):c.3592C>T (p.Arg1198Cys) rs771155432
NM_006267.5(RANBP2):c.3613G>T (p.Asp1205Tyr) rs936822747
NM_006267.5(RANBP2):c.4490C>T (p.Thr1497Ile) rs2149275939
NM_006267.5(RANBP2):c.452T>C (p.Phe151Ser)
NM_006267.5(RANBP2):c.4986C>G (p.Phe1662Leu) rs777676139
NM_006267.5(RANBP2):c.508del (p.Arg170fs) rs2149128467
NM_006267.5(RANBP2):c.5570A>G (p.Gln1857Arg) rs2149279328
NM_006267.5(RANBP2):c.611A>G (p.Asn204Ser) rs2149128791
NM_006267.5(RANBP2):c.637-2A>G rs2149130759
NM_006267.5(RANBP2):c.685C>T (p.Arg229Ter)
NM_006267.5(RANBP2):c.6995T>C (p.Val2332Ala) rs2149283305
NM_006267.5(RANBP2):c.7129G>A (p.Val2377Ile) rs1573820858
NM_006267.5(RANBP2):c.73-1G>T
NM_006267.5(RANBP2):c.7841C>T (p.Pro2614Leu)
NM_006267.5(RANBP2):c.7892A>C (p.Asp2631Ala) rs1677511241
NM_006267.5(RANBP2):c.7961C>A (p.Pro2654His)
NM_006267.5(RANBP2):c.7988G>C (p.Arg2663Thr)
NM_006267.5(RANBP2):c.806_807del (p.Val269fs)
NM_006267.5(RANBP2):c.8516C>G (p.Ser2839Ter)
NM_006267.5(RANBP2):c.8555A>G (p.Asp2852Gly)
NM_006267.5(RANBP2):c.8850G>A (p.Trp2950Ter)
NM_006267.5(RANBP2):c.8923A>G (p.Arg2975Gly)
NM_006267.5(RANBP2):c.8983C>G (p.Pro2995Ala)
NM_006267.5(RANBP2):c.9022T>C (p.Ser3008Pro) rs2149332140
NM_006267.5(RANBP2):c.9041A>C (p.Glu3014Ala)
NM_006267.5(RANBP2):c.9052G>C (p.Glu3018Gln)

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