ClinVar Miner

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

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Total variants: 105
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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 0.00107
NM_006267.5(RANBP2):c.2230G>C (p.Glu744Gln) rs2912840 0.00102
NM_006267.5(RANBP2):c.3226T>G (p.Leu1076Val) rs142768885 0.00068
NM_006267.5(RANBP2):c.7966A>G (p.Thr2656Ala) rs148596328 0.00040
NM_006267.5(RANBP2):c.9346G>A (p.Val3116Ile) rs150721983 0.00034
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.1954A>G (p.Ile652Val) rs560038746 0.00008
NM_006267.5(RANBP2):c.4213C>G (p.Gln1405Glu) rs375021752 0.00007
NM_006267.5(RANBP2):c.4294G>A (p.Val1432Ile) rs1006499929 0.00005
NM_006267.5(RANBP2):c.1309C>T (p.Leu437Phe) rs774972402 0.00003
NM_006267.5(RANBP2):c.2954C>T (p.Pro985Leu) rs368547122 0.00003
NM_006267.5(RANBP2):c.3388G>C (p.Asp1130His) rs765238832 0.00002
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.1702C>T (p.His568Tyr) rs1675916733 0.00001
NM_006267.5(RANBP2):c.1777T>C (p.Tyr593His) rs1373364729 0.00001
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.7129G>A (p.Val2377Ile) rs1573820858 0.00001
NM_006267.5(RANBP2):c.7850-5T>A rs756409669 0.00001
NM_006267.5(RANBP2):c.7982A>G (p.Lys2661Arg) rs746866652 0.00001
NM_006267.5(RANBP2):c.8076del (p.Ser2693fs) rs1164664766 0.00001
NM_006267.5(RANBP2):c.1064-12T>G rs1165835844
NM_006267.5(RANBP2):c.1126T>C (p.Phe376Leu) rs2467478791
NM_006267.5(RANBP2):c.1162G>A (p.Ala388Thr)
NM_006267.5(RANBP2):c.1172C>G (p.Ser391Cys) rs1553487968
NM_006267.5(RANBP2):c.1234C>T (p.Arg412Ter)
NM_006267.5(RANBP2):c.1282C>T (p.Arg428Ter) rs773199480
NM_006267.5(RANBP2):c.1300C>A (p.Leu434Ile)
NM_006267.5(RANBP2):c.1411C>T (p.Leu471Phe)
NM_006267.5(RANBP2):c.141A>T (p.Lys47Asn)
NM_006267.5(RANBP2):c.1436T>C (p.Ile479Thr)
NM_006267.5(RANBP2):c.1440T>A (p.Cys480Ter)
NM_006267.5(RANBP2):c.1640A>G (p.Asn547Ser)
NM_006267.5(RANBP2):c.1685dup (p.Arg563fs) rs1558903136
NM_006267.5(RANBP2):c.1786C>T (p.Arg596Ter) rs2467520894
NM_006267.5(RANBP2):c.178C>T (p.Pro60Ser)
NM_006267.5(RANBP2):c.1836G>T (p.Leu612Phe)
NM_006267.5(RANBP2):c.1894C>T (p.His632Tyr) rs2467521715
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.1966A>G (p.Ile656Val) rs121434504
NM_006267.5(RANBP2):c.2048_2049dup (p.Ala684fs) rs2467526074
NM_006267.5(RANBP2):c.2055+1G>A rs2149233034
NM_006267.5(RANBP2):c.2061dup (p.His688fs) rs2467529652
NM_006267.5(RANBP2):c.2151_2164del (p.Leu718fs)
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) rs2467542011
NM_006267.5(RANBP2):c.2617C>A (p.Pro873Thr) rs2467600123
NM_006267.5(RANBP2):c.270C>A (p.Asn90Lys)
NM_006267.5(RANBP2):c.2808G>C (p.Gln936His) rs755170681
NM_006267.5(RANBP2):c.2831T>C (p.Leu944Ser)
NM_006267.5(RANBP2):c.2872G>T (p.Gly958Cys)
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.3076A>G (p.Thr1026Ala)
NM_006267.5(RANBP2):c.335G>A (p.Gly112Glu) rs2467290624
NM_006267.5(RANBP2):c.3548A>T (p.Glu1183Val)
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.4064G>C (p.Trp1355Ser)
NM_006267.5(RANBP2):c.4490C>T (p.Thr1497Ile) rs2149275939
NM_006267.5(RANBP2):c.452T>C (p.Phe151Ser) rs2467333632
NM_006267.5(RANBP2):c.497A>G (p.His166Arg)
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.5650T>A (p.Ser1884Thr)
NM_006267.5(RANBP2):c.6043C>G (p.Pro2015Ala)
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) rs1695564496
NM_006267.5(RANBP2):c.6995T>C (p.Val2332Ala) rs2149283305
NM_006267.5(RANBP2):c.73-1G>T rs1470243501
NM_006267.5(RANBP2):c.7460_7474delinsCAG (p.Asp2487_Thr2492delinsAlaAla)
NM_006267.5(RANBP2):c.782+1G>T
NM_006267.5(RANBP2):c.7841C>T (p.Pro2614Leu) rs1350325862
NM_006267.5(RANBP2):c.7892A>C (p.Asp2631Ala) rs1677511241
NM_006267.5(RANBP2):c.7940T>G (p.Leu2647Arg)
NM_006267.5(RANBP2):c.7961C>A (p.Pro2654His) rs2467675563
NM_006267.5(RANBP2):c.7988G>C (p.Arg2663Thr) rs2467675816
NM_006267.5(RANBP2):c.806_807del (p.Val269fs) rs1695994911
NM_006267.5(RANBP2):c.8114A>G (p.Asp2705Gly)
NM_006267.5(RANBP2):c.821G>A (p.Gly274Glu)
NM_006267.5(RANBP2):c.8516C>G (p.Ser2839Ter) rs1677945982
NM_006267.5(RANBP2):c.8555A>G (p.Asp2852Gly) rs2467719482
NM_006267.5(RANBP2):c.8684A>T (p.Glu2895Val) rs2467751848
NM_006267.5(RANBP2):c.8850G>A (p.Trp2950Ter) rs2467758007
NM_006267.5(RANBP2):c.8923A>G (p.Arg2975Gly) rs2467758634
NM_006267.5(RANBP2):c.8983C>G (p.Pro2995Ala) rs373123838
NM_006267.5(RANBP2):c.9022T>C (p.Ser3008Pro) rs2149332140
NM_006267.5(RANBP2):c.9041A>C (p.Glu3014Ala) rs2467760832
NM_006267.5(RANBP2):c.9052G>C (p.Glu3018Gln) rs2467760886
NM_006267.5(RANBP2):c.9551_9552del (p.Asp3183_Phe3184insTer)
NM_006267.5(RANBP2):c.9656C>G (p.Thr3219Arg) rs2467772229
NM_006267.5(RANBP2):c.970T>G (p.Phe324Val)

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