ClinVar Miner

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

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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_006267.5(RANBP2):c.1209C>T (p.Ser403=) rs140275032 0.00951
NM_006267.5(RANBP2):c.1632-16T>C rs147266881 0.00948
NM_006267.5(RANBP2):c.2173A>G (p.Ser725Gly) rs17414315 0.00940
NM_006267.5(RANBP2):c.5941T>A (p.Ser1981Thr) rs61748150 0.00849
NM_006267.5(RANBP2):c.3411A>C (p.Pro1137=) rs76461420 0.00790
NM_006267.5(RANBP2):c.3162G>T (p.Gln1054His) rs141230513 0.00290
NM_006267.5(RANBP2):c.3163C>T (p.Pro1055Ser) rs140860785 0.00290
NM_006267.5(RANBP2):c.8407A>G (p.Ile2803Val) rs61758804 0.00272
NM_006267.5(RANBP2):c.4760G>T (p.Gly1587Val) rs148677577 0.00204
NM_006267.5(RANBP2):c.783-6T>C rs138540027 0.00108
NM_006267.5(RANBP2):c.9369+4G>A rs139387463 0.00108
NM_006267.5(RANBP2):c.2243C>T (p.Ser748Leu) rs200940828 0.00072
NM_006267.5(RANBP2):c.2212C>T (p.Pro738Ser) rs201793011 0.00045
NM_006267.5(RANBP2):c.2405G>A (p.Arg802Gln) rs187011794 0.00036
NM_006267.5(RANBP2):c.7340C>T (p.Ser2447Phe) rs200750445 0.00022
NM_006267.5(RANBP2):c.2383-3dup rs542446071
NM_006267.5(RANBP2):c.3162_3163delinsTT (p.Gln1054_Pro1055delinsHisSer) rs1553494411
NM_006267.5(RANBP2):c.6613G>C (p.Gly2205Arg) rs755789696
NM_006267.5(RANBP2):c.7849+936G>T

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