ClinVar Miner

List of variants in gene PRX reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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Total variants: 27
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HGVS dbSNP gnomAD frequency
NM_181882.3(PRX):c.3373G>A (p.Gly1125Ser) rs148939995 0.00191
NM_181882.3(PRX):c.2254G>A (p.Glu752Lys) rs147587689 0.00185
NM_181882.3(PRX):c.3947C>T (p.Ala1316Val) rs142762689 0.00138
NM_181882.3(PRX):c.1574T>C (p.Val525Ala) rs149715830 0.00136
NM_181882.3(PRX):c.823C>A (p.Leu275Ile) rs200033507 0.00108
NM_181882.3(PRX):c.3186G>T (p.Lys1062Asn) rs139188673 0.00105
NM_181882.3(PRX):c.3496C>T (p.Pro1166Ser) rs147826200 0.00093
NM_181882.3(PRX):c.2548C>G (p.Pro850Ala) rs141686828 0.00078
NM_181882.3(PRX):c.3769G>A (p.Gly1257Arg) rs200332462 0.00058
NM_181882.3(PRX):c.3209G>A (p.Arg1070Gln) rs146222815 0.00019
NM_181882.3(PRX):c.3656C>T (p.Pro1219Leu) rs201393544 0.00017
NM_181882.3(PRX):c.16C>G (p.Arg6Gly) rs759056060 0.00010
NM_181882.3(PRX):c.2909G>A (p.Arg970Gln) rs764162630 0.00010
NM_181882.3(PRX):c.4129C>T (p.Arg1377Cys) rs768524850 0.00009
NM_181882.3(PRX):c.1479G>C (p.Glu493Asp) rs367946424 0.00006
NM_181882.3(PRX):c.3886G>C (p.Gly1296Arg) rs769014032 0.00006
NM_181882.3(PRX):c.727G>A (p.Gly243Arg) rs774726424 0.00006
NM_181882.3(PRX):c.1837G>A (p.Val613Met) rs773222045 0.00005
NM_181882.3(PRX):c.2816C>T (p.Ser939Leu) rs761769929 0.00003
NM_181882.3(PRX):c.1170A>T (p.Arg390Ser) rs1288181008 0.00001
NM_181882.3(PRX):c.13A>G (p.Ser5Gly) rs767350599 0.00001
NM_181882.3(PRX):c.1490C>T (p.Pro497Leu) rs1167411868 0.00001
NM_181882.3(PRX):c.1900_1914del (p.629MKLPE[1]) rs575492732
NM_181882.3(PRX):c.3705G>C (p.Glu1235Asp)
NM_181882.3(PRX):c.4207G>A (p.Val1403Ile) rs139051512
NM_181882.3(PRX):c.4366G>T (p.Ala1456Ser) rs149093940
NM_181882.3(PRX):c.682C>G (p.Arg228Gly) rs751238438

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