ClinVar Miner

List of variants in gene PRX reported by Athena Diagnostics Inc

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Gene type:
ClinVar version:
Total variants: 40
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HGVS dbSNP
NM_020956.2(PRX):c.*1028C>A rs200033507
NM_020956.2(PRX):c.*1421G>A rs117336941
NM_020956.2(PRX):c.*1486C>T rs76960467
NM_020956.2(PRX):c.*1688G>C rs146789340
NM_020956.2(PRX):c.*2105_*2119del rs575492732
NM_020956.2(PRX):c.*2459G>A rs147587689
NM_020956.2(PRX):c.*2501G>A rs763619423
NM_020956.2(PRX):c.*2654C>T rs147441856
NM_020956.2(PRX):c.*2674G>A rs61733450
NM_020956.2(PRX):c.*2753C>G rs141686828
NM_020956.2(PRX):c.*2850T>C rs268671
NM_020956.2(PRX):c.*2860T>C rs268672
NM_020956.2(PRX):c.*2968A>G rs268673
NM_020956.2(PRX):c.*3097C>G rs758668778
NM_020956.2(PRX):c.*3391G>T rs139188673
NM_020956.2(PRX):c.*3414G>A rs146222815
NM_020956.2(PRX):c.*3423A>G rs61733451
NM_020956.2(PRX):c.*3453C>G rs3745202
NM_020956.2(PRX):c.*3453C>T rs3745202
NM_020956.2(PRX):c.*3491_*3561del rs1555800610
NM_020956.2(PRX):c.*3599G>A rs268674
NM_020956.2(PRX):c.*3701C>T rs147826200
NM_020956.2(PRX):c.*3785C>G rs149732789
NM_020956.2(PRX):c.*3816del rs776887800
NM_020956.2(PRX):c.*3927G>A rs139120811
NM_020956.2(PRX):c.*4051G>A rs143289108
NM_020956.2(PRX):c.*4152C>T rs142762689
NM_020956.2(PRX):c.*4264_*4266GGA[5] rs139624657
NM_020956.2(PRX):c.*4322C>T rs766729202
NM_020956.2(PRX):c.*704C>T rs10425452
NM_020956.2(PRX):c.134G>A (p.Arg45Gln) rs751441856
NM_020956.2(PRX):c.306C>T (p.Thr102=) rs744389
NM_181882.3(PRX):c.104C>A (p.Ala35Glu) rs138047753
NM_181882.3(PRX):c.1752G>C (p.Glu584Asp) rs759029769
NM_181882.3(PRX):c.2787del (p.Lys930fs) rs754521978
NM_181882.3(PRX):c.2857C>T (p.Arg953Ter) rs104894714
NM_181882.3(PRX):c.3873C>G (p.Tyr1291Ter) rs765769524
NM_181882.3(PRX):c.625G>A (p.Ala209Thr) rs769143653
NM_181882.3(PRX):c.631G>A (p.Ala211Thr) rs112973322
NM_181882.3(PRX):c.899T>C (p.Leu300Ser) rs748380935

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