ClinVar Miner

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

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Total variants: 36
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HGVS dbSNP
NM_020956.2(PRX):c.121G>A (p.Gly41Arg) rs879254307
NM_020956.2(PRX):c.16C>G (p.Arg6Gly) rs759056060
NM_020956.2(PRX):c.361C>T (p.Arg121Trp) rs750435566
NM_020956.2(PRX):c.85G>A (p.Val29Ile) rs879254074
NM_181882.2(PRX):c.1483_1560del (p.469_494ELPKVSEMKLPKVPEMAVPEVRLPEV[1]) rs1555801137
NM_181882.2(PRX):c.1546C>T (p.Arg516Trp) rs144305922
NM_181882.2(PRX):c.1651G>A (p.Val551Met) rs61733448
NM_181882.2(PRX):c.1658A>G (p.Glu553Gly) rs879254301
NM_181882.2(PRX):c.1825C>T (p.Pro609Ser) rs759927281
NM_181882.2(PRX):c.1900A>G (p.Met634Val) rs201204029
NM_181882.2(PRX):c.1911_1925del (p.Glu638_Pro642del) rs759376968
NM_181882.2(PRX):c.2215G>A (p.Asp739Asn) rs779294844
NM_181882.2(PRX):c.2278G>A (p.Val760Met) rs548905150
NM_181882.2(PRX):c.2282_2284del (p.Pro761_Lys762delinsGln) rs1131691425
NM_181882.2(PRX):c.2449C>T (p.Arg817Cys) rs147441856
NM_181882.2(PRX):c.2681T>A (p.Val894Glu) rs778360076
NM_181882.2(PRX):c.3145G>A (p.Gly1049Ser) rs186086914
NM_181882.2(PRX):c.3186G>T (p.Lys1062Asn) rs139188673
NM_181882.2(PRX):c.3209G>A (p.Arg1070Gln) rs146222815
NM_181882.2(PRX):c.3580C>G (p.Leu1194Val) rs149732789
NM_181882.2(PRX):c.3656C>T (p.Pro1219Leu) rs201393544
NM_181882.2(PRX):c.3769G>A (p.Gly1257Arg) rs200332462
NM_181882.2(PRX):c.3845C>T (p.Ser1282Leu) rs753530396
NM_181882.2(PRX):c.3947C>T (p.Ala1316Val) rs142762689
NM_181882.2(PRX):c.4112G>A (p.Arg1371Gln) rs377009047
NM_181882.2(PRX):c.4129C>T (p.Arg1377Cys) rs768524850
NM_181882.2(PRX):c.4157C>A (p.Pro1386His) rs372582520
NM_181882.2(PRX):c.4219T>G (p.Ser1407Ala) rs146468976
NM_181882.2(PRX):c.445G>A (p.Ala149Thr) rs142436391
NM_181882.2(PRX):c.485A>G (p.Lys162Arg) rs879254072
NM_181882.2(PRX):c.682C>T (p.Arg228Cys) rs751238438
NM_181882.2(PRX):c.707T>C (p.Leu236Pro) rs876661240
NM_181882.2(PRX):c.716C>T (p.Pro239Leu) rs528907584
NM_181882.2(PRX):c.727G>A (p.Gly243Arg) rs774726424
NM_181882.2(PRX):c.823C>A (p.Leu275Ile) rs200033507
NM_181882.2(PRX):c.892C>T (p.Pro298Ser) rs185112635

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