ClinVar Miner

List of variants in gene PRX reported as uncertain significance for not specified

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Total variants: 13
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HGVS dbSNP
NM_020956.2(PRX):c.134G>A (p.Arg45Gln) rs751441856
NM_181882.2(PRX):c.1651G>A (p.Val551Met) rs61733448
NM_181882.2(PRX):c.2296G>A (p.Val766Met) rs763619423
NM_181882.2(PRX):c.2449C>T (p.Arg817Cys) rs147441856
NM_181882.2(PRX):c.2892C>G (p.Ile964Met) rs758668778
NM_181882.2(PRX):c.3209G>A (p.Arg1070Gln) rs146222815
NM_181882.2(PRX):c.3248C>T (p.Pro1083Leu) rs3745202
NM_181882.2(PRX):c.3373G>A (p.Gly1125Ser) rs148939995
NM_181882.2(PRX):c.3496C>T (p.Pro1166Ser) rs147826200
NM_181882.2(PRX):c.4059_4061GGA[5] (p.Glu1360_Glu1361del) rs139624657
NM_181882.2(PRX):c.4219T>G (p.Ser1407Ala) rs146468976
NM_181882.2(PRX):c.823C>A (p.Leu275Ile) rs200033507
NM_181882.2(PRX):c.892C>T (p.Pro298Ser) rs185112635

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