ClinVar Miner

List of variants in gene PRX reported by Athena Diagnostics Inc

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Total variants: 30
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HGVS dbSNP
NM_181882.2(PRX):c.1216G>A (p.Ala406Thr) rs117336941
NM_181882.2(PRX):c.1281C>T (p.Ile427=) rs76960467
NM_181882.2(PRX):c.134G>A (p.Arg45Gln) rs751441856
NM_181882.2(PRX):c.1483G>C (p.Glu495Gln) rs146789340
NM_181882.2(PRX):c.2254G>A (p.Glu752Lys) rs147587689
NM_181882.2(PRX):c.2296G>A (p.Val766Met) rs763619423
NM_181882.2(PRX):c.2548C>G (p.Pro850Ala) rs141686828
NM_181882.2(PRX):c.2645T>C (p.Val882Ala) rs268671
NM_181882.2(PRX):c.2655T>C (p.Pro885=) rs268672
NM_181882.2(PRX):c.2763A>G (p.Ile921Met) rs268673
NM_181882.2(PRX):c.2787del (p.Lys930Serfs) rs754521978
NM_181882.2(PRX):c.2857C>T (p.Arg953Ter) rs104894714
NM_181882.2(PRX):c.2892C>G (p.Ile964Met) rs758668778
NM_181882.2(PRX):c.306C>T (p.Thr102=) rs744389
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.3218A>G (p.Glu1073Gly) rs61733451
NM_181882.2(PRX):c.3248C>G (p.Pro1083Arg) rs3745202
NM_181882.2(PRX):c.3248C>T (p.Pro1083Leu) rs3745202
NM_181882.2(PRX):c.3286_3356del71 (p.Ile1096Trpfs) rs1555800610
NM_181882.2(PRX):c.3394G>A (p.Gly1132Arg) rs268674
NM_181882.2(PRX):c.3496C>T (p.Pro1166Ser) rs147826200
NM_181882.2(PRX):c.3611del (p.Leu1204Argfs) rs776887800
NM_181882.2(PRX):c.3722G>A (p.Gly1241Asp)
NM_181882.2(PRX):c.3846G>A (p.Ser1282=) rs143289108
NM_181882.2(PRX):c.3947C>T (p.Ala1316Val) rs142762689
NM_181882.2(PRX):c.4074_4079delGGAGGA (p.Glu1360_Glu1361del) rs139624657
NM_181882.2(PRX):c.4077_4079delGGA (p.Glu1361del) rs139624657
NM_181882.2(PRX):c.499C>T (p.Arg167Cys) rs10425452
NM_181882.2(PRX):c.823C>A (p.Leu275Ile) rs200033507

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