ClinVar Miner

List of variants in gene PRX studied for not provided

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Total variants: 72
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HGVS dbSNP
NM_020956.2(PRX):c.*1028C>A rs200033507
NM_020956.2(PRX):c.*1688G>C rs146789340
NM_020956.2(PRX):c.*1688_*1765del rs1555801137
NM_020956.2(PRX):c.*2116_*2130del rs759376968
NM_020956.2(PRX):c.*2487_*2489del rs1131691425
NM_020956.2(PRX):c.*3578G>A rs148939995
NM_020956.2(PRX):c.*3701C>T rs147826200
NM_020956.2(PRX):c.*4512G>A rs368827070
NM_020956.2(PRX):c.-199+7G>A
NM_020956.2(PRX):c.-242-208G>A
NM_020956.2(PRX):c.-99-20C>G
NM_020956.2(PRX):c.121G>A (p.Gly41Arg) rs879254307
NM_020956.2(PRX):c.123_124dup (p.Ile42fs) rs1555802173
NM_020956.2(PRX):c.16C>G (p.Arg6Gly) rs759056060
NM_020956.2(PRX):c.185-167C>T
NM_020956.2(PRX):c.27+274G>A
NM_020956.2(PRX):c.28-52G>A
NM_020956.2(PRX):c.354G>A (p.Lys118=) rs1044654884
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.1102C>T (p.Arg368Ter) rs104894715
NM_181882.2(PRX):c.1174C>T (p.Arg392Ter) rs773009397
NM_181882.2(PRX):c.1216G>A (p.Ala406Thr) rs117336941
NM_181882.2(PRX):c.1222C>T (p.Pro408Ser) rs150244426
NM_181882.2(PRX):c.1281C>T (p.Ile427=) rs76960467
NM_181882.2(PRX):c.1441G>T (p.Val481Leu) rs747179548
NM_181882.2(PRX):c.1546C>T (p.Arg516Trp) rs144305922
NM_181882.2(PRX):c.1574T>C (p.Val525Ala) rs149715830
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.1951G>A (p.Asp651Asn) rs3814290
NM_181882.2(PRX):c.2097G>A (p.Met699Ile) rs886042156
NM_181882.2(PRX):c.2145T>A (p.Cys715Ter) rs104894707
NM_181882.2(PRX):c.2215G>A (p.Asp739Asn) rs779294844
NM_181882.2(PRX):c.2254G>A (p.Glu752Lys) rs147587689
NM_181882.2(PRX):c.2278G>A (p.Val760Met) rs548905150
NM_181882.2(PRX):c.2496A>T (p.Val832=)
NM_181882.2(PRX):c.2548C>G (p.Pro850Ala) rs141686828
NM_181882.2(PRX):c.2620G>A (p.Ala874Thr) rs145790961
NM_181882.2(PRX):c.2681T>A (p.Val894Glu) rs778360076
NM_181882.2(PRX):c.2787del (p.Lys930fs) rs754521978
NM_181882.2(PRX):c.2853dup (p.Gly952fs) rs1568704829
NM_181882.2(PRX):c.2857C>T (p.Arg953Ter) rs104894714
NM_181882.2(PRX):c.3110A>G (p.Glu1037Gly)
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.3218A>G (p.Glu1073Gly) rs61733451
NM_181882.2(PRX):c.3286_3356del (p.Ile1096fs) rs1555800610
NM_181882.2(PRX):c.3343del (p.Ala1115fs) rs1064797244
NM_181882.2(PRX):c.3346G>T (p.Val1116Leu)
NM_181882.2(PRX):c.3580C>G (p.Leu1194Val) rs149732789
NM_181882.2(PRX):c.3611del (p.Leu1204fs) rs776887800
NM_181882.2(PRX):c.3656C>T (p.Pro1219Leu) rs201393544
NM_181882.2(PRX):c.3722G>A (p.Gly1241Asp)
NM_181882.2(PRX):c.3769G>A (p.Gly1257Arg) rs200332462
NM_181882.2(PRX):c.3772G>T (p.Gly1258Cys) rs781392383
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.445G>A (p.Ala149Thr) rs142436391
NM_181882.2(PRX):c.485A>G (p.Lys162Arg) rs879254072
NM_181882.2(PRX):c.499C>T (p.Arg167Cys) rs10425452
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.731C>T (p.Ala244Val) rs118071705
NM_181882.2(PRX):c.839C>T (p.Pro280Leu) rs557355077

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