ClinVar Miner

List of variants in gene PRX reported as likely benign for not provided

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Gene type:
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Total variants: 59
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HGVS dbSNP
NM_020956.2(PRX):c.*2185G>A rs777413169
NM_020956.2(PRX):c.*2459G>A rs147587689
NM_020956.2(PRX):c.*2473G>A rs570227186
NM_020956.2(PRX):c.*2701A>T rs777527307
NM_020956.2(PRX):c.*2824C>T rs761066015
NM_020956.2(PRX):c.*2846C>A rs375201649
NM_020956.2(PRX):c.*3148G>A rs142228732
NM_020956.2(PRX):c.*3391G>T rs139188673
NM_020956.2(PRX):c.*3701C>T rs147826200
NM_020956.2(PRX):c.*802C>T rs144157275
NM_020956.2(PRX):c.*888G>A rs562108874
NM_020956.2(PRX):c.*936C>T rs118071705
NM_020956.2(PRX):c.-199+7G>A rs541213273
NM_020956.2(PRX):c.-99-20C>G rs148577357
NM_020956.2(PRX):c.185-167C>T rs117182727
NM_020956.2(PRX):c.237C>T (p.Asp79=) rs376174896
NM_020956.2(PRX):c.354G>A (p.Lys118=) rs1044654884
NM_020956.2(PRX):c.75G>A (p.Ala25=) rs766160977
NM_181882.3(PRX):c.1011G>C (p.Leu337=) rs1156439031
NM_181882.3(PRX):c.108C>G (p.Gly36=) rs771407657
NM_181882.3(PRX):c.1113A>G (p.Glu371=) rs137930942
NM_181882.3(PRX):c.1269C>G (p.Pro423=) rs201031197
NM_181882.3(PRX):c.135G>C (p.Arg45=) rs779875514
NM_181882.3(PRX):c.1515A>G (p.Pro505=) rs1234698192
NM_181882.3(PRX):c.1689T>C (p.Ala563=) rs751183515
NM_181882.3(PRX):c.185-4G>A rs1322328826
NM_181882.3(PRX):c.2340G>A (p.Pro780=) rs147618050
NM_181882.3(PRX):c.2421C>T (p.Pro807=) rs752259641
NM_181882.3(PRX):c.2784T>C (p.Ser928=) rs766519481
NM_181882.3(PRX):c.2820G>A (p.Gly940=) rs1599652236
NM_181882.3(PRX):c.286C>T (p.Leu96=) rs149325913
NM_181882.3(PRX):c.2913G>A (p.Val971=) rs1599652077
NM_181882.3(PRX):c.3261T>C (p.Ala1087=) rs1412558420
NM_181882.3(PRX):c.3270C>T (p.Thr1090=) rs764866078
NM_181882.3(PRX):c.3306C>T (p.Val1102=) rs774667067
NM_181882.3(PRX):c.3309G>T (p.Thr1103=) rs557336965
NM_181882.3(PRX):c.3315C>T (p.Gly1105=) rs762102597
NM_181882.3(PRX):c.333C>G (p.Thr111=) rs764439512
NM_181882.3(PRX):c.3441G>A (p.Pro1147=) rs777344023
NM_181882.3(PRX):c.3459A>G (p.Pro1153=) rs1599650963
NM_181882.3(PRX):c.3486G>A (p.Glu1162=) rs764466921
NM_181882.3(PRX):c.3726G>T (p.Gly1242=) rs775170011
NM_181882.3(PRX):c.3831C>T (p.Pro1277=) rs577796628
NM_181882.3(PRX):c.3843C>A (p.Leu1281=) rs369372933
NM_181882.3(PRX):c.3885G>A (p.Glu1295=) rs776947855
NM_181882.3(PRX):c.3900C>G (p.Ala1300=) rs757223803
NM_181882.3(PRX):c.3963G>A (p.Glu1321=) rs781159482
NM_181882.3(PRX):c.4200G>A (p.Lys1400=) rs760540823
NM_181882.3(PRX):c.4377G>A (p.Ala1459=) rs377062046
NM_181882.3(PRX):c.444C>G (p.Pro148=) rs765210929
NM_181882.3(PRX):c.468C>T (p.Val156=) rs543875999
NM_181882.3(PRX):c.618G>T (p.Arg206=) rs1599656533
NM_181882.3(PRX):c.627C>T (p.Ala209=) rs761085934
NM_181882.3(PRX):c.639C>G (p.Pro213=) rs1479088366
NM_181882.3(PRX):c.732G>A (p.Ala244=) rs769735682
NM_181882.3(PRX):c.762C>A (p.Pro254=) rs546448969
NM_181882.3(PRX):c.81C>T (p.Thr27=) rs988404691
NM_181882.3(PRX):c.840G>A (p.Pro280=) rs773272074
NM_181882.3(PRX):c.870C>A (p.Ile290=) rs758097995

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