ClinVar Miner

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

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Total variants: 62
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HGVS dbSNP gnomAD frequency
NM_181882.3(PRX):c.731C>T (p.Ala244Val) rs118071705 0.01410
NM_181882.3(PRX):c.-243+159C>A rs268665 0.01116
NM_181882.3(PRX):c.1483G>C (p.Glu495Gln) rs146789340 0.01068
NM_181882.3(PRX):c.185-167C>T rs117182727 0.00882
NM_181882.3(PRX):c.382-96C>T rs77238923 0.00553
NM_181882.3(PRX):c.1216G>A (p.Ala406Thr) rs117336941 0.00456
NM_181882.3(PRX):c.554G>A (p.Arg185His) rs76756143 0.00292
NM_181882.3(PRX):c.3846G>A (p.Ser1282=) rs143289108 0.00288
NM_181882.3(PRX):c.892C>T (p.Pro298Ser) rs185112635 0.00262
NM_181882.3(PRX):c.445G>A (p.Ala149Thr) rs142436391 0.00193
NM_181882.3(PRX):c.3373G>A (p.Gly1125Ser) rs148939995 0.00191
NM_181882.3(PRX):c.2254G>A (p.Glu752Lys) rs147587689 0.00185
NM_181882.3(PRX):c.719G>A (p.Arg240Gln) rs77917609 0.00140
NM_181882.3(PRX):c.3947C>T (p.Ala1316Val) rs142762689 0.00138
NM_181882.3(PRX):c.1574T>C (p.Val525Ala) rs149715830 0.00136
NM_181882.3(PRX):c.823C>A (p.Leu275Ile) rs200033507 0.00108
NM_181882.3(PRX):c.3110A>G (p.Glu1037Gly) rs148600818 0.00099
NM_181882.3(PRX):c.3496C>T (p.Pro1166Ser) rs147826200 0.00093
NM_181882.3(PRX):c.2548C>G (p.Pro850Ala) rs141686828 0.00078
NM_181882.3(PRX):c.2494G>C (p.Val832Leu) rs116139153 0.00077
NM_181882.3(PRX):c.1651G>A (p.Val551Met) rs61733448 0.00047
NM_181882.3(PRX):c.966G>T (p.Val322=) rs139544245 0.00042
NM_181882.3(PRX):c.2101G>A (p.Val701Met) rs116855701 0.00041
NM_181882.3(PRX):c.540G>A (p.Pro180=) rs371243093 0.00036
NM_181882.3(PRX):c.3708G>A (p.Ala1236=) rs202119177 0.00035
NM_181882.3(PRX):c.285C>T (p.Cys95=) rs531527827 0.00032
NM_181882.3(PRX):c.993G>A (p.Pro331=) rs146323928 0.00022
NM_181882.3(PRX):c.1624C>T (p.Arg542Trp) rs201337455 0.00018
NM_181882.3(PRX):c.3549C>T (p.Tyr1183=) rs367876251 0.00017
NM_181882.3(PRX):c.2265G>A (p.Leu755=) rs370753668 0.00009
NM_181882.3(PRX):c.1369G>A (p.Glu457Lys) rs142064826 0.00008
NM_181882.3(PRX):c.2164A>G (p.Met722Val) rs376309142 0.00005
NM_181882.3(PRX):c.1222C>T (p.Pro408Ser) rs150244426 0.00004
NM_181882.3(PRX):c.2715C>A (p.Thr905=) rs188765166 0.00004
NM_181882.3(PRX):c.3775G>A (p.Glu1259Lys) rs751742049 0.00004
NM_181882.3(PRX):c.1539G>A (p.Pro513=) rs187786861 0.00003
NM_181882.3(PRX):c.3939G>A (p.Leu1313=) rs140109585 0.00003
NM_181882.3(PRX):c.2496A>T (p.Val832=) rs777527307 0.00002
NM_181882.3(PRX):c.3423G>A (p.Ala1141=) rs370800046 0.00002
NM_181882.3(PRX):c.1113A>G (p.Glu371=) rs137930942 0.00001
NM_181882.3(PRX):c.1251G>T (p.Leu417=) rs751470543 0.00001
NM_181882.3(PRX):c.1749T>G (p.Pro583=) rs1234792110 0.00001
NM_181882.3(PRX):c.2804A>C (p.Lys935Thr) rs1179595016 0.00001
NM_181882.3(PRX):c.354G>A (p.Lys118=) rs1044654884 0.00001
NM_181882.3(PRX):c.4350G>A (p.Pro1450=) rs768051108 0.00001
NM_181882.3(PRX):c.825C>T (p.Leu275=) rs753268672 0.00001
NM_181882.3(PRX):c.834G>A (p.Pro278=) rs759984063 0.00001
NC_000019.10:g.40413554dup rs112426896
NM_181882.3(PRX):c.-199+7G>A rs541213273
NM_181882.3(PRX):c.-99-20C>G rs148577357
NM_181882.3(PRX):c.1689T>C (p.Ala563=) rs751183515
NM_181882.3(PRX):c.1863G>A (p.Val621=)
NM_181882.3(PRX):c.1944T>C (p.Ala648=)
NM_181882.3(PRX):c.1953T>C (p.Asp651=)
NM_181882.3(PRX):c.2820G>A (p.Gly940=) rs1599652236
NM_181882.3(PRX):c.2859A>G (p.Arg953=)
NM_181882.3(PRX):c.2913G>T (p.Val971=) rs1599652077
NM_181882.3(PRX):c.3606T>G (p.Gly1202=)
NM_181882.3(PRX):c.3831C>G (p.Pro1277=) rs577796628
NM_181882.3(PRX):c.618G>T (p.Arg206=) rs1599656533
NM_181882.3(PRX):c.876C>G (p.Val292=)
NM_181882.3(PRX):c.993G>T (p.Pro331=) rs146323928

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